Flutizal - Pills Blog, Flutizal

Description

Advair Diskus (30 doses) is used for long-term treatment of asthma and chronic obstructive pulmonary disease (COPD) in certain patients.

Active Ingredient: fluticasone salmeterol

Advair Diskus (Flutizal) as known as: Adoair, Advair, Albeoler, Alergonase, Alerxem, Allegro, Allermist, Anasma, Apo-fluticasone, Arotide, Asmatil, Asmo-lavi, Atmadisc, Atmadisc diskus, Avamys, Axotide, Axotide nebules, Bexitrol, Bioflutikazon, Brexonase, Brexovent, Brisair, Brisair accuhaler, Brisomax, Brisovent, Cutisone, Cutivat, Dalman aq, Dermocort, Eustidil, Flaso, Flihaler, Flixocort, Flixoderm, Flixotaide, Flomist, Flonaspray, Florads, Flosal, Fluamar, Flucomix, Flucortis, Flusona, Flusona nasal, Flusonal, Fluspiral, Flutaide, Flutarzole, Fluti-k, Flutica-teva, Fluticapen, Fluticaps, Fluticason, Fluticasonpropionaat, Fluticort, Flutide, Flutide diskus, Flutiderm, Flutikason, Flutinasal, Flutinase, Flutirin, Flutizal, Fluxone, Forair, Foxair, Inalacor, Inaladuo, Inhaloflucort, Lidil, Lutisone, Maizar, Medicort, Milicarett, Nasaclear, Nasofan, Nebulex, Novex, Perinase, Phavi, Plusvent, Plusvent accuhaler, Potencort, Proair, Proticasone, Raffonin, Ratio-fluticasone, Rinisona, Rinosal, Rinosone, Rontilona, Saltikan, Seretaide, Seretide, Skyron, Ticas, Ticason, Ticavent, Trialona, Ubizol, Veramyst, Veraspir, Viani, Zoberto diskus

Cheap Flutizal 125 mcg no prescription

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Flutizal diseases

Product description

Safety information

Side effects

Advair Diskus is used for long-term treatment of asthma and chronic obstructive pulmonary disease (COPD) in certain patients. It may also be used to treat other breathing conditions as determined by your doctor. Advair Diskus is a long-acting corticosteroid and bronchodilator combination. It works by reducing inflammation and widening the airways in the lungs, which helps you breath more easily.

Use Advair Diskus as directed by your doctor.

Do not use a spacer with Advair Diskus.

Always ready and use this device in a level, flat position.

Hold the device in one hand and put the thumb of your other hand on the thumb grip. Push your thumb away from you as far as it will go until the mouthpiece appears and snaps into position.

Hold the device in a level, flat position with the mouthpiece toward you. Slide the lever away from you as far as it will go until it clicks.

Do NOT close or tilt the device, play with the lever, or move the lever more than 1 time. This may release or waste extra doses.

Hold the device away from your mouth and breathe out fully. Do NOT breathe into the inhaler. Put the mouthpiece to your lips. Breathe in quickly and deeply through the device.

Remove the device from your mouth. Hold your breath for about 10 seconds, or as long as is comfortable. Then breathe out slowly.

Close the device. Put your thumb on the thumb grip and slide it back toward you as far as it will go. The device will click shut and the lever will return to its original position.

Your dose of medicine is a very fine powder. Most, but not all, patients can taste or feel the dose. Do NOT use another dose if you do not taste or feel the medicine. If you are not sure if you are receiving your dose, contact your doctor or pharmacist.

Rinse your mouth with water after using Advair Diskus. DO NOT swallow the rinse solution. Spit the rinse water out.

If you are using other inhaled medicines, wait a few minutes between using Advair Diskus and other inhalers, unless directed otherwise by your doctor.

Take your doses of Advair Diskus about 12 hours apart, unless your doctor tells you otherwise.

Never wash the mouthpiece or any other part of the inhaler. Keep it dry. Store Advair Diskus in a dry place.

Throw Advair Diskus away 1 month after you remove it from the foil pouch, or after the dose indicator reads "0," whichever comes first.

You may breathe more easily after the first dose of Advair Diskus. However, it may take 1 week or longer to achieve the most benefit.

Use Advair Diskus on a regular schedule to get the most benefit from it. Using Advair Diskus at the same time each day will help you remember to use it. Do not stop using Advair Diskus even if you feel better unless your doctor tells you.

If you miss a dose of Advair Diskus, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any question you may have about how to use Advair Diskus.

Store Advair Diskus between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Advair Diskus out of the reach of children and away from pets.

Active Ingredient: Fluticasone propionate, Salmeterol xinafoate.

Do NOT use Advair Diskus if:

you are allergic to any ingredient in Advair Diskus or to milk proteins

you are having an asthma attack (eg, sudden, severe onset or worsening of asthma symptoms such as chest tightness, cough, shortness of breath, wheezing)

you are using another type of long-acting inhaled bronchodilator (eg, formoterol inhalation powder, salmeterol inhalation powder)

you are taking an azole antifungal (eg, ketoconazole), certain HIV protease inhibitors (eg, ritonavir), a macrolide antibiotic (eg, clarithromycin), nefazodone, or telithromycin.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Advair Diskus. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you are taking a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) or tricyclic antidepressant (eg, amitriptyline), or if you have taken either of these medicines within the last 14 days

if you have high blood acid levels (eg, ketoacidosis) or a history of diabetes, glaucoma, or increased pressure in the eye, heart problems (eg, fast or irregular heartbeat, heart blood vessel problems), high blood pressure, nervous system problems, liver problems, low blood potassium levels, seizures, thyroid problems, or an adrenal gland tumor

if you are having a COPD flare-up, have recently been to an emergency room for asthma, have a history of frequent hospitalizations for asthma, or have ever had a life-threatening asthma attack

if you have a fungal, bacterial, or parasitic infection; a viral infection (eg, measles, chickenpox, shingles); herpes virus infection of the eye; tuberculosis (TB); a history of a positive TB skin test; or immune system problems; or if you have had a recent vaccination

if you have weak bones (osteoporosis) or have risk factors for osteoporosis (eg, a family history of osteoporosis, tobacco use, long-term use of corticosteroids or certain seizure medicines, limited physical exercise, poor nutrition).

Some medicines may interact with Advair Diskus. Tell your health care provider if you are taking any other medicines, especially any of the following:

Diuretics (eg, hydrochlorothiazide, furosemide) or long-acting inhaled bronchodilators (eg, salmeterol inhalation powder, formoterol inhalation powder) because the risk of low blood potassium or irregular heartbeat may be increased

Beta-blockers (eg, propranolol) because they may decrease Advair Diskus's effectiveness

Azole antifungals (eg, ketoconazole), catechol-O-methyltransferase (COMT) inhibitors (eg, entacapone), delavirdine, HIV protease inhibitors (eg, ritonavir), macrolide antibiotics (eg, clarithromycin), MAOIs (eg, phenelzine), nefazodone, short-acting beta-agonist bronchodilators (eg, albuterol), telithromycin, or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Advair Diskus's side effects.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Advair Diskus may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Advair Diskus may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Advair Diskus with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

Advair Diskus will not stop an asthma attack once one has started. Be sure to carry a short-acting bronchodilator with you at all times to treat any breathing problems that may occur between doses of Advair Diskus (eg, severe or sudden onset of wheezing or shortness of breath).

If you have been regularly using a short-acting bronchodilator inhaler (eg, albuterol), talk with your doctor about how to use it with Advair Diskus. Short-acting bronchodilators are normally only used with Advair Diskus to treat breathing problems that may occur between doses.

Talk with your doctor or pharmacist about all of your asthma medicines and how to use them. Do not start, stop, or change the dose of any asthma medicine unless your doctor tells you to.

If your symptoms do not get better within 1 week or if they get worse after you start using Advair Diskus, check with your doctor.

Tell your doctor or dentist that you take Advair Diskus before you receive any medical or dental care, emergency care, or surgery.

Tell your doctor at once if you notice your short-acting bronchodilator inhaler does not work as well, if you need to use it more often (eg, more than 4 times a day for more than 2 days in a row, or 1 whole canister within 8 weeks' time), or if you have a decrease in your peak meter flow results.

The risk of serious heart problems (eg, irregular heartbeat) may be greater if you use Advair Diskus in high doses. Do NOT use more than the recommended dose or use for longer than prescribed without checking with your doctor.

Advair Diskus may sometimes cause severe breathing problems right after you use a dose. If this happens, use your short-acting bronchodilator inhaler. Seek medical care at once if your breathing does not improve after you use the short-acting bronchodilator. Tell your doctor about this reaction.

Use caution if you switch from an oral steroid (eg, prednisone) to Advair Diskus. It may take several months for your body to make enough natural steroids to handle events that cause physical stress. Such events may include injury, surgery, infection, a sudden asthma attack, or severe fluid or electrolyte loss. These may be severe and sometimes fatal. Contact your doctor right away if any of these events occur. You may need to take an oral steroid (eg, prednisone) again.

If you have not had chickenpox, shingles, or measles, avoid contact with anyone who does. Contact your doctor at once if you have contact with anyone who has these infection.

Check with your doctor before you receive any vaccine while you are using Advair Diskus.

Diabetes patients - Advair Diskus may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Lab tests, including lung function tests and eye exams, may be performed while you use Advair Diskus. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Advair Diskus with caution in the elderly.

Corticosteroids may affect growth rate in children and teenagers in some cases. They may need regular growth checks while they use Advair Diskus.

Advair Diskus should not be used in children younger than 4 years old; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Advair Diskus while you are pregnant. It is not known if Advair Diskus is found in breast milk. If you are or will be breast-feeding while you use Advair Diskus, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Diarrhea; dizziness; headache; mild muscle or bone pain; nausea; nervousness; throat irritation; tremor; vomiting.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); behavior changes; blurred vision or other vision changes; chest pain; choking; fast or irregular heartbeat; hoarseness; numbness or tingling in hands or feet; seizures; severe muscle weakness, cramps, or spasms; severe or persistent bone pain; severe or persistent dizziness or headache; signs of infection (eg, fever, chills, persistent headache/sore throat, ear pain, increased mucus production or change in mucus color); swelling or tightness in the throat; trouble sleeping; unusual tiredness or weakness; vaginal odor or discharge; weight gain; white patches or sores on the tongue or mouth; worsening of asthma symptoms (eg, increased wheezing, coughing, chest tightness, shortness of breath).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Customers who bought this product also bought:

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Advair Diskus (Flutizal) Delivery

Residents of the USA can order Advair Diskus (Flutizal) to any city, to any address, for example to Ashburn, Atlanta, Denver or Pittsburgh. You can order delivery of a Advair Diskus (Flutizal) to the Sweden, Japan, Hong Kong or any other country in the world.

Flagyl Er - Woman S Health, Korincare

METRONIDAZOLE is an antiinfective. This medicine is used to treat many kinds of infections, like respiratory, skin, gastrointestinal, and bone and joint infections. It will not work for colds, flu, or other viral infections.

What should my health care professional know before I take this medicine?

They need to know if you have any of these conditions: anemia or other blood disorders disease of the nervous system fungal or yeast infection if you drink alcohol containing drinks liver disease seizures an unusual or allergic reaction to metronidazole, or other medicines, foods, dyes, or preservatives pregnant or trying to get pregnant breast-feeding

How should I take this medicine?

Take this medicine by mouth with a full glass of water. Take your medicine at regular intervals. Do not take your medicine more often than directed. Take all of your medicine as directed even if you think you are better. Do not skip doses or stop your medicine early.

Talk to your pediatrician regarding the use of this medicine in children. Special care may be needed.

If you think you have taken too much of this medicine contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

Do not take this medicine with any of the following: alcohol or any product that contains alcohol amprenavir oral solution disulfiram paclitaxel injection ritonavir oral solution sertraline oral solution sulfamethoxazole-trimethoprim injection

This medicine may also interact with the following: cimetidine lithium phenobarbital phenytoin warfarin

This list may not describe all possible interactions. Give your health care providers a list of all the medicines, herbs, non-prescription drugs, or dietary supplements you use. Also tell them if you smoke, drink alcohol, or use illegal drugs. Some items may interact with your medicine.

What should I watch for while taking this medicine?

Tell your doctor or health care professional if your symptoms do not improve or if they get worse.

You may get drowsy or dizzy. Do not drive, use machinery, or do anything that needs mental alertness until you know how this medicine affects you. Do not stand or sit up quickly, especially if you are an older patient. This reduces the risk of dizzy or fainting spells.

Avoid alcoholic drinks while you are taking this medicine and for three days afterward. Alcohol may make you feel dizzy, sick, or flushed.

If you are being treated for a sexually transmitted disease, avoid sexual contact until you have finished your treatment. Your sexual partner may also need treatment.

What side effects may I notice from this medicine?

Side effects that you should report to your doctor or health care professional as soon as possible: allergic reactions like skin rash or hives, swelling of the face, lips, or tongue confusion, clumsiness dark or white patches in the mouth fever, infection numbness, tingling, pain or weakness in the hands or feet pain when passing urine seizures if you are unusually weak or tired vaginal irritation or discharge

Side effects that usually do not require medical attention (report to your doctor or health care professional if they continue or are bothersome): diarrhea headache metallic taste nausea stomach pain or cramps

This list may not describe all possible side effects.

Where can I keep my medicine?

Keep out of the reach of children.

Store at room temperature below 25 degrees C (77 degrees F). Protect from light. Keep the container tightly closed. Throw away any unused medicine after the expiration date.

Diflucan Uses, Dosage - Side Effects, Flucan

Diflucan

Diflucan (fluconazole) is an antifungal medicine.

Diflucan is used to treat infections caused by fungus, which can invade any part of the body including the mouth, throat, esophagus, lungs, bladder, genital area, and the blood.

Diflucan is also used to prevent fungal infection in people who have a weak immune system caused by cancer treatment, bone marrow transplant. or diseases such as AIDS .

Important information

Certain other drugs can cause unwanted or dangerous effects when used with Diflucan, especially cisapride, erythromycin, pimozide, and quinidine. Tell each of your healthcare providers about all medicines you use now, and any medicine you start or stop using.

Before taking Diflucan, tell your doctor if you have liver disease, kidney disease, a heart rhythm disorder, or a history of Long QT syndrome.

Take Diflucan for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antifungal medication. Diflucan will not treat a viral infection such as the common cold or flu.

Before taking this medicine

You should not use Diflucan if you are allergic to fluconazole, or if you also take cisapride, erythromycin, pimozide, or quinidine.

To make sure Diflucan is safe for you, tell your doctor if you have:

heart disease or heart rhythm disorder;

a personal or family history of Long QT syndrome;

kidney disease; or

if you are allergic to other antifungal medicine (such as ketoconazole, itraconazole, miconazole, posaconazole, voriconazole, and others).

Diflucan oral suspension (liquid) contains sucrose. Talk to your doctor before using this form of fluconazole if you have a problem digesting sugars or milk.

A single dose of Diflucan taken to treat a vaginal yeast infection is not expected to harm an unborn baby.

Do not take more than 1 dose of Diflucan if you are pregnant. Long-term use of high doses fluconazole can harm an unborn baby or cause birth defects. Tell your doctor if you become pregnant during treatment.

Diflucan can make birth control pills less effective. Ask your doctor about using non hormonal birth control (condom, diaphragm with spermicide) to prevent pregnancy while taking Diflucan for more than 1 dose.

Fluconazole can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I take Diflucan?

Take Diflucan exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Your dose will depend on the infection you are treating. Vaginal infections are often treated with only one pill. For other infections, your first dose may be a double dose. Carefully follow your doctor's instructions.

You may take Diflucan with or without food.

Shake the oral suspension (liquid) well just before you measure a dose. Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one.

Use this medicine for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Diflucan will not treat a viral infection such as the flu or a common cold.

Call your doctor if your symptoms do not improve, or if they get worse while using Diflucan.

Store the tablets at room temperature away from moisture and heat.

You may store liquid Diflucan in a refrigerator, but do not allow it to freeze. Throw away any leftover liquid medicine that is more than 2 weeks old.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. Overdose symptoms may include confusion or unusual thoughts or behavior.

What should I avoid while taking Diflucan?

Follow your doctor's instructions about any restrictions on food, beverages, or activity.

This medicine may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Diflucan side effects

Get emergency medical help if you have any signs of an allergic reaction to Diflucan . hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have:

headache with chest pain and severe dizziness, fainting, fast or pounding heartbeats;

fever, chills, body aches, flu symptoms;

easy bruising or bleeding, unusual weakness;

liver problems--nausea, upper stomach pain, itching, tired feeling, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

skin rash or skin lesions; or

severe skin reaction--fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Common Diflucan side effects may include:

stomach pain, diarrhea, upset stomach;

changes in your sense of taste.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Diflucan?

Certain other drugs can cause unwanted or dangerous effects when used with Diflucan. Your doctor may need to change your treatment plan if you use any of the following drugs:

Dimethyl Sulfoxide Indications, Side Effects, Warnings, Dimetil

Dimethyl sulfoxide

Before using dimethyl sulfoxide:

Some medical conditions may interact with dimethyl sulfoxide. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have cancer of the bladder or urinary tract

Some MEDICINES MAY INTERACT with dimethyl sulfoxide. However, no specific interactions with dimethyl sulfoxide are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if dimethyl sulfoxide may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use dimethyl sulfoxide:

Use dimethyl sulfoxide as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Dimethyl sulfoxide is usually administered at your doctor's office, hospital, or clinic. If you are using dimethyl sulfoxide at home, carefully follow the procedures taught to you by your health care provider.

If you have severe symptoms or an especially sensitive bladder, the first few treatments may be performed while you are under anesthesia.

Dimethyl sulfoxide is placed into the bladder by catheter or special syringe. An analgesic gel may be applied prior to insertion of the catheter to help prevent spasms and discomfort.

This treatment may be repeated every 2 weeks until relief of symptoms occurs, unless prescribed differently by your doctor. After you experience relief, the treatment may be repeated less often as determined by your doctor.

It may take several weeks for the full benefit of dimethyl sulfoxide to be seen. Do not stop using dimethyl sulfoxide without talking with your doctor.

If you miss a dose of dimethyl sulfoxide, contact your doctor immediately.

Ask your health care provider any questions you may have about how to use dimethyl sulfoxide.

Important safety information:

A garlic-like taste may appear a few minutes after use. This taste may last several hours. Garlic odor on the skin or breath may last up to 72 hours.

The discomfort associated with treatment usually lessens with additional treatments.

Dimethyl sulfoxide may be harmful if swallowed. If you may have taken dimethyl sulfoxide by mouth, contact your local poison control center or emergency room immediately.

LAB TESTS, including eye exams, liver function tests, kidney function tests, and complete blood counts, may be performed to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use dimethyl sulfoxide with extreme caution in CHILDREN. Safety and effectiveness have not been confirmed.

PREGNANCY and BREAST-FEEDING: If you become pregnant while taking dimethyl sulfoxide, discuss with your doctor the benefits and risks of using dimethyl sulfoxide during pregnancy. It is unknown if dimethyl sulfoxide is excreted in breast milk. If you are or will be breast-feeding while you are using dimethyl sulfoxide, check with your doctor or pharmacist to discuss the risks to your baby.

Possible side effects of dimethyl sulfoxide:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Bladder discomfort; garlic odor on breath or skin for up to 72 hours; garlic taste for several hours.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); eye pain or burning; vision changes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately.

Proper storage of dimethyl sulfoxide:

Store dimethyl sulfoxide at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Protect from light. Do not store in the bathroom. Keep dimethyl sulfoxide out of the reach of children and away from pets.

General information:

If you have any questions about dimethyl sulfoxide, please talk with your doctor, pharmacist, or other health care provider.

Dimethyl sulfoxide is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take dimethyl sulfoxide or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about dimethyl sulfoxide. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to dimethyl sulfoxide. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using dimethyl sulfoxide.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about dimethyl sulfoxide

Licostan Dosis Obat, Licostan

licostan

kandungan

tiap kemasan licostan mengandung zat aktif (nama generik) sebagai berikut :

asam mefenamat (mefenamic acid) 500 mg / kaplet

Sekilas tentang zat aktif (nama generik)

asam mefenamat (mefenamic acid) adalah derivat asam antranilat (atau fenamate) yang termasuk nonsteroidal anti-inflammatory drug (NSAID). asam mefenamat (mefenamic acid) bekerja dengan cara menghambat kerja enzim siklooksigenase (COX). Enzim ini berfungsi untuk membantu pembentukan prostaglandin saat terjadinya luka dan menyebabkan rasa sakit dan peradangan. Dengan menghalangi kerja enzim COX, prostaglandin lebih sedikit diproduksi, yang berarti rasa sakit dan peradangan akan mereda.

Indikasi licostan

Kegunaan licostan (asam mefenamat) adalah untuk mengobati nyeri ringan sampai sedang pada sakit gigi dan setelah cabut gigi, sakit kepala, sakit telinga, nyeri otot, nyeri sendi, demam, nyeri setelah operasi, termasuk nyeri haid, dan kadang – kadang digunakan untuk mencegah migrain berkaitan dengan menstruasi (pengobatan dalam jangka pendek, tidak lebih dari 7 hari)

Ada bukti yang mendukung penggunaan licostan (asam mefenamat) untuk perimenstrual migraine headache prophylaxis . pengobatan dimulai 2 hari sebelum timbulnya menstruasi dilanjutkan selama terjadinya menstruasi.

Kontra indikasi

jangan menggunakan licostan (asam mefenamat) untuk pasien yang memiliki riwayat alergi terhadap licostan (asam mefenamat), aspirin atau NSAID lainnya (misalnya, ibuprofen, celecoxib)

pasien yang akan atau telah menjalani operasi by-pass jantung sebaiknya jangan menggunakan licostan (asam mefenamat)

obat ini juga dikontraindikasikan untuk pasien yang memiliki masalah ginjal, hati, pasien yang menderita asma, urtikaria, atau radang / tukak pada lambung atau usus

pasien yang sedang hamil terutama di 3 bulan terakhir, sebaiknya tidak menggunakan licostan (asam mefenamat)

Efek Samping licostan

efek samping licostan (asam mefenamat) yang relatif ringan seperti sakit kepala, gugup dan muntah

Efek samping yang serius dapat berupa diare, hematemesis (muntah darah), hematuria (darah dalam urin), penglihatan kabur, ruam kulit, gatal dan bengkak, sakit tenggorokan dan demam

Pada tahun 2008 label pada kemasan obat ini di USA telah diperbarui dengan peringatan tentang resiko licostan (asam mefenamat) pada kehamilan.

NSAID termasuk licostan (asam mefenamat) dapat menyebabkan peningkatan resiko infark miokardial dan stroke yang bisa berakibat fatal. Resiko ini dapat meningkatkan jika obat digunakan dalam jangka waktu lama

NSAID termasuk licostan (asam mefenamat) menyebabkan gangguan pada saluran gastrointestinal misalnya. perdarahan, ulserasi, dan perforasi lambung atau usus yang bisa berakibat fatal. jika pemakaian dalam dosis tinggi atau untuk waktu yang lama, merokok, atau minum alkohol, meski licostan (asam mefenamat) digunakan bersama makanan tidak akan mengurangi efek samping ini.

gangguan berat pada organ hati seperti penyakit kuning dan hepatitis, juga dilaporkan terjadi akibat pemakaian NSAID termasuk licostan (asam mefenamat). Jika tes hati yang abnormal menetap atau memburuk, jika tanda-tanda dan gejala yang konsisten dengan penyakit hati klinis terjadi, atau jika manifestasi sistemik terjadi (misalnya. eosinofilia, ruam, dan lain – lain), pemakaian licostan (asam mefenamat) harus dihentikan.

Anemia juga dilaporkan terjadi pada pasien yang menggunakan NSAID termasuk licostan (asam mefenamat). Pasien pada pengobatan jangka panjang, kadar hemoglobin dan hematokrit harus diperiksa jika mereka menunjukkan tanda-tanda gejala anemia.

Reaksi dermatologis seperti dermatitis eksfoliatif, sindrom Stevens-Johnson, dan nekrolisis epidermal toksik, yang dapat berakibat fatal, dapat terjadi selama pemakaian NSAID termasuk licostan (asam mefenamat). Pengobatan harus dihentikan jika tanda – tanda seperti ruam atau hipersensitivitas muncul.

Perhatian

licostan (asam mefenamat) sebaiknya dipakai setelah makan atau bersama makanan

Jangan menggunakan licostan (asam mefenamat) pada pasien yang memiliki fungsi hati dan ginjal yang buruk, sedang atau pernah memiliki sakit jantung

Jika pasien menderita hipertensi tekanan darah harus dipantau selama pengobatan

Karena NSAID dapat menyebabkan retensi cairan dan edema, perhatian harus diberikan pada pasien dengan gagal jantung atau yang sudah pernah mengalami retensi cairan

Pasien harus cukup terhidrasi (cukup cairan) sebelum menggunakan licostan (asam mefenamat)

licostan (asam mefenamat) dapat menyebabkan pusing atau mengantuk, yang akan lebih buruk jika pasien juga mengkonsumsi alkohol. Jangan mengemudi atau menyalakan mesin selama pemakaian obat ini

Keamanan dan kemanjuran pada anak-anak < 14 tahun belum diketahui

Penggunaan pada pasien lanjut usia harus lebih hati – hati karena mereka lebih sensitif terhadap efek obat ini, terutama perdarahan perut dan masalah ginjal

licostan (asam mefenamat) ditemukan dalam ASI. Jangan menyusui saat menggunakan obat ini

Toleransi terhadap kehamilan

Penelitian pada reproduksi hewan telah menunjukkan efek buruk pada janin dan tidak ada studi yang memadai dan terkendali dengan baik pada manusia, namun jika potensi keuntungan dapat dijamin, penggunaan obat pada ibu hamil dapat dilakukan meskipun potensi resiko sangat besar.

interaksi obat

Antikoagulan (misalnya, warfarin), aspirin, kortikosteroid (misalnya prednisone), heparin, atau selective serotonin reuptake inhibitor (SSRI) (misalnya, fluoxetine) karena obat – obat ini meningkatkan resiko perdarahan lambung

Magnesium hidroksida (misalnya, antasida) atau probenesid karena obat – obat ini meningkatkan efek samping licostan (asam mefenamat)

Siklosporin, lithium, methotrexate, kuinolon (misalnya, ciprofloxacin ), atau sulfonilurea (misalnya, glipizide) karena efek samping obat – obat ini meningkat jika diberikan bersamaan dengan licostan (asam mefenamat)

Angiotensin-converting enzyme (ACE) inhibitor (misalnya, enalapril) atau diuretik (misalnya, furosemide, hydrochlorothiazide) karena efektivitas obat – obat ini menurun jika diberikan bersama licostan (asam mefenamat)

Dosis licostan

licostan (asam mefenamat) diberikan dengan dosis :

Dosis lazim dewasa untuk Nyeri : 500 mg secara oral selanjutnya 250 mg setiap 6 jam sesuai kebutuhan, tidak melebihi 7 hari

Dosis lazim dewasa untuk Dismenore : 500 mg secara oral selanjutnya 250 mg setiap 6 jam dimulai saat timbulnya menstruasi

Dosis lazim Pediatric untuk Nyeri : 14 – 18 tahun. 500 mg secara oral diikuti oleh 250 mg setiap 6 jam sesuai kebutuhan, tidak melebihi 7 hari

Penyesuaian dosis : dosis yang lebih rendah harus dipertimbangkan pada orang tua

Terkait

Jika informasi ini berguna, bagikan ke teman – teman anda

Tolep, Tolep

Dr. Kenneth Tolep MD

Overview

Dr. Kenneth Tolep is a pulmonologist in Fort Myers, Florida and is affiliated with multiple hospitals in the area, including Gulf Coast Medical Center and Lee Memorial Hospital. He received his medical degree from State University of New York Upstate Medical University and has been in practice for more than 20 years. Dr. Tolep accepts several types of health insurance, listed below. He is one of 19 doctors at Gulf Coast Medical Center and one of 16 at Lee Memorial Hospital who specialize in Pulmonary Disease.

(239) 985-1925 Phone Number

21+ Years in Practice

Board Certifications. Critical Care Medicine, Internal Medicine, Pulmonary Disease

Are You Dr. Tolep? Claim/Edit Your Profile

Office Location & Contact

7335 Gladiolus Drive Fort Myers, FL 33908 [MAP]

(239) 985-1925

Phone Number

(239) 321-6044

Fax Number

Insurance Accepted

Aetna Choice POS II

Aetna HMO

AvMed Health Open Access

BCBS Blue Card PPO

BCBS Florida BlueCare HMO

BCBS Florida NetworkBlue

BCBS Florida Preferred Patient Care PPO

BCBS Illinois PPO

CIGNA HMO

CIGNA Open Access

CIGNA PPO

Coventry Florida - Employer Group PPO

First Health PPO

Great West PPO

Humana ChoiceCare Network PPO

Multiplan PHCS PPO

Multiplan PPO

United Healthcare - Direct Choice Plus POS

United Healthcare - Direct Options PPO

Hospital Affiliation

Dr. Tolep is affiliated with the following hospitals. Affiliation usually means doctors can admit patients to a hospital.

Fort Myers, FL

Gulf Coast Medical Center in Fort Myers, FL is not nationally ranked in any specialty. more

19 Doctors in Specialty 5/10 Survival 4/5 Patient Safety

Fort Myers, FL

Lee Memorial Hospital in Fort Myers, FL is not nationally ranked in any specialty. more

16 Doctors in Specialty 6/10 Survival 2/5 Patient Safety

Specialties & Qualifications

Specialty: Pulmonary Disease

Pulmonologists treat ailments of the lungs and respiratory system, such as asthma, pneumonia, tuberculosis, complicated chest infections and chronic obstructive pulmonary diseases including emphysema.

Subspecialties: General Pulmonary Medicine, Critical Care Medicine, Sleep Medicine

Education & Medical Training

Thomas Jefferson University Residency. Internal Medicine

Temple University Hospital Fellowship. Pulmonary Disease and Critical Care Medicine

State University of New York Upstate Medical University Medical School

Certifications & Licensure

American Board of Internal Medicine Certified in Critical Care Medicine

American Board of Internal Medicine Certified in Internal Medicine

American Board of Internal Medicine Certified in Pulmonary Disease

FL State Medical License Active through 2018

Awards, Honors & Recognitions

CMS Stage 1 EHR 2012

CMS Stage 1 EHR 2013

Checkbook Top Doc

Gulfshore Life Magazine: Top Doctors 2014

Gulfshore Life Magazine: Top Doctors 2013

Gulfshore Life Magazine: Top Doctors 2012

Gulfshore Life Magazine: Top Doctors 2011

Publications & Presentations

Lam, C. P. Tolep, K. A. Metke, M. P. Glockner, J. Cooper, L. T. "Coronary sarcoidosis presenting as acute coronary syndrome.." Clin Cardiol

Mantz, C. A. Dosoretz, D. E. Rubenstein, J. H. Blitzer, P. H. Katin, M. J. Garton, G. R. Nakfoor, B. M. Siegel, A. D. Tolep, K. A. Hannan, S. E. Dosani, R. Feroz, A. Maas, C. Bhat, S. Panjikaran, G. Lalla, S. Belani, K. Ross, R. H. "Endobronchial brachytherapy and optimization of local disease control in medically inoperable non-small cell lung carcinoma: a matched-pair analysis.." Brachytherapy

See All Publications

Pulmonary Disease Resources

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License & Identifications

A medical license is required for a doctor to practice medicine in a particular state. Requirements vary by state but most require, at a minimum, post-graduate training in the doctor’s specific specialty. An NPI number is a national identifier unique to an individual health care provider and is managed by the Center for Medicare & Medicaid Services (CMS).

Learn more about Dr. Kenneth Tolep:

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Patient Reviews

Patient comments (2)

The overall average patient rating of Dr. Kenneth Tolep is Average . Dr. Tolep has been reviewed by 6 patients who have provided 2 comments. The rating is 3 out of 5 stars.

Dr. Kenneth Tolep

Dr. Tolep has been taking care of patients with pulmonary problems in Fort Myers since January 1997. Prior to his arrival in South West Florida, he was on the faculty at Temple University School of Medicine in Philadelphia, where he completed his fellowship in Pulmonary and Critical Care Medicine. Dr. Tolep earned his medical degree from S. U.N. Y. Upstate Medical University in Syracuse, N. Y. and completed his residency in Internal Medicine at Thomas Jefferson University Hospital, in Philadelphia. He is board certified in Internal Medicine, Pulmonary Medicine, Critical Care and Sleep Disorders. He is a Fellow of the American College of Chest Physicians and of the American Academy of Sleep Medicine. He is a current member of the American Thoracic Society. He has been included on the list of Best Doctors in America (since 2005) and Castle Connolly’s list of Top Doctors (since 2011)Areas of interest and expertise include: • COPD and Asthma • Pulmonary Hypertension • Lung cancer • Sleep Apnea

Loradamed Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Loratimed

Loradamed

Uses

Loratadine does not prevent hives or prevent/treat a serious allergic reaction (e. g. anaphylaxis ). Therefore, if your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use loratadine in place of your epinephrine.

If you are self-treating with this medication, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions section.)

Do not use this medication in children younger than 6 years unless directed by the doctor. If you are using the chewable tablets, do not use in children younger than 2 years unless directed by your doctor.

How to use Loradamed

If you are using the over-the-counter product to self-treat, read all the directions on the product package before taking this medication. If your doctor has prescribed this medication, follow your doctor's directions and the instructions on your prescription label. If you have any questions, consult your doctor or pharmacist.

Take this medication by mouth with or without food, usually once a day or as directed by your doctor or the product package. If you are using the chewable tablets, chew each tablet well and swallow. Dosage is based on your age, condition, and response to treatment. Do not increase your dose or take this drug more often than directed. Do not take more of this medication than recommended for your age.

Tell your doctor if your allergy symptoms do not improve after 3 days of treatment or if your hives last more than 6 weeks. Seek immediate medical attention if your condition worsens or you think you have a serious medical problem (e. g. very serious allergic reaction /anaphylaxis).

Side Effects

This drug usually has no side effects. If you have any unusual effects, contact your doctor or pharmacist promptly.

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any symptoms of a serious allergic reaction, including: rash. itching/swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing .

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking loratadine, tell your doctor or pharmacist if you are allergic to it; or to desloratadine; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history. Do not self-treat with this medication without consulting your doctor first if you have certain medical conditions such as: kidney disease. liver disease.

Loratadine does not usually cause drowsiness when used at recommended doses. However, do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely.

If you have hives and your doctor has prescribed loratadine, or if you are considering using this drug to treat your own hives, tell your doctor right away if you have any of these other symptoms because they may be signs of a more serious condition: hives that are an unusual color, hives that look bruised or blistered, hives that do not itch.

The chewable tablets may contain aspartame. If you have phenylketonuria (PKU) or any other condition that requires you to restrict your intake of aspartame (or phenylalanine ), consult your doctor or pharmacist about using this drug safely.

Older adults may be more sensitive to the side effects of this drug, especially drowsiness, or confusion. These side effects can increase the risk of falling.

During pregnancy. this medication should be used only when clearly needed and as directed by your doctor. Discuss the risks and benefits with your doctor before taking this drug.

This medication passes into breast milk. However, it is unlikely to harm a nursing infant. Consult your doctor before breastfeeding .

Interactions

Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage of any medicines without your doctor's approval.

Loratadine is very similar to desloratadine. Do not use medications containing desloratadine while using loratadine.

This medication may interfere with certain laboratory tests (including allergy skin testing ), possibly causing false test results. Make sure laboratory personnel and all your doctors know you use this drug.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: severe drowsiness.

Notes

If your doctor has prescribed this medication for you, do not share it with others.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Different brands/strengths of this medication may have different storage requirements. Read the package labeling or ask your pharmacist for the storage requirements for the product you are using. Protect from light. Do not store in the bathroom. Keep all medicines away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

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CONDITIONS OF USE: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for you or anyone else. A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.

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Kopen Ciclobiotico (Sumycin) Zonder Recept, Ciclobiotico

Ciclobiotico (Sumycin) Kopen Online Zonder Recept

Ciclobiotico (Sumycin) Toelichting

Ciclobiotico wordt gemaakt door professionals drug-store om de problemen met schadelijke bacteriele infecties verspreiden via ziektekiemen hebben. Focus op geassocieerd met Ciclobiotico zou zijn om te beheren, te verdedigen tegen, te beeindigen evenals ziektekiemen te elimineren.

Ciclobiotico kan gaan als een goede anti-infectie behandeling. Ciclobiotico werkt door het elimineren van bacterien die zich voortplant door besmetting.

Ciclobiotico is echt een tetracycline.

Ciclobiotico samen met andere antibiotica voorkomen behandelt virusachtige bacteriele infecties (griep, koud en andere).

General titel geassocieerd met Ciclobiotico is eigenlijk Tetracycline.

Merken geassocieerd met Ciclobiotico neiging om Ciclobiotico, Panmycin, Robitet vijfhonderd, Ala-Tet, Ciclobiotico Syrup, Emtet-500, TetraCon, Brodspec, Tetracap zijn.

Ciclobiotico (Sumycin) Dosis

Ciclobiotico komt in:

250mg lagere dosis frictiemateriaal

500mg normale dosis frictiemateriaal

Ciclobiotico wordt gebruikt 2-4 keer per dag 1 uur voorafgaand aan het diner of misschien meer uren recht daarna.

Het is raadzaam om Ciclobiotico tegelijkertijd overwegen op vacant buik.

Meestal niet gebruiken Ciclobiotico in het geval u consumeren of zelfs te consumeren zuivelproducten (kaas, vetvrije yoghurt, zuivel, gletsjers room).

Het is echt onaanvaardbaar Ciclobiotico overwegen door middel van kinderen onder de acht jaren.

Meestal niet stoppen met het gebruik van Ciclobiotico ineens.

Ciclobiotico (Sumycin) ontbreekt in verband met de dosering

Meestal krijgt niet de dubbele dosering. In het geval u de dosering die u nodig hebt om het te dragen als je eenmaal in het achterhoofd te houden met betrekking tot uw ontbreekt overslaan. Wanneer het tijd is voor de dosering die u nodig hebt om te dragen op je eigen normale dosering routine.

Ciclobiotico (Sumycin) Overdose

In het geval dat u een overdosis Ciclobiotico en je ook voorkomen dat geweldig je nodig hebt om direct te controleren uw arts of zelfs arts. Geassocieerd met Ciclobiotico overdosering: kokhalzen, diarree, misselijkheid of braken.

Ciclobiotico (Sumycin) Opslagruimte

Shop in de ruimte een temperatuur tussen 10 en 30 niveaus D (59 en zesentachtig niveaus F) tegen vocht, verlichting en temperatuur. Versterken elke vorm van ongerepte medicatie na het verstrijken dag. Handhaven van het bereiken van kinderen.

Ciclobiotico (Sumycin) Negatieve effecten

Ciclobiotico biedt de negatieve effecten. De meest typische neiging om:

ontstoken taal frictiemateriaal

zure reflux frictiemateriaal

brandende frictiemateriaal

wijzigen geassocieerd met huidskleur frictiemateriaal

matige misselijkheid of braken frictiemateriaal

zure reflux frictiemateriaal

de inname kwestie frictiemateriaal

ontsteking of zelfs zweren frictiemateriaal

genitale jeuk frictiemateriaal

diarree frictiemateriaal

kokhalzen frictiemateriaal

Veel minder typische en ernstige negatieve gevolgen hele behulp Ciclobiotico:

allergische reactie reacties (urticaria, en uitademen problemen, allergie, evenals eruptie) frictiemateriaal

problemen met het gezichtsvermogen frictiemateriaal

sensatie slaperig frictiemateriaal

ernstige migraine frictiemateriaal

temperatuur frictiemateriaal

hele lichaam pijn frictiemateriaal

porien en de huid oude frictiemateriaal

onvoldoende honger frictiemateriaal

geelzucht frictiemateriaal

ongewoon enige zwakte frictiemateriaal

pee geassocieerd met darkish kleur frictiemateriaal

verbijsterd gemoedstoestand frictiemateriaal

rillingen frictiemateriaal

jeuk frictiemateriaal

ernstige uitputting frictiemateriaal

griepachtige verschijnselen en symptomen frictiemateriaal

ongemak in verband met de buik frictiemateriaal

beklemming geassocieerd met belangrijke gewrichten frictiemateriaal

het plassen problemen frictiemateriaal

onregelmatig bloedverlies frictiemateriaal

Negatieve effecten zijn er aanwijzingen afhankelijk zijn van medicijnen die u zou kunnen gebruiken, maar bovendien rekenen op uw welzijn conditie en andere aspecten.

Ciclobiotico (Sumycin) Contra-indicaties

Meestal niet Ciclobiotico te gebruiken in het geval dat u gevoelig bent om Ciclobiotico elementen.

Meestal krijgt niet Ciclobiotico wanneer u verwacht en hebben nurseling.

Ciclobiotico werkt alleen in de richting van ziektekiemen, zal zich niet bezig met virusachtige bacteriele infecties.

Het is echt onaanvaardbaar Ciclobiotico overwegen door middel van kinderen onder de acht jaren.

Meestal niet gebruiken Ciclobiotico in het geval u consumeren of zelfs te consumeren zuivelproducten (kaas, vetvrije yoghurt, zuivel, gletsjers room).

speelt de rol van voorzichtig met Ciclobiotico gebruik bij het krijgen nier - of zelfs ziekten in de lever, allergische reacties, diabetes, ademhalingsmoeilijkheden.

speelt de rol van voorzichtig met Ciclobiotico gebruik bij gebruik bloedbaan slanker bijvoorbeeld isotretinoine (bijvoorbeeld omdat Accutane); colestipol (bijvoorbeeld omdat Colestid) of zelfs cholestyramine (bijvoorbeeld omdat Questran, Prevalite); bloedbaan slanker (bijvoorbeeld omdat warfarine (Coumadin)); tretinoine (bijvoorbeeld omdat Vesanoid, Renova, Retin-A); nutrienten (zoals omdat metaal, zink, voedingsstoffen voedingssupplementen, calcium mineralen, otc supplement, magnesium); cholesterolverlagende geneesmiddelen bijvoorbeeld maagzuurremmer (zoals omdat Zuivel geassocieerd met Magnesia, Tums, Maalox, Rolaids); items die bismutsubsalicylaat bevatten (zoals omdat Pepto-Bismol); penicilline antibiotica (amoxicilline (zoals omdat Trimox, Amoxil), dicloxacilline (bijvoorbeeld omdat Dynapen), penicilline (bijvoorbeeld omdat Pen-Vee erenigde koninkrijk, Veetids, BeePen-VK), oxacillin (bijvoorbeeld omdat Bactocill), carbenicilline (bijvoorbeeld omdat Geocillin ).

Junk anticonceptie (bijvoorbeeld anticonceptie pillen) is misschien niet zo mooi als je gebruik te maken van Ciclobiotico. Om te voorkomen dat ze zwanger te handelen, hoe aanvullende vorm van anticonceptie (bijvoorbeeld condooms gebruiken).

Speel de rol van voorzichtige, samen met zonnestralen. Ciclobiotico kunnen porien en de huid delicaat om de zon. Safeguard porien en de huid door de zon. Gebruik Ciclobiotico nauwgezet in het geval u wenst te gaan door middel van een chirurgische ingreep (tandheelkunde of voor sommige soort van andere).

Voorkom alcoholische dranken.

Het kan schadelijk zijn voor Ciclobiotico te voorkomen met behulp van ineens.

Ciclobiotico (Sumycin) Veelgestelde vragen

Queen: Precies wat doet Ciclobiotico impliceren?

De: Ciclobiotico is echt een hoge klasse geneesmiddel dat wordt verbruikt in de therapie evenals einde van het contract van de belangrijke microbiele ziektes bijvoorbeeld bacteriele infecties geassocieerd met urine: evenals de ademhalingswegen, gonorroe, chlamydia, acne breakouts. Ciclobiotico effectief weert afstand evenals eindigt enkele andere schadelijke bacteriele infecties veroorzaakt door kiemen bijvoorbeeld clou, Lyme ziekte, buik ulcers. A

Queen: Wat zijn precies merknaam evenals algemene merken geassocieerd met Ciclobiotico ?

De: General titel geassocieerd met Ciclobiotico is eigenlijk Tetracycline. Merken geassocieerd met Ciclobiotico neiging om Ciclobiotico, Panmycin, Robitet vijfhonderd, Ala-Tet, Ciclobiotico Syrup, Emtet-500, TetraCon, Brodspec, Tetracap. A zijn

Queen: Kan vrouwen die zwanger zijn gebruiken Ciclobiotico?

De: Meestal maken geen gebruik van Ciclobiotico wanneer u verwacht en hebben nurseling. A

Queen: We worden getroffen door influenza. Mag ik pakken het door Ciclobiotico?

De: Ciclobiotico samen met andere anti-biotica don "t deal met virusachtige bacteriele infecties (griep, kille evenals andere).A

Queen: Precies wat moet ik te voorkomen bij het gebruik van Ciclobiotico

De. Speel de rol van voorzichtige, samen met zonnestralen Ciclobiotico kan porien en de huid delicaat om zon Safeguard porien en de huid door de zon Gebruik Ciclobiotico nauwgezet in het geval u. wenst te gaan door middel van een chirurgische ingreep (tandheelkundige of een soort van andere). Meestal maken geen gebruik van Ciclobiotico in het geval u consumeren of zelfs te consumeren zuivelproducten (kaas, vetvrije yoghurt, zuivel, gletsjers room).A

Queen. Wat zijn precies ernstige negatieve effecten

De: Echter in de situatie in verband met zijn afgewezen in verband met Ciclobiotico componenten die u in staat om meer ernstige negatieve effecten (allergie reacties tegenkomen zijn (urticaria, en uitademen als evenals de inname van problemen, allergie, evenals uitbarsting), problemen met het gezichtsvermogen, gevoel slaperig, ernstige migraine, temperatuur, hele lichaam pijn, porien en de huid oud, onvoldoende honger, geelzucht, ongewoon enige zwakte, plassen geassocieerd met donkere kleur, verbijsterd gemoedstoestand, rillingen, jeuk, ernstige uitputting, griepachtige verschijnselen en symptomen, ongemak in verband met de buik, benauwdheid geassocieerd met belangrijke gewrichten, plassen problemen, onregelmatige bloeden).A

Queen: echt Ciclobiotico bezitten leeftijdsgroep te beperken?

De: Het is echt onaanvaardbaar Ciclobiotico overwegen door middel van kinderen onder de acht veel years. A

Kopen Ciclobiotico (Sumycin) online, kopen Ciclobiotico (Sumycin) online zonder voorschrift, kopen Ciclobiotico (Sumycin) zonder recept, kopen Ciclobiotico (Sumycin) goedkoop, kopen Ciclobiotico (Sumycin) zonder voorschrift, kopen Ciclobiotico (Sumycin) uit Canada, kopen Ciclobiotico (Sumycin) Canada, inkopen Ciclobiotico (Sumycin) online, inkopen Ciclobiotico (Sumycin) online no prescription, bestelling Ciclobiotico (Sumycin) zonder recept, Ciclobiotico (Sumycin) orale pil

Zoeken

Actisuny, Actisuny

Diclofenac is used to treat pain or inflammation caused by arthritis or ankylosing spondylitis. Diclofenac may also be used for purposes other than those listed in this medication guide.

Use Diclofenac as directed by your doctor.

Take Diclofenac by mouth with or without food. Ask your health care provider any questions you may have about how to use Diclofenac.

Drug Class and Mechanism

Diclofenac is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Diclofenac works by reducing hormones that cause inflammation and pain in the body.

If you miss a dose of Diclofenac, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Store Diclofenac at room temperature between 68 and 77 degrees F (20 and 25 degrees C) in a tightly closed container. Brief periods at temperatures of 59 to 86 degrees F (15 to 30 degrees C) are permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diclofenac out of the reach of children and away from pets.

Do not use Diclofenac if:

you are allergic to any ingredient in Diclofenac; you have had a severe allergic reaction (e. g. severe rash, hives, breathing difficulties, dizziness) to another NSAID (e. g. ibuprofen, naproxen, celecoxib) or aspirin. Contact your doctor or health care provider right away if any of these apply to you.

Important : Diclofenac may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Diclofenac with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Before you start any new medicine, check the label to see if it has Actisuny or another nonsteroidal anti-inflammatory drug (NSAID) medicine in it too. If it does or if you are not sure, check with your doctor or pharmacist. Diclofenac should not be used in children; safety and effectiveness in children have not been confirmed. Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Diclofenac while you are pregnant. It is not known if Diclofenac is found in breast milk. Do not breast-feed while using Diclofenac.

Possible Side Effects

Check with your doctor if any of these most common side effects persist or become bothersome:

burning or stinging; discharge; eye redness, irritation, or itching. Seek medical attention right away if any of these severe side effects occur:

severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred or distorted vision; eye infection; eyelid swelling or redness; sensitivity to glare or light.

Diclofenac is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

High Quality Led Grow Lights For Sale, Opticol

LED Grow Lights | By Optic Lighting

Optic Vero LED Grow Lights use only top quality Bridgelux Vero LED Chips Powered by Efficient Meanwell drivers. The new frame makes it extremely easy for anyone to change out parts if needed. All modules are independent so upgrades are made very easy. Optics Detachable X3 Lens allows the user to choose two different coverage areas. Attach the X3 Lens For deeper penetration, or remove the X3 lens for more coverage area. The Vero comes with a 5 Year Warranty .

Optic CXB3070 LED Grow Lights use only top quality Cree CXB LED Chips Powered by Efficient Meanwell drivers. The new frame makes it extremely easy for anyone to change out parts if needed. All modules are independent so upgrades are made very easy. Optics Detachable X3 Lens allows the user to choose two different coverage areas. Attach the X3 Lens For deeper penetration, or remove the X3 lens for more coverage area. The CXB comes with a 5 Year Warranty .

To Learn More About LED Grow Lights and what Our LED Grow Lights Can Do For You Please See Our About LED Grow Light Page

Our mission is to help clients and businesses adopt environmental practices that are sustainable as well as profitable. We achieve our mission by continuing to provide access to information about LED technology and by offering the best quality LED lights at a low cost.

Optic Lighting is a LED lighting company that has been investing in LED technology since 2005. We strongly believe in the future of LED lighting and the impact that it will have on energy efficiency in your home, business, and the environment. We are proud to say that our indoor LED Grow Lights can help you save significant amounts of money off your lighting bill, take away the stress and hassle of frequent replacement of "regular" bulbs and its high costs, and can last up to 10x's longer than HPS grow lights, all while meeting the standards of being clean and environmentally friendly.

Optic Lighting also serves as an energy reduction company. We work with businesses to show the beneficial investment opportunities that come with switching to LED lighting. Some companies see their return on investments as soon as 4 months and continue to see savings month after month.

If you would like to know what LED lighting can do for you & your business, please call us to book a free consultation. We will be happy to show you the difference it can make for you.

Oftan Akvakol, Oftan Akvakol

Package Leaflets (PL) for Human medicinal products

The package leaflet (PL) provides users with information about the medicinal product and its correct use. The package leaflets contain instructions in both Finnish and Swedish.

The package leaflets can be searched from alphabetical list, with the name, marketing authorisation number and the Anatomical Therapeutic Chemical, i. e. ATC Code of the Summary of Product Characteristics, SPC.

The package leaflets processed as part of the EU centralised marketing authorisation procedure are published by the European Medicines Agency, EMA. Fimea's service contains links to the documents on medicinal products (EPAR PI) on the EMA website. Drugs belonging to the centralised authorisation procedure can be searched in Fimea's service by using an alphabetical list or by entering the product name or ATC code.

The material being published is not necessarily complete or up-to-date due to the technical quality of files submitted to the Finnish Medicines Agency Fimea or earlier to the National Agency for Medicines and the delays in delivery. For this reason, Fimea cannot guarantee that the document on the Internet fully complies with the summary of product characteristics and package leaflet officially approved by a desicion for a marketing authorisation. Only the hard copies of the SPCs and the PLs, which are in accordance with the marketing authorisation, are conclusive.

Search with the first character of the name of the medicinal product: o

Product Information Leaflets 1 - 30 of 234

Diflucan - Anti Fungal, Fluconamerck

Product Description Common use Diflucan is an anti-fungal antibiotic which is used to treat fungal infections called candidiasis. This medication is prescribed for the treatment of such type of infections as vaginal, throat and fungal infections, infections of the urinary tract, peritonitis, and pneumonia. Diflucan works by killing sensitive fungi by interfering with the formation of the fungal cell membrane.

Dosage and direction Take it orally once a day, with or without food using the measuring spoon. Take it at the same time each day with a full glass of water if you want to get the best result. Diflucan make you feel better after 24 hours. However, your symptoms will go away completely just after few days. If there is no change in your health after a few days consult your doctor immediately. The dosage for adults may vary from type of infection: 1) Genital thrush - 150mg as a single dose 2) Mucosal thrush - dose depends on where the infection is located 50mg once daily during month. 3)Fungal skin infections - 50mg once daily for 2-4 weeks ; 4) Internal fungal infections 400mg on the first day then 200-400mg once daily for 6-8 weeks or longer if needed. 5) To stop you from getting fungal infections - 50-400mg once daily while you have risk to get an infection; 6) To stop infection caused by Cryptococcus from coming back - 100-200mg once daily indefinitely The dosage for children 4 weeks to 15 years old may also vary from type of infection: 1) mucosal infections - 3mg/kg once daily; 2)internal fungal infections - 6-12mg/kg once daily; 3)prevention of fungal infections - 3-12mg/kg once daily while at risk of getting an infection. For children 2-4 weeks old it is same dose as above but given once every 2 days. A maximum dose of 12mg/kg every 2 days. For children less than 2 weeks old it is same dose as above but given once every 3 days. Do not give more then 12mg/kg every 3 days. Note: this instruction presented here is just for review. It's very necessary to consult your doctor before using. It will help you to get best results.

For vaginal yeast infections, doctors usually prescribe a single dose of Diflucan. If the yeast infection does not improve after 5 days, contact your doctor as soon as possible. Be careful with this medication if your medical history include liver disease or kidney disease. Although uncommon, this drug may make you dizzy, so be more attentive while you are driving or using machinery. Limit alcohol intake. Diflucan should not be used during pregnancy, lactation or if you plan to become pregnant without a doctor's advice. Do not use before breast-feeding without a doctor's advice.

Contraindications Diflucan is not allowed to people who have hypersensitivity to Fluconazole or other anti fungal azole preparations, eg clotrimazole, ketoconazole, itraconazole and other. Also Diflucan contraindicated in: Kidney and liver disorders; Cardiovascular diseases including heart diseases(heart rate or rhythm disturbances); Low blood levels of calcium, magnesium or potassium.

Possible side effect

They may include an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Also the most possible side effects include: nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); fever, chills, body aches, flu symptoms; severe blistering, peeling, and red skin rash; easy bruising or bleeding, unusual weakness; or seizure (convulsions). Less serious include: mild nausea, vomiting, diarrhea, or upset stomach; headache; dizziness; unusual or unpleasant taste in your mouth; or skin rash or itching. If you experience one of them stop using Diflucan and tell your doctor as soon as possible. Also consult your doctor about any side effect that seems unusual.

Drug interaction Diflucan interact with such medication as: a blood thinner such as warfarin (Coumadin) cyclosporine (Gengraf, Sandimmune, Neoral); an oral diabetes medicine such as glipizide (Glucotrol), glyburide (Diabeta, Micronase, Glynase), tolbutamide (Orinase), tolazamide (Tolinase), chlorpropamide (Diabinese), and others; rifabutin (Mycobutin) or rifampin (Rifadin, Rifater, Rifamate, Rimactane); a sedative such as diazepam (Valium), lorazepam (Ativan), alprazolam (Xanax), or midazolam (Versed); seizure medication such as phenytoin (Dilantin) or valproic acid (Depakene); tacrolimus ((Prograf); theophylline (Theo-Dur, Theolair, Theochron, Elixophyllin, Slo-Phyllin, others). Also note that interaction between two medications does not always mean that you must stop taking one of them. Usually it affects the the effect of drugs, so consult your doctor about the way these interactions are being managed or should be managed.

Missed dose If you forgot to take your dose in time, please do it as soon as you remember. But do not take if it is too late or almost time for your next dose. Do not take double or extra doses. Take your usual dose next day in the same time.

Overdose Symptoms of Diflucan overdose may include: confusion or unusual thoughts or behavior. If you experience one of them call your doctor immediately.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Diflucan is an anti-fungal antibiotic which is used to treat fungal infections called candidiasis. This medication is prescribed for the treatment of such type of infections as vaginal, throat and fungal infections, infections of the urinary tract, peritonitis, and pneumonia. Diflucan works by killing sensitive fungi by interfering with the formation of the fungal cell membrane.

Dosage and direction Take it orally once a day, with or without food using the measuring spoon. Take it at the same time each day with a full glass of water if you want to get the best result. Diflucan make you feel better after 24 hours. However, your symptoms will go away completely just after few days. If there is no change in your health after a few days consult your doctor immediately. The dosage for adults may vary from type of infection: 1) Genital thrush - 150mg as a single dose 2) Mucosal thrush - dose depends on where the infection is located 50mg once daily during month. 3)Fungal skin infections - 50mg once daily for 2-4 weeks ; 4) Internal fungal infections 400mg on the first day then 200-400mg once daily for 6-8 weeks or longer if needed. 5) To stop you from getting fungal infections - 50-400mg once daily while you have risk to get an infection; 6) To stop infection caused by Cryptococcus from coming back - 100-200mg once daily indefinitely The dosage for children 4 weeks to 15 years old may also vary from type of infection: 1) mucosal infections - 3mg/kg once daily; 2)internal fungal infections - 6-12mg/kg once daily; 3)prevention of fungal infections - 3-12mg/kg once daily while at risk of getting an infection. For children 2-4 weeks old it is same dose as above but given once every 2 days. A maximum dose of 12mg/kg every 2 days. For children less than 2 weeks old it is same dose as above but given once every 3 days. Do not give more then 12mg/kg every 3 days. Note: this instruction presented here is just for review. It's very necessary to consult your doctor before using. It will help you to get best results.

For vaginal yeast infections, doctors usually prescribe a single dose of Diflucan. If the yeast infection does not improve after 5 days, contact your doctor as soon as possible. Be careful with this medication if your medical history include liver disease or kidney disease. Although uncommon, this drug may make you dizzy, so be more attentive while you are driving or using machinery. Limit alcohol intake. Diflucan should not be used during pregnancy, lactation or if you plan to become pregnant without a doctor's advice. Do not use before breast-feeding without a doctor's advice.

Contraindications Diflucan is not allowed to people who have hypersensitivity to Fluconazole or other anti fungal azole preparations, eg clotrimazole, ketoconazole, itraconazole and other. Also Diflucan contraindicated in: Kidney and liver disorders; Cardiovascular diseases including heart diseases(heart rate or rhythm disturbances); Low blood levels of calcium, magnesium or potassium.

Possible side effect

They may include an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Also the most possible side effects include: nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); fever, chills, body aches, flu symptoms; severe blistering, peeling, and red skin rash; easy bruising or bleeding, unusual weakness; or seizure (convulsions). Less serious include: mild nausea, vomiting, diarrhea, or upset stomach; headache; dizziness; unusual or unpleasant taste in your mouth; or skin rash or itching. If you experience one of them stop using Diflucan and tell your doctor as soon as possible. Also consult your doctor about any side effect that seems unusual.

Drug interaction Diflucan interact with such medication as: a blood thinner such as warfarin (Coumadin) cyclosporine (Gengraf, Sandimmune, Neoral); an oral diabetes medicine such as glipizide (Glucotrol), glyburide (Diabeta, Micronase, Glynase), tolbutamide (Orinase), tolazamide (Tolinase), chlorpropamide (Diabinese), and others; rifabutin (Mycobutin) or rifampin (Rifadin, Rifater, Rifamate, Rimactane); a sedative such as diazepam (Valium), lorazepam (Ativan), alprazolam (Xanax), or midazolam (Versed); seizure medication such as phenytoin (Dilantin) or valproic acid (Depakene); tacrolimus ((Prograf); theophylline (Theo-Dur, Theolair, Theochron, Elixophyllin, Slo-Phyllin, others). Also note that interaction between two medications does not always mean that you must stop taking one of them. Usually it affects the the effect of drugs, so consult your doctor about the way these interactions are being managed or should be managed.

Missed dose If you forgot to take your dose in time, please do it as soon as you remember. But do not take if it is too late or almost time for your next dose. Do not take double or extra doses. Take your usual dose next day in the same time.

Overdose Symptoms of Diflucan overdose may include: confusion or unusual thoughts or behavior. If you experience one of them call your doctor immediately.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Diflucan is an anti-fungal antibiotic which is used to treat fungal infections called candidiasis. This medication is prescribed for the treatment of such type of infections as vaginal, throat and fungal infections, infections of the urinary tract, peritonitis, and pneumonia. Diflucan works by killing sensitive fungi by interfering with the formation of the fungal cell membrane.

Dosage and direction Take it orally once a day, with or without food using the measuring spoon. Take it at the same time each day with a full glass of water if you want to get the best result. Diflucan make you feel better after 24 hours. However, your symptoms will go away completely just after few days. If there is no change in your health after a few days consult your doctor immediately. The dosage for adults may vary from type of infection: 1) Genital thrush - 150mg as a single dose 2) Mucosal thrush - dose depends on where the infection is located 50mg once daily during month. 3)Fungal skin infections - 50mg once daily for 2-4 weeks ; 4) Internal fungal infections 400mg on the first day then 200-400mg once daily for 6-8 weeks or longer if needed. 5) To stop you from getting fungal infections - 50-400mg once daily while you have risk to get an infection; 6) To stop infection caused by Cryptococcus from coming back - 100-200mg once daily indefinitely The dosage for children 4 weeks to 15 years old may also vary from type of infection: 1) mucosal infections - 3mg/kg once daily; 2)internal fungal infections - 6-12mg/kg once daily; 3)prevention of fungal infections - 3-12mg/kg once daily while at risk of getting an infection. For children 2-4 weeks old it is same dose as above but given once every 2 days. A maximum dose of 12mg/kg every 2 days. For children less than 2 weeks old it is same dose as above but given once every 3 days. Do not give more then 12mg/kg every 3 days. Note: this instruction presented here is just for review. It's very necessary to consult your doctor before using. It will help you to get best results.

For vaginal yeast infections, doctors usually prescribe a single dose of Diflucan. If the yeast infection does not improve after 5 days, contact your doctor as soon as possible. Be careful with this medication if your medical history include liver disease or kidney disease. Although uncommon, this drug may make you dizzy, so be more attentive while you are driving or using machinery. Limit alcohol intake. Diflucan should not be used during pregnancy, lactation or if you plan to become pregnant without a doctor's advice. Do not use before breast-feeding without a doctor's advice.

Contraindications Diflucan is not allowed to people who have hypersensitivity to Fluconazole or other anti fungal azole preparations, eg clotrimazole, ketoconazole, itraconazole and other. Also Diflucan contraindicated in: Kidney and liver disorders; Cardiovascular diseases including heart diseases(heart rate or rhythm disturbances); Low blood levels of calcium, magnesium or potassium.

Possible side effect

They may include an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Also the most possible side effects include: nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); fever, chills, body aches, flu symptoms; severe blistering, peeling, and red skin rash; easy bruising or bleeding, unusual weakness; or seizure (convulsions). Less serious include: mild nausea, vomiting, diarrhea, or upset stomach; headache; dizziness; unusual or unpleasant taste in your mouth; or skin rash or itching. If you experience one of them stop using Diflucan and tell your doctor as soon as possible. Also consult your doctor about any side effect that seems unusual.

Drug interaction Diflucan interact with such medication as: a blood thinner such as warfarin (Coumadin) cyclosporine (Gengraf, Sandimmune, Neoral); an oral diabetes medicine such as glipizide (Glucotrol), glyburide (Diabeta, Micronase, Glynase), tolbutamide (Orinase), tolazamide (Tolinase), chlorpropamide (Diabinese), and others; rifabutin (Mycobutin) or rifampin (Rifadin, Rifater, Rifamate, Rimactane); a sedative such as diazepam (Valium), lorazepam (Ativan), alprazolam (Xanax), or midazolam (Versed); seizure medication such as phenytoin (Dilantin) or valproic acid (Depakene); tacrolimus ((Prograf); theophylline (Theo-Dur, Theolair, Theochron, Elixophyllin, Slo-Phyllin, others). Also note that interaction between two medications does not always mean that you must stop taking one of them. Usually it affects the the effect of drugs, so consult your doctor about the way these interactions are being managed or should be managed.

Missed dose If you forgot to take your dose in time, please do it as soon as you remember. But do not take if it is too late or almost time for your next dose. Do not take double or extra doses. Take your usual dose next day in the same time.

Overdose Symptoms of Diflucan overdose may include: confusion or unusual thoughts or behavior. If you experience one of them call your doctor immediately.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Diflucan is an anti-fungal antibiotic which is used to treat fungal infections called candidiasis. This medication is prescribed for the treatment of such type of infections as vaginal, throat and fungal infections, infections of the urinary tract, peritonitis, and pneumonia. Diflucan works by killing sensitive fungi by interfering with the formation of the fungal cell membrane.

Dosage and direction Take it orally once a day, with or without food using the measuring spoon. Take it at the same time each day with a full glass of water if you want to get the best result. Diflucan make you feel better after 24 hours. However, your symptoms will go away completely just after few days. If there is no change in your health after a few days consult your doctor immediately. The dosage for adults may vary from type of infection: 1) Genital thrush - 150mg as a single dose 2) Mucosal thrush - dose depends on where the infection is located 50mg once daily during month. 3)Fungal skin infections - 50mg once daily for 2-4 weeks ; 4) Internal fungal infections 400mg on the first day then 200-400mg once daily for 6-8 weeks or longer if needed. 5) To stop you from getting fungal infections - 50-400mg once daily while you have risk to get an infection; 6) To stop infection caused by Cryptococcus from coming back - 100-200mg once daily indefinitely The dosage for children 4 weeks to 15 years old may also vary from type of infection: 1) mucosal infections - 3mg/kg once daily; 2)internal fungal infections - 6-12mg/kg once daily; 3)prevention of fungal infections - 3-12mg/kg once daily while at risk of getting an infection. For children 2-4 weeks old it is same dose as above but given once every 2 days. A maximum dose of 12mg/kg every 2 days. For children less than 2 weeks old it is same dose as above but given once every 3 days. Do not give more then 12mg/kg every 3 days. Note: this instruction presented here is just for review. It's very necessary to consult your doctor before using. It will help you to get best results.

For vaginal yeast infections, doctors usually prescribe a single dose of Diflucan. If the yeast infection does not improve after 5 days, contact your doctor as soon as possible. Be careful with this medication if your medical history include liver disease or kidney disease. Although uncommon, this drug may make you dizzy, so be more attentive while you are driving or using machinery. Limit alcohol intake. Diflucan should not be used during pregnancy, lactation or if you plan to become pregnant without a doctor's advice. Do not use before breast-feeding without a doctor's advice.

Contraindications Diflucan is not allowed to people who have hypersensitivity to Fluconazole or other anti fungal azole preparations, eg clotrimazole, ketoconazole, itraconazole and other. Also Diflucan contraindicated in: Kidney and liver disorders; Cardiovascular diseases including heart diseases(heart rate or rhythm disturbances); Low blood levels of calcium, magnesium or potassium.

Possible side effect

They may include an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Also the most possible side effects include: nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); fever, chills, body aches, flu symptoms; severe blistering, peeling, and red skin rash; easy bruising or bleeding, unusual weakness; or seizure (convulsions). Less serious include: mild nausea, vomiting, diarrhea, or upset stomach; headache; dizziness; unusual or unpleasant taste in your mouth; or skin rash or itching. If you experience one of them stop using Diflucan and tell your doctor as soon as possible. Also consult your doctor about any side effect that seems unusual.

Drug interaction Diflucan interact with such medication as: a blood thinner such as warfarin (Coumadin) cyclosporine (Gengraf, Sandimmune, Neoral); an oral diabetes medicine such as glipizide (Glucotrol), glyburide (Diabeta, Micronase, Glynase), tolbutamide (Orinase), tolazamide (Tolinase), chlorpropamide (Diabinese), and others; rifabutin (Mycobutin) or rifampin (Rifadin, Rifater, Rifamate, Rimactane); a sedative such as diazepam (Valium), lorazepam (Ativan), alprazolam (Xanax), or midazolam (Versed); seizure medication such as phenytoin (Dilantin) or valproic acid (Depakene); tacrolimus ((Prograf); theophylline (Theo-Dur, Theolair, Theochron, Elixophyllin, Slo-Phyllin, others). Also note that interaction between two medications does not always mean that you must stop taking one of them. Usually it affects the the effect of drugs, so consult your doctor about the way these interactions are being managed or should be managed.

Missed dose If you forgot to take your dose in time, please do it as soon as you remember. But do not take if it is too late or almost time for your next dose. Do not take double or extra doses. Take your usual dose next day in the same time.

Overdose Symptoms of Diflucan overdose may include: confusion or unusual thoughts or behavior. If you experience one of them call your doctor immediately.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Terbinafine Indications, Side Effects, Warnings, Terbinafin

Terbinafine

Before using terbinafine:

Some medical conditions may interact with terbinafine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver problems, lupus, depression, psoriasis, alcohol abuse or dependence, or blood problems (eg, anemia)

if you have a weakened immune system or low white blood cell counts

Some MEDICINES MAY INTERACT with terbinafine. Tell your health care provider if you are taking any other medicines, especially any of the following:

Amiodarone, cimetidine, fluconazole, or ketoconazole because they may increase the risk of terbinafine's side effects

Rifampin because it may decrease terbinafine's effectiveness

Antiarrhythmics (eg, flecainide, propafenone), beta-blockers (eg, metoprolol), dextromethorphan, monoamine oxidase type B (MAO-B) inhibitors (eg, selegiline), selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine), or tricyclic antidepressants (eg, amitriptyline, desipramine) because the risk of their side effects may be increased by terbinafine

Anticoagulants (eg, warfarin) because their effectiveness may be decreased or the risk of their side effects may be increased by terbinafine

Cyclosporine or tamoxifen because their effectiveness may be decreased by terbinafine

This may not be a complete list of all interactions that may occur. Ask your health care provider if terbinafine may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use terbinafine:

Use terbinafine as directed by your doctor. Check the label on the medicine for exact dosing instructions.

To use the tablets: Take by mouth with or without food.

The tablets are taken for different amounts of time depending on your condition. The full benefit may not be seen for several months after stopping treatment. This includes the time period necessary for healthy nails to grow.

To use the nail lacquer: Use at bedtime, unless your doctor tells you otherwise. Wash and dry the affected nails, then apply a thin coat of medicine.

Do not apply the nail lacquer to a wound, or to broken or damaged skin.

Use the nail lacquer until a new, healthy nail has grown, unless your doctor tells you otherwise. This usually takes 6 to 12 months, depending on your condition.

To clear up your infection completely, take terbinafine for the full course of treatment. Keep taking it even if you begin to see improvement before the end of your therapy.

If you miss a dose of terbinafine, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use terbinafine.

Important safety information:

If you experience dizziness while taking terbinafine, use caution. Do not drive or perform other possibly unsafe tasks.

Terbinafine only works against fungal infections; it does not treat bacterial or viral infections (eg, the common cold).

Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Be sure to use terbinafine for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The fungus could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Very bad skin reactions (eg, Stevens-Johnson syndrome/toxic epidermal necrolysis) that include skin rash with or without liver, lung, kidney, and/or heart problems have occurred in patients taking terbinafine. These reactions can cause very bad health problems that may not go away and sometimes death. Get medical help right away if you have red, swollen, blistered, or peeling skin; fever; red or irritated eyes; sores in your mouth, throat, nose, or eyes; or swollen lymph glands (with or without other unusual side effects).

Terbinafine may lower the ability of your body to fight infection. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.

Tell your doctor or dentist that you take terbinafine before you receive any medical or dental care, emergency care, or surgery.

Before using terbinafine, tell your doctor if you take a medicine that contains caffeine or if you consume large amounts of food or drink that contain caffeine (eg, coffee, tea, cocoa, cola, chocolate).

Taste changes (eg, taste loss) or changes in smell (eg, loss of smell) have been reported in patients taking terbinafine. These effects may resolve after you stop taking terbinafine, but may last for a long time (eg, more than 1 year), or may become permanent. Tell your doctor right away if you experience changes in smell, taste changes, poor appetite, unwanted weight loss, anxiety, or mood changes (eg, symptoms of depression).

Terbinafine may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to terbinafine. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

Rarely, terbinafine may cause severe or even fatal liver problems. If liver problems occur, they may be more severe in patients who have other active liver problems or a history of long-term liver problems. Discuss any questions or concerns with your doctor.

The nail lacquer is for external use only. Do not get it in your eyes, nose, or mouth. If you get it in any of these areas, rinse right away with cool water.

You may apply nail polish on top of the nail lacquer.

Unless you are washing your hands, use gloves while using water or chemical substances to avoid accidentally washing the nail lacquer off. Wearing cotton under the gloves is preferred.

The nail lacquer is flammable. Do not store or use near an open flame or while smoking.

Lab tests, including liver function and complete blood cell counts, may be performed while you use terbinafine. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Terbinafine should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed.

PREGNANCY and BREAST-FEEDING: It is not known if terbinafine can cause harm to the fetus. Do not start taking terbinafine during pregnancy without talking with your doctor. If you think you may be pregnant, contact your doctor right away. You will need to discuss the benefits and risks of using terbinafine while you are pregnant. Terbinafine is found in breast milk. Do not breast-feed while taking terbinafine.

Possible side effects of terbinafine:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Diarrhea; gas; headache; indigestion; mild stomach pain; nausea.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing or swallowing; tightness in the chest; swelling of the mouth, face, lips, throat, or tongue; unusual hoarseness); burning, numbness, or tingling; mental or mood changes (eg, depression, restlessness, sadness, worthlessness); new or worsening symptoms of lupus (eg, butterfly-shaped rash on the face, joint pain, seizures, skin color changes, unusual sensitivity to the sun); pale skin or nail beds; severe muscle or joint pain or tenderness; severe or persistent stomach pain (with or without nausea or vomiting); sleep problems; symptoms of liver problems (eg, dark urine; loss of appetite; pale stools; unexplained, persistent nausea; vomiting; yellowing of the skin or eyes); unusual bruising or bleeding; unusual tiredness or weakness; vision or hearing changes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately. Symptoms may include dizziness; frequent urination; rash; severe headache or nausea; stomach pain; vomiting.

Proper storage of terbinafine:

Store the tablets at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Store the nail lacquer at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not store near an open flame. Keep terbinafine out of the reach of children and away from pets.

General information:

If you have any questions about terbinafine, please talk with your doctor, pharmacist, or other health care provider.

Terbinafine is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take terbinafine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about terbinafine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to terbinafine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your health care provider for complete information about the risks and benefits of using terbinafine.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about terbinafine

Automated Testing Of The Diagnostic Protocol, Candiva

Automated Testing of the Diagnostic Protocol in ECUs with CANoe. DiVa

DiVa is a CANoe extension for automated testing of diagnostic software implementations in ECUs. Reproducible test cases are generated based on an ECU diagnostic description.

Functions

CANoe. DiVa consists of a configuration tool with a dedicated user interface, test case generator and runtime library for extended CANoe test functionality. The generator uses diagnostic descriptions in ODX or CANdela format to generate comprehensive test cases (good and bad cases). It generates the test environment that is loaded in CANoe, as well as a test specification with details on the test flow and the individual tests.

Advantages

Automatic generation of test cases and their specification with comprehensive test coverage based on ECU diagnostic descriptions in ODX or CANdela format

Automated execution of test cases and generation of a test report

Supports different diagnostic standards

Easy to configure test contents

Full integration in the CANoe test environment

Highlights of CANoe. DiVa 4.0

Support of flash tests using the Vector tool vFlash

Import of CANoe. DiVa test cases in vTESTstudio

Extended OEM support

Application Areas

The generation of test cases and automation of test execution are two important trends in testing. The system supplier needs extensive tests to support development as well as regression and release tests. Automotive OEMs also need systematic tests, especially in integration and release on the vehicle level. CANoe. DiVa was designed to be used by automotive OEMs and suppliers.

Lamex Food Group, Lamez

LAMEX FOOD GROUP

One of the world’s largest privately owned frozen and chilled food importers/exporters

LAMEX FOOD GROUP

are committed to being the strongest link in any supply chain

LAMEX FOOD GROUP

have the ability to supply product in line with specific customer requirements, factory standards and welfare systems

Lamex sources poultry worldwide, importing into the EU from lower cost origins such as Brazil and Thailand and exporting to high volume consumers such as China, Vietnam and Russia from Brazil and the USA.

Lamex sources from all the world’s major meat production centres. We procure and supply product to this fast-changing and challenging sector where total consumption continues to rise rapidly.

Lamex created a seafood division in 2009 and now has a varied global supply and customer base with products ranging from shrimps from India to cod from China.

Lamex’s procurement divisions follow the sun to ensure that every crop opportunity is maximised and that every plant with which we work is audited.

Lamex is one of the world’s largest buyers of honey - more than 20,000 tons of bulk honey was sourced by the company last year from countries such as Brazil, Argentina, China and Vietnam.

Working closely with its fruit division, Lamex buys juices, purees and concentrates from all over the world, for some of the most important brands on the planet. These range from exotic juices in South America to red fruit juices in Europe to apple and pear juice from China.

Lamex Foods Europe supplies dairy products and solutions to the dairy industry with a product range of milk powders, butter fats and cheeses.

The worldwide network

A From TO B

Inegy, Inegy

Why register with MediGuard?

We are a free monitoring service designed for patients like you who want to be in the driver seat of your medical treatment. We have a community of more than 2.6 million members and offer the services below.

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Inegy

Share your story! Tell us how MediGuard has helped you or someone you love. Download the MediGuard Mobile App to manage your prescription and over-the-counter medications, for free. Taking multiple medications puts you at risk for possible drug-drug interactions Monitor the medical treatment of you and your loved ones.

DISCLAIMER: MediGuard is not intended to be a substitute for professional medical advice. MediGuard cannot and does not take into consideration every possible interaction or account for individual responses to medicine. Different individuals may respond to medication in different ways. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective, or appropriate for any given patient. Always seek the advice of a qualified health provider with any questions you may have before making any changes to your treatment. The use of the MediGuard site and its content is at your own risk. The MediGuard site and the information contained in it is intended for users in the United States and information in other countries may be different.

© Quintiles 2016

Inegy

Inegy tablets contain two active ingredients, simvastatin and ezetimibe. Both these medicines are used to lower cholesterol. They work in different and complementary ways.

What is Inegy?

Inegy is a medicine used to lower levels of total cholesterol, “bad” cholesterol (LDL cholesterol), and fatty substances called triglycerides in the blood. In addition, Inegy raises levels of “good” cholesterol (HDL cholesterol). It is used for patients who cannot control their cholesterol levels by diet alone. You should stay on a cholesterol-lowering diet while taking this medicine. Inegy works to reduce your cholesterol in two ways. It reduces the cholesterol absorbed in your digestive tract, as well as the cholesterol your body makes by itself. Inegy does not help you lose weight.

Inegy is used in addition to diet if you have:

a raised cholesterol level in your blood (primary hypercholesterolaemia or elevated fat levels in your blood (mixed hyperlipidaemia):

that is not well controlled with a statin alone

for which you have used a statin and ezetimibe as separate tablets

a hereditary illness (homozygous familial hypercholesterolaemia) that increases the cholesterol level in your blood. You may also receive other treatments.

Do not take Inegy if:

you are allergic (hypersensitive) to ezetimibe, simvastatin. or any of the other ingredients of Inegy Tablets

you currently have liver problems

you are pregnant or breast-feeding

you are taking one or more than one of the following drugs at the same time:

itraconazole, ketoconazole, or posaconazole (medicines for fungal infections)

erythromycin, clarithromycin (antibiotics for infections)

HIV protease inhibitors such as indinavir, nelfinavir, ritonavir, and saquinavir (HIV protease inhibitors are used for HIV infections)

boceprevir or telaprevir (medicines for hepatitis C virus infection)

nefazodone (a medicine for depression)

gemfibrozil (a medicine for lowering cholesterol)

ciclosporin (a medicine often used in organ transplant patients)

danazol (a man-made hormone used to treat endometriosis).

Ask your doctor if you are not sure if your medicine is listed above.

Take special care with Inegy

Tell your doctor about all your medical conditions including allergies .

Tell your doctor if you drink large amounts of alcohol or have ever had liver disease. Inegy may not be right for you.

Tell your doctor if you are due to have an operation. You may need to stop taking Inegy tablets for a short time.

Your doctor should do a blood test before you start taking Inegy and if you have any symptoms of liver problems while you take Inegy. This is to check how well your liver is working.

Your doctor may also want you to have blood tests to check how well your liver is working after you start taking Inegy.

While you are on this medicine your doctor will monitor you closely if you have diabetes or are at risk of developing diabetes. You are likely to be at risk of developing diabetes if you have high levels of sugars and fats in your blood, are overweight and have high blood pressure. Tell your doctor if you have severe lung disease.

The combined use of Inegy and fibrates (medicines for lowering cholesterol) should be avoided since the combined use of Inegy and fibrates has not been studied.

Contact your doctor immediately if you experience unexplained muscle pain, tenderness, or weakness. This is because on rare occasions, muscle problems can be serious, including muscle breakdown resulting in kidney damage; and very rare deaths have occurred. The risk of muscle breakdown is greater at higher doses of Inegy, particularly the 10/80-mg dose. The risk of muscle breakdown is also greater in certain patients.

Talk with your doctor if any of the following applies:

you have kidney problems

you have thyroid problems

you are 65 years or older

you are female

you have ever had muscle problems during treatment with cholesterol lowering medicines called “statins ” (like simvastatin. atorvastatin. and rosuvastatin) or fibrates (like gemfibrozil and bezafibrate)

you or close family members have a hereditary muscle disorder

Taking other medicines

It is particularly important to tell your doctor if you are taking any of the following drugs. Taking Inegy with any of these drugs can increase the risk of muscle problems (some of these have already been listed in the above section “Do not take Inegy if").

ciclosporin (a medicine often used in organ transplant patients)

danazol (a man-made hormone used to treat endometriosis)

medicines like itraconazole, ketoconazole, fluconazole or posaconazole (medicines for fungal infections)

fibrates like gemfibrozil and bezafibrate (medicines for lowering cholesterol)

erythromycin. clarithromycin. telithromycin, or fusidic acid (medicines for bacterial infections)

HIV protease inhibitors such as indinavir, nelfinavir, ritonavir, and saquinavir (medicines for AIDS )

boceprevir or telaprevir (medicines for hepatitis C virus infection)

nefazodone (a medicine for depression)

amiodarone (a medicine for an irregular heartbeat)

verapamil, diltiazem, or amlodipine (medicines for high blood pressure. chest pain associated with heart disease, or other heart conditions)

large amounts (1 gram or more each day) of niacin or nicotinic acid (medicines for lowering cholesterol)

colchicine (a medicine used to treat gout ) .

Also tell your doctor if you are taking niacin (nicotinic acid) or a niacin-containing product and are Chinese. As well as the medicines listed above, tell your doctor or pharmacist i f you are taking or have recently taken any other medicines, including those obtained without prescription. In particular, tell your doctor if you are taking any of the following:

medicines to prevent blood clots, such as warfarin. fluindione, phenprocoumon or acenocoumarol (anticoagulants)

colestyramine (a medicine for lowering cholesterol), because it affects the way Inegy works

fenofibrate (another fibric acid derivative)

rifampicin (a medicine used to treat tuberculosis).

You should also tell any doctor who is prescribing a new medicine for you that you are taking Inegy.

Taking Inegy with food and drink

Grapefruit juice contains one or more components that alter the metabolism of some medications, including Inegy. Consuming grapefruit juice should be avoided as it may increase your risk of muscle problems.

Pregnancy and Breast-feeding

Do not take Inegy if you are pregnant, are trying to get pregnant or think you may be pregnant. If you get pregnant while taking Inegy, stop taking it immediately and tell your doctor. Do not take Inegy if you are breast-feeding, because it is not known if the medicine is passed into breast milk. Ask your doctor or pharmacist for advice before taking any medicine.

Children

Inegy is not recommended for children under age 10.

Driving and using machines

Inegy is not expected to interfere with your ability to drive or to use machinery. However, it should be taken into account that some people get dizzy after taking Inegy.

Important information about some of the ingredients of Inegy

Inegy tablets contain a sugar called lactose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

HOW to take Inegy

Always take Inegy exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

Before starting Inegy, you should be on a diet to lower your cholesterol.

You should keep on this diet while taking Inegy.

For adults the dose is 1 tablet (1 INEGY 10 mg/10 mg, 10 mg/20 mg, 10 mg/40 mg, or 10 mg/80 mg tablet) by mouth once a day.

For adolescents (10 to 17 Years of age), the dose is 1 tablet (1 INEGY 10 mg/10 mg, 10 mg/20 mg or 10 mg/40 mg tablet) by mouth once a day.

The tablets are not scored and should not be divided. The 10 mg/80 mg dose is only recommended for adult patients with very high cholesterol levels and at high risk of heart disease problems who have not reached their cholesterol goal on lower doses. Your doctor will determine the appropriate tablet strength for you, depending on your current treatment and your personal risk status. Take Inegy in the evening. You can take it with or without food.

If your doctor has prescribed Inegy along with colestyramine or any other bile acid sequestrant (medicines for lowering cholesterol), you should take Inegy at least 2 hours before or 4 hours after taking the bile acid sequestrant.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

Possible side effects

Like all medicines, Inegy can cause side effects, although not everybody gets them.

The following common side effects were reported (observed in 1 or more in 100 and less than 1 in 10 patients treated):

muscle aches

elevations in laboratory blood tests of liver (transaminases) and/or muscle (CK) function

The following uncommon side effects were reported (observed in 1 or more in 1000 and less than 1 in 100 patients treated):

elevations in blood tests of liver function; elevations in blood uric acid; elevations in the time it takes for blood to clot; protein in urine; weight decreased

dizziness ; headache ; tingling sensation

abdominal pain; indigestion; flatulence; nausea; vomiting; abdominal bloating; diarrhoea; dry mouth; heartburn. rash; itching ; hives, joint pain, muscle pain, tenderness, weakness or spasms; neck pain; pain in arms and legs; back pain

unusual tiredness or weakness ; feeling tired; chest pain; swelling, especially in the hands and feet

sleep disorder ; trouble sleeping

Additionally, the following side effects have been reported in people taking either Inegy or ezetimibe or simvastatin tablets:

low red blood cell count (anaemia ); reduction in blood cell counts, which may cause bruising/bleeding (thrombocytopenia)

numbness or weakness of the arms and legs; poor memory, memory loss, confusion

breathing problems including persistent cough and/or shortness of breath or fever

constipation ; inflammation of the pancreas often with severe abdominal pain

inflammation of the liver with the following symptoms: yellowing of the skin and eyes, itching ,

dark coloured urine or pale coloured stool, feeling tired or weak, loss of appetite; liver failure; gallstones or inflammation of the gallbladder (which may cause abdominal pain, nausea, vomiting)

hair loss; raised red rash. sometimes with target-shaped lesions

a hypersensitivity reaction including some of the following: hypersensitivity (allergic reactions including swelling of the face, lips, tongue and/or throat which may cause difficulty in breathing or swallowing and requires treatment immediately, pain or inflammation of the joints, inflammation of blood vessels, unusual bruising, skin eruptions and swelling, hives, skin sensitivity to the sun, fever. flushing, shortness of breath and feeling unwell, lupus - like disease picture (including rash, joint disorders, and effects on white blood cells))

muscle pain, tenderness, weakness or cramps; muscle breakdown; tendon problems, sometimes complicated by rupture of the tendon

decreased appetite

hot flush; high blood pressure

pain

erectile dysfunction

depression

alterations in some laboratory blood tests for liver function

Additional possible side effects reported with some statins :

sleep disturbances. including nightmares

sexual difficulties

diabetes. This is more likely if you have high levels of sugars and fats in your blood, are overweight and have high blood pressure. Your doctor will monitor you while you are taking this medicine

Contact your doctor immediately if you experience unexplained muscle pain, tenderness, or weakness. This is because on rare occasions, muscle problems can be serious, including muscle breakdown resulting in kidney damage; and very rare deaths have occurred. If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

How to store Inegy

Keep out of the reach and sight of children.

Do not use Inegy after the expiry date which is stated on the carton or container after [EXP].

Do not store Inegy Tablets above 30°C.

Blisters: Store in the original package in order to protect from moisture and light.

Bottles: Keep bottles tightly closed in order to protect from moisture and light.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

References:

Toplep 25 Tablets; Toplep 50 Tablets; Toplep 100 Tablets; Toplep 200 Tablets, Toplep

PROPRIETARY NAME (and dosage form):

TOPLEP 25 Tablets TOPLEP 50 Tablets TOPLEP 100 Tablets TOPLEP 200 Tablets

COMPOSITION TOPLEP 25 Each tablet contains topiramate 25 mg. TOPLEP 50 Each tablet contains topiramate 50 mg. TOPLEP 100 Each tablet contains topiramate 100 mg. TOPLEP 200 Each tablet contains topiramate 200 mg. Sugar free.

PHARMACOLOGICAL CLASSIFICATION A.2.5 Anticonvulsants, including anti-epileptics.

PHARMACOLOGICAL ACTION Mechanism of action Topiramate is an antiepileptic agent classified as a sulfamate-substituted monosaccharide. Three pharmacological properties of topiramate have been identified that may contribute to its anticonvulsant activity:

Topiramate reduces the frequency at which action potentials are generated when the neurons are subjected to a sustained depolarisation indicative of a state-dependent blockade of voltage-sensitive sodium channels.

Topiramate markedly enhances the activity of GABA at some types of GABA receptors, thereby enhancing GABA-induced influx of chloride into neurons.

Topiramate weakly antagonises the excitatory activity of kainate/AMPA subtype of glutamate receptor but has no apparent effect on the activity of N-methyl-D-asparate (NMDA) at the NMDA receptor subtype.

Topiramate also inhibits some isoenzymes of carbonic anhydrase, This pharmacological effect is generally weak and may not be a major contributing factor to the antiepileptic activity of topiramate. Pharmacokinetics Topiramate is well absorbed after oral administration. The relative bioavailability is about 80%. Food does not affect the bioavailability of topiramate. Protein binding is low, 13 to 17%. The time to peak concentration (T max ) is approximately 2 hours following administration of a 400 mg oral dose. The volume of distribution is 0,6 –0,8L/kg with values for women circa 50% of those for males. In patients with normal renal function, steady state is reached in about 4 days. The pharmacokinetics of topiramate are linear, with dose-proportional increases in plasma concentration over the range of 200 to 800 mg a day. The mean elimination half-life (t½) is 21 hours, following single or multiple dosing. Approximately 70% of an administered dose is excreted unchanged in the urine and the remainder undergoes metabolism by hydroxylation, hydrolysis and glucuronidation with no one metabolite accounting for more than 5% of an oral dose. Topiramate clearance is reduced by 42% in patients with moderate renal function impairment and by 54% in patients with severe renal impairment as compared with the clearance in subjects with normal renal function. Children exhibit a higher clearance and shorter elimination half-life than adults. Consequently, the plasma concentration of topiramate for the same mg/kg dose may be lower in children compared to adults. The clearance of topiramate may be decreased in patients with impaired hepatic function.

INDICATIONS Toplep tablets are indicated as adjunctive therapy for adults and children over 4 years old who are inadequately controlled on conventional first line antiepileptic medicines for:

partial onset seizures with or without secondarily generalized seizures

seizures associated with Lennox-Gastaut syndrome.

primary generalized tonic clonic seizures.

CONTRA-INDICATIONS Hypersensitivity to Toplep or any components of the preparation. Children under 4 years (as safety and efficacy of Toplep has not yet been established). Pregnancy and lactation

WARNINGS A syndrome consisting of acute myopia associated with secondary angle closure glaucoma has been reported in patients receiving Toplep . Symptoms include acute onset of decreased visual acuity and/or ocular pain. Ophthalmic findings can include myopia, anterior chamber shallowing, ocular hyperemia (redness) and increased intraocular pressure. Mydriasis may or may not occur. This syndrome may be associated with supraciliary effusion resulting in anterior displacement of the lens and iris, with secondary angle closure glaucoma. Symptoms typically occur within one month of initiating Toplep therapy. Secondary angle closure glaucoma associated with Toplep has been reported in paediatric patients as well as adult patients. Treatment includes discontinuation of Toplep . as rapidly as possible and appropriate measures to reduce intraocular pressure. Metabolic Adidosis Hyperchloremic, non-anion gap, metabolic acidosis (i. e. decreased serum bicarbonate below the normal reference range in the absence of respiratory alkalosis) is associated with topiramate treatment. This decrease in serum bicarbonate is due to the inhibitory effect of topiramate on renal carbonic anhydrase and consequent renal bicarbonate wasting. These decreases are usually mild to moderate (average decrease of 4 mmol/L at doses of 100 mg/day or above in adults and at approximately 6 mg/kg/day in paediatric patients). However, patients have experienced decreases to values below 10 mmol/l. Conditions or therapies that predispose to acidosis (such as renal disease, severe respiratory disorders, status epilepticus, diarrhoea, surgery, ketogenic or certain drugs) may be addictive to bicarbonate lowering effects of topiramate. Chronic metabolic acidosis in paediatric patients can reduce growth rate. Chronic metabolic acidosis can lead to nephrolithiasis and increased risk of fractures. Evaluation of bicarbonate levels is recommended with topiramate therapy. If metabolic acidosis develops and persists, consideration should be given to reducing the dose or discontinuing topiramate. (see dose tapering)

INTERACTIONS Effects of Toplep on other anti-epileptic medicines If Toplep is taken concomitantly with other anti-epileptic medicines (phenytoin, carbamazepine, valproic acid, phenobarbital, primidone), there is no effect on their steady-state plasma concentrations, except in very rare cases where the addition of Toplep to phenytoin may result in an increase of plasma concentrations of phenytoin. Consequently, any patient on phenytoin, taking Toplep, in addition, should have phenytoin levels monitored.

Effects of other anti-epileptic medicines on Toplep Phenytoin and carbamazepine decrease the plasma concentration of Toplep . The addition or withdrawal of phenytoin or carbamazepine to Toplep therapy may require an adjustment in dosage of Toplep . This should be done by titrating to clinical effect. The withdrawal or addition of valproic acid does not produce clinically significant changes in plasma concentrations of Toplep and, therefore, dosage adjustment of Toplep is not necessary. Digoxin Serum digoxin levels have decreased with concomitant administration of Toplep . When Toplep is added or withdrawn in patients on digoxin therapy, careful attention should be given to the routine monitoring of serum digoxin. Oral Contraceptives Efficacy of oral contraceptives may be compromised when used concurrently with Toplep . Bearing in mind the potential risk of teratogenicity, patients should receive a shapeType1fFlipH0fFlipV0lTxid131072dxTextLeft0dyTextTop0dxTextRight0dyTextBottom0fFilled0lineWidth0fLine0fShadow0fLayoutInCell0fLayoutInCell0

preparation containing not less than 50 micrograms of oestrogen or use some alternative non-hormonal method of contraception as Toplep increases plasma clearance of the oestrogenic component significantly. Patients on oral contraceptives are advised to report any change in their bleeding patterns. Others Concomitant use of Toplep with agents predisposing to nephrolithiasis (renal stone formation) should be avoided.

PREGNANCY AND LACTATION Pregnancy (see Contra-indications) Studies have not been done in humans, therefore, the safety in pregnancy has not been established. Hypospadias in male infants exposed in utero to Toplep . with or without other anticonvulsants, has been reported. However, a causal relationship has not been established. Lactation (see Contra-indications) It is not known if Toplep is excreted in human milk. Mothers taking Toplep should not breast feed their babies.

DOSAGE AND DIRECTIONS FOR USE For optimal seizure control, in both adults and children, it is recommended that therapy be initiated at a low dose, followed by titration to an effective dose. It is recommended that film-coated tablets not be broken. Toplep can be taken without meals. Adults Therapy should begin at 25-50 mg nightly for one week. Subsequently, the dose should be increased at weekly intervals by 25-50 mg/day and taken in two divided doses. Dose titration should be guided by clinical outcome. Some patients may achieve efficacy with once-a-day dosing. The effective dose is usually within the range of 200 mg (minimum dose) to 400 mg daily taken in two divided doses; some patients may require up to 800 mg (maximum dose) daily. It is recommended that therapy be initiated at a low dose, followed by titration to an effective dose. Since Toplep is removed from plasma by haemodialysis, an additional dosage equal to approximately one-half of the daily dose should be administered on haemodialysis days. The additional dose should be administered in divided doses at the beginning and completion of the haemodialysis procedure. The additional doses may vary based on the dialysis equipment being used. No dosage adjustment is necessary in elderly patients. For patients with underlying renal disease, see “ Special Precautions ”.

Children 4 years and over The initial dose for children is 25 mg for the first week, increased at intervals of 1 – 2 weeks by increments of 1 to 3 mg/kg/day, administered in two divided doses if more than 25 mg per day. The recommended dose thereafter is about 5 –9 mg/kg/day in two divided doses. Dose titration should be guided by clinical outcome.

SIDE-EFFECTS AND SPECIAL PRECAUTIONS Side-effects The adverse events considered at least possibly related to the treatment are listed below by body system, organ class and frequency (wherever applicable). Frequencies are defined as very common (>1/10), common (>1/100, =1/10), uncommon (>1/1000, =1/100), rare (>1/10000, =1/1000), very rare (=1/10000) or frequency unknown. Blood and lymphatic system disorders Less frequent: Leucopenia Frequency unknown: Purpura. Anaemia and thrombocytopenia, alone or in combination with leucopenia. Thrombolic events have been reported although a causal association with Toplep has not been established. Immune system disorders Frequency unknown: Viral infection. Metabolism and nutritional disorders Less frequent: Weight decrease, anorexia. Psychiatric disorders Frequent: Somnolence, nervousness, psychomotor slowing, difficulty with memory not otherwise specified, confusion, difficulty with concentration/attention, anorexia, depression, mood problems, personality changes, insomnia. Less frequent: Agitation, cognitive problems not otherwise specific, emotional lability, apathy, psychosis/psychotic symptoms, hallucination, aggressive reaction/behaviour, suicidal ideas or attempts. Nervous system disorders Frequent: Paresthesia, ataxia, dizziness, speech disorders/related speech problems, language problems, tremor, hyperkinesias. Co-ordination problems. Eye disorders Frequent: Abnormal vision, diplopia, nystagmus, acute and secondary angle closure glaucoma. Rare: Conjunctivitis. Ear and labyrinth disorders Rare: Tinnitus. Vascular disorders Frequency unknown: Hypotension and postural hypotension. Respiratory, thoracic and mediastinal disorders Less frequent: Pharyngitis. Frequency unknown: Rhinitis, pneumonia, Dyspneoa. Gastro-intestinal disorders Frequent: Nausea. Less frequent: Constipation, dyspepsia, abdominal pain. Frequency unknown: Increased saliva production. Hepato-biliary disorders Frequency unknown: Hepatic failure, hepatitis. Skin and subcutaneous tissue disorders Less frequent: Gingivitis, increased sweating. Rare: Pruritus. Frequency unknown: Bullous skin and mucosal reactions, including erythema multiforme, pemphigus, Stevens-Johnson syndrome and toxic epidermal necrolysis. Renal and urinary disorders Less frequent: Nephrolithiasis (kidney stones). Rare: Dysuria, urinary frequency, incontinence. Frequency unknown: Renal failure, haematuria, General disorders and administration site conditions Frequent: Asthenia, fatigue. Frequency unknown: Injury.

Special Precautions Toplep should be withdrawn gradually to minimize the potential of increased seizure frequency. Toplep should be used with caution in patients with renal or hepatic impairment. Renal elimination is dependent on renal function and is independent of age. Patients with moderate or severe renal impairment may take 10 to 15 days to reach steady-state plasma concentrations as compared to 4 to 8 days in patients with normal renal function. The titration schedule should be guided by clinical outcome (i. e. seizure control and avoidance of side-effects). In patients with hepatic impairment, Toplep should be administered with caution as it may be decreased. Some patients, especially those with a predisposition to nephrolithiasis, may be at risk for renal stone formation. Concomitant use of Toplep with agents predisposing to nephrolithiasis (renal stone formation) should be avoided. Adequate hydration while using Toplep is very important. Hydration can reduce the risk of nephrolithiasis or developing renal calculi. Proper hydration prior to and during activities such as exercise or exposure to warm temperatures may reduce the risk of heat related adverse events. Effects on driving ability and use of machinery Toplep may produce central nervous system related events such as: drowsiness, dizziness or other related symptoms. Caution is advised when driving or operating machinery. Toplep may be more sedating than other antiepileptic medicines.

KNOWN SYMPTOMS OF OVERDOSAGE AND PARTICULARS OF ITS TREATMENT Headache, agitation, drowsiness, lethargy, metabolic acidosis and hypokalemia occurred after overdosing. At very high doses, coma, lasting 20-24 hours followed by full recovery after 3 to 4 days, may occur. Treatment is symptomatic and supportive. An attempt should be made to remove undigested Toplep from the gastro-intestinal tract using gastric lavage, induction of emesis or activated charcoal. Hemodialysis has been shown to be an effective means to remove Toplep from the body. The patient should be well hydrated.

IDENTIFICATION TOPLEP 25 White, film coated, circular tablets debossed with ‘TP1’ on one side and plain on the other side with intact coating. TOPLEP 50 Yellow coloured, film coated, circular tablets debossed with ‘TP2’ on one side and plain on the other side with intact coating. TOPLEP 100 Yellow coloured, film coated, circular tablets debossed with ‘TP3’ on one side and plain on the other side with intact coating. TOPLEP 200 Peach coloured, film coated, circular tablets debossed with ‘TP4’ on one side and plain on the other side with intact coating.

PRESENTATION Cartons contain a white opaque HDPE bottle containing 60 tablets.

STORAGE INSTRUCTIONS Store below 25°C in the original package, protected from moisture. KEEP OUT OF REACH OF CHILDREN.

REGISTRATION NUMBERS TOPLEP 25 . 40/2.5/0348 TOPLEP 50 . 40/2.5/0349 TOPLEP 100 . 40/2.5/0350 TOPLEP 200 . 40/2.5/0351

NAME AND BUSINESS ADDRESS OF THE HOLDER OF THE CERTIFICATE OF REGISTRATION RANBAXY (SA) (PTY) LTD Third Floor Outspan House 1006 Lenchen Avenue North Centurion.

DATE OF PUBLICATION OF THE PACKAGE INSERT June 2007

New addition to this site: December 2007 Source: Pharmaceutical Industry SAEPI HOME PAGE TRADE NAME INDEX GENERIC NAME INDEX FEEDBACK Information presented by Malahyde Information Systems © Copyright 1996-2014

Floxin (Ofloxacin) Side Effects, Interactions, Warning, Dosage & Uses, Ofloxin

Fluoroquinolones, including FLOXIN® (ofloxacin). are associated with an increased risk of tendinitis and tendon rupture in all ages. This risk is further increased in older patients usually over 60 years of age, in patients taking corticosteroid drugs, and in patients with kidney, heart or lung transplants (See WARNINGS ).

Fluoroquinolones, including FLOXIN® (ofloxacin). may exacerbate muscle weakness in persons with myasthenia gravis. Avoid FLOXIN® (ofloxacin) in patients with a known history of myasthenia gravis (See WARNINGS ).

To reduce the development of drug-resistant bacteria and maintain the effectiveness of FLOXIN® (ofloxacin tablets) Tablets and other antibacterial drugs, FLOXIN® (ofloxacin tablets) Tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

DRUG DESCRIPTION

FLOXIN® (ofloxacin tablets) Tablets is a synthetic broad-spectrum antimicrobial agent for oral administration. Chemically, ofloxacin, a fluorinated carboxyquinolone, is the racemate, (±)-9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid. The chemical structure is:

Its empirical formula is C 18 H 20 FN 3 O 4 . and its molecular weight is 361.4 Ofloxacin is an off-white to pale yellow crystalline powder. The molecule exists as a zwitterion at the pH conditions in the small intestine. The relative solubility characteristics of ofloxacin at room temperature, as defined by USP nomenclature, indicate that ofloxacin is considered to be soluble in aqueous solutions with pH between 2 and 5. It is sparingly to slightly soluble in aqueous solutions with pH 7 (solubility falls to 4 mg/mL) and freely soluble in aqueous solutions with pH above 9. Ofloxacin has the potential to form stable coordination compounds with many metal ions. This in vitro chelation potential has the following formation order: Fe +3 > Al +3 > Cu +2 > Ni +2 > Pb +2 > Zn +2 > Mg +2 > Ca +2 > Ba +2 .

FLOXIN® (ofloxacin) Tablets contain the following inactive ingredients: anhydrous lactose, modified corn starch, hydroxypropyl cellulose, hypromellose, magnesium stearate, polyethylene glycol, polysorbate 80, sodium starch glycolate, titanium dioxide and may also contain synthetic yellow iron oxide.

What are the possible side effects of ofloxacin (Floxin)?

Get emergency medical help if you have any of these signs of an allergic reaction . hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Stop using ofloxacin and call your doctor at once if you have a serious side effect such as:

diarrhea that is watery or bloody;

seizure (convulsions);

confusion, hallucinations, anxiety, feeling resltess, tremors, insomnia, nightmares, unusual thoughts or behavior, feeling light-headed;

severe dizziness, fainting, fast or pounding heartbeat;

sudden pain, snapping or popping sound.

What are the precautions when taking ofloxacin (Floxin)?

See also Warning section.

Before taking ofloxacin, tell your doctor or pharmacist if you are allergic to it; or to other quinolone antibiotics (such as ciprofloxacin, levofloxacin); or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: seizure disorder, conditions that increase your risk of seizures (such as brain/head injury, brain tumors), nerve problems (such as peripheral neuropathy), kidney disease, liver disease, myasthenia gravis, joint/tendon problems (such as tendonitis, bursitis).

Ofloxacin may cause a condition that affects the heart.

Last reviewed on RxList: 4/15/2011 This monograph has been modified to include the generic and brand name in many instances.

Negaflox Lb Tab Buy Medicines India S Best Online Pharmacy Network, Negaflox

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NEGAFLOX LB TAB

Brief Info About Medicine

All Information published below is from public sources and cannot be used as expert's opinion. We request you to consult your doctor for more information

1 Why Is it Used ?

NORFLOXACIN :

Adult: PO Uncomplicated gonorrhoea 800 mg once daily. Susceptible infections 400 mg twice daily. Duration: Chronic bacterial prostatitis: 28 days; Complicated UTI: 10-21 days; Gastroenteritis: 3-5 days; Uncomplicated UTI caused by susceptible Escherichia coli, Klebsiella pneumoniae, roteus mirabilis species: 3 days; Uncomplicated UTI caused by other susceptible bacteria: 7-10 days. Chronic relapsing UTI 400 mg twice daily, up to 12 wk, may reduce to once daily if adequate suppression w/in 1st 4 wk. Ophth Conjunctivitis As 0.3% soln: Instill 1-2 drops 4 times/day for up to 7 days. May increase to 2 hrly for the 1st day in more severe infections.

2 What are the Side Effects ?

NORFLOXACIN :

Nausea, vomiting, heartburn, constipation, diarrhoea, abdominal cramping, anorexia; headache, dizziness; depression, insomnia; phototoxicity; rash, fever, arthralgia; elevated liver enzymes, urea and creatinine. Eosinophilia, neutropenia, thrombocytopenia and anaemia; hyperhidris; tendon rupture; QT prolongation. Potentially Fatal: Anaphylaxis, acute renal failure, seizures.

3 What Precautions should be taken ?

NORFLOXACIN :

Renal impairment; history of CNS disorders; myasthaenia gravis. Pregnancy. QT prolongation; discontinue if signs of neuropathy occur.

4 Do not take this if you have any of the below.

NORFLOXACIN :

Hypersensitivity to quinolones; children TROPENOR TAB

10 TAB in Strip

Moraceae Pharmaceuticals Pvt. Ltd.

Torsemide - Heart Disease, Furogamma

Torsemide is used for treatment of edema (swelling) associated with heart, kidney, or liver failure, or conditions when there is excess of body water. It is also used alone or with other medicines to treat high blood pressure.

It may also be used to treat certain conditions as determined by your doctor, which may not be listed in the professional package insert.

Use Torsemide as directed by your doctor.

Take Torsemide by mouth with or without food. Torsemide may increase the amount of urine or cause you to urinate more often when you first start taking it. To keep this from disturbing your sleep, try to take your dose before 6 pm. If you also take cholestyramine, do not take it within 4 hours before or after taking Torsemide. Check with your doctor if you have questions. Avoid eating licorice or Korean ginseng while taking Torsemide. Ask your health care provider any questions you may have about how to use Torsemide.

Drug Class and Mechanism

Torsemide is a loop diuretic. It works by making the kidney eliminate larger amounts of electrolytes (especially sodium and potassium salts) and water than normal (diuretic effect).

If you miss a dose of Torsemide and are using it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Store Torsemide between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Torsemide out of the reach of children and away from pets.

Do not use Torsemide if:

you are allergic to any ingredient in Torsemide or to sulfonylureas (e. g. glyburide); you are unable to urinate. Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Torsemide. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines or other substances if you have fluid in your abdomen, hearing impairment, diabetes mellitus, low urine output, high blood uric acid levels, a blood disorder, kidney disease, lupus, had a heart attack, are dehydrated, or have liver disease or heart failure

Some MEDICINES MAY INTERACT with Torsemide. Tell your health care provider if you are taking any other medicines, especially any of the following: Aminoglycosides (eg, gentamicin) or cisplatin because the risk of temporary or permanent hearing loss may be increased Nonsteroidal anti-inflammatory drugs (NSAIDs; eg, ibuprofen, naproxen) or probenecid because they may decrease the effectiveness of Torsemide Chloral hydrate, digitalis (eg, digoxin), lithium, suramin because side effects may be increased by Torsemide Nondepolarizing muscle relaxants (eg, pancuronium) because its actions and side effects may be increased or decreased by Torsemide

Possible Side Effects

Check with your doctor if any of these most common side effects persist or become bothersome:

constipation; dizziness or lightheadedness when sitting up or standing; excessive urination; headache; increased coughing; nasal inflammation; nausea.

Seek medical attention right away if any of these severe side effects occur: severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; diarrhea; dry mouth or unusual thirst; hearing loss or ringing in the ears; loss of appetite; muscle pain or cramps; rapid or irregular heartbeat; rectal bleeding; restlessness; unusual tiredness or weakness; vomiting.

If you have any questions about Torsemide, please talk with your doctor, pharmacist, or other health care provider.

Torsemide is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Apo-Glimepiride - London Drugs Pharmacy, Apo-Glimep

Medications

DIN (Drug Identification Number)

02295377 APO-GLIMEPIRIDE 1MG TABLET 02295385 APO-GLIMEPIRIDE 2MG TABLET 02295393 APO-GLIMEPIRIDE 4MG TABLET

Glimepiride belongs to a group of medications known as oral hypoglycemics . It is used to control blood sugar for people with type 2 diabetes. It is used when diet, exercise, and weight reduction have not been found to control blood sugar well enough on their own. Glimepiride increases the amount of insulin released by the pancreas and helps the body use insulin more efficiently.

Glimepiride may be used in combination with metformin or insulin when diet and exercise and the use of these medications on their own do not provide adequate control of blood sugar.

This medication may be available under multiple brand names and/or in several different forms. Any specific brand name of this medication may not be available in all of the forms or approved for all of the conditions discussed here. As well, some forms of this medication may not be used for all of the conditions discussed here.

Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Do not stop taking this medication without consulting your doctor.

Do not give this medication to anyone else, even if they have the same symptoms as you do. It can be harmful for people to take this medication if their doctor has not prescribed it.

1 mg Each pink, flat-faced, bevelled-edge, indented capsule-shaped tablet, engraved "GLM" deep bisect "1" on one side, "APO" deep bisect "APO" on the other side, contains glimepiride 1 mg. Nonmedicinal ingredients: anhydrous lactose, corn starch, magnesium stearate, and red ferric oxide.

2 mg Each green, flat-faced, bevelled-edge, indented capsule-shaped tablet, engraved "GLM" deep bisect "2" on one side, "APO" deep bisect "APO" on the other side, contains glimepiride 2 mg. Nonmedicinal ingredients: anhydrous lactose, corn starch, magnesium stearate, indigotine aluminum lake, and yellow ferric oxide.

4 mg Each blue, flat-faced, bevelled-edge, indented capsule-shaped tablet, engraved "GLM" deep bisect "4" on one side, "APO" deep bisect "APO" on the other side, contains glimepiride 4 mg. Nonmedicinal ingredients: anhydrous lactose, corn starch, magnesium stearate, and indigotine aluminum lake.

The usual starting dose is 1 mg once daily to be taken with breakfast or the first main meal. After reaching a dose of 2 mg, further increases should be done in increments of no more than 1 mg at one-week to 2-week intervals, based on the response. The usual maintenance adult dose ranges from 1 mg to 4 mg once daily to be taken with breakfast or the first main meal of the day. The maximum daily dose is 8 mg.

Gilmepiride tablets should be swallowed whole with approximately ½ glass of liquid. Do not chew or crush this medication.

Many things can affect the dose of medication that a person needs, such as body weight, other medical conditions, and other medications. If your doctor has recommended a dose different from the ones listed here, do not change the way that you are taking this medication without consulting your doctor.

It is important to take this medication exactly as prescribed by your doctor. If you miss a dose, take it as soon as possible and continue with your regular schedule. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to make up for a missed one. If you are not sure what to do after missing a dose, contact your doctor or pharmacist for advice.

Store this medication at room temperature, protect it from light and moisture, and keep it out of the reach of children.

Do not dispose of medications in wastewater (e. g. down the sink or in the toilet) or in household garbage. Ask your pharmacist how to dispose of medications that are no longer needed or have expired.

Do not take glimepiride if you:

are allergic to glimepiride or any ingredients of the medication

are pregnant or breast-feeding

have type 1 diabetes (i. e. insulin-dependent diabetes)

have diabetic ketoacidosis, with or without coma

What side effects are possible with this medication?

Many medications can cause side effects. A side effect is an unwanted response to a medication when it is taken in normal doses. Side effects can be mild or severe, temporary or permanent.

The side effects listed below are not experienced by everyone who takes this medication. If you are concerned about side effects, discuss the risks and benefits of this medication with your doctor.

The following side effects have been reported by at least 1% of people taking this medication. Many of these side effects can be managed, and some may go away on their own over time.

Contact your doctor if you experience these side effects and they are severe or bothersome. Your pharmacist may be able to advise you on managing side effects.

Although most of the side effects listed below don't happen very often, they could lead to serious problems if you do not check with your doctor or seek medical attention.

Check with your doctor as soon as possible if any of the following side effects occur:

blurred vision

fever

general feeling of illness

increased skin sensitivity or skin rashes following sun exposure

signs of bleeding (e. g. bleeding gums, blood in the urine, dark tarry stools, easy bruising, nosebleeds, vomiting blood)

signs of high blood sugar ( hyperglycemia ; e. g, dry mouth, dry skin, flushing, frequent urination, loss of appetite, thirst, tiredness, trouble breathing)

signs of low blood sugar ( hypoglycemia ; e. g. blurred vision, dizziness, fatigue, headache, numbness or tingling of the mouth, pale colour, rapid heartbeat, shakiness, sudden hunger, sweating or confusion, weakness)

signs of liver damage (e. g. abdominal pain, dark urine, fatigue, fever, loss of appetite, yellow skin or eyes)

skin redness, itching, or rash

sore throat

swelling of the hands or feet

unusual tiredness or weakness

Stop taking the medication and seek immediate medical attention if any of the following occur:

chest pain

signs of a severe skin reaction such as blistering, peeling, a rash covering a large area of the body, a rash that spreads quickly, or a rash combined with fever or discomfort

signs of a serious allergic reaction (e. g. abdominal cramps, difficulty breathing, nausea and vomiting, or swelling of the face and throat)

signs of very low blood sugar (e. g. convulsions or seizures, loss of consciousness)

Some people may experience side effects other than those listed. Check with your doctor if you notice any symptom that worries you while you are taking this medication.

Before you begin taking a medication, be sure to inform your doctor of any medical conditions or allergies you may have, any medications you are taking, whether you are pregnant or breast-feeding, and any other significant facts about your health. These factors may affect how you should use this medication.

Allergy: Some people who are allergic to sulfonamide antibiotics or other similar diabetes medications also experience allergic reactions to glimepiride. Before you take glimepiride inform your doctor about any previous adverse reactions you have had to medications, especially to antibiotics or other diabetes medications. Contact your doctor at once if you experience signs of an allergic reaction, such as skin rash, itching, difficulty breathing or swelling of the face and throat.

Drowsiness/reduced alertness: Due to the effect of glimepiride on blood sugar, it may affect the mental or physical abilities needed to drive or operate machinery. Avoid driving, operating machinery, or performing other hazardous tasks until you have determined how this medication affects you.

Hypoglycemia (low blood sugar): Hypoglycemia is a condition in which blood sugar levels are abnormally low. Symptoms of hypoglycemia include:

dizziness

drowsiness

headache

lack of energy

nervousness

numbness or tingling of the mouth

shakiness

sweating

weakness

People with more severe hypoglycemia can experience blurred vision, confusion, and an inability to concentrate. If left untreated, severe hypoglycemia can lead to convulsions (seizures) and unconsciousness within minutes. People who are more likely to become hypoglycemic include seniors, people with reduced liver or kidney function, people who are malnourished, or people taking beta-blockers or other medications that lower blood sugar. Low blood sugar is more likely to occur when food intake is inadequate, or after strenuous or prolonged physical exercise. Blood sugar should be monitored regularly and an emergency source of sugar (e. g. a sugar packet, orange juice, or hard candy) and glucagon kit should be made available in case the need arises to increase blood sugar levels.

Loss of blood sugar control: People on glimepiride may experience loss of blood sugar control during illness or stressful situations such as fever, infection, trauma, or surgery. Under these conditions, your doctor may consider stopping the medication and prescribing insulin until your blood sugar is controlled and within target levels. For some people, their doctor may prescribe insulin or metformin in combination with glimepiride to control blood sugar.

Proper diet: Glimepiride is a treatment to be used in combination with a proper diet. Glimepiride is not as a substitute for a proper diet.

Worsening of condition: Over time, glimepiride may become less effective because of the worsening of diabetes. Talk to your doctor if glimepiride no longer controls your blood glucose to target levels. Your doctor may ask you to stop this medication, or continue this medication and take an additional antidiabetic medication to help control your blood sugar.

Pregnancy: This medication should not be used during pregnancy. If you become pregnant while taking this medication, contact your doctor immediately.

Breast-feeding: It is not known if glimepiride passes into breast milk. If you are a breast-feeding mother and are taking this medication, it may affect your baby. Talk to your doctor about whether you should continue breast-feeding.

Children: The safety and effectiveness of using this medication have not been established for children.

Seniors: The side effects of this medication may be more noticeable in seniors. People who are over 65 years old should discuss with their doctor how this medication may affect them and whether any special monitoring is needed.

There may be an interaction between glimepiride and any of the following:

acetylsalicylic acid (ASA)

alcohol

amiodarone

anabolic steroids

angiotensin receptor blockers (ARBs; e. g. candasartan, irbesartan, losartan)

aprepitant

"azole" antifungals (e. g. itraconazole, ketoconazole, voriconazole)

barbiturates (e. g. phenobarbital, secobarbital)

beta-blockers (e. g. atenolol, metoprolol)

bosentan

buserelin

carbamazepine

capecitabine

chloramphenicol

clarithromycin

clonidine

inhaled corticosteroids (e. g. budesonide, ciclesonide, fluticasone)

oral corticosteroids (e. g. dexamethasone, hydrocortisone, prednisone)

corticosteroids (e. g. budesonide, hydrocortisone, prednisone)

cyclophosphamide

cyclosporine

dabrafenib

other diabetes medications (e. g. chlorpropamide, glipizide, glyburide, insulin, metformin, nateglinide, rosiglitazone)

diazoxide

disopyramide

diuretics (e. g. furosemide, hydrochlorothiazide, acetazolamide)

epinephrine

estrogens (e. g. conjugated estrogens)

fibrates (e. g. fenofibrate, gemfibrozil)

fluorouracil

fluvastatin

glucagon

goserelin

guanethidine

H2-receptor antagonists (e. g. ranitidine)

HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs; e. g. delaviridine, efavirenz, etravirine, nevirapine)

laxatives (after prolonged use)

leflunomide

monoamine oxidase inhibitors (MAOIs; e. g. moclobemide, phenelzine, rasagiline, selegiline, tranylcypromine)

milk thistle

nilotinib

nonsteroidal anti-inflammatory drugs (e. g. ibuprofen, naproxen)

omeprazole

peginterferon Alfa-2b

phenytoin

phenothiazines (e. g. chlorpromazine)

phenylbutazone

porfimer

primidone

probenecid

progestogens (e. g. medroxyprogesterone)

propranolol

pyrimethamine

quinine

quinolone antibiotics (e. g. ciprofloxacin, norfloxacin, ofloxacin)

reserpine

rifampin

salicylates (e. g. ASA, salsalate)

selective serotonin reuptake inhibitors (SSRIs; e. g. citalopram, duloxetine, fluoxetine, paroxetine, sertraline)

somatropin

sorafenib

sulfonamides (e. g.,sulfadiazine, sulfamethoxazole, sulfasoxazole)

sympathometics (cough, cold or allergy medication)

testosterone

tetracyclines (e. g. tetracycline, minocycline)

thyroid hormones (e. g. levothyroxine)

ticagrelor

tolbutamide

tricyclic antidepressasnts (e. g. amitriptyline, clomipramine, desipramine, trimipramine)

trimethoprim

warfarin

zafirlukast

If you are taking any of these medications, speak with your doctor or pharmacist. Depending on your specific circumstances, your doctor may want you to:

stop taking one of the medications,

change one of the medications to another,

change how you are taking one or both of the medications, or

leave everything as is.

An interaction between two medications does not always mean that you must stop taking one of them. Speak to your doctor about how any drug interactions are being managed or should be managed.

Medications other than those listed above may interact with this medication. Tell your doctor or prescriber about all prescription, over-the-counter (non-prescription), and herbal medications that you are taking. Also tell them about any supplements you take. Since caffeine, alcohol, the nicotine from cigarettes, or street drugs can affect the action of many medications, you should let your prescriber know if you use them.

All material © 1996-2016 MediResource Inc. Terms and conditions of use. The contents herein are for informational purposes only. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.

Docusol, Docusol

Docusol

docusate sodium

Apo-Docusate Sodium (CA), Colace, Correctol, Correctol Stool Softener (CA), Diocto, Dioctyl (UK), Docusol (UK), Dom-Docusate Sodium (CA), D. O.S. Softgels, Docu-Soft, DOK, D-S-S, DulcoEase (UK), Dulcolax Stool Softener, Enemeez, Genasoft Softgels, Norgalax (UK), Novo Docusate (CA), PHL-Docusate Sodium (CA), PMS-Docusate Sodium, Ratio-Docusate Sodium (CA), Selax (CA), Silace

Pharmacologic class: Emollient

Therapeutic class: Stool softener, surfactant

Pregnancy risk category C

Action

Increases absorption of liquid into stool, resulting in softening of fecal mass. Also promotes electrolyte and water secretion into colon.

Availability

Capsules: 240 mg

Capsules (soft gels ): 240 mg

Rectal solution: 283 mg/5 ml

Capsules: 50 mg, 100 mg, 250 mg

Capsules (soft gels ): 100 mg, 250 mg

Liquid: 150 mg/15 ml

Syrup: 50 mg/15 ml, 60 mg/15 ml, 20 mg/5 ml, 100 mg/30 ml, 150 mg/15 ml

⊘ Indications and dosages

➣ Stool softener

Adults and children older than age 12: 240 mg (docusate calcium) or 50 to 200 mg (docusate sodium) P. O. daily until bowel movements are normal

Children ages 6 to 12: 40 to 120 mg (docusate sodium) P. O. daily

Children ages 3 to 6: 20 to 60 mg (docusate sodium) P. O. daily

Contraindications

• Hypersensitivity to drug • Abdominal pain, nausea, or vomiting • Intestinal obstruction

Precautions

Use cautiously in: • pregnant or breastfeeding patients.

Administration

• Give tablets and capsules with full glass of water. • Give liquid solution with milk or fruit juice. • Be aware that excessive or long-term use may lead to laxative dependence.

Adverse reactions

EENT: throat irritation

GI: nausea, diarrhea, mild cramps

Other: bitter taste, decreased appetite, laxative dependence

Interactions

Drug-drug. Mineral oil: increased mineral oil absorption, causing toxicity

Warfarin: decreased warfarin effects (with high doses)

Patient monitoring

• If diarrhea occurs, withhold drug and notify prescriber. • Know that therapeutic efficacy usually becomes apparent 1 to 3 days after first dose.

Patient teaching

• Instruct patient to drink sufficient fluids with each dose and to increase fluid intake during the day. • Advise patient to prevent constipation by increasing fluids and consuming more dietary fiber (as in fruits and bran). • Inform patient that excessive or prolonged use may lead to laxative dependence. • As appropriate, review all other significant adverse reactions and interactions, especially those related to the drugs mentioned above.

Docusol

Link to this page:

Flutamide Indications, Side Effects, Warnings, Flutaide

Flutamide

Generic Name: flutamide (FLEW-tuh-mide) Brand Name: Generic only. No brands available.

Flutamide may cause serious, even life-threatening, liver problems. Tell your doctor if you have a history of liver disease. Notify your doctor immediately if you develop nausea, vomiting, stomach pain, loss of appetite, fever, yellowing eyes or skin, dark urine, or unusual fatigue. Laboratory tests (eg, liver function tests) should be performed before and during use of flutamide. Your doctor will be monitoring your treatment closely.

Flutamide is used for:

Treating prostate cancer, along with other medicines. Flutamide is not intended for use in women.

Flutamide is an anti-androgen. It works by interfering with antigen activity in the prostate, which stops tumor growth and allows the tumor to shrink.

Do NOT use flutamide if:

you are allergic to any ingredient in flutamide

you are female

you have severe liver disease

Contact your doctor or health care provider right away if any of these apply to you.

Before using flutamide:

Some medical conditions may interact with flutamide. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have blood or blood sugar problems, liver problems, or you smoke

Some MEDICINES MAY INTERACT with flutamide. Tell your health care provider if you are taking any other medicines, especially any of the following:

Blood thinners (eg, warfarin) because the actions and side effects may be increased by flutamide

This may not be a complete list of all interactions that may occur. Ask your health care provider if flutamide may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use flutamide:

Use flutamide as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Flutamide may be taken with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

Take flutamide with a full glass of water (8 oz/240 mL).

Flutamide comes with an additional patient leaflet. Read it carefully and reread it each time you get flutamide refilled.

If you miss a dose of flutamide, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use flutamide.

Important safety information:

Flutamide may cause diarrhea. Do not use laxatives while using flutamide, unless directed by your doctor. If diarrhea occurs, ask your doctor or pharmacist to recommend a treatment for you.

LAB TESTS, such as liver function tests, may be required to monitor treatment or to check for side effects. Be sure to keep all doctor and lab appointments.

Flutamide is not recommended for use in CHILDREN; safety and effectiveness have not been confirmed.

PREGNANCY and BREAST-FEEDING: Flutamide is not recommended for use in women.

Possible side effects of flutamide:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Blood in the urine; breast growth; decreased sex drive or ability; diarrhea; hot flashes; inflamed prostate; nausea; rash; rectal bleeding; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); brown urine; flu-like symptoms; impotence; loss of appetite; muscle aches or soreness; nausea; severe diarrhea; stomach pain/tenderness; unusual tiredness; vomiting; yellowing of skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately. Symptoms may include decreased activity; goose bumps; loss of appetite; slow breathing; tearing; trouble walking; vomiting.

Proper storage of flutamide:

Store flutamide at room temperature, 59 to 86 degrees F (15 to 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep flutamide out of the reach of children and away from pets.

General information:

If you have any questions about flutamide, please talk with your doctor, pharmacist, or other health care provider.

Flutamide is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take flutamide or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about flutamide. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to flutamide. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using flutamide.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about flutamide

Calan Sr (Verapamil Oral) Medical Facts From, Isoptina Sr

Calan SR

antifungal medication--itraconazole, ketoconazole, posaconazole, voriconazole;

cholesterol lowering medicines called "statins"--atorvastatin, fluvastatin, lovastatin, pitavastatin, pravastatin, rosuvastatin, simvastatin;

heart medication--nicardipine, quinidine;

hepatitis C medications--boceprevir, telaprevir;

HIV/AIDS medication--atazanavir, delavirdine, efavirenz, fosamprenavir, indinavir, nelfinavir, nevirapine, ritonavir, saquinavir;

seizure medication--carbamazepine, fosphenytoin, oxcarbazepine, phenobarbital, phenytoin, primidone; or

tuberculosis medication--isoniazid, rifabutin, rifampin, rifapentine.

This list is not complete and many other drugs can interact with verapamil. This includes prescription and over-the-counter medicines, vitamins, and herbal products. Give a list of all your medicines to any healthcare provider who treats you.

More about Calan SR (verapamil)

Consumer resources

Professional resources

Other formulations

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about verapamil.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2012 Cerner Multum, Inc. Version: 13.01. Revision Date: 2013-06-13, 10:21:08 AM.

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Cpap Community - View Topic - Re-Ponaris Nasal Emollient, Ponaris

I bought a bottle yesterday at Walgreen's-anybody want it? Didn't work for me at all. Made my nasal passages cooler and moisturized, but it made me so sick at my stomach, I was wrenching and hurling all night. It drained down the back of my throat into my stomach. Wow. can still taste that nasty oil. Did not open up my nose at all-was still stuffed up. By the way--$15.99 plus tax was cost. Hope it was cheaper at the other pharmacy!

Additional Comments: HC100 HH. Activa Orig. (w/Activa LT cushion), Activa LT, Pur Sleep, Pad A Cheeks,

Started using cpap Sept. 12, 2007 Respironics PR System One Bi-Pap Auto w/Flex, pressure of 9/15, do not use ramp

by Guest on Wed Dec 19, 2007 8:36 pm

Joyce are you allergic to most cough suppressant that contain eucalyptus/menthol oils that are usually found in most cough suppressant? Some people do have trouble with these type of oils. For me the oil had a soothing effect on my sinuous and throat. The taste was similar to the Halls Plus cough suppressants that I take when I have a cold. My cost was $13.00 plus tax, a little cheaper here. Sorry you had a bad reaction to the oils.

Anonymous wrote: Joyce are you allergic to most cough suppressant that contain eucalyptus/menthol oils that are usually found in most cough suppressant? Some people do have trouble with these type of oils. For me the oil had a soothing effect on my sinuous and throat. The taste was similar to the Halls Plus cough suppressants that I take when I have a cold. My cost was $13.00 plus tax, a little cheaper here. Sorry you had a bad reaction to the oils.

Actually no, I have taken most all cough medicines, I have suffered with bronchitis most all my life. When I read the post on here last week I think, not sure, anyway, got me curious. Since I am trying to get away from nasal sprays, I thought that would be the trick! But it just didnt work for me. Was soothing, but that was about all. Sure glad you got a better price! I nearly flipped when she told me $16 plus!

Additional Comments: HC100 HH. Activa Orig. (w/Activa LT cushion), Activa LT, Pur Sleep, Pad A Cheeks,

Started using cpap Sept. 12, 2007 Respironics PR System One Bi-Pap Auto w/Flex, pressure of 9/15, do not use ramp

Forgot to log in, Joyce I forgot to ask if you tried Ayr-gel that is a nasal gel that can be applied with a cotton swap inside the nostrils, to help keep them moisturized? It's cheaper and there is no problem with it going down your throat, no nasty taste.

Celebrate It™ Occasions™ Tulle With Glitter, Glitter-M

Celebrate It™ Occasions™ Tulle with Glitter

Rated 4.1 out of 5 by 23 reviewers.

Rated 5 out of 5 by Snowee55 Excellent product for crafting This item was perfect for making my daughter a tutu for her upcoming birthday. And so many wonderful colors to choose from! September 7, 2016

Rated 5 out of 5 by Empress Made a great tutu. My 11 year old granddaughter wanted to make a tutu to wear to a concert. She had seen one on You Tube made with a mesh headband and strips of tulle. She and the friend she was going with wanted hot pink and neon green. The pink was available at my local Michaels, but I had to drive to a store 50 miles away to get the green. (To order on line required a minimum of six rolls, which would have been stupid.) Once she had the tulle, my granddaughter worked diligently and the tutu was really cute. August 13, 2016

Rated 4 out of 5 by JamieJ Pretty, but glitter mess I used this to created a sign for my daughters 2nd bday by wrapping a cut out of the number two in the tulle. Only negative was with every manipulation or folding of the tulle TONS of glitter fell off. There was still plenty on the finished sign and I would use this again, I just had to vacuum my floor and couch a few times to clean it all up, and I still find random bits on my kid and dog, lol. August 3, 2016

Rated 5 out of 5 by esullivan glittery tulle shines Tulle can sometimes be dull, but having glitter on tulle makes it eye catching. Love the shine. July 16, 2016

Rated 5 out of 5 by FashionMom Sparkle Great item. Works great and has multiple uses. Beware of the glitter it will get everywhere June 29, 2016

Rated 1 out of 5 by Sunshine This product was very messy I wanted a glittery tutu but I thought the glitter wasn't going to come off. It was such a hassle putting my tutu together. The glitter was falling off everywhere. The finish product looked pretty but I would try and avoid glitter tutu next time. June 27, 2016

Rated 5 out of 5 by Tanna86 Love the color Great tulle plus it was buy 1 get 1 so it was even better. Made great tulle balls for party decorations. June 4, 2016

Rated 5 out of 5 by Gallegos10 Tulle I've bought over 15 and the tulle is not thin like other places sell. I can even sew it an it still holds up May 19, 2016

2016-09-18 T07:39:44.374-05:00

bvseo_lps, prod_bvrr, vn_prr_5.6

cp-1, bvpage1

co_hasreviews, tv_23, tr_23

loc_en_US, sid_M10217906, prod, sort_default

Simple Uv Spectrophotometric Assay Of Clarithromycin, Klaribact

Simple UV spectrophotometric assay of Clarithromycin

Clarithromycin belongs to semi-synthetic macrolide antibiotic class of drugs that inhibits bacterial protein synthesis. Our aim of study is to develop a efficient least time consuming and simple spectrophotometric method for the assay of clarithromycin. Comparision of assay of five different brands of clarithromycin (klaricid, klaribact, rithmo, clariteck, E-clark) available in public medical store of Karachi, Pakistan has also been done. The assay is based on the ultraviolet UV absorbance maxima at about 210nm wavelength of mefenamic acid, water is used as solvent. A sample of drug was dissolved in water to produce a solution containing mefenamic acid. Similarly, a sample of ground tablets of different brand were dissolved in water and various dilutions were made. The absorbance of sample preparation was measured at 210nm against the solvent blank and the assay was determined by comparing with the absorbance of available brand. Our results reveals that among all the five brands of clarithromycin (klaricid, klaribact, rithmo, clariteck, E-clark) Klaribact shows highest percentage assay i. e 115.3846%. Klaricid and Claritecl shows percentage assay of 107.693%. Rithmo shows a percent assay of 92.307% while E-clark shows lowest value for percentage assay 84.6153%.Keywords — clarithromycin, assay, UV spectrophotometry INTRODUCTION Clarithromycin is a semi-synthetic macrolide antibiotic. It is bacterial protein synthesis inhibitor. It is better absorbed and acid-stable. It is widely used in regimens of anti-helicobacter pylori (h pylori). The sustained-release (sr) and immediate-release (ir) clarithromycin formulations available on the market. [1] It decreases activity of CYP3A4 enzyme and thus slowly inhibits of coadministered drugs and its own metabolism. Clarithromycin is a broad-spectrum antibiotic and it is widely used for the treatment of upper and lower respiratory tract and many other infections.[2] It interacts with many drugs on the level of CYP3A hepatic and intestinal metabolizing enzymes.[3]Clarithromycin is rapidly and completely absorbed from the gastrointestinal tract (GI). As chlarithromycin undergoese first-pass metabolism, bioavalibility of an oral dose as clarithromycin is fifty% to fifty five% in the systemic circulation. It is widely distributed throughout the body and has an apparent volume of distribution that ranges from 126 to 306 liters. Approximately 22% of an oral dose is recovered as the parent compound, 4% being recovered in the feces with 18% being recovered in the urine. The elimination half-life of clarithromycin is time and dose dependent and ranges from 2.7 to 4.8 hours. The average total body clearance ranges is found to be from 29 to 58 liters/hour and the average renal clearance ranges from 6.7 to 12.8 liters/hours in healthy subjects depending on the the number of doses and dose .[4] clarithromycin has been associated with fetal loss in animals. A study shows a doubling in the frequency of miscarriages among pregnant women using clarithromycin.[5] Clarithromycin acts by binding to the peptidyl transferase region of 23S rRNA and inhibits bacterial protein synthesis. Clarithromycin resistance results from structural changes in the 23S rRNA molecule caused by mutation of the 23S rRNA gene. Transitions of Adenine to guanine at positions 2142 and 2143 are the main 23S rRNA mutations in clarithromycin-resistant isolates[6]. We have already done these types of assay for different drugs [7-10].

Do you want to read the rest of this article.

[Show abstract] [Hide abstract] ABSTRACT: To evaluate the patterns of use of clarithromycin for gastrointestinal disease treatment and promote its rational use. Using a structured pro forma, we conducted a two-month survey of the electronic prescriptions containing immediate-release (IR) or sustained-release (SR) product of clarithromycin for outpatients with gastrointestinal diseases in a 2200-bed general hospital. Suitability of the prescription was audited retrospectively. One hundred and sixty-four prescriptions of SR product and 110 prescriptions of IR product were prescribed for gastrointestinal disease treatment. Among prescriptions for anti-Helicobacter pylori (H pylori) therapy, triple therapy take the dominant position (91.8%), followed by quadruple therapy (4.3%) and dual therapy (3.9%). Amoxicillin was the most frequently co-prescribed antibiotic. Furazolidone and levofloxacin are used more widely than metronidazole or tinidazole. Clarithromycin SR was administered at inappropriate time points in all prescriptions. Fifty percent of all prescriptions of clarithromycin SR, and 6.4% of prescriptions of clarithromycin IR, were prescribed at inappropriate dosing intervals. Surprisingly, disconcordance between diagnoses and indications was observed in all prescriptions of clarithromycin SR which has not been approved for treating H pylori infection although off-label use for this purpose was reported in literature. On the contrary, only one prescription (0.9%) of clarithromycin IR was prescribed for unapproved indication (i. e. gastro-oesophageal reflux disease). 1.4% of prescriptions for chronic gastritis or peptic ulcer treatment were irrational in that clarithromycin was not co-prescribed with gastric acid inhibitors. Clinical significant CYP3A based drug interactions with clarithromycin were identified. There is a great scope to improve the quality of clarithromycin prescribing in patients with gastrointestinal disease, especially with regard to administration schedule, concordance between indications and diagnoses and management of drug interactions.

Article · Nov 2008

[Show abstract] [Hide abstract] ABSTRACT: The in vitro and in vivo antibacterial activity of A-56268 (TE-031), the 6-O-methyl derivative of erythromycin, was compared with those of erythromycin and other reference drugs. A-56268 had the same spectrum of antibacterial activity as erythromycin. A-56268 was generally 1 log2 dilution more potent or equal to erythromycin against all organisms except haemophilus influenzae and Propionibacterium acnes, for which A-56268 was 1 log2 dilution and 3 log2 dilutions, respectively, less potent. The MBC of A-56268 and erythromycin was not significantly different from the MIC against Streptococcus pyogenes, Streptococcus pneumoniae, Staphylococcus epidermidis, and H. influenzae but was more than 2 log2 dilutions higher than the MICs for some Staphylococcus aureus strains. Human serum at a concentration of 50% did not change the in vitro potency of A-56268 or erythromycin. A-56268 was similar to erythromycin in being more active at pH 8.0 than at the physiologic pH of 7.3. The activity of A-56268 was synergistic with sulfamethoxazole against 4 of 12 strains of H. influenzae. In mouse protection tests, when administered orally A-56268 was more potent than erythromycin against H. influenzae, S. pyogenes, S. pneumoniae, and S. aureus. After subcutaneous administration the potencies of A-56268 and erythromycin were not statistically different from each other. A-56268 was more potent than erythromycin against Legionella infection in guinea pigs. The concentration of A-56268 in the serum and lung was higher than that of erythromycin after intraperitoneal administration. In A-56268 in the serum and lung was higher than that of erythromycin after intraperitoneal administration. In mice, the peak levels in serum of A-56268 and erythromycin were similar after subcutaneous administration and seven times higher for A-56268 after oral administration. The serum half-life of A-56268 was approximately twice that of erythromycin after administration by both routes.

Article · Jan 1987

[Show abstract] [Hide abstract] ABSTRACT: Objective To assess the relative contribution of intestinal and hepatic CYP3A inhibition to the interaction between the prototypic CYP3A substrates midazolam and clarithromycin. Methods On day 1, 16 volunteers (eight men and eight women; age range, 20 to 40 years; weight range, 45 to 100 kg) received simultaneous doses of midazolam intravenously (0.05 mg/kg over 30 minutes) and orally (4 mg of a stable isotope, 15N3-midazolam). Starting on day 2, 500 mg clarithromycin was administered orally twice daily for 7 days. On day 8, intravenous and oral doses of midazolam were administered 2 hours after the final clarithromycin dose. Blood and urine samples were assayed for midazolam, 15N3-midazolam, and metabolites by gas chromatography-mass spectrometry. ResultsThere was no significant (p > 0.05) difference in the urinary excretion of 1?-hydroxymidazolam after intravenous and oral dosing on day 1 or day 8, indicating that the oral dose was completely absorbed into the gut wall. The oral clearance of midazolam was found to be significantly greater in female subjects (1.9 ± 1.0 versus 1.0 ± 0.3 L/hr/kg; p < 0.05) than in male subjects but not systemic clearance (0.35 ± 0.1 versus 0.44 ± 0.1 L/hr/kg). For women not receiving oral contraceptives (n = 6) a significant gender-related difference was observed for systemic and oral clearance and for area under the curve and elimination half-life after oral administration. A significant (p < 0.05) reduction in the systemic clearance of midazolam from 28 ± 9 L/hr to 10 ± 3 L/hr occurred after clarithromycin administration. Oral midazolam availability was significantly increased from 0.31 ± 0.1 to 0.75 +- 0.2 after clarithromycin dosing. Likewise, intestinal and oral availability were significantly increased from 0.42 ± 0.2 to 0.83 ± 0.2 and from 0.74 ± 0.1 to 0.90 ± 0.04, respectively. A significant correlation was observed between intestinal and oral availability (n = 32, r = 0.98, p < 0.05). After clarithromycin administration, a significant correlation was observed between the initial hepatic or intestinal availability and the relative increase in hepatic or intestinal availability, respectively. Female subjects exhibited a greater extent of interaction after oral and intravenous dosing than male subjects (p < 0.05).Conclusion These data indicate that in addition to the liver, the intestine is a major site of the interaction between oral midazolam and clarithromycin. Interindividual variability in first-pass extraction of high-affinity CYP3A substrates such as midazolam is primarily a function of intestinal enzyme activity. Clinical Pharmacology & Therapeutics (1998) 64, 133-143; doi:

Article · Aug 1998

Kop Avedox-Fc (Ventolin) Utan Recept, Avedox-Fc

Kopa Avedox-fc (Ventolin) Natet Utan Recept

Avedox-fc (Ventolin) Forklaring

Avedox-fc ar en kategori av lakemedel kallas bronkdilaterare. Avedox-fc ar faktiskt papekas for lindring samt undvikande i samband med luftpassage blockering (bronkospasm) inom de drabbade tillsammans med andningssvarigheter och lider tillsammans med anstrangningsutlosta andningsbesvar. Avedox-fc kan ocksa anvandas for de drabbade tillsammans med emfysem samt ihallande bronkit nar deras egna tecken och symtom tenderar att vara forknippade med alterluftpassagen blockering.

Albuterol, ar den faktiska aktiva komponenten i Avedox-fc verkligen en krasen betaadrenerg bronkdilaterare anvands for att hantera allvarliga allvarliga andningssvarigheter samt ihallande bronkospasm vackt den av nagra andra lung obstruktiva problem som inte riktigt tas om hand omedelbart andra stilar i samband med behandling.

Allmanna varumarken som forknippas med Avedox-fc tenderar att vara Albuterol, Salbutamol.

Avedox-fc kan ocksa kallas Albuterol, Salbutamol, Ventorlin, Asthalin, Proventil, ProAir, Salamol, Aerolin.

Avedox-fc (Ventolin) Dose

Avedox-fc kommer in:

2 mg lagre dos friktionsmaterial

4 mg Regular Dos friktionsmaterial

Den faktiska instruktioner nar det galler att anvanda denna medicinering tillhandahalls av din lakare. Utnyttja Avedox-fc precis som riktar sig.

Utnyttja detta lakemedel oralt eftersom syftar fran din lakare.

Vanligtvis inte slipa eller ens tugga upp detta. Konsumera p-piller hela. Mosa eller ens knapra Avedox-fc kommer sakert forneka sjalva skjutit upp lanseringen systemet fran medicinen.

-Den normala effektiv dosering ar faktiskt 4 mg, 3 eller 4 ganger per dag. friktionsmaterial

-Om tillracklig bronkdilatation inte riktigt forvarvas, kan alla ensamma dosering forbattras langsamt upp till 8 mg. friktionsmaterial

-Vissa drabbade forvarva tillracklig lindring tillsammans med tva milligram 3 eller 4 ganger varje dag. friktionsmaterial

2-6 manga ar: Den faktiska minimala borjan dosen ar faktiskt 1 mg 3 ganger dagligen. Detta skulle kunna forbattras for att 2 mg (1 tablett), 3 eller 4 ganger varje day. A friktionsmaterial

sex - mer an ett decennium: Den faktiska minimala borjan dosen ar faktiskt 2 mg 3 ganger dagligen. Detta skulle kunna forbattras for att 4 ganger varje day. A friktionsmaterial

Fler an mer an ett decennium: Den faktiska minimala borjan dosen ar faktiskt 2 mg 3 ganger dagligen. Detta skulle kunna forbattras for att 4 mg (2 tabletter), 3 eller 4 ganger varje day. A friktionsmaterial

Inom seniorer sjuka eller till och med inom alla de som anses vara generellt kansliga for att beta-adrenerga stimulerande lakemedel, bor du borja behandlingen tillsammans med tva milligram salbutamol 3 eller 4 ganger varje dag. friktionsmaterial

Avedox-fc (Ventolin) I brist forknippas med dosering

Vanligtvis far inte dubbel dos. Om du hoppar over dosen du behover for att bara den nar du kom ihag nar det galler din saknas. Nar det ar dags for dosering du behover bara pa din egen normal dosering rutin.

Avedox-fc (Ventolin) Overdosering

Om du overdoserar Avedox-fc och du undviker ocksa stor att du behover kolla din lakare eller ens lakare omedelbart.

Avedox-fc (Ventolin) Lagringsutrymme

Shoppa i ett utrymme temperaturer som inte riktigt gar over trettio nivaer D (86 nivaer F) fran fukt, belysning samt temperatur. Starka sjalva efter utgangen dagen. Behall fran uppna barnen.

Avedox-fc (Ventolin) Negativa effekter

Avedox-fc erbjuder de negativa effekterna. Den mest typiska tenderar att vara:

huvudvark friktionsmaterial

skakningar, vanligtvis fran fingrarna (tremor) friktionsmaterial

orolig tryckfriktionsmaterial

forstaelse for dina egna hjartslag (hjartklappning) friktionsmaterial

muskelmassa kramper friktionsmaterial

lagre blodomloppet kaliumgrad (hypokalemi) friktionsmaterial

Mycket mindre typiska och allvarliga negativa effekter i hela anvander Avedox-fc:

allergiska reaktion reaktioner (hudutslag, nasselutslag, klada, svart att andas in och andas, tryck over brostet, inflammation fran munnen omrade, mote, lapparna, eller till och med spraket, for mycket klada, yrsel) friktionsmaterial

hjartproblem friktionsmaterial

onormal hjartrytm friktionsmaterial

ovantade Forsamrade samband med inandning och utandning problem / astma (paradoxal bronkospasm) friktionsmaterial

Negativa effekter tyder forlitar pa medicin du kanske anvander men dessutom lita pa ditt valbefinnande villkor och en annan aspekter.

Avedox-fc (Ventolin) Kontraindikationer

Vanligtvis inte far Avedox-fc om du ar kanslig for att Avedox-fc element.

Det ar langt ifran erkand huruvida Avedox-fc sakert kommer att skada en bra vaxande foster. Vanligtvis anvander sig inte av detta lakemedel utan att ha en egen lakares vagledning om du vantar eller ens amning.

Var forsiktig tillsammans med Avedox-fc for dem som har diabetes, hjartproblem, hogt blodtryck (hypertoni), hypertyreos, ar battre an (arytmier) onormala hjart.

Avedox-fc kan gora en person yrsel. Vanligtvis inte genererar, anvander utrustning, eller ens ga atgard som behover uppmarksamhet om du tenderar att vara saker pa att du har mojlighet att utfora den har typen av atgarder ordentligt.

Vanligtvis inte sluta behandlingen, ser kanslan mycket battre, om inte naturligtvis din lakare later dig veta for att. Det kan ta natter eller ens langre innan du bestammer dig for att ha full kontroll over den verkliga medicinen.

Forhindra alkoholhaltiga drycker.

Vanligtvis inte sluta anvanda Avedox-fc plotsligt.

Avedox-fc (Ventolin) Vanliga fragor

Queen: Vad exakt ar Avedox-fc?

Avedox-fc ar verkligen en hog effektiv medicin som pekas ut for lindring samt undvikande i samband med luftpassage blockering (bronkospasm) inom de drabbade tillsammans med andningssvarigheter och lider tillsammans med anstrangningsutlost andning svarigheter. Avedox-fc kan ocksa anvandas for de drabbade tillsammans med emfysem samt ihallande bronkit nar deras egna tecken och symtom tenderar att vara forknippade med alterluftpassage blockage. A

Queen: Har de erbjuder en dart dos for barnen ?

Allt beror pa ditt barns aldersgrupp. 2-6 manga ar: Den faktiska minimala borjan dosen ar faktiskt 1 mg 3 ganger dagligen. Detta skulle kunna forbattras for att 2 mg (1 tablett), 3 eller 4 ganger varje dag. sex - mer an ett decennium: Den faktiska minimala borjan dosen ar faktiskt 2 mg 3 ganger dagligen. Detta skulle kunna forbattras for att 4 ganger varje dag. Mer an mer an ett decennium: Den faktiska minimala borjan dosen ar faktiskt 2 mg 3 ganger dagligen. Detta skulle kunna forbattras for att 4 mg (2 tabletter), 3 eller 4 ganger varje day. A

Queen: Exakt vad ska jag fag situationen i samband med saknar doseringen?

Vanligtvis blir inte dubbel dos. Om du hoppar over dosen du behover for att bara den nar du kom ihag nar det galler din saknas. Nar det ar dags for dosering du behover bara pa din egen normal dosering routine. A

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Halo Nation, Halo

Find out more about Halo Nation on the About page.

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Kromicin, Kromicin

Product Description Common use Zithromax is a semi-synthetic macrolide antibiotic chemically related to erythromycin which is effective against majority of species of gram positive and gram negative microorganisms such as genus Staphylococcus; S. aureus, S. pneumoiane, S. pyogenes, S. agalactiae, Haemophilus influenzae and parainfluenzae, Moraxela catarrhalis, Bacteroides fragilis, Escherichia coli, Bordetella ssp. Borrelia burgdorferi, Haemophilus ducreui, Nisseria gonorrhoeae Ø Chlamidia trachomati. In vitro it showed activity against Legionella pneumophila, Mycoplasma pneumoia Ø hominis, Helicobacter pylori, Toxoplasma gondii, Ureaplasma urealiticum. As a Macrolide antibiotic Zithromax inhibits bacterial protein synthesis and prevents bacteria from growth and propagation. It is used to treat infections of upper and low respiratory organs (tonsillitis, otitis, sinusitis, pneumonia), urogenital infections (urethritis, prostatitis, cervicitis, adnexitis caused by chlamydia, gonorrhea, early syphilis), intestinal infections, ulcer of stomach and duodenum.

Dosage and directions Take exactly as prescribed and do not discontinue your treatment even if you feel fine and your symptoms improved without your doctor's permission. Take Zithromax tablet with a big glass of water. To prepare a liquid suspension form one dose packet mix one packet with 2 ounces of water, shake and drink at once. Do not use the suspension which was prepared longer than 12 hours ago. Tablets and suspension can be taken with or without food while capsules should be taken on an empty stomach 2 hours before or after a meal.

Precautions There are no evidences if Zithromax affects an unborn baby or excretes in a breast milk. This medication should be used by pregnant and breastfeeding women only if expected benefit prevails over potential risk for the baby.

Hypersensitivity to Zithromax and related drugs such as azithromycin or erythromycin.

Possible side effect Among side effects may be diarrhea or loose stools, nausea, abdominal pain, and vomiting, uneven heartbeats, loss of appetite, dark urine, clay-colored stools, jaundice, fever, rash, red skin, headache. You should call your doctor and inform about such symptoms or get immediate medical attention.

Drug interaction Zithromax is not recommended to take with aluminum - or magnesium - based antacids, such as Mylanta or Maalox as they decrease its absorption in the intestine.

Missed dose Take the missed dose when you remember. If it is almost time of the next intake just skip it and return to your schedule.

Overdose Symptoms of overdose may appear as nausea, vomiting, diarrhea, and stomach discomfort. In this case look for immediate medical attention.

Storage Store at room temperature between 59-77 F (15-25 C) away from light and moisture, kids and pets. Do not store the liquid longer than 10 days.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Zithromax is a semi-synthetic macrolide antibiotic chemically related to erythromycin which is effective against majority of species of gram positive and gram negative microorganisms such as genus Staphylococcus; S. aureus, S. pneumoiane, S. pyogenes, S. agalactiae, Haemophilus influenzae and parainfluenzae, Moraxela catarrhalis, Bacteroides fragilis, Escherichia coli, Bordetella ssp. Borrelia burgdorferi, Haemophilus ducreui, Nisseria gonorrhoeae Ø Chlamidia trachomati. In vitro it showed activity against Legionella pneumophila, Mycoplasma pneumoia Ø hominis, Helicobacter pylori, Toxoplasma gondii, Ureaplasma urealiticum. As a Macrolide antibiotic Zithromax inhibits bacterial protein synthesis and prevents bacteria from growth and propagation. It is used to treat infections of upper and low respiratory organs (tonsillitis, otitis, sinusitis, pneumonia), urogenital infections (urethritis, prostatitis, cervicitis, adnexitis caused by chlamydia, gonorrhea, early syphilis), intestinal infections, ulcer of stomach and duodenum.

Dosage and directions Take exactly as prescribed and do not discontinue your treatment even if you feel fine and your symptoms improved without your doctor's permission. Take Zithromax tablet with a big glass of water. To prepare a liquid suspension form one dose packet mix one packet with 2 ounces of water, shake and drink at once. Do not use the suspension which was prepared longer than 12 hours ago. Tablets and suspension can be taken with or without food while capsules should be taken on an empty stomach 2 hours before or after a meal.

Precautions There are no evidences if Zithromax affects an unborn baby or excretes in a breast milk. This medication should be used by pregnant and breastfeeding women only if expected benefit prevails over potential risk for the baby.

Hypersensitivity to Zithromax and related drugs such as azithromycin or erythromycin.

Possible side effect Among side effects may be diarrhea or loose stools, nausea, abdominal pain, and vomiting, uneven heartbeats, loss of appetite, dark urine, clay-colored stools, jaundice, fever, rash, red skin, headache. You should call your doctor and inform about such symptoms or get immediate medical attention.

Drug interaction Zithromax is not recommended to take with aluminum - or magnesium - based antacids, such as Mylanta or Maalox as they decrease its absorption in the intestine.

Missed dose Take the missed dose when you remember. If it is almost time of the next intake just skip it and return to your schedule.

Overdose Symptoms of overdose may appear as nausea, vomiting, diarrhea, and stomach discomfort. In this case look for immediate medical attention.

Storage Store at room temperature between 59-77 F (15-25 C) away from light and moisture, kids and pets. Do not store the liquid longer than 10 days.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Dolofen

Eqv. To Diclofenac sodium BP 10mg

Rheumatoid arthritis, osteoarthritis, low back pain, Ankylosing Spondylitis, Acute musculoskeletal disorders such as peri-arthritis including frozen shoulder. Tendinitis, tenosynovitis, bursitis, Sprains and sislocation, painful post-operative conditions. Pain following dental surgery. Painful inflammatory conditions in Gynaecology and primary dysmenorrhoea, inflammatory disease of the eye.

Patients having active or recurrent peptic ulcer, Hypersensitivity to diclofenac sodium, Asthmatic patients in whom attacks of asthma are precipitated by aspirin or other NSAIDs, Pregnancy and Lactation.

Patients having a history of GI ulceration, haematemesis or malaena. Ulcerative colitis, Crohris disease. Cardiac and renal insufficiency, Elderly patients.

Epigastric pain, Nausea, Diarrhoea, Tiredness, Insomnia, Skin rash, Itching, Retention of fluid.

Increase blood levels of lithium and digoxin, inhibits diuretics but potentiates potassium sparing diuretics, Methotrexate toxicity enhanced.

Dolofen 100 SR 1 tablet daily after a meal

Dolofen 50 1 tablet 2-3 times daily after a meals

Dolofen Gel Gently rub on the skin over the painful and inflamed

Buy Rasoltan Losartan Online Without Prescriptions, Rasoltan

Cozaar is used for treating high blood pressure alone or with other medicines. It is used in certain patients to decrease the risk of stroke. It is used in certain patients to treat kidney problems caused by diabetes (diabetic nephropathy). Cozaar is an angiotensin II receptor blocker (ARB). It works by relaxing blood vessels. This helps to lower blood pressure.

Use Cozaar as directed by your doctor.

Take Cozaar by mouth with or without food.

Take Cozaar on a regular schedule to get the most benefit from it. Taking Cozaar at the same time each day will help you remember to take it.

Continue to take Cozaar even if you feel well. Do not miss any dose.

If you miss a dose of Cozaar, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Cozaar.

Store Cozaar at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Cozaar out of the reach of children and away from pets.

Active Ingredient: Losartan potassium.

Do NOT use Cozaar if:

you are allergic to any ingredient in Cozaar

you are in your second or third trimester of pregnancy

the patient is a child with severe kidney problems.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Cozaar. Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you are able to become pregnant

if you have a history of angioedema (swelling of the hands, face, lips, eyes, throat, or tongue; difficulty swallowing or breathing; or hoarseness), including angioedema caused by treatment with an angiotensin-converting enzyme (ACE) inhibitor (eg, lisinopril)

if you have a history of heart problems (eg, heart failure), blood vessel problems, blood flow problems, liver or kidney problems, or diabetes

if you have a history of stroke or recent heart attack

if you are dehydrated or have low blood volume

if you have electrolyte problems (eg, high blood potassium levels, low blood sodium levels) or are on a low-salt (sodium) diet

if you are on dialysis or are scheduled to have major surgery.

Some medicines may interact with Cozaar. Tell your health care provider if you are taking any other medicines, especially any of the following:

Diuretics (eg, furosemide, hydrochlorothiazide) because the risk of low blood pressure may be increased

Potassium-sparing diuretics (eg, spironolactone, triamterene) or potassium supplements because the risk of high blood potassium levels may be increased

Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen, indomethacin, celecoxib) or rifampin because they may decrease Cozaar's effectiveness

Lithium because the risk of its side effects may be increased by Cozaar.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cozaar may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Cozaar may cause dizziness, lightheadedness, or fainting. These effects may be worse if you take it with alcohol or certain medicines. Use Cozaar with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Cozaar may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

Cozaar may cause a serious side effect called angioedema. Contact your doctor at once if you develop swelling of the hands, face, lips, eyes throat, or tongue; difficulty swallowing or breathing; or hoarseness.

Cozaar may not work as well to reduce the risk of stroke in black patients. Discuss any questions or concerns with your doctor.

Dehydration, excessive sweating, vomiting, or diarrhea may increase the risk of low blood pressure. Contact your health care provider at once if any of these occur.

Check with your doctor before you use a salt substitute or a product that has potassium in it.

Tell your doctor or dentist that you take Cozaar before you receive any medical or dental care, emergency care, or surgery.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

If you have high blood pressure, do not use nonprescription products that contain stimulants. These products may include diet pills or cold medicines. Contact your doctor if you have any questions or concerns.

Diabetes patients - This may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Lab tests, including blood pressure, blood electrolyte levels, and heart, kidney, or liver function, may be performed while you use Cozaar. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Cozaar should not be used in children younger 6 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Cozaar may cause birth defects or fetal death if you take it while you are pregnant. If you think you may be pregnant, contact your doctor right away. It is not known if Cozaar is found in breast milk. Do not breastfeed while taking Cozaar.

Atovarol Cbg, Atovarol

ATOVAROL CBG C?psula blanda ATORVASTATINA

COMPOSICIÓN Cada CÁPSULA BLANDA contiene: Atorvastatina cálcica, equivalente a atorvastatina base 10 mg. Excipientes, c. s.p. Atorvastatina cálcica, equivalente a atorvastatina 20 mg. Excipientes, c. s.p.

INDICACIONES Tratamiento de la hiperlipidemia: Los inhibidores de la (3-hidroxi-3-metilglutaril) coenzima A (HMG-CoA) reductasa, como la atorvastatina, están indicados como adjunto a la dieta en el tratamiento de hipercolesterolemia primaria (heterocigoto familiar y no familiar) y dislipidemia mixta (hiperlipoproteinemia tipo IIa y IIb), causada por la elevada concentración de colesterol lipoproteínico de baja densidad (LDL-C) en pacientes con un riesgo significativo de enfermedad arterio-coronaria, solamente a quienes no responden a la dieta u otro régimen. Los inhibidores de la HMG-CoA reductasa (atorvastatina) también pueden ser usados en la reducción de las concentraciones elevadas de LDL-C en pacientes con hipercolesterolemia combinada con hipertrigliceridemia, y para la reducción de colesterol total, LDL-C, apolipoproteína B (Apo B), y triglicérido (TG) y el incremento de los níveles de HDL-C en pacientes con hipercolesterolemia combinada y dislipidemia mixta. Atorvastatina además, está indicada como un tratamiento adjunto con otros disminuidores de lípidos (por ejemplo LDL aféresis), en hipercolesterolemia homocigótica familiar para reducir el colesterol total (Total-C) y el LDL-C. Atorvastatina también está indicado para el tratamiento de disbetalipoproteinemia (hiperlipoproteinemia tipo III), en pacientes que no responden a una adecuada dieta. Atorvastatina está indicada adjunto a la dieta para el tratamiento de pacientes con elevados niveles séricos de triglicéridos (hiperlipoproteinemia tipo IV).

CONTRAINDICACIONES Las consideraciones médicas y/o contraindicaciones incluidas han sido seleccionadas sobre la base de su potencial significación clínica. Excepto bajo circunstancias especiales, esta medicación no debería ser usada cuando existan los siguientes problemas médicos: Enfermedad hepática activa. La relación riesgo-beneficio debe ser considerada cuando existan los siguientes problemas médicos: • Utilícese con precaución en pacientes con historia de consumo importante de alcohol. • Antecedentes de enfermedad hepática, elevación persistente de las transaminasas séricas (más de tres veces el límite normal superior). • Transplante de órgano con terapia inmunosupresora (incrementa el riesgo de rabdomiólisis y el deterioro renal). • Hipersensibilidad a sus componentes. • Condiciones serias de predisposición para el desarrollo del deterioro renal secundario a rabdomiólisis, tal como hipotensión, infección severa aguda, desórdenes endocrinos, electrolíticos o metabólicos severos, ataques no controlados, cirugía mayor, o trauma.

ACCIÓN FARMACOLÓGICA La forma activa de los inhibidores de la HMG-CoA reductasa (como la atorvastatina), el ácido beta-hidroxi; inhibe en forma competitiva la enzima HMG-CoA reductasa. Atorvastatina es administrada en forma activa (ácido abierto). La inhibición de HMG-CoA reductasa previene la conversión de HMG-CoA a mevalonato, el paso-límite en la biosíntesis del colesterol. El lugar primario de acción de atorvastatina es el hígado. La inhibición de síntesis de colesterol en el hígado conduce a una alta regulación de los receptores LDL y a un incremento en el catabolismo del colesterol LDL. Puede haber también alguna reducción en la producción de LDL como resultado de la inhibición de síntesis hepática de lipoproteína de muy baja densidad (VLDL), precursor de LDL. Los inhibidores de HMG-CoA reductasa (atorvastatina) reducen el colesterol LDL, colesterol VLDL, y en menor grado, concentraciones de triglicérido del plasma, y ligeramente el aumento de las concentraciones de lipoproteínas de alta densidad (HDL).

INTERACCIONES MEDICAMENTOSAS Las siguientes interacciones con drogas y/o problemas relacionados han sido seleccionadas sobre la base de su potencial significación clínica: Anticoagulantes cumarínicos o derivados de la indandiona: Concurrente uso de atorvastatina puede incrementar el tiempo de protrombina o sangría; el tiempo de protrombina debería ser monitorizado antes y durante el tratamiento, en pacientes que tienen terapia concurrente de atorvastatina con anticoagulantes. Sin embargo, cuando atorvastatina se administra con warfarina, el efecto del tiempo de protrombina no tiene efecto significativo. Colestiramina o colestipol: Su concurrente uso puede disminuir la biodisponibilidad de atorvastatina; por lo tanto cuando estos agentes son usados con atorvastatina para un beneficio terapéutico, es recomendable que atorvastatina se tome 2 a 4 horas después de colestiramina o colestipol. Antifúngicos azólicos, ciclosporina, gemfibrozilo u otros fibratos, inmunosupresores, antibióticos macrólidos, niacina: Concurrente uso con atorvastatina puede asociarse con un incremento en el riesgo de rabdomiólisis y deterioro renal agudo; aunque estos casos se han reportado solo con lovastatina. En terapia combinada de atorvastatina con gemfibrozilo, otros fibratos, niacina, o inmunosupresores, debería monitorizarse cuidadosamente los síntomas de miopatía o rabdomiólisis. Antiácidos: Su concurrente uso puede disminuir la concentración en plasma de atorvastatina en un 35% aproximadamente. Contraceptivos orales: Su concurrente uso con atorvastatina puede incrementar el valor de la concentración plasmática-tiempo del área bajo la curva (AUC) de noretindrona y etinil estradiol, en aproximadamente 30% y 20% respectivamente. Digoxina: La administración concurrente con atorvastatina puede incrementar la concentración plasmática. Jugo de toronja: El uso concurrente de grandes cantidades de jugo de toronja reporta un significativo incremento de atorvastatina a nivel sérico y en la concentración plasmática-tiempo del área bajo la curva (AUC). En un estudio de 12 pacientes a quienes se les administró doble concentración de jugo de toronja, 200 mL, tres veces al día, provocó una disminución aproximadamente del 24% de atorvastatina activa. Un incremento del AUC de atorvastatina activa fue en un 23%. El tiempo para Cmáx. (Tmáx.), se incrementó desde 1 hora a 4 horas. El jugo de toronja u otros productos de toronja en grandes dosis no deberían tomarse antes o después de la administración de atorvastatina.

PRECAUCIONES Carcinogenicidad: Un estudio de 2 años sobre carcinogenicidad en ratas a las que se les aplicó dosis de 10, 30, y 100 mg por kg de peso corporal (mg/kg) diario, halló 2 tumores poco comunes (rabdomiosarcoma y fibrosarcoma) con altas dosis en ratas hembras (concentraciones plasmáticas de la droga aproximadamente de 16 veces a la concentración de droga en el plasma humano luego de una dosis oral de 80 mg). La administración por 2 años de atorvastatina con dosis de 100, 200, o 400 mg/kg diarios en ratones (que producen 6 veces los valores en plasma, luego de una dosis oral de 80 mg en humanos), resultó en un incremento significativo, en machos, de adenomas de hígado y en hembras, de carcinomas de hígado. Embarazo y reproducción • Fertilidad: A dosis hasta de 175 mg/kg (15 veces la exposición en humanos) en ratas, no se observaron cambios en la fertilidad. Se encontraron casos de aplasia y aspermia en el epidídimo y bajo peso epididimal, a dosis de 100 mg/kg diarios (16 veces la exposición en humanos con dosis de 80 mg). A dosis de 30 y 100 mg/kg se observó disminución del peso testicular. En ratas machos que tomaron 100 mg/kg diarios por 11 semanas, previo al apareamiento, se observó: Disminución de la motilidad del espermatozoide, decrecimiento de la concentración de la cabeza del espermatozoide, y un incremento en el número de espermatozoides anormales. En perros que tomaron dosis de 10, 40, o 120 mg/kg por 2 años, no se hallaron efectos adversos sobre los parámetros seminales o histopatología en los órganos reproductivos. • Embarazo: No se ha establecido seguridad en el embarazo. Se han registrado casos raros de anormalidades congénitas seguidas de exposición intrauterina a los inhibidores de reductasa HMG-CoA. Los inhibidores de reductasa de HMG-CoA no se recomiendan durante el embarazo. Se debe llevar un intervalo de un mes desde la suspensión del tratamiento de atorvastatina hasta la concepción en caso de tener planeado el embarazo. Según FDA, categoría X. Lactancia: El uso de atorvastatina no es recomendado en lactancia, por el potencial de efectos adversos serios en el niño lactante. Se desconoce que atorvastatina se distribuya en la leche materna. En el plasma e hígado de rata lactante se encontró niveles de atorvastatina de 50% y 40%, respectivamente, comparado con los niveles de la leche materna. Pediátricas: Estudios apropiados relacionados a la edad no se han realizado en población pediátrica. Su seguridad y eficacia no han sido establecidas. Experiencias limitadas de uso de atorvastatina en jóvenes de 18 años de edad, parecen indicar que esta medicación es bien tolerada y puede ser usada en hipercolesterolemia severa pediátrica cuando sea necesaria. Sin embargo, la seguridad en el tratamiento largo con niños no ha sido estudiada. El uso de estos agentes terapéuticos en casos severos deberían estar bajo el cuidado de un especialista. Se recomienda precaución al usar agentes disminuidores de colesterol en niños de 10 años de edad. Geriátricas: Estudios realizados a la fecha en un número limitado de pacientes de 65 o más años de edad no demostraron problemas específicos que limiten la utilidad de atorvastatina en ancianos.

INCOMPATIBILIDADES: No se han reportado.

REACCIONES ADVERSAS Los siguientes efectos adversos han sido seleccionados sobre la base de su potencial significación clínica: Las siguientes reacciones adversas necesitan de atención médica: • Incidencias menos frecuentes o raras: Mialgia, miositis o rabdomiólisis (fiebre, dolor o calambre muscular, inusual cansancio o debilidad). Nota: Rabdomiólisis puede conducir a deterioro renal. Puede incrementarse la incidencia en pacientes que son tratados con inmunosupresores, gemfibrozilo, eritromicina o niacina. Su aparición puede ocurrir semanas o meses después de iniciado el tratamiento. El paciente debería ser advertido de reportar al médico algún dolor muscular, debilidad o cansancio sin explicación, especialmente si esta acompañado de fiebre o malestar. Las siguientes reacciones adversas necesitan de atención médica solo si continúan o causan molestia: • Incidencias más frecuentes: Estreñimiento, diarrea, gases, ardor de estómago, dolor de estómago, mareos, cefalea, náusea, rash dérmico. • Incidencias raras: Impotencia (disminución de la habilidad sexual), insomnio (molestia en el sueño).

ADVERTENCIAS: Es importante no usar más o menos medicación que la cantidad prescrita. En la pérdida de dosis, tomar tan pronto como sea posible; luego retomar el programa de dosis regular. No duplicar la dosis. Cumplir la dieta prescrita. Las mujeres en edad fértil deben utilizar un método anticonceptivo adecuado y no tener planes de quedar embarazadas. Debe administrarse la dosificación establecida. Su tratamiento debe ser monitorizado por el médico.

TRATAMIENTO EN CASOS DE SOBREDOSIS: Como no existe antídoto específico en tratamiento de sobredosis, será sintomático y de soporte. Los pacientes con sospecha de sobredosis intencional, deberán ser diferidos a un centro psiquiátrico.

DOSIS Y VÍAS DE ADMINISTRACIÓN Dosis usual adultos • Antihiperlipidemia: Hipercolesterolemia heterocigótica familiar y no familiar, y dislipidemia mixta (Frederickson tipo IIa y IIb). – Inicial: Oral, 10 mg una vez al día. La dosis puede ser ajustada después que se ha evaluado la respuesta del tratamiento en 2 a 4 semanas. – Mantenimiento: Oral, 10 a 80 mg al día. • Hipercolesterolemia homocigótica familiar: Oral, 10 a 80 mg diarios. Nota: Atorvastatina debería ser usado en tratamientos adjuntos con reducidores de lípidos tales como aféresis LDL, o si cada tratamiento no es disponible. Dosis usual pediátrica • Antihiperlipidémico: Hipercolesterolemia homocigótica familiar: La dosificación no ha sido establecida.

FORMAS DE PRESENTACIÓN ATOVAROL CBG 10 mg • Cajas conteniendo 7, 10, 14, 20, 28, 30, 50 y 100 cápsulas blandas tipo blíster. • Cajas dispensadoras conteniendo 84, 100 y 200 cápsulas blandas tipo blíster. ATOVAROL CBG 20 mg • Cajas conteniendo 7, 10, 14, 20, 28, 30, 50 y 100 cápsulas blandas tipo blíster. • Cajas dispensadora conteniendo 84, 100 y 200 cápsulas blandas tipo blíster.

ALMACENAMIENTO: Almacenar a temperatura entre 20 y 25 ºC.

UNIMED DEL PERÚ S. A. Calle Los Libertadores 155, Piso 7 - San Isidro Teléfono: 611-5500 Fax: 628-9540 Lima-Perú

Oleptro Er Oral Reviews And User Ratings Effectiveness, Ease Of Use, And Satisfaction, Oleptro

User Reviews & Ratings - Oleptro ER oral

« Oleptro ER oral Information

Comment: I was very tired and disoriented. I also experienced a very fast heart beat. It scared me and I had a fever. Stopped taking after 3 days on it.

Comment: I was very tired and disoriented. I also experienced a very fast heart beat. It scared me and I had a fever. Stopped taking after 3 days on it. Hide Full Comment

4 people found this review helpful. Was this review helpful? Yes | No

Condition: Major Depressive Disorder

2/5/2012 9:15:19 PM

Reviewer: Austin, 19-24 Male on Treatment for less than 1 month (Patient)

Current Rating: 5

Current Rating: 5

Current Rating: 5

Comment: I had been on numerous SSRI medications and was not too happy with the side effects, mostly sexual side effects. I initially tried Instant release Trazodone, and found it helped, but It always found myself in a fog in the mornings. I stumbled on Oleptro after some internet research, so I decided to give it a try(300mg), Its been much better, I wake up feeling refreshed and my depression has been m. Show Full Comment

Comment: I had been on numerous SSRI medications and was not too happy with the side effects, mostly sexual side effects. I initially tried Instant release Trazodone, and found it helped, but It always found myself in a fog in the mornings. I stumbled on Oleptro after some internet research, so I decided to give it a try(300mg), Its been much better, I wake up feeling refreshed and my depression has been much more tolerable, and I still get the great sleep I got from taking the instant release version. Id recommend this to anyone who traditional SSRI's were ineffective or who ever doesn't like the side effects. Hide Full Comment

4 people found this review helpful. Was this review helpful? Yes | No

Condition: Major Depressive Disorder

10/13/2011 7:38:20 PM

Reviewer: 2pu3ik, 55-64 Female on Treatment for 1 to 6 months (Patient)

Current Rating: 5

Current Rating: 5

Current Rating: 4

Comment: Difficult to get to sleep. Trouble with muscle pain. No weight gain.

Comment: Difficult to get to sleep. Trouble with muscle pain. No weight gain. Hide Full Comment

2 people found this review helpful. Was this review helpful? Yes | No

Condition: Major Depressive Disorder

8/22/2011 9:54:44 PM

Reviewer: gator, 55-64 Male on Treatment for 6 months to less than 1 year (Patient)

Current Rating: 4

Current Rating: 5

Current Rating: 4

Comment: I've been on Oleptro for 6 months. The really good news for me is that I have no/minimal side effects (as compared with Cymbalta). It does a fairly good job with my depression - at least as good as Cymbalta.

Comment: I've been on Oleptro for 6 months. The really good news for me is that I have no/minimal side effects (as compared with Cymbalta). It does a fairly good job with my depression - at least as good as Cymbalta. Hide Full Comment

3 people found this review helpful. Was this review helpful? Yes | No

Condition: Major Depressive Disorder

6/16/2011 11:30:22 PM

Reviewer: Pain4real, 35-44 Female on Treatment for less than 1 month (Patient)

Current Rating: 2

Current Rating: 5

Current Rating: 3

Comment: I've been on this for a week and my ankles are swollen, I'm retaining water and constantly have the chills. I also have been light headed, my equilibrium is off and my mouth and hands tingle. As of last night, I went to bed and could not get up this morning. Have had bizarre dreams as well, but I do not wake up a bazillion times either. So far I'm on the fence with this and need to co. Show Full Comment

Comment: I've been on this for a week and my ankles are swollen, I'm retaining water and constantly have the chills. I also have been light headed, my equilibrium is off and my mouth and hands tingle. As of last night, I went to bed and could not get up this morning. Have had bizarre dreams as well, but I do not wake up a bazillion times either. So far I'm on the fence with this and need to contact my DR. Hide Full Comment

7 people found this review helpful. Was this review helpful? Yes | No

Stadaquel, Stadaquel

Stadaquel

Stadaquel anvendes til behandling af

skizofreni og andre psykoser.

Anvendes desuden til behandling og forebyggelse af

mani og

depression ved bipolar affektiv sindslidelse.

Findes som tabletter.

Dosis er individuel og afh?nger af sygdommens sv?rhedsgrad.

Voksne. Begyndelsesdosis. 50 mg 1. dag, 100 mg 2. dag, 200 mg 3. dag og 300 mg 4. dag. Dosis fordeles pa 2 daglige doser. Derefter justeres dosis afh?ngig af virkningen til vedligeholdelsesdosis: S?dvanligvis 300-450 mg i dognet fordelt pa 2 daglige doser. Dosis ma ikke overskride 1200 mg i dognet.

Voksne. 1. dag: 100 mg, 2. dag: 200 mg, 3. dag: 300 mg og 4. dag: 400 mg. Dosis fordeles pa 2 daglige doser. Derefter justeres dosis afh?ngig af virkningen med hojst 200 mg i dognet. Vedligeholdelsesdosis er s?dvanligvis i intervallet 400-800 mg fordelt pa 2 doser. Dosis ma ikke overskride 1200 mg i dognet.

Depression ved bipolar lidelse:

Voksne under 65 ar . 1. dag: 50 mg, 2. dag 100 mg, 3. dag: 200 mg og 4. dag: 300 mg. Dosis tages s?dvanligvis ved sengetid. Derefter kan dosis justeres afh?ngig af virkningen til hojst 600 mg i dognet.

Forebyggelse af mani eller depression ved bipolar lidelse:

S?dvanligvis samme dosis som er brugt ved tidligere mani eller depression.

Til ?ldre og ved darligt fungerende lever:

Begyndelsesdosis 25 mg i dognet. Dosis oges med 25-50 mg dgl.

Bor ikke anvendes til born og unge under 18 ar pga. mulig oget risiko for bivirkninger.

Nedbrydning af muskelv?v

Allergisk h?velse i ansigtet samt mundhulen og strubehovedet, Anafylaktisk chok - en akut alvorlig allergisk tilstand

Bivirkninger fra bev?geapparatet er set ved korttidsbehandling af depression. Hyppigheden ser ud til, at v?re oget ved samtidig behandling med lithium (middel mod bipolar lidelse).

Sovnapno (pauser i vejrtr?kningen under sovn) er forekommet.

Sovnighed forekommer oftest i lobet af de forste 2 uger og forsvinder som regel, hvis man forts?tter behandlingen.

I sj?ldne tilf?lde forekommer sakaldt malignt neuroleptikasyndrom - en alvorlig tilstand med feber, bevidsthedssloring og flere af de ovenn?vnte bivirkninger. Denne tilstand kr?ver ojeblikkelig l?gehj?lp.

Ufrivillige bev?gelser forekommer oftest ved langtidsbehandling. Disse vil normalt svinde efter ophor med midlet, hos enkelte er de dog vedvarende.

Ved behandling med midler mod psykoser, er set s?rlige forstyrrelser af hjerterytmen (QT C - forl?ngelse), som i enkelte tilf?lde kan fore til pludselig dod.

En r?kke bivirkninger er set med oget hyppighed hos born og unge under 18 ar, bl. a. besvimelsesanfald.

Ma kun anvendes under visse foruds?tninger.

Kan om nodvendigt anvendes.

Denne tekst afviger fra indl?gssedlen.

Ma ikke tappes. 3 maneders karant?ne efter endt behandling.

Virker ved at ?ndre aktiviteten af flere signalstoffer i hjernen, sa overforslen af nerveimpulser i hjernen h?mmes. Midlet har saledes en beroligende og antipsykotisk virkning uden at virke helbredende. Den antipsykotiske virkning kan forst forventes efter behandling i 1-2 uger, undertiden 1-2 maneder. Virkningen kan vare flere uger, efter at behandlingen er ophort.

Tabletter. 1 tablet (filmovertrukken) indeholder 25 mg, 100 mg (delek?rv), 200 mg eller 300 mg (delek?rv) quetiapin (som fumarat).

Midlet skal anvendes med forsigtighed:

Til ?ldre

Ved tidligere krampeanfald

Ved sygdom i hjernen

Ved darligt fungerende lever

Ved hjerte - og kredslobslidelser

Hvis man lider af eller tidligere har lidt af gron st?r, forhojet tryk i ojet eller manglende vandladning

Hvis man tidligere har haft selvmordstanker.

Hvis man har

diabetes eller risiko for at udvikle diabetes, skal man lobende til kontrol hos l?gen.

Bmi og taljemal bor folges under behandlingen pga. risikoen for v?gtogning.

Storre m?ngder grapefrugtjuice kan oge virkningen af midlet.

Alkohol forst?rker midlets slovende virkning.

Der er set storre dodelighed end normalt, nar man behandler ?ldre med demens med antipsykotika.

Blodpropper kan ses ved behandling med antipsykotika. Man skal v?re ekstra opm?rksom, hvis man har forhojet risiko for at fa blodpropper.

Antipsykotika kan i nogle tilf?lde oge m?ngden af hormonet prolaktin, som har betydning for udviklingen af brystkr?ft. Hvis man er i behandling for brystkr?ft, skal midlet anvendes med forsigtighed.

Ved ophor af behandling skal dosis neds?ttes gradvis over 1-2 uger, idet der ved pludseligt ophor kan ses bl. a. sovnloshed, opkastning og svimmelhed.

Hvis man far symptomer pa forstyrrelser af hjerterytmen (fx hjertebanken, svimmelhed, besvimelsesanfald), skal man kontakte l?gen.

Depression . I starten af behandlingen, kan der forekomme oget risiko for selvmordsforsog og selvmordstanker. Hos unge under 25 ar kan der generelt v?re en oget risiko for selvmordsforsog.

Brug af anden medicin

Det er vigtigt at informere l?gen om alle de l?gemidler, du tager.

Midlet ma ikke bruges, hvis man samtidig bruger visse typer l?gemidler, heriblandt visse midler mod HIV (proteaseh?mmere), visse antibiotika (clarithromycin og erythromycin) samt visse midler mod svamp.

Stadaquel kan neds?tte virkningen af levodopa (middel mod Parkinsons sygdom).

Epilepsimidler (carbamazepin og phenytoin) neds?tter virkningen af Stadaquel.

Generel forsigtighed ved brug af andre l?gemidler der kan forstyrre hjerterytmen - fx lithium (middel mod bipolar lidelse), visse antibiotika, visse midler mod depression, visse midler mod hjerterytmeforstyrrelser samt visse midler mod psykoser. En del af disse midler skal helt undgas. Det g?lder: Chlorprothixen og pimozid (midler mod psykoser), moxifloxacin (antibiotikum), amiodaron og dronedaron (midler mod hjerterytmeforstyrrelser), droperidol (middel mod kvalme) samt vandetanib (middel mod kr?ft).

Visse bivirkninger (fx mundtorhed, forstoppelse, manglende vandladning, svimmelhed) ved andre midler (fx midler mod overfolsomhed og midler mod parkinsons sygdom) kan forst?rkes.

Tilskud, udlevering, pakninger og priser

Seroquel is used for treating schizophrenia or bipolar disorder. It may also be used for other conditions as determined by your doctor.

Use Seroquel as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Seroquel by mouth with or without food. Taking Seroquel at the same time each day will help you remember to take it. Take Seroquel on a regular schedule to get the most benefit from it. It may take a few weeks for you to notice the benefits of Seroquel. Continue to take Seroquel even if you feel good. Do not miss any doses. Drug Class and Mechanism

Seroquel is an antipsychotic. It works by altering the balance of certain chemicals that occur naturally in the brain, which are responsible for thinking and behavior.

If you miss a dose of Seroquel, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Store Seroquel at 77 degrees F (25 degrees C). Brief storage between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Seroquel out of the reach of children and away from pets.

Do not use Seroquel if:

you are allergic to any ingredient in Seroquel. Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Seroquel. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you or a family member has a history of bipolar disorder (manic depression), suicidal thoughts or attempts, mental or mood problems, or diabetes if you drink alcohol or have a history of alcohol or substance abuse if you have Alzheimer disease, dementia, or trouble swallowing, or you are very overweight if you have a history of heart problems (eg, heart attack, heart failure, irregular heartbeat), stroke, blood vessel problems, high blood cholesterol levels, or high or low blood pressure if you have history of blood problems (eg, low white blood cells), liver problems, thyroid problems, cataracts, narrow-angle glaucoma, seizures, neuroleptic malignant syndrome (NMS), high blood prolactin levels, or breast cancer

Some MEDICINES MAY INTERACT with Seroquel. Tell your health care provider if you are taking any other medicines, especially any of the following: Alpha-blockers (eg, doxazosin) or medicine for high blood pressure because the risk of low blood pressure and fainting may be increased Azole antifungals (eg, ketoconazole), fluvoxamine, macrolide antibiotics (eg, erythromycin), or telithromycin because they may increase the risk of Seroquel 's side effects Barbiturates (eg, phenobarbital), carbamazepine, corticosteroids (eg, prednisone), phenytoin, rifampin, or thioridazine because they may decrease Seroquel 's effectiveness Dopamine receptor agonists (eg, pramipexole) or levodopa because their effectiveness may be decreased by Seroquel.

Possible Side Effects

Check with your doctor if any of these most common side effects persist or become bothersome:

agitation; back pain; constipation; dizziness; drowsiness; dry mouth; headache; indigestion; runny nose; sore throat; stomach pain; weakness; weight gain. Seek medical attention right away if any of these severe side effects occur: severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); altered mental abilities, including lack of response to your surroundings; high blood sugar (eg, thirst, increased urination, confusion, drowsiness, flushing, rapid breathing, or fruity breath odor); increased or irregular heartbeat; involuntary, uncontrolled muscle movements; lightheadedness when rising from a seated or lying position; muscle stiffness; sweating; tremor; unexplained fever; vision changes.

Seroquel is to be used only by the patient for whom it is prescribed. Do not share it with other people.

Seroquel is used for treating schizophrenia or bipolar disorder. It may also be used for other conditions as determined by your doctor.

Use Seroquel as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Seroquel by mouth with or without food. Taking Seroquel at the same time each day will help you remember to take it. Take Seroquel on a regular schedule to get the most benefit from it. It may take a few weeks for you to notice the benefits of Seroquel. Continue to take Seroquel even if you feel good. Do not miss any doses. Drug Class and Mechanism

Seroquel is an antipsychotic. It works by altering the balance of certain chemicals that occur naturally in the brain, which are responsible for thinking and behavior.

If you miss a dose of Seroquel, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Store Seroquel at 77 degrees F (25 degrees C). Brief storage between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Seroquel out of the reach of children and away from pets.

Do not use Seroquel if:

you are allergic to any ingredient in Seroquel. Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Seroquel. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you or a family member has a history of bipolar disorder (manic depression), suicidal thoughts or attempts, mental or mood problems, or diabetes if you drink alcohol or have a history of alcohol or substance abuse if you have Alzheimer disease, dementia, or trouble swallowing, or you are very overweight if you have a history of heart problems (eg, heart attack, heart failure, irregular heartbeat), stroke, blood vessel problems, high blood cholesterol levels, or high or low blood pressure if you have history of blood problems (eg, low white blood cells), liver problems, thyroid problems, cataracts, narrow-angle glaucoma, seizures, neuroleptic malignant syndrome (NMS), high blood prolactin levels, or breast cancer

Some MEDICINES MAY INTERACT with Seroquel. Tell your health care provider if you are taking any other medicines, especially any of the following: Alpha-blockers (eg, doxazosin) or medicine for high blood pressure because the risk of low blood pressure and fainting may be increased Azole antifungals (eg, ketoconazole), fluvoxamine, macrolide antibiotics (eg, erythromycin), or telithromycin because they may increase the risk of Seroquel 's side effects Barbiturates (eg, phenobarbital), carbamazepine, corticosteroids (eg, prednisone), phenytoin, rifampin, or thioridazine because they may decrease Seroquel 's effectiveness Dopamine receptor agonists (eg, pramipexole) or levodopa because their effectiveness may be decreased by Seroquel.

Possible Side Effects

Check with your doctor if any of these most common side effects persist or become bothersome:

agitation; back pain; constipation; dizziness; drowsiness; dry mouth; headache; indigestion; runny nose; sore throat; stomach pain; weakness; weight gain. Seek medical attention right away if any of these severe side effects occur: severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); altered mental abilities, including lack of response to your surroundings; high blood sugar (eg, thirst, increased urination, confusion, drowsiness, flushing, rapid breathing, or fruity breath odor); increased or irregular heartbeat; involuntary, uncontrolled muscle movements; lightheadedness when rising from a seated or lying position; muscle stiffness; sweating; tremor; unexplained fever; vision changes.

Seroquel is to be used only by the patient for whom it is prescribed. Do not share it with other people.

Constulose, Constulose

lactulose

a synthetic disaccharide used as a cathartic and to enhance the excretion of ammonia in treatment of hepatic encephalopathy .

lactulose

Apo-Lactulose (CA), Constulose, Duphalac (UK), Enulose, Euro-Lac (CA), Generlac, Gen-Lac (CA), GPI-Lactulose (CA), Kristalose, Lactugal (UK), Lactulax (CA), Lemlax (UK), PMS-Lactulose (CA), Ratio-Lactulose (CA), Regulose (UK)

Pharmacologic class: Osmotic

Therapeutic class: Laxative

Pregnancy risk category B

Action

Produces osmotic effect, which increases water content in colon and enhances peristalsis. Breakdown products in colon lead to acidification of colonic contents, softening of feces, and decreased ammonia absorption from colon to systemic circulation. These effects reduce blood ammonia level in portal-system encephalopathy.

Availability

Powder (single-use packets): 10 g, 20 g

Syrup: 10 g/15 ml

⊘ Indications and dosages

Adults: 10 to 20 g (15 to 30 ml) P. O. daily; may increase to 60 ml daily p. r.n.

➣ Portal-system encephalopathy

Adults: 20 to 30 g (30 to 45 ml) P. O. three or four times daily until two or three soft stools are produced daily. Therapy may continue over long term. Or, 300 ml P. O. with 700 ml of water or normal saline solution. Or, as retention enema by rectal balloon catheter, repeated q 4 to 6 hours.

Contraindications

• Patients requiring low-galactose diet

Precautions

Use cautiously in: • diabetes mellitus • elderly patients • pregnant or breastfeeding patients • children.

Administration

• Don't give concurrently with other laxatives. • Dissolve contents of single-use packet in 4 oz of water or juice. • Dilute syrup with water or fruit juice to mask taste.

Adverse reactions

GI: nausea, vomiting, diarrhea, intestinal cramps, abdominal distention, flatulence

Metabolic: hyperglycemia (in diabetic patients), hypokalemia, hypernatremia

Interactions

Drug-drug. Anti-infectives: decreased lactulose efficacy

Other laxatives: interference with response to lactulose (in patients with hepatic encephalopathy)

Drug-diagnostic tests. Blood ammonia: 25% to 50% decrease

Glucose: increased level (in diabetic patients)

Potassium: decreased level

Sodium: increased level

Patient monitoring

• Watch for adverse GI reactions. • Check stool consistency and frequency. • Monitor electrolyte levels, especially in elderly patients. • Check blood glucose level in diabetic patients.

Patient teaching

• Instruct patient to dissolve contents of single-use packet in 4 oz of water or juice. • Suggest that patient dilute syrup with water or juice to mask taste. • Tell patient drug may cause flatulence and intestinal cramps at first, but these symptoms usually subside. • Inform patient that excessive use may cause diarrhea and excessive fluid loss. • Encourage patient to drink adequate fluids and to report signs and symptoms of dehydration. • As appropriate, review all other significant adverse reactions and interactions, especially those related to the drugs and tests mentioned above.

lac·tu·lose

A synthetic disaccharide used to treat hepatic encephalopathy and chronic constipation.

lactulose

/lac·tu·lose/ ( lak?tu-lōs ) a synthetic disaccharide used as a laxative and to enhance excretion or formation of ammonia in the treatment of hepatic encephalopathy.

lactulose

a nonabsorbable synthetic disaccharide, 4-0-beta - d - galactopyranosyl - D - fructose, C 12 H 22 O 11 . It is hydrolyzed in the colon by bacteria primarily to lactic acid and small amounts of formic and acetic acids, which results in increased osmotic pressure and acidification of the colonic contents. It is used as a cathartic in chronic constipation. Because the acidification causes ammonia to be removed from the blood to form ammonium ion, it is also used in the treatment of hepatic coma. Its ability to increase fecal water content, however, may also cause diarrhea.

lactulose

A synthetic disaccharide used to treat hepatic encephalopathy, which is administered by mouth, acting as a laxative; lactulose reduces intraluminal NH3 which, via the extracellular fluid, reduces NH3 in the blood.

lac·tu·lose

A synthetic disaccharide used to treat hepatic encephalopathy and chronic constipation.

lactulose

A disaccharide sugar that acts as a gentle but effective LAXATIVE. It is not absorbed or broken down but remains intact until it reaches the colon where it is split by bacteria and helps to retain water, thereby softening the stools. Brand names are Duphalac, Lactugal and Regulose.

lactulose

a synthetic disaccharide used as a cathartic and to enhance the excretion of ammonia in the treatment of hepatic encephalopathy.

Link to this page:

Back Pain Causes, Symptoms And Treatments - Medical News Today, Back Pain

Back Pain: Causes, Symptoms and Treatments

Back pain is a very common complaint. According to the Mayo Clinic, approximately 80% of all Americans will have low back pain at least once in their lives.

Back pain is a common reason for absence from work and doctor visits. Although back pain may be painful and uncomfortable, it is not usually serious.

Even though back pain can affect people of any age, it is significantly more common among adults aged between 35 and 55 years. Experts say that back pain is associated with the way our bones, muscles and ligaments in our backs work together.

Pain in the lower back may be linked to the bony lumbar spine, discs between the vertebrae, ligaments around the spine and discs, spinal cord and nerves, lower back muscles, abdomen and pelvic internal organs, and the skin around the lumbar area. Pain in the upper back may be due to disorders of the aorta, tumors in the chest, and spine inflammation.

Contents of this article:

You will also see introductions at the end of some sections to any recent developments that have been covered by MNT's news stories. Also, look out for links to information about related conditions.

Risk factors for back pain

A risk factor is something which increases the likelihood of developing a condition or disease. For example, obesity significantly raises the risk of developing diabetes type 2. Therefore, obesity is a risk factor for diabetes type 2.

The following factors are linked to a higher risk of developing low back pain:

A mentally stressful job

Pregnancy - pregnant women are much more likely to get back pain

A sedentary lifestyle

Age - older adults are more susceptible than young adults or children

Anxiety

Depression

Gender - back pain is more common among females than males

Obesity/overweight

Smoking

Strenuous physical exercise (especially if not done properly)

Strenuous physical work.

Signs and symptoms of back pain

A symptom is something the patient feels and reports, while a sign is something other people, such as the doctor detect. For example, pain may be a symptom while a rash may be a sign.

The main symptom of back pain is, as the name suggests, an ache or pain anywhere on the back, and sometimes all the way down to the buttocks and legs. In most cases signs and symptoms clear up on their own within a short period.

If any of the following signs or symptoms accompanies a back pain your should see your doctor:

Weight loss

Elevated body temperature (fever )

Inflammation (swelling) on the back

Persistent back pain - lying down or resting does not help

Pain down the legs

Pain reaches below the knees

A recent injury, blow or trauma to your back

Urinary incontinence - you pee unintentionally (even small amounts)

Difficulty urinating - passing urine is hard

Fecal incontinence - you lose your bowel control (you poo unintentionally)

Numbness around the genitals

Numbness around the anus

Numbness around the buttocks.

According to the National Health Service (NHS), UK, the following groups of people should seek medical advice if they experience back pain:

People aged less than 20 and more than 55 years

Patients who have been taking steroids for a few months

Drug abusers

Patients with cancer

Patients who have had cancer

Patients with low immune systems.

Causes of back pain

The human back is composed of a complex structure of muscles, ligaments, tendons, disks and bones - the segments of our spine are cushioned with cartilage-like pads. Problems with any of these components can lead to back pain. In some cases of back pain, its cause is never found.

Strain - the most common causes of back pain are:

Lifting something in an improper manner is a common cause of back pain.

Strained muscles

Strained ligaments

Lifting something improperly

Lifting something that is too heavy

The result of an abrupt and awkward movement

A muscle spasm.

Structural problems - the following structural problems may also result in back pain:

Ruptured disks - each vertebra in our spine is cushioned by disks. If the disk ruptures there will be more pressure on a nerve, resulting in back pain.

Bulging disks - in much the same way as ruptured disks, a bulging disk can result in more pressure on a nerve.

Sciatica - a sharp and shooting pain that travels through the buttock and down the back of the leg, caused by a bulging or herniated disk pressing on a nerve.

Arthritis - patients with osteoarthritis commonly experience problems with the joints in the hips, lower back, knees and hands. In some cases spinal stenosis can develop - the space around the spinal cord narrows.

Abnormal curvature of the spine - if the spine curves in an unusual way the patient is more likely to experience back pain. An example is scoliosis. when the spine curves to the side.

Osteoporosis - bones, including the vertebrae of the spine, become brittle and porous, making compression fractures more likely.

Below are some other causes of back pain:

Cauda equina syndrome - the cauda equine is a bundle of spinal nerve roots that arise from the lower end of the spinal cord. People with cauda equine syndrome feel a dull pain in the lower back and upper buttocks, as well as analgesia (lack of feeling) in the buttocks, genitalia and thigh. There are sometimes bowel and bladder function disturbances.

Cancer of the spine - a tumor located on the spine may press against a nerve, resulting in back pain.

Infection of the spine - if the patient has an elevated body temperature (fever) as well as a tender warm area on the back, it could be caused by an infection of the spine.

Sleep disorders - individuals with sleep disorders are more likely to experience back pain, compared to others.

Shingles - an infection that can affect the nerves.

Bad mattress - if a mattress does not support specific parts of the body and keep the spine straight, there is a greater risk of developing back pain.

Everyday activities or poor posture.

Back pain can also be the result of some everyday activity or poor posture. Examples include:

We live in a world of computers. Adopting a very hunched sitting position when using computers can result in increased back and shoulder problems over time.

Bending awkwardly

Pushing something

Pulling something

Carrying something

Lifting something

Standing for long periods

Bending down for long periods

Twisting

Coughing

Sneezing

Muscle tension

Over-stretching

Sitting in a hunched position for long periods (e. g. when driving)

Long driving sessions without a break (even when not hunched).

On the next page we look at how back pain is diagnosed, the treatment options and how back pain can be prevented.

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Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Kop Aconip (Indocin) Utan Recept, Aconip

Kopa Aconip (Indocin) Natet Utan Recept

Aconip (Indocin) Forklaring

Aconip ar verkligen en idealisk behandling, som hjalper dig att bekampa obehag eller ens svullnad vackt den av manga omstandigheter till exempel gikt smarta, ankyloserande spondylit, ledsjukdom, bursit, eller till och tendinit.

Aconip verkar genom att minska kroppens hormoner som utloser svullnad samt obehag i kroppen.

Aconip kan ocksa kallas Indometacin, Indocid, Inmecin, Indochron ER, Aconip-SR, Flexin CONTINUS, Indolar, Indomax, Indomod, Pardelprin, Rheumacin, Rimacid, Slo-Indo.

Det ar verkligen icke-steroida antiinflammatoriska lakemedel.

Allmant titeln i samband med Aconip faktiskt Indometacin.

Varumarke associerade med Aconip tenderar att vara Aconip, Aconip SR.

Aconip (Indocin) Dose

Aconip kommer in:

25mg lagre dos friktionsmaterial

50mg Regular Dos friktionsmaterial

Darra sjalva vatskan typ av Aconip fore utnyttjande.

Get Aconip piller samt vatskekontaktformular genom munnen tillsammans med dricksvatten.

Get Aconip ett par ganger varje dag samtidigt.

Vanligtvis inte slipa eller ens tugga upp detta.

Om du vill astadkomma basta resultaten brukar inte sluta anvanda Aconip helt plotsligt.

Aconip (Indocin) I brist forknippas med doserings

Vanligtvis far inte dubbel dos. Om du hoppar over dosen du behover for att bara den nar du kom ihag nar det galler din saknas. Nar det ar dags for dosering du behover bara pa din egen normal dosering rutin.

Aconip (Indocin) Overdosering

Om du overdoserar Aconip och du undviker ocksa stor att du behover kolla din lakare eller ens lakare omedelbart. Forknippas med Aconip overdosering: kasta upp, migran, yrsel, missforstand, svar trotthet, en kansla av stickningar, stickande, brannande upp, smyga i porerna och huden, provokation, trotthet.

Aconip (Indocin) Lagringsutrymme

Shop i rymden temperaturer mellan 10 och 30 nivaer D (59 samt 86 nivaer F) fran fukt och temperatur. Behall text ordentligt stangd. Starka nagon form av orord medicinering efter utgangen dagen. Behall fran uppna barnen.

Aconip (Indocin) Negativa effekter

Aconip erbjuder de negativa effekterna. Den mest typiska tenderar att vara:

yrsel friktionsmaterial

kastar upp friktionsmaterial

costiveness friktionsmaterial

obehag fran rumpan friktionsmaterial

kontinuerlig en kansla av att det ar nodvandigt att vakant faktiska tarmfriktionsmaterial

ringande oron friktionsmaterial

migran friktionsmaterial

diarre friktionsmaterial

Mycket mindre typiska och allvarliga negativa effekter i hela anvander Aconip:

allergisk reaktion svar (urtikaria, inandning och utandning fragor, allergi, samt utbrott) friktionsmaterial

varm friktionsmaterial

montage friktionsmaterial

klada friktionsmaterial

inflammation fran ogat, moter. sprak, lapparna, tonsiller, fingrar, fot, skenben, kalvar friktionsmaterial

problem med att andas in och andas ut eller till och med intag av friktionsmaterial

HESHET friktionsmaterial

ljus hud friktionsmaterial

for mycket trotthet friktionsmaterial

ovanlig blodforlust eller ens stoter friktionsmaterial

otillracklig effekt friktionsmaterial

trotthet friktionsmaterial

minskad hunger friktionsmaterial

influensaliknande symtom friktionsmaterial

gulsot friktionsmaterial

dyster friktionsmaterial

fargade, eller ens vekling kissa friktionsmaterial

smarta i nedre ryggen friktionsmaterial

hart eller ens obehagligt peeing friktionsmaterial

suddig syn eller till och med en del andra problem med utsikt friktionsmaterial

ovanligt att satta pa vikt friktionsmaterial

obehag i hogra ovre hornet delen av magen friktionsmaterial

snabb hjarta sla friktionsmaterial

Negativa effekter tyder forlitar pa medicin du kanske anvander men dessutom lita pa ditt valbefinnande villkor och en annan aspekter.

Aconip (Indocin) Kontraindikationer

Vanligtvis inte far Aconip om du ar kanslig for att Aconip element.

Vanligtvis inte far Aconip om du vantar annars du tanker ha ett barn, annars ar du verkligen en medicinsk mamma.

Var forsiktig tillsammans med Aconip om du anvander angiotensin 2 radio fiender t. ex. kandesartan (Atacand), eprosartan (Teveten), irbesartan (Avapro), losartan (Cozaar), olmesartan (Benicar), telmisartan ( Micardis), saval som valsartan (Diovan); betablockerare till exempel atenolol (Tenormin), labetalol (normodyne), metoprolol (Lopressor, Toprol xl), nadolol (corgard), liksom propranolol (Inderal); cyklosporin (Sandimmun Neoral, Sandimmune); digoxin (Lanoxin); diuretika (vatske piller ") for exempelvis triamteren (dyrenium, inom dyazide); litium (eskalith, Lithobid); metotrexat (Rheumatrex); fenytoin (Dilantin); liksom probenecid (Benemid), angiotensin-converting kemiska (ACE) - hammare exempelvis benazepril (Lotensin), kaptopril (Capoten), enalapril (Vasotec), fosinopril (Monopril), lisinopril (Prinivil, Zestril), moexipril (univasc), perindopril (Aceon), kinapril (Accupril), ramipril (altace), liksom trandolapril (mavik).

Det kan vara skadligt att anvanda sig av Aconip om du drabbas av och har en kort historia i samband med kramper, parkinsons sjukdom, depressioner eller till och med psykologisk sjukdom, eller ens lever orgel eller ens renal sjukdom.

Var forsiktig tillsammans med Aconip nar du planerar att anvanda sig av indometacin uvulas.

Var forsiktig tillsammans med Aconip om du agde proktit (inflammation fran andtarmen) och har pa sistone upplevt anal blodforlust, andningssvarigheter, regelbunden packade eller nasal nasal omrade eller ens nasa polyper (svullnad fran fodret fran nasan).

Forhindra alkoholhaltiga drycker.

Var forsiktig tillsammans med Aconip om du vill ha en kirurgisk behandling.

Forhindra reser ordning.

Vanligtvis inte sluta bara den helt plotsligt.

Aconip (Indocin) Vanliga fragor

Queen: Exakt vad betyder Aconip innebar?

Aconip ar ett effektivt lakemedel som hjalper dig att slass med vauge smarta eller ens svullnad vackt den av manga omstandigheter till exempel gikt smarta, ankyloserande spondylit, ledsjukdom, bursit, eller ens tendinitis. A

Queen: Vad exakt ar allmanna och varumarken som forknippas med Aconip?

Allman titeln i samband med Aconip faktiskt Indometacin. Varumarken ar forknippade med Aconip tenderar att vara Aconip, Aconip SR. A

Queen: Hur kan verkligen Aconip kora?

Aconip arbetar genom att minska kroppens hormoner som utloser svullnad samt obehag i kroppen. Det ar verkligen icke-steroida antiinflammatoriska medication. A

Queen: Vad exakt ar Aconip negativa effekter?

Aconip erbjuder de typiska negativa effekterna till exempel: yrsel, kasta upp, costiveness, obehag fran rumpan, fortlopande en kansla av att det ar nodvandigt att vakant sjalva tarmen, ringande oron, migran, diarre. Men i situationen i samband med att bli avvisad i samband med Aconip komponenter du har mojlighet att mota mer allvarliga negativa effekter: varmt, montage, klada, inflammation fran ogat, mote, sprak, lapparna, tonsiller, fingrar, fot, skenben, kalvar; problem inandning och utandning eller intag, HESHET, ljus hud, for mycket trotthet, ovanlig blodforlust eller ens gupp, otillracklig effekt, trotthet, minskad hunger, influensaliknande symtom, gulsot, dyster, fargade, eller ens vekling pee; smarta i nedre ryggen, svart eller till och med obehaglig peeing, suddig syn eller ens nagra andra problem med utsikt, ovanliga viktokning, obehag i hogra ovre hornet delen av magen, i samband med allergisk reaktion (svarigheter tillsammans med inandning och utandning, inflammation, porer och huden allergi eller ens nasselfeber), snabb hjarta beat. A

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