Nislev Dosis Obat, Nislev

nislev

golongan . obat keras

kemasan . dos 10 tablet

komposisi . levofloxacin 500 mg

Sekilas tentang zat aktif (nama generik)

levofloksasin (levofloxacin) adalah antibiotik golongan fluorokuinolon yang mempunyai spektrum luas, aktif terhadap bakteri gram negatif maupun gram positif. levofloksasin (levofloxacin) adalah levo isomer dari ofloksasina. seperti semua kuinolon, levofloksasin (levofloxacin) bekerja dengan cara menghambat dua tipe enzim II topoisomerase yaitu DNA Gyrase dan topoisomerase IV. topoisomerase IV memerlukan DNA terpisah yang telah direplikasi sebelum pembelahan sel bakteri. Dengan DNA yang tidak dipisahkan, proses terhenti dan bakteri tidak bisa membagi. Sedangkan DNA gyrase bertanggungjawab untuk supercoil DNA sehingga akan cocok di dalam sel yang baru terbentuk. kombinasi dari dua mekanisme di atas akan membunuh bakteri sehingga levofloksasin (levofloxacin) digolongkan sebagai bakterisida.

Indikasi nislev

Kegunaan nislev (levofloxacin) adalah untuk pengobatan infeksi maksilaris sinusitis akut, eksaserbasi bakteri akut bronkitis kronik, pneumonia komunitas, kulit dan struktur kulit yang kompleks, infeksi saluran kemih, pieloneritis dan infeksi lain yang disebabkan kuman peka terhadap nislev (levofloxacin).

kontra indikasi

nislev (levofloxacin) harus dihindari pada pasien dengan hipersensitivitas terhadap nislev (levofloxacin) atau antibiotik golongan kuinolon lainnya. nislev (levofloxacin) juga kontra indikasi pada pasien dengan epilepsi atau gangguan kejang lainnya. dan pada pasien yang memiliki riwayat pemakaian kuinolon terkait tendon pecah .

Efek Samping nislev

Kebanyakan efek samping nislev (levofloxacin) bersifat ringan sampai sedang. Namun, efek samping serius kadang terjadi. Efek samping yang paling umum seperti gangguan gastrointestinal. mual, muntah, dan sembelit. nislev (levofloxacin) juga menyebabkan intoksifikasi pernafasan, darah dan kelainan hormonal serta kardiovaskuler. efek samping yang yang kadang terjadi meskipun jarang adalah tremor, kegelisahan, ansietas, sakit kepala ringan, kebingungan, halusinasi, paranoid, depresi, mimpi buruk, insomnia.

perhatian

hati-hati pemberian nislev (levofloxacin) pada pasien dengan penyakit hati. efektivitas dan keamanan pemakaian pada anak-anak, wanita hamil dan menyusui belum terbukti.

Toleransi terhadap kehamilan

penelitian pada reproduksi hewan menunjukkan levofloxacin memberikan efek buruk pada janin. Tidak ada studi yang memadai dan terkendali dengan baik pada manusia. tetapi jika manfaat potensial terhadap ibu lebih besar daripada risiko pada janin maka obat ini bisa diberikan.

interaksi obat

penggunaan nislev (levofloxacin) bersama antasida yang mengandung magnesium hidroksida atau aluminium hidroksida, menurunkan penyerapan nislev (levofloxacin) oleh usus. Hal yang sama terjadi jika diberikan bersamaan dengan suplemen zat besi dan multi-vitamin yang mengandung zinc. nislev (levofloxacin) menunjukkan potensi untuk memblokir pemecahan warfarin dan phenprocoumon. Hal ini dapat meningkatkan kerja obat seperti warfarin, sehingga menyebabkan efek samping yang lebih potensial, seperti perdarahan. Dalam dosis tinggi, penggunaan nislev (levofloxacin) bersamaan dengan anti inflamasi non steroid (NSAID) dapat menyebabkan kejang.

Dosis nislev

nislev (levofloxacin) diberikan dengan dosis. dosis oral sama dengan dosis parenteral. pemberian melalui infus dilakukan secara perlahan-lahan. sinusitis maksilaris akut. 500 mg tiap 24 jam selama 10-14 hari. eksaserbasi akut bronkitis kronis. 500 mg tiap 24 jam selama 7 hari; community acquired pneumonia . 500 mg tiap 24 jam selama 7-14 hari. infeksi saluran kemih terkomplikasi, pieloneritis akut. 250 mg tiap 24 jam selama 10 hari. infeksi kulit dan struktur kulit tidak terkomplikasi. 500 mg tiap 24 jam selama 7-10 hari.

Terkait

Rheum - Definition Of Rheum By The Free Dictionary, Arheuma

rheum

I would I had not trusted Malkin to his keeping, for, crippled as I am with the cold rheum. I am undone if aught but good befalls her.

I say four, if not five," answered Don Quixote, "for never in my life have I had tooth or grinder drawn, nor has any fallen out or been destroyed by any decay or rheum .

He turned towards me, and looked into my eyes with two filmy orbs that distilled the rheum of intoxication.

One plant I hope won't follow suit is Rheum palmatum, a giant rhubarb that is flowering in all its glory in the raised beds.

G Tarr, (1) MB BCh, FCP (SA), Cert Rheum (SA), MMed (Int Med); B Hodkinson, (2) MB BCh, FCP (SA), Cert Rheum (SA), PhD; H Reuter, (1, 3) MB ChB, FCP (SA), MMed (Int), FRCP (Edin), PhD

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In the Belgian list, it is stated that, for Cassia and Rheum spp.

But among the subset of patients with at least one swollen joint who fulfill the 2010 criteria, the spontaneous remission rate appears to be much lower, on the order of 10% (Arthritis Rheum .

Rheum palmatum, called Chinese rhubarb, has deeply cut leaves and is best grown in herb gardens.

The ACR list of 19 neuropsychiatric syndromes attributable to SLE includes headache, mood disorders, cognitive dysfunction, and anxiety disorders (Arthritis Rheum .

We were planting jungle-type plants like rheum. gunnera and macleaya so it must have been one of those hairy-leafed blighters.

W B van den Hout, G J Tijhuis, J M W Hazes, F C Breedveld, and T P M Vliet Vlieland Ann Rheum Dis 2003; 62: 308-315.

5 Facts About Ketones, Ketones

Blood Glucose Management: Checking for Ketones

What are ketones?

The human body normally runs on glucose that’s produced when the body breaks down carbohydrates. But when your body doesn’t have enough glucose or insulin to use the glucose, your body starts breaking down fats for energy. Ketones are byproducts of this breakdown. Those with type 1 diabetes are especially at risk for making ketones.

Ketones can make your blood acidic. Acidic blood can cause a serious condition known as diabetic ketoacidosis (DKA). Because the presence of ketones is often one of the signs that a person needs medical help, those with diabetes are often encouraged to check ketones in urine or blood regularly.

Ketone levels can range from negative or none at all to very high levels. While individual testing may vary, some general results for ketone levels can be:

negative: less than 0.6 millimoles per liter (mmol/L)

low to moderate: between 0.6 to 1.5 mmol/L

high: 1.6 to 3.0 mmol/L

very high: greater than 3.0 mmol/L

Call your doctor if your ketones are low to moderate, and seek emergency medical attention if your ketone levels are high to very high.

What are the symptoms of ketone buildup?

If you have diabetes, you need to be especially aware of the symptoms that having too many ketones in your body can cause. Examples of early symptoms of ketone buildup include:

a dry mouth

blood sugar levels greater than 240 milligrams per deciliter

strong thirst

frequent urination

If you don’t get treatment, the symptoms can progress. The symptoms that occur later can include:

confusion

extreme fatigue

flushed skin

a fruity breath odor

nausea

vomiting

stomach pain

trouble breathing

You should always seek immediate medical attention if your ketone levels are high.

What causes ketones to build up?

Ketones are the body’s alternate way of fueling. They build up when you:

don’t have enough insulin

can’t use the insulin you have

aren’t eating enough

This may occur if you aren’t feeling well or you’re trying to diet and you aren’t eating enough.

Your body receives signals to release energy from fats when it:

doesn’t have enough insulin, which occurs in type 1 diabetes

can’t use insulin properly, which occurs in type 2 diabetes

can’t use glucose properly, which occurs in starvation

When these fats reach your liver, it breaks them down into ketones.

The release of ketones can become a cycle. Your body will continue to release energy from fats, and the liver will continue to release ketones. This can cause your blood levels to become too acidic, which can be deadly.

Some diets, such as a low-carbohydrate diet, are intended to release fats and create ketones. Those who don’t have diabetes can usually compensate for these changes. However, the excess ketones can be dangerous for someone with diabetes. This is why doctors recommend that people with diabetes proceed carefully when restricting their diets.

How are ketones tested?

You can use blood or urine tests to test your ketone levels. At-home testing kits are available for both types of tests. Urine tests are available without a prescription at most drugstores, or you can buy them online.

You should test your urine or blood for ketones when any of the following occurs:

your fasting blood sugar is higher than 240 mg/dL

your blood sugar exceeds 300 mg/dL

you feel sick or nauseated, regardless of your blood sugar reading

Urine testing strips contain a special chemical. If the strip interacts with urine that has ketones, it will turn a specific color. Several manufacturers make testing kits for ketone levels. Many of them provide results that indicate no ketones up to a high level of ketones in the body. If a child isn’t potty-trained, a parent can usually press the stick to their child’s wet diaper to test for ketones.

An at-home meter is available to test for blood ketones. This is tested in a similar way to a finger-stick glucose test. You’ll prick your finger with a needle and place a small drop of blood onto the testing area.

Doctors often recommend that people who’ve just been diagnosed with diabetes test their ketones twice daily.

If you have a large amount of blood ketones, usually greater than 3.0 mmol/L, or you have a large amount of ketones in your urine, you should seek emergency medical treatment.

What happens if your ketone levels get too high?

If you don’t get treatment for high ketone levels, DKA can occur. The most serious effects of DKA include:

swelling in the brain

a loss of consciousness

diabetic coma

death

This is why it’s important to have a plan for if your ketone levels are moderate and if they become high.

Treatment for high ketone levels

High ketone levels usually take time to start getting higher. Accordingly, it can take several days to correct DKA. Treatments can include:

Intravenous (IV) fluid replacement

One DKA symptom is increased urination, which can result in fluid loss. Rehydrating with IV fluids can help to dilute the extra glucose in your blood.

Electrolyte replacement

When a person has DKA, the electrolyte levels tend to be low. Examples of electrolytes include potassium, sodium, and chloride. If a person loses too much of these electrolytes, their heart and muscles can’t function as well.

Insulin

People usually receive insulin through an IV to improve their ability to use excess glucose in the blood for energy. This usually involves testing glucose levels on an hourly basis. When your ketones and blood acid level return to normal, IV insulin may no longer be necessary.

Since an underlying illness can also lead to DKA, such as a severe stomach bug that causes vomiting, your doctor may prescribe treatments for that illness as well.

What is the outlook?

Seeking immediate medical treatment when ketone levels are high can ensure a person gets the help they need. You may need hospitalization for several days if you have DKA, but it’s treatable. However, you should evaluate your diet and blood glucose management plan after a DKA episode to help prevent your ketone levels from getting too high again.

Are there ways to prevent high ketone levels?

Careful management of diabetes is the key to preventing high ketone levels. Do the following to keep your blood sugar levels healthy and ketone production to a minimum:

Check blood sugar levels regularly

Your doctor will recommend how frequently you should check your blood sugar levels, but this is typically three to four times per day. You should check your blood sugar more often if:

your blood sugar levels are getting higher

you’re having symptoms of high or low blood sugar

you’re sick

Follow a healthy diet plan

Eating enough food and taking enough insulin for the foods you eat that contain carbohydrates is vital for managing diabetes.

Create a plan for moderate ketone levels

Sometimes, moderate ketone levels can be treated before they worsen. A doctor can help you create a plan when your ketone levels get too high, such as administering additional insulin and drinking more water.

Always keep ketone testing kits available

Keep ketone testing kits with you at home and when you travel so that you have a fast way to check your ketone levels.

Work closely with a diabetes educator and your doctor

Diabetes management takes constant vigilance to ensure your insulin administration and eating plan is working effectively. The medication and insulin combination that works best varies depending on the person. You should talk to your doctor if you’re concerned about your ketone levels being frequently high.

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Hipril-A Tablet Micro Labs Use, Composition, Dosage, Side Effect, Price And Review - Tablet Tree, Hi

Hipril-A

Hipril-A Tablet - Uses, Composition, Dosage, Side Effects & Reviews

Hipril-A is very much effective and gives a new life to you by providing you a shield from high blood pressure. Check your blood pressure one week after starting this drug and conuslt your doctor if it has not improved. It consists of an active ingredient Amlodipine and Lisinopril. This combination of drug acts fantastically with no side effects. The major cardiovascular diseases can be treated with this medication. This combination is used for the management of high blood pressure. Amlodipine is the dihydropyridine derivative calcium-channel blocker, used for treating hypertension and brining it to normal level.

Lisinopril is angiotensin-converting-enzyme (ACE) inhibitor. It acts by inhibiting production of chemical angiotensin II resulting in relaxation of blood vessels, and thus, reduces blood pressure. It is also used in patients of diabetes with kidney failure. Buy Hipril-A online from Tablet Tree to get heavy discounts.

Hipril-A Tablet Uses

Amlodipine: belongs to a class of drugs called calcium channel blocker. It reduces the amount of calcium that enters the smooth muscles of the blood vessels and heart. As muscle cells require calcium to contract, reducing the flow of calcium causes the muscle cells to relax and blood vessels to dilate, reducing blood pressure, force and rate of the heartbeat. It improves blood and oxygen supply to the heart muscles.

Lisinopril: is a known angiotensin-converting-enzyme (ACE) inhibitor. It is used to relax blood vessels. It prevents an enzyme in your body from producing angiotensin II, that works by narrowing your blood vessels and releasing hormones that can raise your blood pressure.

Hipril-A Tablet Composition

Amlodipine……… 5 mg

Hipril-A Tablet Dosage

The usual initial dosage is one tablet daily.

If blood pressure control is inadequate after a week or two, the dose may be increased to two tablets daily. The dosage, however, should be individualized.

The correct dosage and prescription commonly depend on the patient and the condition being treated. Do not adjust your dosage without the approval of your healthcare provider. Please consult your doctor and follow his or her recommendations. Please do not self medicate.

Hipril-A Tablet Side Effects

Body As A Whole - Fatigue, weakness, and fainting

Heart - Low blood pressure

Gastrointestinal - Diarrhea, nausea, vomiting, and indigestion

Musculoskeletal - Muscle cramps

Central Nervous System - Headache, dizziness, tingling and decreased sexual activity

Respiratory - Cough, cold and respiratory tract infection

Skin - Rash and psoriasis

Genitourinary - Impotence

Other Information on Hipril-A Tablet:

Pharmaceutical Form

Precautions

Avoid excess dosage

Keep all medicines out of the reach of children and never share your medicine with anyone

Not to be used in untreated phaeochromocytoma

Drug – Drug Interaction

This medication is known to interact with the following drugs and increases or decreases its own potency:

Decreased effect with aluminum and calcium salts, barbiturates, cholestyramine, NSAIDs, ampicillin, rifampicin.

Potentially Fatal: May increase effects of drugs which slow AV conduction (digoxin, verapamil, diltiazem).

Overdose

If you think there is an overdose, here are the general symptoms of such an overdose:

Symptoms: rapid heartbeats, severe dizziness, and fainting

Management: Seek emergency medical attention if you think you have taken too much of this medicine

Contraindications

Contraindicated in patients who shows:

Hypersensitivity to either component

History of angioedema related to ACE inhibitor

Patients with hereditary or idiopathic angioedema

Pregnancy

Lactation

Storage

Store the medicine at room temperature, away from heat, moisture, and direct light

Manufacturer

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The information contained on this page is only an educational aid. This information does not intend to be medical advice for individual conditions or treatment. Every effort has been made to ensure that the information provided is accurate, up-to-date and complete, but no guarantee is made to that effect. This information is not a substitute for a medical exam, doctor visit or any services provided by medical or healing professionals. Only your doctor can provide you safe and effective advice based on your own physical conditions or symptoms. The use of the www. tablettree. com is at your risk. These products or information are provided as-is and without any warranties of any kind, either expressed or implied. www. tablettree. com makes no representation or warranty to the accuracy or completeness of any of the information. www. tablettree. com makes no warranties to the opinions or services or data that you may access as a result of using our website. All implied warranties are hereby excluded. www. tablettree. com does not assume any responsibility or risk for your use of www. tablettree. com.

Maxilerg, Maxilerg

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 Maxilerg 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.

Buy Pain Relief - Contra-Schmerz P (Brand Name Anacin) Online - Order Cheap Aspirin, Caffeine - Purc

Anacin is a pain reliever intended for the temporary relief of minor aches and pains. Anacin is a combination salicylate and stimulant. It works by blocking several different chemical processes within the body that cause pain, inflammation, and fever. It also reduces the tendency for blood to clot.

Availability: In Stock (17 packs)

Anacin is used for treating pain including, headache, muscle aches, sprains, tooth extraction and toothache, menstrual cramps, arthritis and rheumatism, and pain and fever of the common cold. It may also be used for other conditions as determined by your doctor.

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

Take Anacin by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation. Taking it with food may not decrease the risk of stomach or bowel problems (eg, bleeding, ulcers) that may occur while taking Anacin.

Take Anacin with a full glass of water (8 oz/240 mL). Do not lie down for 30 minutes after taking Anacin.

Use Anacin exactly as directed on the package, unless instructed differently by your doctor. If you are taking Anacin without a prescription, follow any warnings and precautions on the label.

If you miss a dose of Anacin and you are taking 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.

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

Store Anacin at room temperature, 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 Anacin out of the reach of children and away from pets.

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

Avoid large amounts of food or drink that have caffeine (eg, coffee, tea, cocoa, cola, chocolate). This includes any medicines that contain caffeine.

Anacin has aspirin in it. Before you start any new medicine, check the label to see if it has aspirin in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Talk to your doctor before you take Anacin or other pain relievers/fever reducers if you drink more than 3 drinks with alcohol per day. Serious stomach ulcers or bleeding can occur with the use of Anacin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Anacin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor. Taking more than the recommended dose or taking Anacin regularly may be habit-forming.

Anacin may reduce the number of clot-forming cells (platelets) in your blood. To prevent bleeding, avoid situations in which bruising or injury may occur. Report any unusual bleeding, bruising, blood in stools, or dark, tarry stools to your doctor.

Aspirin has been linked to a serious illness called Reye syndrome. Do not give Anacin to a child or teenager who has the flu, chickenpox, or a viral infection. Contact your doctor with any questions or concerns.

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

If Anacin has a strong vinegar-like smell upon opening, do not use. It means the medicine is breaking down. Throw the bottle away safely and out of the reach of children; contact your pharmacist and replace.

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

Do not take Anacin for at least 7 days after any surgery unless directed by your health care provider.

Do not take Anacin for more than 10 days for pain or for more than 3 days for fever unless directed to do so by your health care provider.

Different brands of Anacin may have different dosing instructions for CHILDREN. Follow the dosing instructions on the package labeling. If your doctor has given you instructions, follow those. If you are unsure of the dose to give a child, check with your doctor or pharmacist.

Do NOT use Anacin if:

you are allergic to any ingredient in Anacin

you are a child or teenager with influenza (flu) or chickenpox

you have bleeding problems such as hemophilia, von Willebrand disease, or low blood platelets, or you have active severe bleeding

you have had a severe allergic reaction (eg, severe rash, hives, breathing difficulties, dizziness) to aspirin, tartrazine, or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

you are taking anticoagulants (eg, heparin, warfarin) or methotrexate

Before using Anacin:

Some medical conditions may interact with Anacin. 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 alcoholism or if you consume 3 or more alcohol-containing drinks every day

if you have asthma, bleeding or clotting problems, growths in the nose (nasal polyps), kidney or liver problems, stomach or intestinal problems (eg, ulcer, inflammation), heart problems, heartburn, upset stomach, stomach pain, hives, influenza (flu) or chickenpox, or vitamin K deficiency

if you have anxiety, trouble sleeping, or heart problems

if you are a child with a stroke, a weakened blood vessel (cerebral aneurysm) or bleeding in the brain, rheumatic disease (eg, rheumatoid arthritis), or Kawasaki syndrome (a rare inflammation causing heart problems in children)

Some MEDICINES MAY INTERACT with Anacin. Tell your health care provider if you are taking any other medicines.

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Anacin while you are pregnant. Anacin is not recommended during the last 3 months (third trimester) of pregnancy because it may cause harm to the fetus. Anacin is found in breast milk. If you are or will be breast-feeding while you use Anacin, 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. Anacin's side effects may include dizziness, heartburn, irritability, nausea, nervousness, rashes, hives, bloody stools, drowsiness, hearing loss, ringing in the ears, and trouble sleeping.

Check with your doctor if any of the listed above most COMMON side effects persist or become bothersome.

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); black or bloody stools; confusion; diarrhea; drowsiness; hearing loss; ringing in the ears; severe or persistent dizziness; severe or persistent stomach pain or heartburn; shakiness; trouble sleeping; vomiting.

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.

Iquix - Fda Prescribing Information, Side Effects And Uses, Iquix

Iquix

Iquix Description

Iquix ® (levofloxacin ophthalmic solution) 1.5% is a sterile topical ophthalmic solution. Levofloxacin is a fluoroquinolone antibacterial active against a broad spectrum of Gram-positive and Gram-negative ocular pathogens. Levofloxacin is a fluorinated 4-quinolone containing a six-member (pyridobenzoxazine) ring from positions 1 to 8 of the basic ring structure. Levofloxacin is the pure(-)-( S )-enantiomer of the racemic drug substance, ofloxacin. It is more soluble in water at neutral pH than ofloxacin.

Chemical Name: (-)( S )-9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7 H - pyrido[1,2,3-de]-1,4 benzoxazine-6-carboxylic acid hemihydrate.

Levofloxacin (hemihydrate) is a yellowish-white crystalline powder.

Each mL of Iquix ® contains 15.36 mg of levofloxacin hemihydrate equivalent to 15 mg levofloxacin.

Contains

Active: Levofloxacin 1.5% (15 mg/mL); Inactives: glycerin and water. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH to approximately 6.5. Iquix ® solution is isotonic with an osmolality of approximately 290 mOsm/kg.

Iquix - Clinical Pharmacology

Pharmacokinetics

Levofloxacin concentration in plasma was measured in 14 healthy adult volunteers during a 16-day course of treatment with Iquix ® solution. The dosing schedule was 1-2 drops per eye once in the morning on Days 1 and 16; 1-2 drops per eye every two hours Days 2 through 8; and 1-2 drops per eye every four hours Days 9 through 15. The mean levofloxacin concentration in plasma 1 hour postdose ranged from 3.13 ng/mL on Day 1 to 10.4 ng/mL on Day 16. Maximum mean levofloxacin concentrations increased from 3.22 ng/mL on Day 1 to 10.9 ng/mL on Day 16, which is more than 400 times lower than those reported after standard oral doses of levofloxacin.

Levofloxacin concentration in tears was measured in 100 healthy adult volunteers at various time points following instillation of 2 drops of Iquix ® solution. Mean tear concentration measured 15 minutes after instillation was 757 µg/mL.

Microbiology

Levofloxacin is the L - isomer of the racemate, ofloxacin, a quinolone antimicrobial agent. The antibacterial activity of ofloxacin resides primarily in the L - isomer. The mechanism of action of levofloxacin and other fluoroquinolone antimicrobials involves the inhibition of bacterial topoisomerase IV and DNA gyrase (both of which are type II topoisomerases), enzymes required for DNA replication, transcription, repair, and recombination.

Levofloxacin has in vitro activity against a wide range of Gram-negative and Gram-positive microorganisms and is often bactericidal at concentrations equal to or slightly greater than inhibitory concentrations.

Fluoroquinolones, including levofloxacin, differ in chemical structure and mode of action from β-Iactam antibiotics and aminoglycosides, and therefore may be active against bacteria resistant to β-Iactarn antibiotics and aminoglycosides. Additionally, β-Iactam antibiotics and aminoglycosides may be active against bacteria resistant to levofloxacin. Resistance to levofloxacin due to spontaneous mutation in vitro is a rare occurrence (range: 10 -9 to 10 -10 ).

Levofloxacin has been shown to be active against most strains of the following microorganisms, both in vitro and in clinical infections as described in the INDICATIONS AND USAGE section:

AEROBIC GRAM-POSITIVE MICROORGANISMS:

AEROBIC GRAM-NEGATIVE MICROORGANISMS:

The following in vitro data are also available, but their clinical significance in ophthalmic infections is unknown. The safety and effectiveness of levofloxacin in treating ophthalmological infections due to these microorganisms have not been established in adequate and well-controlled trials.

These organisms are considered susceptible when evaluated using systemic breakpoints. However, a correlation between the in vitro systemic breakpoint and ophthalmological efficacy has not been established. The list of organisms is provided as guidance only in assessing the potential treatment of corneal ulcer. Levofloxacin exhibits in vitro minimal inhibitory concentrations (MICs) of 2 µg/mL or less (systemic susceptible breakpoint) against most (≥90%) strains of the following ocular pathogens:

AEROBIC GRAM-POSITIVE MICROORGANISMS:

Enterococcus faecalis (many strains are only moderately susceptible)

Streptococcus (Group C/F)

Streptococcus (Group G)

AEROBIC GRAM-NEGATIVE MICROORGANISMS:

Clinical Studies

In two randomized, double-masked, multicenter controlled clinical trials of 280 patients with positive cultures, subjects were dosed with Iquix ® or ofloxacin 0.3% ophthalmic solution. Dosing occurred on Days 1 through 3 every two hours while awake and 4 and 6 hours after retiring. Dosing occurred on Day 4 through treatment completion 4 times daily while awake. Clinical cure was defined as complete re-epithelialization and no progression of the infiltrate for two consecutive visits. The Iquix ® treated subjects had an approximately equal mean clinical cure rate of 80% (73% to 87%) compared to 84% (82% to 86%) for the subjects treated with ofloxacin 0.3% ophthalmic solution.

Indications and Usage for Iquix

Iquix ® solution is indicated for the treatment of corneal ulcer caused by susceptible strains of the following bacteria:

* Efficacy for this organism was studied in fewer than 10 infections.

Viridans group streptococci*

Contraindications

Iquix ® solution is contraindicated in patients with a history of hypersensitivity to levofloxacin, to other quinolones, or to any of the components in this medication.

Warnings

NOT FOR INJECTION.

Iquix ® solution should not be injected subconjunctivally, nor should it be introduced directly into the anterior chamber of the eye.

In patients receiving systemic quinolones, serious and occasionally fatal hypersensitivity (anaphylactic) reactions have been reported, some following the first dose. Some reactions were accompanied by cardiovascular collapse, loss of consciousness, angioedema (including laryngeal, pharyngeal or facial edema), airway obstruction, dyspnea, urticaria, and itching. If an allergic reaction to levofloxacin occurs, discontinue the drug. Serious acute hypersensitivity reactions may require immediate emergency treatment. Oxygen and airway management should be administered as clinically indicated.

Precautions

General

As with other anti-infectives, prolonged use may result in overgrowth of non-susceptible organisms, induding fungi. If superinfection occurs, discontinue use and institute alternative therapy. Whenever clinical judgment dictates, the patient should be examined with the aid of magnification, such as slit-lamp biomicroscopy, and, where appropriate, fluorescein staining.

Patients should be advised not to wear contact lenses if they have signs and symptoms of corneal ulcer.

Information for Patients

Avoid contaminating the applicator tip with material from the eye, fingers or other source.

Systemic quinolones have been associated with hypersensitivity reactions, even following a single dose. Discontinue use immediately and contact your physician at the first sign of a rash or allergic reaction.

Drug Interactions

Specific drug interaction studies have not been conducted with Iquix ®. However, the systemic administration of some quinolones has been shown to elevate plasma concentrations of theophylline, interfere with the metabolism of caffeine, and enhance the effects of the oral anticoagulant warfarin and its derivatives, and has been associated with transient elevations in serum creatinine in patients receiving systemic cyclosporine concomitantly.

Carcinogenesis, Mutagenesis, Impairment of Fertility

In a long term carcinogenicity study in rats, levofloxacin exhibited no carcinogenic or tumorigenic potential following daily dietary administration for 2 years; the highest dose (100 mg/kg/day) was 100 times the highest recommended human ophthalmic dose.

Levofloxacin was not mutagenic in the following assays: Ames bacterial mutation assay (S. typhimurium and E. coli). CHO/HGPRT forward mutation assay, mouse micronucleus test, mouse dominant lethal test, rat unscheduled DNA synthesis assay, and the in vivo mouse sister chromatid exchange assay. It was positive in the in vitro chromosomal aberration (CHL cell line) and in vitro sister chromatid exchange (CHL/IU cell line) assays.

Levofloxacin caused no impairment of fertility or reproduction in rats at oral doses as high as 360 mg/kg/day, corresponding to 400 times the highest recommended human ophthalmic dose.

Pregnancy

Pregnancy Category C

Levofloxacin at oral doses of 810 mg/kg/day in rats, which corresponds to approximately 1000 times the highest recommended human ophthalmic dose, caused decreased fetal body weight and increased fetal mortality.

No teratogenic effect was observed when rabbits were dosed orally as high as 50 mg/kg/day, which corresponds to approximately 60 times the highest recommended maximum human ophthalmic dose, or when dosed intravenously as high as 25 mg/kg/day, corresponding to approximately 30 times the highest recommended human ophthalmic dose.

There are, however, no adequate and well-controlled studies in pregnant women. Levofloxacin should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nursing Mothers

Levofloxacin has not been measured in human milk. Based upon data from ofloxacin, it can be presumed that levofloxacin is excreted in human milk. Caution should be exercised when Iquix ® is administered to a nursing mother.

Pediatric Use

Safety and effectiveness in children below the age of six years have not been established. Oral administration of systemic quinolones has been shown to cause arthropathy in immature animals. There is no evidence that the ophthalmic administration of levofloxacin has any effect on weight bearing joints.

Geriatric Use

No overall differences in safety or effectiveness have been observed between elderly and other adult patients.

Adverse Reactions

The most frequently reported adverse events in the overall study population were headache and a taste disturbance following instillation. These events occurred in approximately 8–10% of patients.

Adverse events occurring in approximately 1–2% of patients included decreased/blurred vision, diarrhea, dyspepsia, fever, infection, instillation site irritation/discomfort, ocular infection, nausea, ocular pain/discomfort, and throat irritation.

Other reported ocular reactions occurring in less than 1% of patients included chemosis, corneal erosion, corneal ulcer, diplopia, floaters, hyperemia, lid edema, and lid erythema.

Iquix Dosage and Administration

Days 1 through 3

Instill one to two drops in the affected eye(s) every 30 minutes to 2 hours while awake and approximately 4 and 6 hours after retiring.

Day 4 through treatment completion

Instill one to two drops in the affected eye(s) every 1 to 4 hours while awake.

How is Iquix Supplied

Iquix ® (levofloxacin ophthalmic solution) 1.5% is supplied in a white, low density polyethylene bottle with a controlled dropper tip and a tan, high density polyethylene cap in the following size:

5 mL fill in 5 cc container– NDC 68669-145-05

Storage

Store at 15° – 25°C (59°– 77°F).

Manufactured by: Santen Oy, P. O. Box 33, FIN-33721 Tampere, Finland

Marketed by: VISTAKON ® Pharmaceuticals, LLC Jacksonville, FL 32256 USA

Licensed from: Daiichi Sankyo Co. Ltd. Tokyo, Japan

U. S. PAT. NO 5,053,407

April 2007 Version

PRINCIPAL DISPLAY PANEL - 5mL Carton

Iquix ® (levofloxacin ophthalmic solution) 1.5%

VISTAKON ® PHARMACEUTICALS, LLC

About Us, Innovair

About Us

After a successful career leading several major data-driven direct marketing firms – while simultaneously volunteering his time to help numerous causes and associations – Don decided to combine his professional skills with his personal passions and joined Innovairre. Now Don's favorite quote is, "Your cause is our cause."

Don has extensive experience building integrated, multichannel marketing services organizations – with several thousand employees and more than a dozen locations – through leadership development, business turnaround/transformation and progressive growth strategies.

Previously, Don served as president and CEO for these leading organizations: SourceLink, Direct Group, CC3, Petsky Prunier and a division of Advo. Over the years, Don has contributed his expertise to the marketing industry, serving on many industry boards. This includes being elected vice chairman of the Direct Marketing Association, the world's largest trade association supporting both nonprofit and commercial direct marketers with more than 2,600 member organizations. Don is also is a frequent speaker on emerging trends in big data and integrated communications.

Don and his wife, Nancy, are proud parents. In their spare time, they have worked diligently to serve their church. Nancy, a nurse, also does volunteer work at a free health clinic.

John joined Innovairre in 2016 and has worked in the print/packaging/distribution/digital space for 32 years in progressive senior level operational and business unit leadership positions. He has supported several multinational CPG's as well as the Global Pharmaceutical 'Top 20' during his career.

Most of the last 20 years have been spent working with private equity backed companies. He is 54 years old and has both an MBA and a BS in Management/Computer Science.

Drew brings together experience managing the financial complexities of a $1+ billion public company with an understanding of the unique challenges of nonprofits. Throughout his career, Drew has held various leadership positions with educational, health and community nonprofits. At Innovairre, it's our clients who benefit.

Drew spent 24 years as a CFO, treasurer and corporate secretary at Pulse Electronics, an international, NYSE-listed public manufacturing company. During this time, he developed strong capital markets experience and was responsible for corporate finance, accounting, strategic planning and governance. In addition, as a business segment CEO of a 1,700-person global manufacturing operation, Drew gained direct operating experience as he grew revenue and operating profit substantially in the segment.

Drew is results-oriented, informal, candid and inspires credibility and accountability in others. He is also passionate about local institutions and causes. He has served on the board of directors of both the Philadelphia Zoo and Penn Foundation, which is a foundation that uses the healing power of hope and the possibility of recovery to treat the mental health, substance abuse and intellectual disability needs of individuals and families in his community.

Drew is based in our New Jersey office and lives in Philadelphia, PA. When he isn't busy with Innovairre, he enjoys fitness, community causes and keeping up with the activities of his teenage daughters.

Helping nonprofits is what Dawn does, personally and professionally.

Dawn offers our clients more than 18 years of experience improving fundraising performance through the development of innovative strategic plans, multichannel integration, the unique application of analytics and strong fiscal management.

At Innovairre, Dawn leads a team of forward-thinking strategists dedicated to exceeding our clients' fundraising goals through holistic or targeted plans that can include direct mail, digital, CRM, major gifts and/or planned giving. In this role, Dawn was the mastermind behind several proprietary analytical tools that drive exceptional fundraising results.

Before joining Innovairre, Dawn served as senior vice president, fundraising and client services at Barton Cotton.

Dawn is active in her community, helping local non-profit organizations. Dawn resides in Maryland with her husband, Andrew, and their two children.

Matt is a marketing executive with a passion for data and marketing technology. He is certainly in the right place at the right time.

Matt's unique expertise is the intersection of data and evolving digital technologies that increase marketing effectiveness through integrated, multichannel engagement.

At Innovairre, Matt leads data-driven digital strategy and innovation for nonprofit marketing/fundraising success. This includes data modeling and analytics; database-driven marketing automation; high-speed, full-color, variable digital print; online, interactive marketing; social awareness and fundraising; and mobile engagement

Prior to joining Innovairre, Matt held strategic and technology leadership positions at several highly respected marketing/production companies, including SourceLink, CC3, Direct Group and Budco where he provided strategic support for their transformation from traditional print and mail service providers to data-driven, technology-enabled marketing services agencies.

When Matt is not pioneering the latest and greatest in smart marketing solutions, he keeps busy with his six kids (preschool through high school) and all the schooling, sports and community volunteer work that goes with it.

Born and raised in France and currently living in the Netherlands with her husband and four children, Rebecca built our branch office in Amsterdam from the ground up by combining passion, creativity, tenacity, knowledge and integrity with a strong entrepreneurial drive.

Having traveled the world extensively and built numerous partnerships with communication agencies and nonprofit organizations around the globe, Rebecca brings her diverse experience to everything she does. And it doesn’t hurt that she speaks three languages fluently: French, English and Dutch.

Believing there is nothing greater than helping those in need, Rebecca envisioned and pioneered the International Network of Fundraising Agencies (INFA) network, which partners fundraising agencies around the world. INFA’s primary goal is to redefine fundraising and be at the leading edge of a new culture dedicated to fundraising.

Her approach is hands-on, results-driven but also people-oriented. Her communication style is open and combined with a healthy dose of humor and sense of perspective. Rebecca is a visionary. She strives to add value and bring innovation wherever she goes and in all that she does. That’s her philosophy.

Because she believes in the power of trust, she greatly values the relationships she builds with nonprofits and takes great pride and satisfaction in aiding them on their missions.

Mark has a fascinating, comprehensive background, having worked in the nonprofit and commercial markets; in government, as a presidential appointee; and on the client and agency side of the fundraising market. Currently, Mark leads our integrated fundraising and marketing activities on behalf of more than 50 full-service clients.

Prior to joining Innovairre, Mark served for 10 years as the associate executive director for development, marketing and communications at the Paralyzed Veterans of America, where he was responsible for more than 15 revenue-generating programs and all branding and communications efforts. Mark served as a presidential appointee during both the Reagan and the first Bush administrations. As director of business finance for the State of Florida, Mark was responsible for all economic and community development financing throughout the state.

Active in his community and local nonprofits, Mark currently resides in Manassas, Virginia, with his wife of 30 years, Susan, a local artist, and two of their four children.

Adam is driven by a passion to help the world's leading nonprofits maximize net revenue to fund their critical missions. As a fundraising futurist, Adam evolves time-tested, direct marketing best practices through data insights, analytics and technology.

As the chair of the Direct Marketing Association's Committee on the Environment and Social Responsibility and a member of the DMA Ethics Policy Committee, Adam believes that sustainable business is the new business as usual, particularly for mission-driven organizations.

He has collaborated with more than 60 leading nonprofits and agencies in the UK, Canada and U. S. markets where his ideas and vision led to advances in donor acquisition and retention marketing results.

Adam has a Masters in Sustainability Management from Columbia University and a Bachelor of Science in Marketing from Penn State.

Michael has an unwavering passion to provide scalable and collaborative multinational solutions to his domestic and international fundraising partners. His entrepreneurial vision has spanned over 21 years in manufacturing, operations and marketing. Michael uses his keen focus on exceeding clients’ goals and his “get it done” business vigor to lead successful start-ups and turnarounds in both the nonprofit and commercial sectors.

At Innovairre, Michael serves as the SVP/General Manager leading our client-centric operations team located in New Jersey, Maryland, Italy and Amsterdam. His diverse team is made up of project managers, data processors, mailing services, logistics and fundraising professionals from eight different countries with a single focus on providing exceptional client experiences.

Prior to joining Innovairre, Michael spent 16 years with a leading solutions provider, RR Donnelley & Sons, where he served in a number of senior-level positions around the world, which included director of fulfillment operations, regional vice president of business operations and platform vice president for their short-run digital, direct mail and fulfillment division.

Michael is very active in his community, aiding his local church and community sports organization with their fundraising efforts. Michael resides in Pennsylvania with his wife of nearly 20 years, Kelly, and their two children.

Jill offers our clients more than 16 years of direct marketing and fundraising experience. She is an innovator and strategic thinker; her approach includes campaign planning, package innovation and multichannel integration leading to the goal of raising money for non-profits.

Currently, Jill focuses her energy on leading our CSI (Creative, Strategy and Innovation) team. A group instrumental in our organization, they work to create breakthrough print, premium and digital campaigns for non-profits and their agencies.

Jill's background is diverse. Her manufacturing and premium sourcing experience allows her and her team to work closely with our overseas teams, bringing cost-effective and innovative package solutions to our clients.

Jill studied at Boston University and Bryant University. She is active in her community, volunteering regularly in her community. She resides in Rhode Island with her husband and son.

Innovairre's Chairman of the Board, Robert "Kam" Kamerschen, is an experienced outside director of public and private companies. Kam is also a senior advisor/consultant and a retired Chairman & CEO with a track record of being a very successful change leader in a number of industries.

Kam served as Chairman & CEO of Advo, Inc. (NYSE), the nation's largest direct mail services' company, with annual revenues of more than $5 billion, where he led an approximate 13-fold increase in total shareholder return over his 10-year tenure. Following his retirement from Advo, he accepted a CEO assignment to navigate a firm, DIMAC, through the C-11 process, which he did successfully.

Prior to joining ADVO, Kam was President & CEO of RKO/Six Flags; President & COO of Marketing Corporation of America; EVP & Group Executive of Norton Simon, Inc. where he was responsible for five companies: Hunt Wesson Foods, Max Factor, Halston Enterprises, McCall Pattern and United Can, as well as President & CEO of Max Factor; President of Chanel and Christian Dior Parfums; and has held senior marketing executive assignments at Scott Paper Company, Dunkin' Donuts and Revlon.

Regarding his public board experience, Kam has served on the Board of Directors of MDC Partners (NASDAQ & TSE) as its Presiding Director as well as Chairman of the Nominating and Governance Committee. His other public corporate directorships, where he served in committee chairmanship roles in virtually all of them, were R. H. Donnelley/Now DexOne (NYSE); IMS Health (NYSE); RadioShack (NYSE); Linens n' Things (NYSE); Vertrue (NASDAQ); Synavant (NASDAQ); Maxxcom (NASDAQ & TSE); Coolsavings (NASDAQ); Micrografx, Inc. (NASDAQ); MECA Software (NASDAQ); and Playboy Enterprises (NYSE). Kam is also currently serving as an investor board member on a number of private companies, primarily backed by prominent private equity firms. He has also served as a panelist and speaker in a number of certified corporate governance conferences.

Additionally, Kam served as a Dean's Associate at Miami's School of Business Advisory Council; participated in the University of Georgia's Distinguished Lecturer/Practitioner program; and has lectured at a number of leading business schools. He also served as Trustee at Emerson College, Columbia College and Hartford University, as well as at Wadsworth Atheneum Museum of Art and Bushnell Theater.

Kam has been registered in Who's Who in America for a number of years and, more recently, Who's Who in the World. He received his B. S. and MBA with Beta Gamma Sigma honors at Miami University in Oxford, Ohio.

Innovairre Board Member, Robert "Rob" Janes is an important part of our team for both his financial accumen and active board management experience.

Currently, Rob is an active board member of the following organizations: Beckman Production Services/RedZone Coil Tubing, Davis Standard, Megtec and EiKO.

In addition, Rob is Managing Director for Stephens Capital Partners, the highly respected financial services firm founded in 1933.

As a specialist in the Corporate Finance Department of Stephens Inc. he has assisted with several major transactions, including Stephens' acquisition of Donrey Media Group (now Stephens Media) in 1993.

Rob earned a BBA degree from SMU and an MBA from The Wharton School.

Innovairre Board Member, Rakesh K. Kaul is a highly skilled Chief Executive Officer, Board Member and Senior Advisor, with a long-standing commitment to community service.

Rakesh K. Kaul is currently a Board Member of Life Line Screening, Income Discovery and Estee Advisors and is Chairman and Founder of Spherenomics.

Previously, Rakesh served as Senior Advisor to The Carlyle Group (Consumer and Retail Group) and as Senior Advisor and Board Member of Oriental Trading Co.

In a management capacity, Rakesh has experience as CEO of TWS and Hanover Direct and Vice Chairman of Fingerhut. He has also held senior roles at Beatrice/Hunt-Wesson and Shaklee Corporation.

Rakesh's community service has included serving on the boards of the Bay Area United Way and the Ordway Music Theatre, and serving as a Trustee of the Asian Art Museum in San Francisco, as a founding contributor to the Chair of India Studies at Berkeley and CASI at the University of Pennsylvania, as a President's Circle Member of the Asia Society, New York, as a Charter member of TIE and the US Group, as past Board member of the Dwight Englewood School, as Co-Chairman of The Arts of Kashmir Exhibition 2007 at the Asia Society, as Co-Chair for the IIT Delhi Excellence Foundation in North America, and as Head of Fundraising for the $5MM Mattoo Center for India Studies at SUNY, which was inaugurated in December 2013.

Peter thinks big. He has to.

Peter supervises more than 3,000 employees in two vertically integrated printing and production facilities in Southern China, which cover more than 1.1 million square feet of industrial space.

The operations Peter is responsible for produce hundreds of millions of direct mail packages annually for nonprofit clients located in 20 countries.

Peter has more than 40 years of direct mail manufacturing experience and holds a Masters in EMBA from City University of Hong Kong. He is proud of his active involvement in the fundraising community.

Dean likes to say, "Think big and make a difference." It's that mindset that helps the 4,000+ employees of Innovairre, spread across five continents, service 500+ nonprofit organizations and deliver more than five billion fundraising communications per year.

Dean spent more than 18 years with Quad/Graphics and Quebecor World and held positions as a VP and EVP responsible for numerous facilities across North America. Dean has extensive operations, finance and team-building experience. His passion is leading business operations to new levels of success by achieving lean efficiency, creating growth and ensuring sustainable success.

Through strategic leadership and financial management expertise, Dean excels at transforming organizations through the standardization of operations, the implementation of market expansion initiatives and creating an innovative culture to service clients.

Dean's dedication to good causes doesn't stop with his work at Innovairre. Along with his wife and two children, Dean gives back to his local community with his time and service to several local missions, which support his long-time passion of improving the lives of others.

We plan, analyze, and produce. You prosper.

Innovairre is the worldwide leader in fundraising, supporting partner agencies and nonprofit organizations. We service more than 500 charities, with 4000+ employees, working across five continents. In 2013 alone, Innovairre's operations helped our nonprofit partners and partner agencies raise more than five billion dollars.

Innovairre leverages a scientific marketing approach for fundraising optimization. This includes use of advanced data analytics and insights; progressive digital marketing; leading edge technologies; sophisticated application of personalization; a proven creative and testing methodology; and unsurpassed capabilities in direct mail development, digital printing and premiums for the nonprofit sector.

Innovairre also supports many leading commercial companies and has specialized expertise in the financial, healthcare, insurance, publishing and retail categories.

The employees of Innovairre will proudly donate up to 16,000 hours this year to important nonprofit causes and participate in several mission trips.

To stay current on Innovairre's activities, please read our blog or follow us on Twitter. LinkedIn. and Facebook .

Our Areas of Expertise

Medical Research ? Environmental ? Animal rights ? Humanitarian ? Disaster Relief ? Religious ? Veterans ? The Arts ? Hospitals ? Colleges and Universities

Financial ? Healthcare ? Insurance ? Retail ? Publishing

Losartan Medlineplus Medicinas, Losacor

Losartan

Informe a su medico si esta embarazada o planea quedar embarazada. No tome losartan si esta embarazada. Si queda embarazada mientras esta tomando losartan, deje de tomarlo y llame a su medico de inmediato. El losartan puede provocar la muerte o lesiones graves en el feto cuando se lo toma en los ultimos 6 meses de embarazo.

?Para cuales condiciones o enfermedades se prescribe este medicamento?

El losartan se usa solo o en combinacion con otros medicamentos para tratar la presion arterial alta. El losartan tambien se usa para disminuir el riesgo de accidente cerebrovascular en personas que tienen presion arterial alta y una afeccion del corazon llamada hipertrofia ventricular izquierda (agrandamiento de las paredes del lado izquierdo del corazon). Es posible que el losartan no disminuya el riesgo de accidente cerebrovascular en las personas afroamericanas que tienen estas afecciones. Este medicamento tambien se usa para tratar la enfermedad del rinon en personas que tienen diabetes tipo 2 (afeccion en la que el cuerpo no usa insulina en forma normal y, por lo tanto, no puede controlar la cantidad de azucar en la sangre) y presion arterial alta. El losartan pertenece a una clase de medicamentos llamados antagonistas del receptor de la angiotensina II. Actua bloqueando la accion de determinadas sustancias naturales que contraen los vasos sanguineos, lo que permite que la sangre circule mejor y que el corazon bombee con mayor eficiencia.

La presion arterial alta es una condicion comun, y cuando no es tratada, puede causar danos en el cerebro, el corazon, los vasos sanguineos, los rinones y otras partes del cuerpo. El dano a estos organos puede causar enfermedades del corazon, un ataque cardiaco, insuficiencia cardiaca, accidente cerebrovascular, insuficiencia renal, perdida de la vision, y otros problemas. Ademas de tomar la medicacion, hacer cambios de estilo de vida tambien ayudara a controlar su presion arterial. Estos cambios incluyen comer una dieta que sea baja en grasa y sal, mantener un peso saludable, hacer ejercicio al menos 30 minutos casi todos los dias, no fumar y consumir alcohol con moderacion.

?Como se debe usar este medicamento?

La presentacion del losartan es en tabletas para administrarse por via oral. Generalmente, se toma una o dos veces al dia, con o sin alimentos. Para que no olvide tomar el losartan, tomelo aproximadamente a la misma hora todos los dias. Siga atentamente las instrucciones del medicamento recetado, y pidales a su medico o a su farmaceutico que le expliquen cualquier cosa que no entienda. Tome el losartan segun lo indicado. No aumente ni disminuya la dosis, ni la tome con mas frecuencia que la indicada por su medico.

Es posible que su medico le recete al principio una dosis baja de losartan y la aumente en forma gradual.

Si su hijo no puede tragar una tableta, consulte a su medico o farmaceutico. El farmaceutico puede preparar una forma liquida de este medicamento para su hijo.

El losartan controla la presion arterial alta, pero no la cura. Es posible que su presion arterial disminuya durante la primera semana de su tratamiento, pero quizas transcurran de 3 a 6 semanas antes de que note el beneficio total del losartan. Siga tomando el losartan aunque se sienta bien. No deje de tomar el losartan sin consultar a su medico.

Pidales a su medico o a su farmaceutico una copia de la informacion del fabricante para el paciente.

?Que otro uso se le da a este medicamento?

El losartan tambien se utiliza a veces para tratar la insuficiencia cardiaca congestiva (afeccion en la que el corazon no puede bombear suficiente sangre al resto del cuerpo). Consulte a su medico acerca de los posibles riesgos de usar este medicamento para su afeccion.

Este medicamento puede recetarse para otros usos; pidales mas informacion a su medico o a su farmaceutico.

Cephalexin Medlineplus Drug Information, Cephalex R

Cephalexin

Cephalexin is used to treat certain infections caused by bacteria such as pneumonia and other respiratory tract infections; and infections of the bone, skin, ears. genital, and urinary tract. Cephalexin is in a class of medications called cephalosporin antibiotics. It works by killing bacteria.

Antibiotics such as cephalexin will not work for colds, flu, or other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.

How should this medicine be used?

Cephalexin comes as a capsule, tablet, and suspension (liquid) to take by mouth. It is usually taken with or without food every 6 or 12 hours for 7 to 14 days, depending on the condition being treated. Take cephalexin at around the same times every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take cephalexin exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Shake the liquid well before each use to mix the medication evenly.

You should begin to feel better during the first few days of treatment with cephalexin. If your symptoms do not improve or get worse, call your doctor.

Continue to take cephalexin until you finish the prescription even if you feel better. If you stop taking cephalexin too soon or skip doses, your infection may not be completely treated and the bacteria may become resistant to antibiotics.

Other uses for this medicine

Cephalexin is also sometimes used for certain penicillin allergic patients who have a heart condition and are having a dental or upper respiratory tract (nose, mouth, throat, voice box) procedure, in order to prevent them from developing a heart valve infection.

This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.

What special precautions should I follow?

Before taking cephalexin,

tell your doctor and pharmacist if you are allergic to cephalexin; other cephalosporin antibiotic such as cefaclor, cefadroxil cefazolin (Ancef, Kefzol), cefdinir, cefditoren (Spectracef), cefepime (Maxipime), cefixime (Suprax), cefotaxime (Claforan), cefotetan, cefoxitin (Mefoxin), cefpodoxime, cefprozil, ceftaroline (Teflaro), ceftazidime (Fortaz, Tazicef, in Avycaz), ceftibuten (Cedax), ceftriaxone (Rocephin), and cefuroxime (Zinacef); penicillin antibiotics; or any other medications. Also tell your doctor if you are allergic to any of the ingredients in cephalexin capsules, tablets, or suspension. Ask your pharmacist for a list of the ingredients.

tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention any of the following: anticoagulants ('blood thinners') such as warfarin (Coumadin, Jantoven); metformin (Fortamet, Glucophage, Glumetza, Riomet, in Glucovance, Invokamet, others); and probenecid (Probalan). Your doctor may need to change the doses of your medications or monitor you carefully for side effects.

tell your doctor if you have or have ever had any kind of allergies, gastrointestinal disease (GI; affecting the stomach or intestines), especially colitis (condition that causes swelling in the lining of the colon [large intestine]), or kidney or liver disease.

tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking cephalexin, call your doctor.

What special dietary instructions should I follow?

Unless your doctor tells you otherwise, continue your normal diet.

What should I do if I forget a dose?

Take the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not take a double dose to make up for a missed one.

What side effects can this medication cause?

Cephalexin may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

nausea

diarrhea

vomiting

heartburn

stomach pain

rectal or genital itching

dizziness

extreme tiredness

agitation

confusion

headache

joint pain

Some side effects can be serious. If you experience any of the following symptoms, call your doctor immediately or get emergency medical treatment:

watery or bloody stools, stomach cramps, or fever during treatment or for up to two or more months after stopping treatment

rash

itching

hives

swelling of the face, throat, tongue, lips, and eyes

difficulty breathing or swallowing

wheezing

a return of fever, sore throat, chills, or other signs of infection

hallucinations (seeing things or hearing voices that do not exist)

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www. fda. gov/Safety/MedWatch ) or by phone (1-800-332-1088).

What should I know about storage and disposal of this medication?

Keep this medication in the container it came in, tightly closed, and out of reach of children. Store the capsules and tablets at room temperature and away from excess heat and moisture (not in the bathroom). Keep liquid medicine in the refrigerator, tightly closed, and dispose of any unused medication after 14 days.

Unneeded medications should be disposed of in special ways to ensure that pets, children, and other people cannot consume them. However, you should not flush this medication down the toilet. Instead, the best way to dispose of your medication is through a medicine take-back program. Talk to your pharmacist or contact your local garbage/recycling department to learn about take-back programs in your community. See the FDA's Safe Disposal of Medicines website (http://goo. gl/c4Rm4p ) for more information if you do not have access to a take-back program.

In case of emergency/overdose

In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.

Symptoms of overdose may include:

nausea

vomiting

diarrhea

pink, red, or dark brown urine

stomach pain

Lansoprazole Medlineplus Drug Information, Lanzoprazol

Lansoprazole

Why is this medication prescribed?

Prescription lansoprazole is used to treat gastroesophageal reflux disease (GERD), a condition in which backward flow of acid from the stomach causes heartburn and possible injury of the esophagus (the tube between the throat and stomach). Prescription lansoprazole is used to treat the symptoms of GERD, allow the esophagus to heal, and prevent further damage to the esophagus. Prescription lansoprazole is also used to treat ulcers (sores in the lining of the stomach or intestine), to prevent more ulcers from developing in people whose ulcers have already healed, and to decrease the risk that people who are taking nonsteroidal anti-inflammatory drugs (NSAIDs) will develop ulcers. Prescription lansoprazole is also used to treat conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome. Prescription lansoprazole is also used in combination with other medications to treat and prevent stomach ulcers caused by a certain type of bacteria ( H. pylori ). Nonprescription (over-the-counter) lansoprazole is used to treat frequent heartburn (heartburn that occurs two or more days per week). Lansoprazole is in a class of medications called proton pump inhibitors. It works by decreasing the amount of acid made in the stomach.

How should this medicine be used?

Prescription lansoprazole comes as a delayed-release (releases the medication in the intestine to prevent break-down of the medication by stomach acids) capsule and an orally disintegrating (dissolving) tablet to take by mouth. Nonprescription lansoprazole comes as a delayed-release (releases the medication in the intestine to prevent break-down of the medication by stomach acids) capsule to take by mouth. Prescription lansoprazole is usually taken once a day, before a meal. When taken in combination with other medications to eliminate H. pylori . prescription lansoprazole is taken twice a day (every 12 hours) or three times a day (every 8 hours), before a meal, for 10 to 14 days. Nonprescription lansoprazole is usually taken once a day, in the morning before eating for 14 days. Additional 14-day treatments may be repeated once every 4 months if needed. Take lansoprazole at around the same time(s) every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take lansoprazole exactly as directed. Do not take more or less of it or take it more often or for a longer time than prescribed by your doctor or stated on the package. Tell your doctor if you have taken nonprescription lansoprazole for a longer period of time than stated on the package.

Swallow the prescription capsules whole; do not split, chew, or crush them. If you have difficulty swallowing capsules, you may open the capsule, sprinkle the granules on 1 tablespoon of applesauce, Ensure pudding, cottage cheese, yogurt, or strained pears and swallow the mixture immediately without chewing. You can also open a capsule and pour the contents into 2 ounces (60 milliliters) of orange juice, apple juice or tomato juice, mix briefly, and swallow immediately. After you swallow the mixture, rinse the glass with some additional juice and drink immediately. Then rinse the glass with juice a second time and drink the juice to be sure that you wash all the medication out of the glass.

Swallow the nonprescription capsules whole with a glass of water. Do not split, chew, or crush them.

Do not break, cut or chew the orally disintegrating tablets. Place a tablet on your tongue and wait up to one minute for it to dissolve. After the tablet dissolves, swallow it with or without water. If you cannot swallow the tablet, you may place it in an oral syringe, draw up 4 mL of water for a 15 mg tablet or 10 mL of water for a 30-mg tablet, shake the syringe gently to dissolve the tablet, and squirt the contents into your mouth immediately. Then draw an additional 2 mL of water into the syringe, shake gently, and squirt that water into your mouth. Do not swallow the mixture more than 15 minutes after you dissolve the tablet.

The capsule contents and orally disintegrating tablets can both be given through a feeding tube. If you have a feeding tube, ask your doctor how you should take the medication. Follow these directions carefully.

Do not take nonprescription lansoprazole for immediate relief of heartburn symptoms. It may take 1 to 4 days for you to feel the full benefit of the medication. Call your doctor if your symptoms get worse or do not improve after 14 days or if your symptoms return sooner than 4 months after you finish your treatment. Do not take nonprescription lansoprazole for longer than 14 days or treat yourself with omeprazole more often than once every 4 months without talking to your doctor.

Continue to take lansoprazole even if you feel well. Do not stop taking prescription lansoprazole without talking to your doctor. If your condition does not improve or gets worse, call your doctor.

Ask your doctor or pharmacist for a copy of the manufacturer's information for the patient.

Other uses for this medicine

This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.

What special precautions should I follow?

Before taking lansoprazole,

tell your doctor and pharmacist if you are allergic to lansoprazole, any other medications, or any of the ingredients in lansoprazole capsules or orally disintegrating tablets. Ask your doctor or pharmacist for a list of the ingredients.

tell your doctor if you are taking rilpivirine (Edurant, in Complera, Odefsey). Your doctor will probably tell you not to take lansoprazole if you are taking this medication.

tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention any of the following: certain antibiotics, including ampicillin (Principen), anticoagulants (blood thinners) such as warfarin (Coumadin), atazanavir (Reyataz), digoxin (Lanoxin), diuretics ('water pills'), iron supplements, ketoconazole (Nizoral), methotrexate (Rheumatrex, Trexall), tacrolimus (Prograf), and theophylline (Theo-bid, TheoDur). Your doctor may need to change the doses of your medications or monitor you carefully for side effects.

if you are taking sucralfate (Carafate), take it at least 30 minutes after you take lansoprazole.

you may take antacids with lansoprazole. If you feel you need an antacid, ask your doctor to recommend one and to tell you when and how to take it.

tell your doctor if you have or have ever had a low level of magnesium in your bloodor liver disease.

if you plan to take nonprescription lansoprazole, first tell your doctor if your heartburn has lasted 3 months or longer or if you have experienced any of the following symptoms: lightheadedness, sweating, or dizziness along with your heartburn; chest pain or shoulder pain; shortness of breath or wheezing; pain that spreads to your arms, neck, or shoulders; unexplained weight loss; nausea; vomiting, especially if the vomit is bloody; stomach pain; difficulty swallowing food or pain when you swallow food; or black or bloody stools. You may have a more serious condition that cannot be treated with nonprescription medication.

tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking lansoprazole, call your doctor.

if you are 50 years of age or older, ask your doctor if it is safe for you to use prescription or nonprescription lansoprazole. The risk that you may develop a severe form of diarrhea caused by bacteria or that you may fracture your wrist, hip, or spine may be higher if you are an older adult.

if you have phenylketonuria (PKU, an inherited condition in which a special diet must be followed to prevent mental retardation), you should know that the orally disintegrating tablets may contain aspartame, which forms phenylalanine.

What special dietary instructions should I follow?

Unless your doctor tells you otherwise, continue your normal diet.

What should I do if I forget a dose?

Take the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your dosing schedule. Do not take a double dose to make up for a missed one.

What side effects can this medication cause?

Lansoprazole may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

Some side effects can be serious. If you experience any of the following symptoms, call your doctor immediately:

rash

blistering or peeling skin

hives

swelling of the eyes, face, lips, mouth, tongue, or throat

difficulty breathing or swallowing

hoarseness

irregular, fast, or pounding heartbeat

excessive tiredness

dizziness

lightheadedness

muscle spasms

uncontrollable shaking of a part of the body

seizures

severe diarrhea with watery stools

stomach pain

fever

Lansoprazole may cause other side effects. Call your doctor if you have any unusual problems while you are taking the medication.

People who take proton pump inhibitors such as lansoprazole may be more likely to fracture their wrists, hips, or spine than people who do not take one of these medications. The risk is highest in people who take high doses of one of these medications or take them for 1 year or longer. Talk to your doctor about the risk of taking lansoprazole.

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www. fda. gov/Safety/MedWatch ) or by phone (1-800-332-1088).

What should I know about storage and disposal of this medication?

Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.

In case of emergency/overdose

Benofomin, Benofomin

BENOFOMIN

Perhatian

Hamil.

Hentikan terapi sebelum operasi atau pemeriksaan klinis.

Kondisi yang dapat menyebabkan dehidrasi .

Infeksi serius atau trauma. Interaksi obat : – dapat menyebabkan hipoglikemia (kadara glukosa darah yang rendah) jika digunakan dengan Sulfonilurea atau Insulin. – mengganggu penyerapan Vitamin B12 . – dosis antikoagulan membutuhkan penyesuaian.

Kategori Keamanan Kehamilan B . Baik penelitian reproduksi hewan tidak menunjukkan risiko pada janin maupun penelitian terkendali pada wanita hamil atau hewan coba tidak memperlihatkan efek merugikan (kecuali penurunan kesuburan) dimana tidak ada penelitian terkendali yang mengkonfirmasi risiko pada wanita hamil semester pertama (dan tidak ada bukti risiko pada trisemester selanjutnya).

Dosis 3 kali sehari 500 mg.

Gold Cross Paracetamol, Tandamol

Gold Cross Paracetamol

Chemical Name

Chemical Formula

Other Brand Names

2-A

A-Mycin

A-Per

Abdine

Abrol

Abrolet

Acamol

Acamoli

Ace

Acecat

Acenol

Acephen

Acertol

Acet

Aceta

Acetafen

Acetagen

Acetalgin

Acetalis

Acetamin

Acetaminofen

Acetaminofen

Acetaminofen MK

Acetaminophen

Acetaminophen and Codeine Phosphate

Acetaminophen and Pentazocine hydrochloride

Acetamol

Acetazone Forte

Acetolit

Aceval

Actadol

Actol

Adalgur

Adco-Paracetamol

Adinol

Adol

Adol PM

Adol Sinus

Adolef

Adorem

Aeknil

Afebryl

Agurin

Aldolor

Algiafin

Algicalm

Alginox

Algisedal

Algocod

Algopirina

Algostase

Algostase mono

Algotropyl

Alikal

Alivax

Alphamol

Alvedon

Ametrex

Amifen

Amipar

Amol

Anacin

Anadin Paracetamol

Analgan

Analgiplus

Analper

Ananty

Andox

Anexsia

Anhiba

Anti-Gripe Asclepius

Antidol

Antigriphine

Antigrippine

Anyrume

APA

APAP

Apap C Plus

Apap Extra

Apap Noc

APC-Acetaminophen

Aphlogis

Apiret

Apiretal

Apiretal Codeina

Apo-Acetaminophen

Apo-Oxycodone/Acet

Aporex

Apotel

Apracur Granulado

Apyrene

Arfen

Arthrifen Plus

Asta

Atamel

Atasol

Atenemen

Atmiphen

ATP

Atralidon

Azur

Azur compositum

Baby Rinolo

Babyfever

Becetamol

Ben-u-ron

Benuron

Benylin Cold and Sinus

Beres Febrilin

Besemax

Besenol

Biogesic

Biogrip-T

Bodrex

Bodrex forte

Brexin

Buscopan compositum

Buscopan plus

Butapap

Calapol

Calonal

Calpol

Calpol 6 plus

Calpol Paediatric

Calsil

Capital and Codeine Phosphate

Captin

Catajap

Causalon

Cebion Febbre

Cefecon D

Cefekons

Cemol

Cetadol

Cetafrin

Cetal

Cetalgin

Cetamol

Chefarine

Children's Bufferin

Children's Panadol

Children's Tylenol

Citrosan

Claradol

Co-Becetamol

Co-Becetamol fur Kleinkinder

Co-Dafalgan

Co-Efferalgan

Cocarl

Cod Efferalgan

Codalgin

Codipar

Codipar Plus

Coditam

Coldrex Sinus

Contac

Contac Cold & Sore Throat, Non Drowsy

Contra-Schmerz P

Contraneural

Contratemp

Copyrkal

Cotibin Compuesto

Couldrex

Coxumadol

Crocin

Croix Blanche

Cupanol

Curadies Paracetamol

Curpol

Curpol Junior

Cytramon-P

Dafalgan

Dafalgan Bebe

Dafalgan C

Dafalgan Codeine

Dafalgan Enfant

Dafalgan Odis

Dafalgan Pediatrie

Dafalgan plus C

Daga

Daimeton

Daleron

Daleron C

Daleron C junior

Dalminette

Daro Hoofdpijnpoeder

Daro Paracetamol

Darvocet

Day & Night

Daygrip

Decolgen ACE

Demogripal C

Dentonibsa

Dentopain [+ Ibuprofen>

Depalgos

Depyrin

Dexamol

Dexamol Kid

Dhamol

Dialgine

Dimetapp Daytime Cold Extra Strength

Dirox

Disprol

Distalgesic

Doc Para

Docpara

Docparacod

Docpelin Paracetamol

Dolal

Dolel

Dolevar

Dolex

Dolgesic

Dolgesic Codeina

Doliprane

Dolitabs

Dolko

Dolocare

DoloCitran C

Dolofebril

Dolol Instant

Dolomedil

Dolomol

Dolomolargesico

Dolostop

Dolotec

Dolprone

Doluvital

Dolviran

Dopagan

Dopalgan

Dopalogan

Dopamol

Dorbigot

Doregrippin

Dorocol

Doxyfene

Dozol

Dristan N. D.

Dumin

Duokapton

Duorol

Dymadon

Efagesic

Eferalgan

Efetamol

Effect

Efferalgan

Efferalgan Vitamina C

Efferalganodis

Ekosetol

Emidol

Empacod

Empaped

Emtacetamol

Enddol

Endocet

Enelfa

Enelfa Dr. Henk

Erphamol

Espaven

Ethics Paracetamol

Expandox

FAP

Farmadol

Fast

Fea

Febrax

Febrectal

Febrectal Infantil

Febrex

Febricet

Febridol

Febrilix

Felibrix

Femerital

Fevac

Fevadol

Feverall

Fevrin

Fibrex

Fibrexin

Fibrimol

Filanc

Finimal

Finimal C

Fitamol

Flaviston E

Flectadol

Flogodisten

Fludeten

Fludrex

Fluental

Flutabs

Fortamol

Frenagial

Gabbrocet

Gamatherm

Gelocatil

Gelocatil Codeina

Gelonida

Geluprane

Genapap

Genebs

Geniol-P

Genspir

Geralgine-P

Getol

Gitas Plus

Go-Gesic

Gripakin

Gripostad

Grippex

Grippostad

Grippostad Heissgetrank

Hapacol

Head-O

Hedex

Hepa

Hexplider-C

Hot Coldrex

Hydrocodone bitartrate and Acetaminophen

Ibumol

Ibupain

Infadrops

Infants' Feverall

Infants' Tylenol

Infapain

Influbene C

Influbene N

Intaflam

Iremax

Isalgen Compuesto

Itamol

Itedal

Ixprim

Jagcin

Junior Parapaed

Kafa

Kafa Flashtabs

Kafa plus Koffein

Kapake

Kelvin

Kenox

Kinderparacetamol

Kinderparacetamol CF

Kitadol

Kodipar

Kolibri

Korylan

Lanamol

Lekadol

Lemgrip

Lemsip

Lensen

Liquiprin

Lisopan

Lonarid

Lortab

Lotem

Lupocet

Lusadeina

Mafidol

Mafidol Compuesto

Maganol

Magnidol

Malex

Malidens

Mann

Medamol

Medibudget Schmerztabletten Paracetamol

Medinol

Medinol Paediatric

Medipyrin

Mejorax

Mejorax Infantil

Methoxacet

Mexalen

Midol Night-Time

Midrid

Midrone

Migraeflux MCP

Migralave + MCP

Migrane-Neuridal

Migranerton

Minafen

Minofen

Minoset

Miralgin

Momentum

Muscadol

Myogesic

Mypaid

N-Paracetamol

Nactop

Napa

Napacod

Napafen

Napamol

Naprex

Nasa

Nasamol

Nedolon

Neo Rheumacyl

Neomol

Neopap

Neopyrin

Neverdol

Niocitran

Nodipir

Nodrof

Norco

Norflex CO

Norgesic

Normotemp

Novalsung

Novo Asat

Novo-Gesic

Nufadol

Nuosic

Octadon

Omol

Optalidon Schmerztabletten

Optipyrin

Oskadon

Ottopan

Oxycet

Oxycodone and Acetaminophen

Pacimol

Painamol

Painamol Plus

Paldesic

Pamol

Pamol Flash

Panacare

Panacetamol

Panadeine

Panado

Panadol

Panadol 7+ years

Panadol Actifast

Panadol Adultos

Panadol Antigrippine

Panadol Artrose

Panadol Baby

Panadol Baby & Infant

Panadol C

Panadol Codeine

Panadol Extend

Panadol Extra

Panadol Femina

Panadol Infantil

Panadol Junior

Panadol Night

Panadol Plus

Panadol Rapide

Panadol Zapp

Panaflam

Panagesic Adultos

Panagesic Infantil

Panam Retard

Panamax

Panaram

Panasorbe

Panasorbe (Sanofi-Aventis - Produtos farmaceuticos, S.)

Panets

Panets Baby

Panodil

Panodil Zapp

Para

Para-C

Para-don

Para-G

Para-Suppo

Para-Tabs

Para-z-mol

Paracap

Paracare

Paracen

Paraceon

Paracet

Paracetam

Paracetamol / Ascorbinezuur

Paracetamol / Codeine A

Paracetamol / Codeine PCH

Paracetamol A

Paracetamol Agrand

Paracetamol AL

Paracetamol AL comp.

Paracetamol BC

Paracetamol beta

Paracetamol Brifarma

Paracetamol CF

Paracetamol Cinfamed

Paracetamol Cuve

Paracetamol DM

Paracetamol dura

Paracetamol EG

Paracetamol elac

Paracetamol Elixir

Paracetamol Extra Fort

Paracetamol Fairmed

Paracetamol FLX

Paracetamol for Chlidren

Paracetamol G Gam

Paracetamol G. E.S.

Paracetamol Grunenthal

Paracetamol Hanseler

Paracetamol HTP

Paracetamol Infantil

Paracetamol L. CH.

Paracetamol Lch

Paracetamol Lichtenstein

Paracetamol LPH

Paracetamol Merck

Paracetamol Merck

Paracetamol MK

Paracetamol PCH

Paracetamol PT Copii

Paracetamol Q-Generics

Paracetamol Ranbaxy

Paracetamol Rosch

Paracetamol Roter

Paracetamol SAD

Paracetamol SmithKline Beecham

Paracetamol Tablets

Paracetamol Therapeuticon

Paracetamol Triangle Pharma

Paracetamol Winthrop

Paracetamol Winthrop

Paracetamol Zikidis

Paracetamolis L

Paracetamolo

Paracetol

Paracin Kid Tabs.

Paracof Roter

Paracor

Paracotene

Paradex

Paradol

Paradote

Paradrops

Parafil

Parafludeten

Parafon Forte

Parageniol

Parahexal

Parakapton

Paralen

Paralgan

Paralgin

Paralief

Paralink

Paralyoc

Paramax

Paramed A. L.S.

Paramidol

Paramol

Paramolan

Paranox

Paranox-S

Parapaed

Parapyrol

Parasedol

Parasupp

Paratab

Paratabs

Paratral

Parclen

Parol

Paroma

Parox Meltab

Parsel

Paximol

Pazital

Pe-Tam

Pediatrix

Pendol

Percocet

Perdolan

Perdolan Bebe

Perdolan Codeine

Perdolan Enfant

Perfalgan

Perfalgan Kinder

Perfalgan Paediatric

Perfusalgan

Pharex Paracetamol

Pharmacare Paracetamol

Pharmadol

Phrenilin

Pinex

Pinex Comp.

Pirofen

Piros

Plicet

Plivamed

Plovacal

Pmol

PMS-Oxycodone-Acetaminophen

Polmofen

Pontalsic

Poro

Pracetam

Praxion

Prefer

Primadol

Primiza

Profenal

Progesic

Prolief

Prontopyrin

Propoxi 66

Propoxyphene Hydrochloride and Acetaminophen

Propoxyphene napsylate and Acetaminophen

Propyretic

Pyradol

Pyral

Pyralen

Pyralgin

Pyrex

Pyrexin

Pyrexon

Pyrigesic

Ramol

Rapidol

Rapidon

ratio-Emtec-30

ratio-Oxycocet

Razimol

Relaxibys

Relaxon

Reliv

Remedeine

Remedol

Reset

Resolvebohm

Revanin

Rhinofebryl

Robaxacet

Robaxisal Compuesto [+ Methocarbamol

Rokamol

Roxicet

Roxilox

Rubophen

Salzone

Sanador

Sanaflu

Sanalgin

Sanalgin N

Sanicopyrine

Sanipirina

Sanmol

Sapramol

Saridon

Scopamin Plus

Scopma Plus

Sedalito

Sedo-Febril Pediatrico

Sensamol

Servigesic

Setamol

Sifenol

Silpa

Sinalgia

Sinapol

Sinaspril Paracetamol

Singrips

Sinmol

Sinofree

Sinuclear

Sinugesic

Sinumax

Sinutab

Sinutab Sinus Non Drowsy

Sistenol

Six Plus Parapaed

Snaplets-FR

Solpadol

Spashi Plus

Spasmend

Spectrapain

Spironolactone Altizide EG

Stop Grip

Sudafed Head Cold and Sinus Extra Strength

Sudafed PE Sinus + Pain Relief

Sudafed Sinus Pain

Sudafed Sinus Pain Relief

Supofen

Supracalm

Tachiforte

Tachipirin

Tachipirina

Tafirol

Talacen

Talgo

Talgo Codeina

Talvosilen

Tamen

Tamol

Tandamol

Tapsin

Tapsin Infantil

Tazamol

Teedex

Tempil

Tempol

Tempra

Teralgex

Termacet

Termalgin

Termalgin Codeina

Termalgin Flashtab

Termalgine

Termocatil

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Tetradox

Theraflu Zatoki

Thomapyrin

Tiffy

Tilalgin Efe

Tilderol

Timidal

Tinten

Tiptipot Aldolor

Titretta

Tramacet

Tramadol hydrochloride and Acetaminophen

Tramil

Treupel

Treupel Dolo Paracetamol

Triatec-30

Trimedil

Turpan

Tydenol

Tydol

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Tylex

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Vick Vitapyrena

Vicks Paracetamol

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Xpa

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Zalidar Efe

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Zydone

Astifen Online Without Prescriptions, Ketotilon

Zaditor (Ketotifen) is an antihistamine that inhibits the body's release of a chemical called histamine. Histamine can produce allergy symptoms such as sneezing, runny nose, and watery eyes. Ketotifen ophthalmic is used to treat itching of the eyes caused by allergy to dust, pollen, animals, or other allergens.

Ketotifen ophthalmic may also be used for other purposes not listed in this medication guide.

Zaditor (Ketotifen) is an antihistamine that inhibits the body's release of a chemical called histamine. Histamine can produce allergy symptoms such as sneezing, runny nose, and watery eyes. Ketotifen ophthalmic is used to treat itching of the eyes caused by allergy to dust, pollen, animals, or other allergens.

Ketotifen ophthalmic may also be used for other purposes not listed in this medication guide.

Use this medication exactly as directed on the label, or as it has been prescribed by your doctor. Do not use the medication in larger amounts, or use it for longer than recommended.

Wash your hands before using the eye drops.

If you wear contact lenses, remove them before applying ketotifen ophthalmic. This medication may contain a preservative (benzalkonium chloride) that may cause discoloration of contact lenses.

To apply the eye drops:

Tilt your head back slightly and pull down your lower eyelid. Hold the dropper above the eye with the dropper tip down. Look up and away from the dropper as you squeeze out a drop, then close your eye. Gently press your finger to the inside corner of the eye (near your nose) for about 1 minute to keep the liquid from draining into your tear duct. If you use more than one drop in the same eye, wait about 5 minutes before putting in the next drop. Do not allow the dropper tip to touch any surface, including the eyes or hands. If the dropper becomes contaminated it could cause an infection in your eye, which can lead to vision loss or serious damage to the eye.

After using the eyedrops, wait at least 10 minutes before putting contact lenses into your eyes. Do not use the eye drops if the liquid has changed colors or has particles in it. Call your doctor for a new prescription. Store the drops at room temperature away from heat and moisture. Keep the bottle tightly closed when not in use.

Use this medication exactly as directed on the label, or as it has been prescribed by your doctor.

If you miss a dose of Zaditor, 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 Zaditor at room temperature, 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 in a tight, light-resistant container. Keep Zaditor out of the reach of children and away from pets.

Active Ingredient: Ketotifen (0.025%) (Antihistamine)

Do not use this medication if you are allergic to ketotifen, or if you have an untreated eye infection.

Do not use it if you you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement.

Ketotifen ophthalmic should not be used to treat eye irritation caused by wearing contact lenses.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether ketotifen passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Do not use this medication in a child younger than 3 years old without the advice of a doctor.

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using ketotifen ophthalmic and call your doctor at once if you have any of these serious side effects:

redness, drainage, eyelid swelling, or other signs of infection;

vision changes; or

severe itching of the eyes worse than before using the medication.

Less serious side effects may include:

mild burning, stinging, or eye irritation;

dryness of the eyes; or

increased sensitivity to light.

This is not a complete list of side effects and others may occur. Tell your doctor or health care provider about any unusual or bothersome side effect.

Zaditor 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.

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Amit, Amit

Verb Edit

1646 . Sir Thomas Browne. Pseudodoxia Epidemica [1]. Concerning the Loadstone: And though a loadstone fired doth presently amit its proper virtue, and according to the position in cooling contracts a new verticity from the earth, yet if the same be laid awhile in aqua fortis . or other corrosive water, and taken out before a considerable corrosion, it still reserves its attraction, and will convert the needle according to former polarity.

1848 . Alexander Duff, Commentaries on the recent statutes relative to conveyancing [2]. [ … ] and in the event of the said O. H. failing so to complete his title and grant entry to the petitioner, or to shew reasonable cause why he delays or refuses so to do, to find and declare that the said G. H. has forfeited and amitted all right to the said superiority [ … ]

Etymology Edit

Danoxilin, Danoxilin

Metformin is used for treating type 2 diabetes. It is used along with diet and exercise. It may be used alone or with other anti-diabetic medicines.

Use Metformin as directed by your doctor.

Take Metformin by mouth with food. Take Metformin on a regular schedule to get the most benefit from it. Taking Metformin at the same time each day will help you remember to take it. Continue taking Metformin even if you feel good. Do not miss any doses. Ask your health care provider any questions you may have about its usage.

Drug Class and Mechanism

Metformin is a biguanide antidiabetic. It works by decreasing the amount of sugar that the liver produces and the intestines absorb. It also helps to make your body more sensitive to the insulin that you naturally produce.

If you miss a dose of Metformin 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 Metformin 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 Metformin out of the reach of children and away from pets.

Do not use Metformin if:

you are allergic to any ingredient in Metformin; you have congestive heart failure that is treated by medicine; you have a severe infection, low blood oxygen levels, kidney or liver problems, high blood ketone or acid levels (e. g. diabetic ketoacidosis), or severe dehydration; you have had a stroke or a recent heart attack, or you are in shock; you are 80 years old or older and have not had a kidney function test; you will be having surgery or certain lab procedures. Contact your doctor or health care provider right away if any of these apply to you.

Important : Dizziness may occur while you are taking Metformin. This effect may be worse if you take it with alcohol or certain medicines. Use Metformin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Follow the diet and exercise program given to you by your health care provider. Do not drink large amounts of alcohol while you use Metformin. Talk to your doctor or health care provider before you drink alcohol while you use Metformin. Tell your doctor or dentist that you take Metformin before you receive any medical or dental care, emergency care, or surgery. Be careful not to become dehydrated, especially during hot weather or while you are being active. Dehydration may increase the risk of Metformin 's side effects. Carry an ID card at all times that says you have diabetes. Check your blood sugar levels as directed by your doctor. If they are often higher or lower than they should be and you take Metformin exactly as prescribed, tell your doctor. This medicine does not usually lower your blood sugar levels. Low blood sugar may be more likely to occur if you skip a meal, exercise heavily, or drink alcohol. It may also be more likely if you take Metformin along with certain medicines for diabetes (e. g. sulfonylureas, insulin). It is a good idea to carry a reliable source of glucose (e. g. tablets or gel) to treat low blood sugar. If this is not available, you should eat or drink a quick source of sugar like table sugar, honey, candy, orange juice, or non-diet soda. This will raise your blood sugar level quickly. Tell your doctor right away if this happens. To prevent low blood sugar, eat meals at the same time each day and do not skip meals. Fever, infection, injury, or surgery may increase your risk for high or low blood sugar levels. If any of these occur, check your blood sugar closely and tell your doctor right away. Metformin may commonly cause stomach upset, indigestion, nausea, vomiting, or diarrhea at the beginning of treatment. If you develop unusual or unexpected stomach problems, or if you develop stomach problems later during treatment, contact your doctor at once. This may be a sign of lactic acidosis. Lab tests, including kidney function, fasting blood glucose, hemoglobin A1c, and blood counts, may be performed while you use Metformin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Use Metformin with caution in the elderly; they may be more sensitive to its effects. Low blood sugar levels may also be more difficult to recognize in the elderly. Metformin should not be used in children younger than 10 years old; safety and effectiveness in these 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 Metformin while you are pregnant. It is not known if Metformin is found in breast milk. Do not breast-feed while taking Metformin.

Possible Side Effects

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

Diarrhea; gas; headache; indigestion; nausea; stomach upset; temporary metallic taste; 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); chest pain or discomfort; dizziness or lightheadedness; fast or difficult breathing; feeling of being unusually cold; fever, chills, or persistent sore throat; general feeling of being unwell; muscle pain or weakness; slow or irregular heartbeat; unusual drowsiness; unusual or persistent stomach pain or discomfort; unusual tiredness or weakness.

If you have any questions about Hydrochlorothiazide, please talk with your doctor, pharmacist, or other health care provider. Metformin is to be used only by the patient for whom it is prescribed. Do not share it with other people.

Why register with MediGuard?

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Danoxilin (Amoxicillin)

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The risk of serious side effects for taking this medicine can be different if you take other medicines or if you suffer from a condition. Get your Risk Rating by creating a profile in a few steps.

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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

Metformin is used for treating type 2 diabetes. It is used along with diet and exercise. It may be used alone or with other anti-diabetic medicines.

Use Metformin as directed by your doctor.

Take Metformin by mouth with food. Take Metformin on a regular schedule to get the most benefit from it. Taking Metformin at the same time each day will help you remember to take it. Continue taking Metformin even if you feel good. Do not miss any doses. Ask your health care provider any questions you may have about its usage.

Drug Class and Mechanism

Metformin is a biguanide antidiabetic. It works by decreasing the amount of sugar that the liver produces and the intestines absorb. It also helps to make your body more sensitive to the insulin that you naturally produce.

If you miss a dose of Metformin 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 Metformin 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 Metformin out of the reach of children and away from pets.

Do not use Metformin if:

you are allergic to any ingredient in Metformin; you have congestive heart failure that is treated by medicine; you have a severe infection, low blood oxygen levels, kidney or liver problems, high blood ketone or acid levels (e. g. diabetic ketoacidosis), or severe dehydration; you have had a stroke or a recent heart attack, or you are in shock; you are 80 years old or older and have not had a kidney function test; you will be having surgery or certain lab procedures. Contact your doctor or health care provider right away if any of these apply to you.

Important : Dizziness may occur while you are taking Metformin. This effect may be worse if you take it with alcohol or certain medicines. Use Metformin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Follow the diet and exercise program given to you by your health care provider. Do not drink large amounts of alcohol while you use Metformin. Talk to your doctor or health care provider before you drink alcohol while you use Metformin. Tell your doctor or dentist that you take Metformin before you receive any medical or dental care, emergency care, or surgery. Be careful not to become dehydrated, especially during hot weather or while you are being active. Dehydration may increase the risk of Metformin 's side effects. Carry an ID card at all times that says you have diabetes. Check your blood sugar levels as directed by your doctor. If they are often higher or lower than they should be and you take Metformin exactly as prescribed, tell your doctor. This medicine does not usually lower your blood sugar levels. Low blood sugar may be more likely to occur if you skip a meal, exercise heavily, or drink alcohol. It may also be more likely if you take Metformin along with certain medicines for diabetes (e. g. sulfonylureas, insulin). It is a good idea to carry a reliable source of glucose (e. g. tablets or gel) to treat low blood sugar. If this is not available, you should eat or drink a quick source of sugar like table sugar, honey, candy, orange juice, or non-diet soda. This will raise your blood sugar level quickly. Tell your doctor right away if this happens. To prevent low blood sugar, eat meals at the same time each day and do not skip meals. Fever, infection, injury, or surgery may increase your risk for high or low blood sugar levels. If any of these occur, check your blood sugar closely and tell your doctor right away. Metformin may commonly cause stomach upset, indigestion, nausea, vomiting, or diarrhea at the beginning of treatment. If you develop unusual or unexpected stomach problems, or if you develop stomach problems later during treatment, contact your doctor at once. This may be a sign of lactic acidosis. Lab tests, including kidney function, fasting blood glucose, hemoglobin A1c, and blood counts, may be performed while you use Metformin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Use Metformin with caution in the elderly; they may be more sensitive to its effects. Low blood sugar levels may also be more difficult to recognize in the elderly. Metformin should not be used in children younger than 10 years old; safety and effectiveness in these 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 Metformin while you are pregnant. It is not known if Metformin is found in breast milk. Do not breast-feed while taking Metformin.

Possible Side Effects

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

Diarrhea; gas; headache; indigestion; nausea; stomach upset; temporary metallic taste; 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); chest pain or discomfort; dizziness or lightheadedness; fast or difficult breathing; feeling of being unusually cold; fever, chills, or persistent sore throat; general feeling of being unwell; muscle pain or weakness; slow or irregular heartbeat; unusual drowsiness; unusual or persistent stomach pain or discomfort; unusual tiredness or weakness.

If you have any questions about Hydrochlorothiazide, please talk with your doctor, pharmacist, or other health care provider. Metformin is to be used only by the patient for whom it is prescribed. Do not share it with other people.

Carol Waugh, Skin Care, Balancing Cream, Career Opportunity - Balancing Creams, Prolief

Natural balancing creams are applied to soft tissues including chest, inner arms, neck, face, palms of hands and soles of feet, with the best results from rotating applications to different soft tissues.

"I have been using PhytoProlief for about a month. I visited my doctor and told him about the product and now he is waiting for me to send him information. I am so happy. Thank you so much Arbonne!"

Margaret Sabin: Columbia, TN

PhytoProlief Natural Balancing Cream

A light, greaseless, natural balancing cream to help balance the body naturally and conveniently with an easy, pre-metered pump. Key Ingredients: Chaste tree, dong quai, evening primrose oil, red clover and black cohosh extracts, USP progesterone Skin Types: All

Note: This product is not intended for pregnant or lactating women. People with known medical conditions should consult with a physician prior to using this product.

Prolief Natural Balancing Cream

A natural balancing cream for men and women who want the benefits of a balancing cream without the added herbs, packaged in a precisely-metered pump. Key Ingredients: Sweet almond and sunflower oils, aloe, USP progesterone Skin Types: All

Natural alternatives can be a solution to imbalance, but it's a decision every woman must make for herself. PhytoProlief and Prolief are exactly that ? botanically-based options for natural balance.

PHYTOPROLIEF & PROLIEF: ONE SIMPLE DIFFERENCE

Both products are natural balancing creams, conveniently packaged in a metered pump to supply 1/4 teaspoon of product per dose. PhytoProlief contains added phytoestrogens or plant estrogens, and Prolief does not.

Contains the following phytoestrogen herbs:

? Chaste Tree Berry

? Evening Primrose Oil

ARBONNE'S PERFECT PUMP : PhytoProlief and Prolief come in an incredible container with a ?smart? pump:

? airtight: keeps container free of contaminants, helps maintain potency

? metered: dispenses a 1/4 a tsp. each pump

? convenient: no messy, confusing measuring

? economical: 2.5 oz. more than most products on the market

Note: These products are not intended for pregnant or lactating women. People with known medical conditions should consult with a physician prior to using any of these products.

Clomiphene And Letrozole Restore Ovulation And Correct Fertility Problems, Letroz

CLOMIPHENE CITRATE (brand names Serophene, Clomid)

LETROZOLE (brand name Femara)

Both clomiphene citrate and letrozole are medications used to treat infertile women who have an ovulation problem. These medications work by helping your pituitary gland (located at the base of the brain) improve the stimulation of developing follicles (eggs) in the ovaries. Neither clomiphene citrate nor letrozole may help a woman become more fertile if she is already ovulating normally. For that reason, these medications are most often prescribed to those patients who have been found to have an abnormality with their cycle.

Clomiphene is often referred to as the "fertility pill". Letrozole is very similar to clomiphene in the way it works. However, letrozole is quickly cleared from the body. It only works for the cycle in which it is taken and is less likely to adversely affect the uterine lining and cervical mucous. With clomiphene, one may experience effects 6-8 weeks after stopping the medication. Both medications are prescribed for five days each cycle, usually beginning on day three and continuing through day seven. The usual initial dose for clomiphene is 50 mg, one tablet daily. The number of tablets can be increased to as many as four daily, if a lesser dosage does not result in ovulation. Rarely are more than two tablets required. Clomiphene should be repeated each cycle until pregnancy occurs, or your doctor discontinues it. The usual dosage of letrozole is 2.5 mg. one tablet each day.

Of all women treated with clomiphene, or letrozole, 60% to 80% will ovulate normally. However, only half of those patients who ovulate will become pregnant. It is not known why only half of the women who apparently ovulate with clomiphene or letrozole therapy become pregnant. It is suspected that factors other than inadequate ovulation may be contributing to the fertility problem. Therefore, if you are not pregnant after three or four cycles, additional testing such as hysterosalpingogram or laparoscopy may be necessary. If you have polycystic ovary syndrome, a trial of metformin (Glucophage) therapy may be advised.

Some 10% to 20% of women taking clomiphene or letrozole will experience side effects. By far, most of these are minor and temporary in nature. They include such things as hot flashes, blurred vision, nausea, bloating sensation, and headache. Serious side effects are rarely seen with either medication. There are two side effects associated with clomiphene or letrozole therapy that warrant specific discussion. The first is the possibility of multiple pregnancy. The frequency of twins occurring in women who conceive while taking clomiphene or letrozole has been reported to be as high as 10%. Triplets may occur as frequently as 1 in 400 births, and quadruplets in 1 in 800 births. Neither clomiphene nor letrozole is the "fertility drug" you may have heard in the news bulletins often associated with large numbers of infants, such as quintuplets. Newer studies suggest that long-term use of either clomiphene or letrozole for more than 12 cycles may place you at an increased risk of developing ovarian cancer. Secondly, clomiphene and letrozole have also been associated with the occasional development of ovarian cysts. These cysts are not true growths of the ovary and within a few weeks will resolve without treatment. However, on an extremely rare occasion, these cysts have been known to cause internal bleeding or twist, requiring surgery and removal of the involved ovary. However, I must again emphasize that such a complication is extremely rare.

Clomiphene or letrozole stimulated cycles are not unlike normal cycles in that there is only a 20-25% chance of conception occurring each cycle during the first three to four treatment cycles, even if the medication is working properly. (Results may be lower with unexplained infertility.) This means that at least four to six cycles of treatment are necessary before one has given either medication an adequate trial. Recent studies indicate that if a pregnancy occurs as a result of the clomiphene/letrozole treatment, there is no clinically significant increased risk of miscarriage or congenital birth defects when compared to other infertile couples who conceived without clomiphene/letrozole treatment. However, women with polycystic ovary syndrome may be at higher risk for miscarriage during a pregnancy conceived using either of these medications.

Fluororinil, Fluororinil

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.

Medication Information Personalized Risk Rating Easy to understand overview Serious Side Effects Printable Medication List

Information you can understand Overview on Safety Alerts & Recalls Overview of Medications & Conditions

Community of patients Members’ Feedback Members Treatment Satisfaction

Health condition information Easy to understand overview Commonly Used Medications

Safety checks Safety Alerts & Recalls Drug - Drug Interaction Drug - Condition Interaction

Research participation Option to participate in medical surveys & studies*

Celestamine

What is your Risk Rating for this medicine?

The risk of serious side effects for taking this medicine can be different if you take other medicines or if you suffer from a condition. Get your Risk Rating by creating a profile in a few steps.

Benefits:

We monitor your health and alert you to any safety updates and recalls.

You get to talk directly to other members about their experience.

You can create profiles for you and your loved ones.

Create my Profile Learn more about Risk Ratings

Other Names

Expand to see all

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

Skincare - Fluororinil (Brand name: betnovate)

Betnovate helps to reduce the redness, itching, and swelling of skin conditions such as eczema, psoriasis, contact dermatitis, and seborrhea.

Use Betnovate as directed by your doctor.

This medication is usually applied 2 or 3 times daily or according to the instruction. Enough medication should be applied to completely cover the affected area with a thin film. The medication should be gently and thoroughly massaged into the affected area. In certain conditions, the doctor will order the application to be covered with a dressing. Ask your health care provider any questions you may have about how to use Betnovate.

Drug Class and Mechanism

Betnovate is a corticosteroid that is used for the topical treatment of skin irritations.

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.

Store Betnovate at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Betnovate out of the reach of children and away from pets.

Betnovate should not be taken by anyone who:

is allergic to betamethasone valerate or any of the ingredients of the medication; has chickenpox; has fungal, yeast, or viral skin lesions; has herpes simplex; has tuberculosis of the skin; has vaccinia.

Possible Side Effects

Side effects that you should report to your prescriber or health care professional as soon as possible:

burning or itching of the skin; dark red spots on the skin; infection; lack of healing of the skin condition; painful, red, pus-filled blisters in hair follicles; severe burning and continued itching of the skin; thinning of the skin, with easy bruising, sunburn more likely especially on the face. Other serious side effects can develop if you use Betnovate for a long time, or if you use too much. Contact your prescriber or health care professional if you notice any unusual effects.

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): burning, itching, or irritation of the skin; dry skin; increased redness or scaling of the skin.

Betnovate 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.

Gsk Terms Of Use, Voltarol

GSK Terms of Use

Healthcare information

This website may provide information about medical conditions and their treatment. GSK makes no representation that material in the site is appropriate or available for use outside of the territory of the intended audience. Those who choose to access this site from other locations do so on their own initiative and are responsible for compliance with local laws, if and to the extent that local laws are applicable. In addition, nothing on this website should be construed as providing any kind of medical advice or recommendation, and should not be relied on as the basis for any decision or action. Specific medical advice should always be sought from a qualified medical practitioner

GSK uses reasonable efforts to update this website, but some information may become out of date over time. Except as specifically stated, GSK makes no claims or warranties as to the accuracy, completeness or use of the information contained on this website.

This website has a specific section for members of the public, a specific section for patients and a specific section for healthcare professionals. “Healthcare professional” refers to an individual who in the course of their professional activities may prescribe, supply or administer a medicine or medical devices. [Reference may also be made to other appropriate healthcare staff in accordance with local codes and policies]

The section for the public has been designed as a library resource to provide reference information relating to GSK medicines, including but not limited to, prescription only medicines, to the public within the United Kingdom. Within the public section there are specific patient-only pages for those who have been prescribed the medicine relating to those pages. These pages remain hidden from site navigation and can only be accessed once a member of the public has confirmed they are a patient that has been prescribed a particular medicine.

FOR HEALTHCARE PROFESSIONALS ONLY: Please note that approved prescribing information must guide the appropriate use of all medicines. Before prescribing any medicine, healthcare professionals should consult the approved prescribing information for that medicine in their country.

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Healthcare information

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All intellectual property rights in the material on this site are owned by the GSK group of companies, or they have been granted permission to use such material except where specifically stated otherwise. Reproduction of part or all of the contents in any form is prohibited other than in accordance with the following permissions.

You may read, view, print, download and copy the material on this website for your personal and non-commercial use, but only if you acknowledge the website as the source of the material and include the copyright statement “© GSK group of companies, all rights reserved ”. Unless specifically indicated, no other use of the material is permitted.

Nothing contained in this website should be construed as conferring any licence or right under any intellectual property (including patents, trade marks and copyright) of the GSK group of companies or any third party.

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Communications from users or other material sent through the internet, posted on a GSK website or otherwise (other than those containing personal and/or health-related information, which fall within GSK’s Privacy Policy) are deemed to be non-confidential and non-proprietary, and GSK shall have no obligation of any kind with respect to such information. GSK shall be free to use this information for any purpose it deems appropriate, including reproduction and publication, and may use any ideas, concepts, know-how or techniques contained in such information for any purpose whatsoever, including commercial purposes, without paying users for the right to do so.

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Haltran Oral Drug Information On Uses, Side Effects, Interactions, And User Reviews On Rxlist, Haltr

Haltran oral

Haltran oral Warnings

Nonsteroidal anti-inflammatory drugs (including ibuprofen) may rarely increase the risk for a heart attack or stroke. The risk may be greater if you have heart disease or increased risk for heart disease (for example, due to smoking, family history of heart disease, or conditions such as high blood pressure or diabetes), or with longer use. This drug should not be taken right before or after heart bypass surgery (CABG).

This drug may rarely cause serious (rarely fatal) bleeding from the stomach or intestines. This effect can occur without warning at any time while taking this drug. Older adults may be at higher risk for this effect.

Stop taking ibuprofen and get medical help right away if you notice any of these rare but serious side effects: black/tarry stools, persistent stomach/abdominal pain, vomit that looks like coffee grounds, chest/jaw/left arm pain, shortness of breath, unusual sweating, confusion, weakness on one side of the body, slurred speech, sudden vision changes.

Talk to your doctor or pharmacist about the benefits and risks of taking this drug.

Haltran oral Uses

Ibuprofen is used to relieve pain from various conditions such as headache, dental pain, menstrual cramps, muscle aches, or arthritis. It is also used to reduce fever and to relieve minor aches and pain due to the common cold or flu. Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. This effect helps to decrease swelling, pain, or fever.

If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.

Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

This medication may also be used to treat gout attacks.

How to use Haltran oral

If you are taking the over-the-counter product, read all directions on the product package before taking this medication. If your doctor has prescribed this medication, read the Medication Guide provided by your pharmacist before you start taking ibuprofen and each time you get a refill. If you have any questions, ask your doctor or pharmacist.

Take this medication by mouth, usually every 4 to 6 hours with a full glass of water (8 ounces/240 milliliters) unless your doctor directs you otherwise. Do not lie down for at least 10 minutes after taking this drug. If you have stomach upset while taking this medication, take it with food, milk, or an antacid.

The dosage is based on your medical condition and response to treatment. To reduce your risk of stomach bleeding and other side effects, take this medication at the lowest effective dose for the shortest possible time. Do not increase your dose or take this drug more often than directed by your doctor or the package label. For ongoing conditions such as arthritis, continue taking this medication as directed by your doctor.

When ibuprofen is used by children, the dose is based on the child's weight. Read the package directions to find the proper dose for your child's weight. Consult the pharmacist or doctor if you have questions or if you need help choosing a nonprescription product.

For certain conditions (such as arthritis), it may take up to two weeks of taking this drug regularly until you get the full benefit.

If you are taking this drug "as needed" (not on a regular schedule), remember that pain medications work best if they are used as the first signs of pain occur. If you wait until the pain has worsened, the medication may not work as well.

If your condition persists or worsens, or if you think you may have a serious medical problem, get medical help right away. If you are using the nonprescription product to treat yourself or a child for fever or pain, consult the doctor right away if fever worsens or lasts more than 3 days, or if pain worsens or lasts more than 10 days.

Haltran oral Precautions

Before taking ibuprofen, tell your doctor or pharmacist if you are allergic to it; or to aspirin or other NSAIDs (such as naproxen, celecoxib); 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 taking this medication, tell your doctor or pharmacist your medical history, especially of: asthma (including a history of worsening breathing after taking aspirin or other NSAIDs), blood disorders (such as anemia, bleeding/clotting problems), growths in the nose (nasal polyps), heart disease (such as previous heart attack), high blood pressure, liver disease, stroke, throat/stomach/intestinal problems (such as bleeding, heartburn, ulcers).

Kidney problems can sometimes occur with the use of NSAID medications, including ibuprofen. Problems are more likely to occur if you are dehydrated, have heart failure or kidney disease, are an older adult, or if you take certain medications (see also Drug Interactions section). Drink plenty of fluids as directed by your doctor to prevent dehydration and tell your doctor right away if you have any unusual change in the amount of urine.

This drug may make you dizzy or drowsy. Do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely. Limit alcoholic beverages.

This medicine may cause stomach bleeding. Daily use of alcohol and tobacco, especially when combined with this medicine, may increase your risk for stomach bleeding. Limit alcohol and stop smoking. Consult your doctor or pharmacist for more information.

This medication may make you more sensitive to the sun. Avoid prolonged sun exposure, tanning booths or sunlamps. Use a sunscreen and wear protective clothing when outdoors.

Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products).

Older adults may be more sensitive to the effects of this drug, especially stomach/intestinal bleeding and kidney problems.

Before using this medication, women of childbearing age should talk with their doctor(s) about the benefits and risks (such as miscarriage, trouble getting pregnant). Tell your doctor if you are pregnant or if you plan to become pregnant. During pregnancy, this medication should be used only when clearly needed. It is not recommended for use during the first and last trimesters of pregnancy due to possible harm to the unborn baby and interference with normal labor/delivery.

This medication passes into breast milk, but is unlikely to harm a nursing infant. Consult your doctor before breast-feeding.

Haltran oral 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.

Some products that may interact with this drug include: aliskiren, ACE inhibitors (such as captopril, lisinopril), angiotensin II receptor blockers (such as losartan, valsartan), cidofovir, corticosteroids (such as prednisone), lithium, "water pills" (diuretics such as furosemide).

This medication may increase the risk of bleeding when taken with other drugs that also may cause bleeding. Examples include anti-platelet drugs such as clopidogrel, "blood thinners" such as dabigatran/enoxaparin/warfarin, among others.

Check all prescription and nonprescription medicine labels carefully since many medications contain pain relievers/fever reducers (including aspirin, NSAIDs such as celecoxib, ketorolac, or naproxen). These drugs are similar to ibuprofen and may increase your risk of side effects if taken together. However, if your doctor has directed you to take low-dose aspirin for heart attack or stroke prevention (usually at dosages of 81-325 milligrams a day), you should continue taking the aspirin unless your doctor instructs you otherwise. Daily use of ibuprofen may decrease aspirin's ability to prevent heart attack/stroke. Talk to your doctor about using a different medication (such as acetaminophen) to treat pain/fever. If you must take ibuprofen, talk to your doctor about possibly taking immediate-release aspirin (not enteric-coated/EC) while taking ibuprofen. Take ibuprofen at least 8 hours before or at least 30 minutes after your aspirin dose. Do not increase your daily dose of aspirin or change the way you take aspirin/other medications without your doctor's approval.

Haltran oral 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 stomach pain, trouble breathing, extreme drowsiness.

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

Laboratory and/or medical tests (such as blood pressure, kidney function tests) may be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

Keep all regular medical and laboratory appointments.

If you are taking this drug on a regular schedule (not just "as needed") and 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.

Store at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications 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.

Information last revised May 2016. Copyright(c) 2016 First Databank, Inc.

La Comunicaci - N Asertiva, Sertiva

La comunicación asertiva

By Ana Munoz. Motivación Expert

Updated March 10, 2016.

Algunas personas tienen problemas para hacer valer sus derechos de un modo asertivo y tienden a reaccionar de formas poco apropiadas que les crean problemas en sus relaciones, asi como estres y malestar. Pero la asertividad es una habilidad que puede aprenderse.

Cuando no eres asertivo, tiendes a responder de dos maneras distintas, que a veces se dan en la misma persona, en diferentes momentos:

Continue Reading Below

Pueden ceder, someterse y no hacer valer sus derechos. En este caso, es posible que luego se sientan dolidos, humillados. resentidos o debiles. No es raro que recurran a comportamientos agresivos-pasivos. Es decir, comportamientos con los que tratan de vengarse de un modo indirecto. Por ejemplo, aceptan hacer un favor a alguien pero luego lo "olvidan" o hacen "sin querer" algo que perjudica o molesta a la otra persona afirmando despues no haberse dado cuenta. Esta es una forma inmadura de afrontar este problema y tiende a crear conflictos en las relaciones o destruirlas.

2. Agresividad. En otros casos, reaccionan de manera agresiva, haciendo valer sus derechos con amenazas, insultos, gritos, desprecio hacia la otra persona, etc. no respetan los derechos de los demas ni tienen en cuenta sus opiniones o sentimientos. Algunas personas recurren generalmente a este modo de comportarse, mientras que en otros casos se trata de personas que tienden a ceder y someterse a los deseos o caprichos de los demas, hasta que no pueden mas y entonces estallan con agresividad.

En cualquiera de estos casos, estas personas no han aprendido a comunicarse de manera asertiva y necesitan aprender como hacerlo y practicar.

Continue Reading Below

Asertividad

La comunicacion asertiva implica responder sin agresividad, respetando a la otra persona, al mismo tiempo que te niegas a hacer algo que no deseas hacer o que consideras injusto. No levantas la voz, no muestras ira. y tratas de resolver el conflicto teniendo en cuenta los deseos de ambas partes, buscando compromisos y soluciones, en vez de pretender simplemente salirte con la tuya.

Ser asertivo significa que te respetas a ti mismo y que estas dispuesto a expresarte, a no dejarte avasallar, pedir lo que te corresponde y hacer valer tus derechos. Tambien significa que eres consciente de los derechos de los demas y los respetas. La comunicacion asertiva no es ni demasiado agresiva ni demasiado pasiva.

Cuando la otra persona no entra en razones, solo quiere salirse con la suya y no acepta una negativa, la persona asertiva simplemente interrumpe la conversacion y se marcha, dejando claro que no esta enfadada y que sigue disponible para el otro, pero no va a seguir esa conversacion ni se va a dejar convencer para hacer algo que no desea hacer.

La persona asertiva no recurre a la agresividad ni a comportamientos agresivo-pasivos, suele tener confianza en si misma y una buena autoestima .

Tecnicas y consejos para ser mas asertivo

Utiliza frases en primera persona. Es decir, en vez de decir "estas equivocado", di algo como "No estoy de acuerdo en esto". De este modo, estas expresando tu opinion, mas que rechazando o despreciando la opinion de la otra persona.

Practica el decir no. Tal vez piensas que para negarte a hacer algo tienes que tener una excusa, de manera que cuando no la tienes, no eres capaz de negarte. Pero esta es una idea falsa que va a hacerte mas mal que bien. No necesitas ninguna excusa para negarte. Simplemente puedes negarte a hacer algo porque no deseas hacerlo o no te apetece. Practica cuando surja la ocasion y simplemente di algo como: "no me apetece", "prefiero no hacerlo", "eso no va conmigo", etc.

Cuidado con tu lenguaje corporal. Tu cuerpo dice mucho mas que tus palabras. Si tus palabras dicen no pero tu cuerpo muestra una actitud debil y poco convincente, la otra persona seguira insistiendo hasta que cedas. Por tanto, manten una postura erguida, mira a los ojos directamente, muestra confianza y serenidad, habla con claridad, sin gritar pero con un tono de voz algo elevado. Practica ante el espejo unas cuantas veces hasta que lo hagas con naturalidad.

Cuidado con tus emociones. Si un tema te irrita demasiado y te entran granas de gritar, llorar o tener cualquier reaccion emocional exagerada. calmate primero antes de hablar, y piensa lo que vas a decir y como puedes decirlo de un modo que sea asertivo.

Adenock - Drug Review Dosage, Side Effects, Action, Buy Adenock, Adenock

Adenock

Adenock review

Adenock is the generic name for a medicament that also goes by the brand name Zyloprim. It is prescribed for patients who have primary or secondary gout. and for patients with elevated levels of serum and urinary acidic levels, such as those receiving cancer treatments for leukemia and lymphoma. It can also be used to treat people who have calcium disorders that result in high levels of daily uric acid. Adenock can be given in pill form or as an injection.

The most common side effect of Adenock is a skin rash. These rashes can be mild to very severe, even fatal, and it is recommended that treatment with Adenock be stopped immediately if a rash develops. In addition, if an allergic reaction develops, or if you experience painful or bloody micturition. you should discontinue use of Adenock. Other severe but less common side effects can include pyrexia, chills, jaundice, and either an increase or a decrease in white blood cells. In some cases, taking antibiotics at the same time as Adenock can increase the negative side effects. Other side effects can include diarrhea. nausea or vomiting. an increase in the alakaline levels in the blood. an increase in acute attacks of gout, headache. inflammation of the blood vessels. liver disorders, abdominal pain, inflammation of the stomach. and upset stomach. You may also experience muscle disorders, nerve inflammation, numbness, tingling, or prickling sensations of the skin, sleepiness, nosebleeds, baldness. human immunodeficiency viruses, red spots, skin sensitivity, loss or distortion of taste, kidney failure. swelling of the tongue. loss of appetite. weakness, decreased libido, asthma. rhinorrhea, sweating, cataracts, eye infections, impotence or male infertility. You should see your doctor if you have any of these rare reactions.

It is important during treatment with Adenock that you drink enough water to produce two liters of urine every day. This will help in the prevention of kidney stones and with the absorption of Adenock at the proper levels. If you do not experience immediate relief of your gout, do not stop taking Adenock, since it often takes from two to six weeks to experience optimal results. It is recommended that you take your Adenock after meals in order to minimize stomach irritation.

Adenock is in Pregnancy Category C, which means that it has not been shown to cause harm to developing fetuses. However, these are results from animal studies; conclusive studies have not been done on pregnant women. It has been determined that Adenock passes into breast milk, but the effects on the nursing baby are not known. If you are pregnant or nursing, or plan to become pregnant or to nurse a baby, you should discuss it with your doctor to determine whether the benefits of taking Adenock outweigh any possible negative effects for you or your baby. Adenock is rarely prescribed for children, though there are cases in which a child may have an excess of uric acid due to cancer treatments or genetic conditions. In these cases, Adenock may be indicated for pediatric use.

Adenock has the following structural formula:

• Molecular formula of adenock is C5H4N4O • Chemical IUPAC Name is 3,5,7,8-tetrazabicyclo[4.3.0]nona-3,5,9-trien-2-one • Molecular weight is 136.112 g/mol • Adenock available. 100mg tablets, 300mg tablets

Generic name: Allopurinol

Brand name(s): Ailural. Allo-Puren. Allopur. Allopurinol sodium. Allopurinolum. Allozym. Allural. Aloprim. Alopurinol. Aloral. Alositol. Aluline. Anoprolin. Anzief. Apo-Allopurinol. Apulonga. Apurin. Apurol. Atisuril, Bleminol, Bloxanth, Caplenal, Cellidrin, Cosuric, Dabrosin, Dabroson, Embarin, Epidropal, Epuric, Foligan, Geapur, Gichtex, Gotax, Hamarin, Hexanuret, Ketanrift, Ketobun-A, Ledopur, Lopurin, Lysuron, Milurit, Miniplanor, Monarch, Nektrohan, Progout, Purinol, Remid, Riball, Sigapurol, Suspendol, Takanarumin, Urbol, Uricemil, Uriprim, Uripurinol, Uritas, Urobenyl, Urolit, Urosin, Urtias, Xanturat, Zyloprim. Zyloric

Cyclamen Care How To Take Care Of Cyclamen Plants, Cyclomed

Cyclamen Plant Care – Tips For Taking Care Of A Cyclamen

By Heather Rhoades

Taking care of a cyclamen properly is essential if you wish to keep your cyclamen plant lasting year after year. Their vibrant flowers and interesting leaves make this plant a popular houseplant and many owners ask “How do I take care of a cyclamen plant?” Let’s look at how to take care of cyclamen plants both during and after blooming.

Basic Cyclamen Plant Care

Cyclamen care starts with the correct temperature. In nature, cyclamens grow in cool, humid environments. If the temperature of your house is over 68 F. (20 C.) during the day and 50 F. (10 C.) at night, your cyclamen will start to die slowly. Temperatures that are too high will cause the plant to begin to yellow, and the flowers will fade rapidly.

Cyclamen that are sold as houseplants are tropical and cannot tolerate temperatures below 40 F. (4 C.). Hardy cyclamen, on the other hand, which are sold in garden nurseries for outside use, are typically hardy to USDA Zone 5, but check the plant’s label to see the specific hardiness of the hardy cyclamen variety you are buying.

The next essential part of taking care of a cyclamen is to make sure that it is properly watered. Cyclamen are sensitive to both over and under watering. Make sure the plant has excellent drainage with a potting medium that holds water well. Water your cyclamen plant only when the soil is dry to the touch, but do not leave the plant in this dry state so long that it shows visible signs of not being watered, such as droopy leaves and flowers.

When you water the plant, water from below the leaves so that the water does not touch the stems or leaves. Water on the stems and leaves can cause them to rot. Be sure that when you water the plant, you thoroughly soak the soil and let any excess water drain away.

The next part of cyclamen plant care is fertilizer. Only fertilizer once every one to two months with water soluble fertilizer mixed at half strength. When cyclamen get too much fertilizer, it can affect their ability to rebloom.

Cyclamen Care After Blooming

After a cyclamen blooms, it will go into a dormant state. Going into a dormant state looks very much like the plant is dying, as the leaves will turn yellow and fall off. It is not dead, just sleeping. With proper cyclamen plant care, you can help it through its dormancy and it will rebloom in a few months. (Please note that hardy cyclamen planted outdoors will go through this process naturally and do not need extra care to rebloom.)

When taking care of a cyclamen after blooming, allow the leaves to die and stop watering the plant once you see the signs that the leaves are dying. Place the plant in a cool, somewhat dark place. You can remove any dead foliage, if you would like. Let sit for two months.

Taking Care of a Cyclamen to Get it to Rebloom

Once a cyclamen has finished its dormant period, you can start to water it again and bring it out of storage. You may see some leaf growth, and this is okay. Make sure to completely soak the soil. You may want to set the pot in a tub of water for an hour or so, then make sure any excess water drains away.

Check the cyclamen tuber and make sure that the tuber has not outgrown the pot. If the tuber seems crowded, repot the cyclamen to a larger pot.

Once the leaves start to grow, you can resume normal cyclamen care and it should rebloom shortly.

This article was last updated on 02/13/15

Mercaptopurine Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Mercaptopurinum

mercaptopurine

GENERIC NAME(S): MERCAPTOPURINE

Uses

This medication is used with other drugs to treat a certain type of cancer (acute lymphocytic leukemia ). Mercaptopurine belongs to a class of drugs known as purine antagonists. It works by slowing or stopping the growth of cancer cells.

Talk to the doctor about the risks and benefits of mercaptopurine, especially when used in children and young adults.

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

How to use mercaptopurine

Take this medication by mouth with or without food with a full glass of water (8 ounces or 240 milliliters), usually once daily or as directed by your doctor. Drink plenty of fluids while taking this medication unless otherwise directed by your doctor. Doing so may help decrease the risk of side effects (e. g. kidney stones ).

If you are using the suspension, shake the bottle well for at least 30 seconds before each dose to make sure the medication is well mixed. Carefully measure the dose using a special measuring device/spoon. Do not use a household spoon because you may not get the correct dose. Once opened, the suspension bottle should be used within 6 weeks.

The dosage is based on your body weight. medical condition and response to treatment. Do not increase your dose or take this medication more often than prescribed. Your condition will not improve any faster, and the risk of serious side effects may be increased.

Since this drug may be absorbed through the skin and lungs. women who are pregnant or who may become pregnant should not handle this medication or breathe the dust from the tablets. Properly discard any unused medication. Ask your pharmacist for details.

Side Effects

Nausea. vomiting. diarrhea. and loss of appetite may occur. Temporary hair loss may also occur. Normal hair growth should return after treatment has ended. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

Many people using this medication have serious side effects. However, your doctor has prescribed this drug because he or she has judged that the benefit to you is greater than the risk of side effects. Careful monitoring by your doctor may decrease your risk.

Tell your doctor right away if any of these unlikely but serious side effects occur: easy bruising/bleeding, dizziness /fainting. joint pain /swelling, tongue /mouth sores or pain, unusual tiredness, symptoms of liver disease (such as persistent nausea/vomiting, stomach /abdominal pain. dark urine, yellowing eyes /skin).

Tell your doctor right away if any of these rare but very serious side effects occur: symptoms of possible lymphoma (such as swollen or painful abdomen. persistent fever. night sweats. unexplained weight loss ), signs of kidney problems (such as change in the amount of urine, pain in the lower back/side).

This medication can lower the body's ability to fight an infection. Tell your doctor promptly if you develop any signs of an infection such as fever, chills, or persistent sore throat .

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction. rash. itching /swelling (especially of the face/tongue /throat), 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 mercaptopurine, tell your doctor or pharmacist if you are allergic to it; or to azathioprine ; 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.

This medication should not be used if you have a certain medical condition. Before taking this medicine, consult your doctor or pharmacist if a certain drug (thioguanine ) did not work for you in the past. This may affect how well mercaptopurine works for you.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: other blood disorders (e. g. anemia, low blood cell counts), gout, kidney disease (including kidney stones ), liver disease, pancreatitis. radiation treatment, history of cancer (such as lymphoma).

Do not have immunizations/vaccinations without the consent of your doctor, and avoid contact with people who have recently received oral polio vaccine or flu vaccine inhaled through the nose.

Wash your hands well to prevent the spread of infections.

To lower your risk of getting cut, bruised, or injured, use caution with sharp objects like razors and nail cutters, and avoid activities such as contact sports.

If you need to have surgery or a dental procedure, tell your doctor or dentist that you are using mercaptopurine.

Drinking alcohol may increase the risk of stomach/esophageal irritation or liver damage. Limit alcoholic beverages.

People with a certain inherited problem (lack of thiopurine methyltransferase-TPMT enzyme) may be at increased risk for serious side effects from this medication and may require dosage adjustment. Consult your doctor for details and to discuss whether you should be tested for this inherited problem.

Caution is advised when using this drug in the elderly because they may be more sensitive to the effects of the drug, especially the liver and bone marrow effects.

This medication is not recommended for use during pregnancy. It may harm the unborn baby. It may be particularly harmful during the first 3 months of pregnancy. Consult your doctor for more details and to discuss reliable forms of birth control. If you become pregnant or think you may be pregnant, tell your doctor right away.

It is not known whether this drug passes into breast milk. Because of the possible risk to the infant, breast-feeding while using this drug is not recommended. Consult your doctor before breast-feeding.

Interactions

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with them first.

This drug should not be used within 2 weeks of receiving a live vaccine (e. g. flu, measles, mumps, polio). Before taking this medication, tell your doctor of any planned or recently received vaccines. (See also Precautions section.)

This drug should not be used with the following medication because a very serious interaction may occur: febuxostat.

If you are currently using the medication listed above, tell your doctor or pharmacist before starting mercaptopurine.

Before using this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use, especially of: aminosalicylates (e. g. olsalazine, mesalazine, sulfasalazine), aspirin, "blood thinners" (e. g. warfarin), drugs that may affect the bone marrow (e. g. trimethoprim/sulfamethoxazole, other cancer chemotherapies), drugs that may affect the liver (e. g. amiodarone, erythromycin).

Before using this medication, tell your doctor or pharmacist if you are taking allopurinol. The dose of mercaptopurine may need to be decreased to avoid severe side effects.

If your doctor has directed you to take low-dose aspirin for heart attack or stroke prevention (usually at dosages of 81-325 milligrams a day), you should continue taking it unless your doctor instructs you otherwise. Ask your doctor or pharmacist for more details.

This product can affect the results of certain lab tests (e. g. uric acid), possibly causing false test results. Make sure laboratory personnel and all your doctors know you use this drug.

Mercaptopurine is very similar to azathioprine. Do not use medications containing azathioprine while using mercaptopurine.

This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

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: sudden or severe nausea/vomiting, sudden/severe diarrhea, dark urine, severe abdominal pain, yellowing eyes/skin.

Notes

Do not share this medication with others.

Laboratory and/or medical tests (e. g. complete blood count, liver function tests) should be performed periodically to monitor your progress or check for side effects. Keep all medical/lab appointments. Consult your doctor for more details.

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

Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture. 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.

MEDICAL ALERT: Your condition can cause complications in a medical emergency. For information about enrolling in MedicAlert, call 1-888-633-4298 (US) or 1-800-668-1507 (Canada).

Information last revised May 2016. Copyright(c) 2016 First Databank, Inc.

Images

Selected from data included with permission and copyrighted by First Databank, Inc. This copyrighted material has been downloaded from a licensed data provider and is not for distribution, expect as may be authorized by the applicable terms of use.

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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ADHD Drug Side Effects

Drug Overdose

Abacavir - Bruksanvisning, Beskrivning - Kod J, Efavirenz

Abacavir

Leversjukdom, Tidig barndom (till 3 Manader), amning.

Graviditet och amning.

Kategori atgarder leder till FDA - C. (Studiet av reproduktion hos djur har visat negativa effekter pa fostret, och adekvata och valkontrollerade studier pa gravida kvinnor inte har hallit, Dock de potentiella fordelarna, samband med anvandning av HP hos gravida kvinnor, kan motivera dess anvandning, trots den mojliga risken.)

Fordrojd overkanslighet ( иногда — угрожающие жизни ): feber, sjukdomskansla, uttrottbarhet, gastrointestinala storningar (muntorrhet, illamaende, krakningar, diarre, buksmartor), hosta, andfaddhet, lagt blodtryck, svullnad och smarta i lederna, huvudvark, svaghet, somnstorningar, minskad aptit, gepatomegaliya, leversteatos, pankreatit, laktatacidos, hudutslag.

Mojlig konkurrens for alkoholdehydrogenas med droger, metaboliseras under sitt deltagande (retinoider).

Dosering och administration.

Inuti, oavsett maltiden, i strikt definierade timmar, vuxna och ungdomar over 12 ar - 1 Bord. (300 mg) eller 15 ml (en oformaga eller oformaga att svalja tabletter) 2 en gang om dagen, Barn fran 3 manader till 12 ar - 8 mg / kg kroppsvikt 2 en gang om dagen, men inte mer 600 mg.

Monoterapi ar inte tillatet. Forskrivare kan specialist, med erfarenhet av behandling av HIV-infektion. Innan starten av den aktiva antiretroviral behandling genomfores full klinisk och laboratorieundersokning av patienten, inkl. niva bestams pa virusmangd i plasma och antalet CD4 T-lymfocyter. Under behandlingen en vanlig visar (var 3-6 manad) bedomning av nivan av replikationsprocessen, virusmangd i plasma (определение bДНК и RT-PCR) och nivan av CD4 - celler. I narvaro av kliniska symptom pa HIV-terapi skulle borja utesluta CD4 cellantal och viral belastning pa plasma. Utseendet pa nagra tecken pa overkanslighetsreaktioner (vanligt forekommande i den forsta 6 veckors behandling) pa grund av deras potentiella fara for livet kraver avbrytande (och vidare anvandning av drogen ar oacceptabelt). Patienter bor varnas, att behandlingen inte minskar risken for overforing av HIV till andra.

Beskrivning av interaktion

Zoflut Cream (Fluticasone) - United Pharmacies, Zoflut

Zoflut

Description

Zoflut Cream (Fluticasone) is a medium strength corticosteroid used to decrease swelling, itchiness, redness, and inflammation. It can be used to treat a variety of skin conditions including psoriasis, dermatitis, eczema, and even symptoms caused by a mild allergic reaction. It should also be noted that the cream is not effective in treating severe acne, rosacea, or viral infections such as herpes or chicken pox.

Dosage and Administration

Strictly use Zoflut Cream (Fluticasone) as you have been prescribed by your physician. Never self-medicate. To use the medicine apply the cream directly to the area being treated, gently massage it into the skin, and allow any excess cream to evaporate. Do not apply the cream to the genitals, face, or armpits unless specifically advised to do so by your physician. Always finisht he course of prescribed medication, even if your symptoms have disappeared, as the infection may not be destroyed and can return.

Patients using Zoflut Cream (Fluticasone) may experience irritation, dryness, redness, or itchiness. As your body adjusts to the cream these side effects should stop. If any persist, notify your physician promptly.

Seek medical attention as soon as possible if you notice any of these more serious side effects:

Headaches

Severe weakness or fatigue

Stretch marks

Skin infections

Swelling of the feet or ankles

Increased thirst

Abnormal acne

Abnormal hair growth

Abnormal weight loss

Changes to your urination

Changes to your vision

Zoflut Cream (Fluticasone) may increase the skin`s sensitivity to sun light and other sources of UV rays. Avoid exposure to direct sunlight, and all use of sun lamps and tanning booths.

Disabused - Definition Of Disabused By The Free Dictionary, Diabuse

disabused

References in classic literature ?

And now look again, and see what will naturally follow it' the prisoners are released and disabused of their error.

Influenced by these thoughts, his face wore an expression so benign and tranquil, that the waiter in immediate attendance upon him felt he could almost have died in his defence, and settled in his own mind (until the receipt of the bill, and a very small fee for very great trouble disabused it of the idea) that such an apostolic customer was worth half-a-dozen of the ordinary run of visitors, at least.

I thought so for a time, until my colleague Pete Zelinski disabused me of the notion.

Carwyn Jones needs to be disabused of the opinion that this drug only works in "exceptional" cases or that Irfon Williams demonstrates an "unusual response" to the drug.

creature, I'd say, who has not been disabused of the fairytale idea

IF you've ever harboured any doubt that austerity is serious then you will be disabused of the notion today.

Then I got off the bus and was quickly disabused of that idea.

Which I think is appropriate: If you believe in participative management, you will be disabused of your silly idea.

If Burma's rulers expect to rehabilitate their image abroad with this pretense of magnanimity, they should be disabused of that view.

ANY notion that the bloodstock world lives in a bubble of its own has been swiftly disabused over the last 12 months.

Put it this way: you were certainly pretty quickly disabused of any romantic notions you might have had about the era.

I trust recent events have disabused the public of this view.

Endal Hd Medical Facts From, Enddol

Endal HD

What is this medicine?

Diphenhydramine is an antihistamine that reduces the natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.

Hydrocodone is a narcotic cough medicine.

Phenylephrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).

Diphenhydramine, hydrocodone, and phenylephrine is a combination medicine used to treat runny or stuffy nose, sinus congestion, and cough caused by the common cold or flu.

Diphenhydramine, hydrocodone, and phenylephrine may also be used for purposes not listed in this medication guide.

What is the most important information I should know about Endal HD (diphenhydramine, hydrocodone, and phenylephrine)?

Do not use this medicine if you have taken an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, and tranylcypromine.

You should not use this medicine if you have recently used alcohol, sedatives, tranquilizers, or other narcotic medications.

What should I discuss with my healthcare provider before taking this medicine?

Do not use this medicine if you have taken an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, and tranylcypromine.

You should not use diphenhydramine, hydrocodone, and phenylephrine if you are allergic to it, or if you have recently used alcohol, sedatives, tranquilizers, or other narcotic medications.

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

blockage in your digestive tract (stomach or intestines);

diarrhea, inflammatory bowel disease;

a colostomy or ileostomy;

liver or kidney disease;

bladder obstruction or other urination problems;

a head injury or brain tumor;

asthma, COPD, sleep apnea, or other breathing disorder;

a thyroid disorder;

pheochromocytoma (tumor of the adrenal gland);

low blood pressure; or

if you are dehydrated.

Hydrocodone may be habit forming. Never share this medicine with another person, especially someone with a history of drug abuse or addiction. Keep the medication in a place where others cannot get to it.

FDA pregnancy category C. It is not known whether this medicine will harm an unborn baby. Hydrocodone may cause addiction or withdrawal symptoms in a newborn if the mother takes the medication during pregnancy. Tell your doctor if you are pregnant or plan to become pregnant while using diphenhydramine, hydrocodone, and phenylephrine.

Diphenhydramine, hydrocodone, and phenylephrine can pass into breast milk and may harm a nursing baby. You should not breast-feed while using this medicine.

How should I take Endal HD (diphenhydramine, hydrocodone, and phenylephrine)?

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

You may take this medication with or without food.

Measure liquid medicine with a special dose-measuring spoon or cup, not a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

Store at room temperature away from moisture and heat.

Keep track of the amount of medicine used from each new bottle. Hydrocodone is a drug of abuse and you should be aware if anyone is using your medicine improperly or without a prescription.

What happens if I miss a dose?

Since this medicine is used when needed, you may not be on a dosing schedule. If you are on a schedule, use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use 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. An overdose of hydrocodone can be fatal.

Overdose symptoms may include extreme drowsiness, pinpoint pupils, confusion, cold and clammy skin, weak pulse, shallow breathing, fainting, or breathing that stops.

What should I avoid while taking Endal HD (diphenhydramine, hydrocodone, and phenylephrine)?

This medication may cause blurred vision and may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert and able to see clearly.

Drinking alcohol can increase certain side effects of diphenhydramine, hydrocodone, and phenylephrine.

Endal HD (diphenhydramine, hydrocodone, and phenylephrine) side effects

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

Stop using this medicine and call your doctor at once if you have:

pounding heartbeats or fluttering in your chest;

a light-headed feeling, like you might pass out;

severe anxiety, confusion, fear;

painful or difficult urination;

little or no urinating; or

dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, confusion, chest pain, shortness of breath, uneven heartbeats, seizure).

Common side effects may include:

blurred vision; or

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 Endal HD (diphenhydramine, hydrocodone, and phenylephrine)?

Taking this medicine with other drugs that make you sleepy or slow your breathing can cause dangerous or life-threatening side effects. Ask your doctor before taking diphenhydramine, hydrocodone, and phenylephrine with a sleeping pill, narcotic pain medicine, muscle relaxer, or medicine for anxiety, depression, or seizures.

Other drugs may interact with diphenhydramine, hydrocodone, and phenylephrine, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.

More about Endal HD (diphenhydramine / hydrocodone / phenylephrine)

Consumer resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about diphenhydramine, hydrocodone, and phenylephrine.

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: 3.01. Revision Date: 2013-10-09, 2:12:11 PM.

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Therevac-Sb News - Updates, Therevac-Sb

Therevac-SB News

FDA Medwatch Alert: Oral Liquid Docusate Sodium by PharmaTech. Recall - Contaminated with B. cepacia

Posted 20 Jul 2016 by Drugs. com

ISSUE: The FDA is alerting health care professionals that PharmaTech LLC, Davie, Florida, is voluntarily recalling all non-expired lots of Diocto Liquid, a docusate sodium solution distributed by Rugby Laboratories, Livonia, Michigan. The agency confirmed the product has been contaminated with Burkholderia cepacia, a bacteria linked to an outbreak in five states. In addition, FDA has received several adverse event reports of B. cepacia infections in patients. Some of these reports identify liquid docusate sodium products manufactured by companies other than PharmaTech. FDA and the Centers for Disease Control and Prevention continue to investigate the extent of this issue in order to identify other potentially contaminated liquid docusate sodium products. BACKGROUND: PharmaTech manufactures the oral liquid docusate sodium, which is distributed nationwide by Rugby with a Rugby label in. Read more

Posted 8 Jun 2016 by Drugs. com

-- Laxatives can have unpleasant side effects, especially when overused. The American Academy of Family Physicians says possible problems associated with laxative use include: Abdominal cramps or nausea. Gas, diarrhea or bloating. Electrolyte imbalance, which can affect the muscles, nerves and organs. Those most at risk include children and people with kidney disease or diabetes. Muscle weakness or muscle spasms. Fatigue, confusion, headache or vomiting. Read more

Posted 8 Oct 2014 by Drugs. com

WEDNESDAY, Oct. 8, 2014 – A new study suggests that the type of laxative a person takes might be a factor in their odds for colon cancer. The research indicates that fiber-based laxatives are associated with a lower risk of colorectal cancer, while non-fiber laxatives are linked with a higher risk. The study could only show an association between laxative types and colon cancer risk, it could not prove cause-and-effect, and experts stress that more study is needed. Still, the researchers believe the findings are important because about 20 percent of Americans use laxatives. According to a team led by Jessica Citronberg, a predoctoral fellow at Fred Hutchinson Cancer Research Center in Seattle, non-fiber laxatives are the most widely used in the United States and work by forcing the colon to contract. On the other hand, fiber-based laxatives boost the water content and bulk of the stool. Read more

Posted 28 Jan 2013 by Drugs. com

MONDAY, Jan. 28 – Some treatments are more effective than others for relieving constipation in seniors, according to a new review. And laxatives aren't always enough, researchers say. Constipation is common in seniors and can have serious health consequences and affect quality of life. Excessive straining in frail elderly people can cause them to faint and put them at risk of injury or falling, or restrict blood flow to the heart and brain. Chronic constipation can lead to fecal impaction, a large lump of hard stool that remains stuck in the rectum. Fecal impaction can cause nausea, pain and loss of appetite. "Given the growing proportion of older adults in North America, effective management of constipation by health care professionals will be increasingly necessary," Dr. Dov Gandell, of Sunnybrook Health Sciences Centre in Toronto, and colleagues wrote in an article appearing Jan. 28. Read more

Posted 17 May 2010 by Drugs. com

-- Laxatives are medications usually purchased over-the-counter to help treat constipation. The American Academy of Family Physicians says side effects are rare if laxatives are taken as their labels direct, but sometimes they can trigger: Diarrhea. Nausea. Cramps. Gas. Bloating. Read more

Ask a Question

Motrin - Pain Relief, Ipufen

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. 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 the proper use of Motrin .

Store Motrin at room temperature, 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 Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

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

Some medical conditions may interact with Motrin. 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 product, or dietary supplement

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

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

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

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin 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:

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

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

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

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

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

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can 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:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

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

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the 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.

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. 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 the proper use of Motrin .

Store Motrin at room temperature, 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 Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

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

Some medical conditions may interact with Motrin. 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 product, or dietary supplement

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

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

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

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin 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:

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

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

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

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

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

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can 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:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

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

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the 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.

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. 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 the proper use of Motrin .

Store Motrin at room temperature, 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 Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

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

Some medical conditions may interact with Motrin. 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 product, or dietary supplement

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

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

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

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin 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:

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

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

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

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

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

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can 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:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

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

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the 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.

Mihail Korubin, Corubin

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MIhail Korubin’s limited edition giclee prints, are produced on a museum quality 300 gsm HARMAN 100% cotton fine art paper, printed with Epson UltraChrome K3® Inks on a high end giclee printer. Framed prints are made with solid wood frame, crystal clear glass and high quality paspartu border. These prints are completed with mounting hardware and they are ready to hang.

from Call for pricing <a href="tel:+38970365237"> +389 70 365 237</a> E-mail - for pricing - <a href="mailto:hi@mihailkorubin. com"> hi@mihailkorubin. com</a>

2012 / Oil on canvas / 135cm x 100cm

MIhail Korubin’s limited edition giclee prints, are produced on a museum quality 300 gsm HARMAN 100% cotton fine art paper, printed with Epson UltraChrome K3® Inks on a high end giclee printer. Framed prints are made with solid wood frame, crystal clear glass and high quality paspartu border. These prints are completed with mounting hardware and they are ready to hang.

Kloramixin, Kloramixin

Product Description Common use Decadron is used to treat conditions such as arthritis, blood/hormone/immune system disorders, allergic reactions, certain skin and eye conditions, breathing problems, certain bowel disorders. Also it is used in the treatment of cancers of the white blood cells (leukemias), and lymph gland cancers (lymphomas). Finally, Decadron is used as replacement therapy in patients whose adrenal glands are unable to produce sufficient amounts of corticosteroids.

Dosage and direction Take this medication by mouth as directed by your doctor. The initial oral dose is 0.75 to 9 mg daily depending on the disease. The initial dose should be adjusted according to the response to therapy. Take with food or milk to prevent stomach upset. Take this medication by mouth with food or a full glass of water or milk unless your doctor directs you otherwise. If you take this medication once daily, take it in the morning before 9 AM. Use this medication regularly in order to get the most benefit from it. Take it at the same time(s) each day. It is important to continue taking this medication even if you feel well. Follow the dosing schedule carefully, and take this medication exactly as prescribed. Do not stop taking this medication without consulting your doctor. Inform your doctor if your condition does not improve or worsens.

Precautions Do not get immunizations, vaccinations, or skin tests unless specifically directed by your doctor. Before taking Decadron, tell your doctor or pharmacist if you have any allergies, your medical history: active fungal infections, kidney or liver disease, mental/mood conditions, low blood minerals, thyroid disease, stomach/intestinal problems, high blood pressure, heart problems, diabetes, eye diseases, brittle bones, history of blood clots. If you have been taking this medication for a long time, your body may not make enough natural hormones while you are under physical stress. Your dose may need to be adjusted. If you have stopped taking this drug within the past 12 months, you may need to start taking it again if your body is under physical stress. Before having surgery, tell your doctor or dentist that you are using this medication or have taken it within the last 12 months. If you have a history of ulcers or take large doses of aspirin or other arthritis medication. Limit alcoholic beverages while taking this medication to decrease the risk of stomach/intestinal bleeding. If you have diabetes, this drug may make it harder to control your blood sugar levels. Monitor your blood sugar levels regularly and inform your doctor of the results. During pregnancy, this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor. This drug may pass into breast milk and could have undesirable effects on a nursing infant. Therefore, breast-feeding is not recommended while using this medication. Avoid contact with people who have recently received oral polio vaccine or flu vaccine inhaled through the nose, chickenpox or measles unless you have previously had these diseases (in childhood). If you are exposed to one of these infections and you have not previously had it, seek immediate medical attention.

Contraindications Do NOT use Decadron if you are allergic to any ingredient in Decadron, you have a systemic fungal infection, you are taking mifepristone. Contact your doctor or health care provider immediately if any of these apply to you.

Possible side effects

Side effects of Decadron depend on the dose, the duration and the frequency of administration. Short courses of dexamethasone usually are well tolerated with few and mild side effects. Long term, high dose dexamethasone usually will produce predictable and potentially serious side effects. Whenever possible, the lowest effective dose of dexamethasone should be used for the shortest possible length of time to minimize side effects. Alternate day dosing also can help reduce side effects. Side effects include fluid retention, weight gain, high blood pressure, loss of potassium, headache, muscle weakness, puffiness, and hair growth on the face, thinning and easy bruising of skin, glaucoma, cataracts, peptic ulceration, worsening of diabetes, irregular menses, growth retardation in children, convulsions, stomach upset, headache, dizziness, menstrual changes, trouble sleeping, increased appetite, or weight gain may occur, depression, euphoria, insomnia, mood swings, personality changes, and even psychotic behavior. A very serious allergic reaction to this drug is rare. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Drug interactions Drugs such as phenobarbital, ephedrine, phenytoin (Dilantin), and rifampin (Rifadin, Rimactane) may increase the breakdown of corticosteroids by the liver. As a result it may be lower blood levels and reduced effects. Therefore, the dose of corticosteroid may need to be increased if treatment with any of these agents is begun.

Missed dose If you are taking this medication daily and on a regular schedule, and 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.

Overdose Seek emergency medical attention if you think you have used too much of this medicine.

Storage Decadron should be stored at 68-77 F (20-25 C) and not frozen

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.

Lexor Manufacturer - Spa Pedicure Chairs, Lextor

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You have no obligation to purchase the product once you know the price. You can simply remove the item from your cart.

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Urogesic Blue Indications, Side Effects, Warnings, Eurogesic

Urogesic Blue

Urogesic Blue is used for:

Treating painful and irritating symptoms of the urinary tract due to urinary tract infections or diagnostic procedures.

Urogesic Blue is a urinary antiseptic, urinary acidifier, and antispasmodic combination. It works by helping to kill bacteria in the urine, decreasing inflammation, and reducing muscle spasms in the urinary tract. These actions work together to help relieve discomfort while urinating.

Do NOT use Urogesic Blue if:

you are allergic to any ingredient in Urogesic Blue

you have angle-closure glaucoma, a certain problem with your esophagus (reflux esophagitis), a blockage of your bladder, certain severe bowel problems (eg, toxic megacolon, ulcerative colitis), or myasthenia gravis

you are taking a sulfonamide (eg, sulfamethoxazole) or a solid oral potassium product (eg, tablet)

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

Before using Urogesic Blue:

Some medical conditions may interact with Urogesic Blue. 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 (including other belladonna alkaloids, such as atropine), foods, or other substances

if you have constipation, dehydration, diarrhea, or stomach or bowel problems (eg, blockage, infection, hiatal hernia)

if you have glucose-6-phosphate dehydrogenase (G6PD) deficiency, gout, increased pressure in the eyes or glaucoma, risk factors for glaucoma, an enlarged prostate, or bladder problems, or if you are unable to urinate

if you have a history of liver or kidney problems, an irregular heartbeat, heart blood vessel problems, or other heart problems (eg, congestive heart failure, heart valve problems)

if you are on a low-salt (sodium) diet

if you are taking medicine for a mental or mood problem

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

Anticholinergics (eg, benztropine) because they may increase the risk of Urogesic Blue's side effects

Narcotic pain medicine (eg, codeine) or solid oral potassium products (eg, tablets) because the risk of serious side effects may be increased

Ketoconazole, medicines for myasthenia gravis (eg, ambenonium), phenothiazines (eg, chlorpromazine), sulfonamides (eg, sulfamethoxazole), thiazide diuretics (eg, hydrochlorothiazide), or urinary alkalinizers (eg, sodium bicarbonate) because their effectiveness may be decreased by Urogesic Blue

This may not be a complete list of all interactions that may occur. Ask your health care provider if Urogesic Blue 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 Urogesic Blue:

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

Take Urogesic Blue by mouth with or without food.

Do not take an antacid or antidiarrheal medicine that has loperamide in it within 1 hour before or 1 hour after you take Urogesic Blue.

If you take ketoconazole, wait at least 2 hours after taking it before taking Urogesic Blue.

Drinking extra fluids while you are taking Urogesic Blue is recommended. Check with your doctor for instructions.

If you miss a dose of Urogesic Blue, 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 Urogesic Blue.

Important safety information:

Urogesic Blue may cause dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Urogesic Blue with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

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

Urogesic Blue may discolor the urine or stool a blue-green color. This is normal and not a cause for concern.

Use Urogesic Blue with caution in the ELDERLY; they may be more sensitive to its effects, especially agitation, confusion, drowsiness, and excitement.

Caution is advised when using Urogesic Blue in CHILDREN; they may be more sensitive to its effects.

Urogesic Blue should not be used in CHILDREN younger than 6 years old; safety and effectiveness in these 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 taking Urogesic Blue while you are pregnant. Urogesic Blue is found in breast milk. If you are or will be breast-feeding while you take Urogesic Blue, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Urogesic Blue:

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:

Dry mouth; flushing; nausea; 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); blurred vision; difficulty urinating; dizziness; fast or irregular heartbeat; 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. 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 Urogesic Blue:

Store Urogesic Blue 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 Urogesic Blue out of the reach of children and away from pets.

General information:

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

Urogesic Blue 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 Urogesic Blue 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 Urogesic Blue. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to Urogesic Blue. 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 Urogesic Blue.

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 Urogesic Blue (hyoscyamine / methenamine / methylene blue / sodium biphosphate)

Porphyria Cutanea Tarda Background, Pathophysiology, Epidemiology, Cutanum

Porphyria Cutanea Tarda

Background

Porphyria cutanea tarda (PCT) is a term encompassing a group of acquired and familial disorders in which activity of the heme synthetic enzyme uroporphyrinogen decarboxylase (UROD) is deficient. [1] Approximately 80% of all cases of porphyria cutanea tarda are acquired; 20% are familial, although the ratio may vary among different geographic regions and ethnic groups.

Familial porphyria cutanea tarda most often arises from autosomal dominant inheritance of a single mutation of the UROD gene. Human UROD has been mapped to band 1p34. [2] To date, 121 UROD mutations are listed by the Human Genome Mutation Database. A rare recessive familial type of porphyria cutanea tarda in which both UROD alleles are mutated is termed hepatoerythropoietic porphyria. [3] Familial porphyria cutanea tarda without detectable UROD mutations has been reported. [4, 5]

The common acquired form, sporadic porphyria cutanea tarda, occurs in individuals whose UROD DNA sequences are normal, but who may have other genetically determined susceptibilities to inhibition of UROD activity. Acquired porphyria in large populations exposed to polyhalogenated aromatic hydrocarbon hepatotoxins [6] has been referred to as "epidemic” porphyria cutanea tarda. Hepatic tumors producing excess porphyrins are rare causes of porphyria cutanea tarda–like disorders.

Clinical expression of both sporadic and familial porphyria cutanea tarda most often requires exposure to environmental or infectious agents or the presence of coexisting conditions that adversely affect hepatocytes and result in hepatic siderosis. Ethanol intake, estrogen therapies, hemochromatosis genes, and hepatitis and human immunodeficiency viral infections are among these contributory factors. [1] The increased oxidative stress associated with all of these factors has been shown to reduce hepatic expression of the gene encoding hepcidin, a regulator of iron absorption and metabolism, thus increasing iron absorption and iron overload. [7] Excess iron facilitates formation of toxic oxygen species, thus amplifying porphyrinogenesis by catalyzing formation of oxidative inhibitors of UROD enzyme activity. [8] Accumulating porphyrins in hepatocytes may then further down-regulate hepcidin gene expression. [7] Most patients with porphyria cutanea tarda have increased iron burden; iron-reduction therapies can lead to clinical and biochemical remissions; subsequent reaccumulation of iron stores may lead to symptomatic recurrence.

Reduced UROD activity causes polycarboxylated porphyrinogen intermediaries of heme synthesis to accumulate in hepatocytes; these excess substrates then undergo iron-facilitated spontaneous oxidization to photoactive porphyrins. Porphyrin by-products of the pathway exit the hepatocytes, are distributed throughout the body in blood plasma, mediate photooxidative chemical reactions causing skin lesions, and yield the abnormal excretory porphyrin profiles that characterize porphyria cutanea tarda. Partial oxidation of uroporphyrinogen to the UROD inhibitor uroporphomethene occurs in murine porphyria cutanea tarda models and has been suggested as a pathogenic mechanism in the human disease. [9] Reduction of hepatic UROD activity to approximately 25% of normal, most often reflecting effects of multiple genetic and/or exogenous inhibitory factors, is required for clinical disease expression. [10, 11]

Pathophysiology

When hepatic UROD activity falls below the critical threshold, porphyrin by-products of the heme biosynthetic pathway with 4-8 carboxyl group substituents are overproduced. These porphyrins are reddish pigments that accumulate in the liver and are disseminated in plasma to other organs. Porphyrins with high carboxyl group numbers are water soluble and excreted primarily by renal mechanisms. The porphyrin with 8 carboxyl groups is termed uroporphyrin; 4-carboxyl porphyrins include coproporphyrin and isocoproporphyrin, which are chiefly excreted in feces. Porphyrins are photoactive molecules that efficiently absorb energy in the visible violet spectrum. Photoexcited porphyrins in the skin mediate oxidative damage to biomolecular targets, causing cutaneous lesions.

The most common photocutaneous manifestations of porphyria cutanea tarda are due to increased mechanical fragility after sunlight exposure; erosions and blisters form painful indolent sores that heal with milia, dyspigmentation, and scarring (see images below).

Other common features of porphyria cutanea tarda include hypertrichosis, sclerodermalike plaques that may develop dystrophic calcification, and excretion of discolored urine that resembles port wine or tea, which is due to the presence of porphyrin pigments. [12]

Epidemiology

Frequency

A registry has been established by the NIH-funded Porphyrias Consortium (http://rarediseasesnetwork. epi. usf. edu/registry/direct. htm ) to more accurately enumerate cases of various types of porphyrias occurring in the US population. Until sufficient data have been collected by this registry to allow calculation, approximately 1 case of porphyria cutanea tarda in populations of 10,000-25,000 can be estimated based on data from other countries. Porphyria cutanea tarda is the most common porphyria seen in clinical practice.

Higher prevalences of porphyria cutanea tarda have been reported among various European populations. A high prevalence of porphyria cutanea tarda among South African Bantu people has been linked with a propensity for hepatic siderosis. Fractions of studied porphyria cutanea tarda cases reported as familial vary widely: 14.6% in Spain, [13] 24% in Denmark, [14] and 50% in Chile. [15]

Race

Porphyria cutanea tarda occurs in persons of all ethnic groups.

Sex

Porphyria cutanea tarda occurs in both sexes. Older reports indicated a great preponderance of porphyria cutanea tarda in men; more recent surveys include many women.

Age

Sporadic porphyria cutanea tarda typically manifests in adulthood. Symptoms of familial porphyria cutanea tarda typically first appear in adults heterozygous for a UROD gene mutation, but they have also been reported in heterozygote children. [16] When biallelic mutations are present (homozygotes or compound heterozygotes), symptoms may be severe, with onset in early childhood. [17] Milder phenotypes with somewhat later onset have also been observed. [18, 19]

Porphyria cutanea tarda–like disorders resulting from exposure of large numbers of people to hepatotoxic chemicals have afflicted people of all ages. [6]

About Medscape Drugs & Diseases

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Splosni Pogoji In Pravila, Fidiflex

Splosni pogoji in pravila – FIDIKLUB

Splosni pogoji in pravila – FIDIKLUB

Fidimed je ze 20 let vodilno podjetje na podrocju proizvodnje in prodaje zdravil naravnega izvora ter prehranskih dopolnil. Nase delo vkljucuje pripravo lastnih receptov, saj je vecina izdelkov plod domacega znanja, nekatera prehranska dopolnila in naravna zdravila, pa so plod sodelovanja z uglednimi evropskimi proizvajalci.

Ker zelimo v Fidimedu se najprej nagrajevati vase zaupanje in zvestobo, vam predstavljamo Fidiklubu. Fidiklub je nadgradnja Fidimedovega programa zvestobe, ki je potekal v preteklem letu. In ker je v Fidimedu vase zdravje in dobro pocutje nasa glavna skrb Vas bomo razvajali se z dodatnimi ugodnostmi, novostmi, popusti in zdravstvenimi nasveti.

1.2. KAKO POSTATI CLAN FIDIKLUBA?

Clan Fidikluba lahko postane vsaka polnoletna oseba, ki na sedez podjetja - PharmaSwiss d. o.o, Brodisce 32, 1236 Trzin - poslje popolno izpolnjeno in podpisano pristopno izjavo s pripisom Fidiklub.

Pristopno izjavo vam lahko posljemo na vas naslov, ce poklicete v Fidimedovo posvetovalnico na brezplacno telefonsko stevilko 080 32 35 vsak delavnik med 8. in 15. uro.

Z oddajo pristopne izjave clan sprejema splosne pogoje in pravila Fidikluba.

Vsi, ki ste bili v preteklosti ze del nasega programa zvestobe boste avtomaticno postali clani Fidiklub in lahko neumudoma pricnete koristi ugodnosti. V primeru, da si tega ne zelite vas vljudno naprosamo, da nam na naslov PharmaSwiss d. o.o. Brodisce 32, 1236 Trzin oz. na sloveniainfo@pharmaswiss. com posljete pisno odpoved za izstop iz Fidikluba. Ce posameznik izstopi iz Fidikluba, ne more vec koristiti ugodnosti, ki jih le-ta ponuja.

Namen Fidikluba je, nagraditi zveste uporabnike Fidimedovih izdelkov. Ker zelimo, da bi bili vsi uporabniki zadovoljni z nasimi izdelki in storitvami, bodo:

Vasi podatki pri nas varni in shranjeni v skladu z Zakonom o varstvu osebnih podatkov (ZVOP-1).

Zagotavljamo vam, da vas bomo sproti obvescali o novostih, ugodnih ponudbah, nagradnih igrah, popustih in drugih za zdravje koristnih informacijah.

Za vsa vprasanja o Fidimedovih izdelkih, Fidiklubu smo Vam na voljo od pon.-pet. med 8. In 15. uro na brezplacni telefonski stevilki 080 32 35. Vprasanja pa nam lahko posljete tudi na e-naslov: PharmaSwissSloveniaInfo@valeant. com

1.3. UGODNOSTI FIDIKLUBA

Clan/-ica Fidikluba lahko koristi naslednje ugodnosti:

Brezplacno strokovno svetovanje v Fidimedovi posvetovalnici na brezplacni stevilki 080 32 35

Brezplacno postnino ob nakupu v vrednosti nad 15 €

Obvescanje o novostih

Popusti

Posebne ponudbe

Darila

V izbranih lekarnah in specializiranih prodajalnah Vam ob nakupu Fidimedovih izdelkov izrocijo kartico zvestobe, ki je v izbrani lekarni/specializirani prodajalni unovcljiva do 31.12.2016. Ob nakupu prehranskih dopolnil blagovne znamke Fidimed prejmete Fidinalepke glede na vrednost nakupa po lestvici:

10 €-19,99 € = 1 nalepka

20 € - 29,99 € = 2 nalepki

30 € - 39,99 € = 3 nalepke

Vsak nadaljnji nakup v vrednosti 10 € pa Vam prinese dodatno nalepko.

Program zvestobe NE VELJA ob pri nakupu zdravil BaldriMed®, Fidi koencim 10®, Fidiflex® 1178 mg in Remifemin®.

Ko zberete 20 nalepk . na kartici zvestobe oznacite izdelek iz nabora navedenega na kartici zvestobe, ki ga zelite prejeti in popolno izpolnjeno kartico izrocite osebju v lekarni/specializirani prodajalni, ki Vam bo izbran izdelek podarilo.

Pravila dolocajo pogoje clanstva Fidikluba, ki ga ustanavlja podjetje PharmaSwiss d. o.o. Brodisce 32, 1236 Trzin.

Clan Fidikluba je oseba, ki je bila v preteklosti sodelovala v Programu zvestobe ali oseba, ki je izpolnjeno in podpisano pristopno izjavo poslala na sedez podjetja.

Clan Fidikluba se zavezuje, da bo ustanovitelju Fidikluba – podjetju PharmaSwiss – ustno, pisno ali preko elektronske poste posredoval morebitne spremembe podatkov, kot so: sprememba naslova, telefonske stevilke, itd. ki so bistveni pri obvescanju o novostih in ugodnosti kluba.

V primeru tehnicnih tezav, ki ovirajo nemoteno delovanje racunalniskega sistema, Pharmaswiss za cas sistemskih motenj ne zagotavlja uporabljanja ugodnosti iz naslova Fidikluba, zagotavlja pa naknadni vpis sprememb, nakupov,…

5. FIDIMEDOVA POSVETOVALNICA

Za pomoc, svetovanje in vprasanja o Fidimedovih izdelkih in storitvah je na voljo magistrica farmacije.

** Prodajo vrsi partnerska Lekarna Slovenska Bistrica.

5.1. POMOC CLANOM FIDIKLUBA

Posameznik se lahko za vec informacij oz. pomoc pri vclanitvi v Fidiklub obrne na brezplacno telefonsko stevilko 080 32 35 ali na elektronski naslov PharmaSwissSloveniaInfo@valeant. com

5.2. IZSTOP IZ FIDIKLUBA

Clan/-ica Fidikluba lahko kadarkoli brez navedbe razlogov pisno izstopi iz Fidikluba. Odpoved zacne veljati, ko podjetje prejme pisno odpoved na naslov: PharmaSwiss d. o.o. Brodisce 32, 1236 Trzin s pripisom Fidiklub ali na PharmaSwissSloveniaInfo@valeant. com. Ce posameznik izstopi iz Fidikluba, ne more vec koristiti ugodnosti, ki ji jih le-ta ponuja. Podjetje Pharmaswiss lahko hrani osebne podatke o clanu do preklica oziroma izstopa iz Fidikluba. Upravljavec osebnih podatkov je dolzan pridobljene podatke o clanu Fidikluba izbrisati najkasneje v 15 delovnih dneh od dneva prejema odjave oz. preklica in o tem posameznika, ki je to zahteval tudi pisno obvestiti.

5.3. SPREMEMBE SPLOSNIH POGOJEV POSLOVANJA

Podjetje PharmaSwiss d. o.o. lahko v vsakem trenutku spremeni splosne pogoje in pravila Fidikluba, ce to zahtevajo vzroki tehnicne, komercialne narave ali vzroki, ki so na strani javnosti.

O spremembi splosnih pogojev in pravil Fidikluba mora podjetje PharmaSwiss d. o.o clane Fidikluba pisno obvestiti.

Smatramo, da clan, v primeru da ne poslje pisne odpovedi na sedez podjetja PharmaSwiss d. o.o. soglasa s spremembo splosnih pogojev in pravil Fidikluba.

Ko PharmaSwiss clana Fidikluba pisno obvesti o spremembi splosnih pogojev in pravil Fidikluba, nadaljnjo koriscenje ugodnosti pomeni, da se clan strinja s spremenjenimi splosnimi pogoji in pravili.

PharmaSwiss d. o.o. si pridrzuje pravico, da lahko Fidiklub kadarkoli in brez navedbe razlogov pisno odpove.

VARSTVO OSEBNIH PODATKOV

Z izpolnitvijo pristopne izjave posameznik dovoljuje, da podjetje Pharmaswiss d. o.o. Brodisce 32, 1236 Trzin, kot upravljavec zbirke osebnih podatkov vse posredovane podatke in podatke o vsebini nakupov obdeluje v skladu z Zakonom o varstvu osebnih podatkov (ZVOP-1).

Pharmaswiss d. o.o. zagotavlja, da osebne podatkov clanov Fidikluba in vse ostale podatke, zbrane v postopku vclanitve, sciti pred razkritjem in posredovanjem nepooblascenim tretjim osebam. Vsi podatki clanov Fidikluba so zaupni.

Z vnosom svojih osebnih podatkov na pristopni izjavi za vclanitev v Fidiklub ter s sprejetjem splosnih pogojev in pravil le-tega clan izrecno soglasa, da Pharmaswiss d. o.o. lahko posreduje nekatere podatke o clanu Fidikluba pooblascenim tretjim osebam na ozemlju Republike Slovenije (npr. tiskarji, IT podjetja, ki skrbijo za podatkovno bazo upravljavca).

Poleg podatkov, ki jih posameznik vnese ob izpolnitvi pristopne izjave, se zbirajo tudi naslednji podatki: naziv izdelka, kolicina, vrednost nakupa, cas nakupa, stanje nakupov, uveljavljene ugodnosti, poslana darila, popusti.

Podatki o nakupu se zbirajo zaradi prilagoditve ponudbe posameznim clanom Fidikluba. Zbrani podatki se lahko uporabijo v naslednje namene: statisticne obdelave, trzenjske raziskave, posiljanje oglasnega materiala, vabil, telefonsko, pisno ali elektronsko anketiranje.

Clan Fidikluba z izpolnitvijo pristopne izjave in sprejetjem splosnih pogojev in pravil tudi potrjuje, da je seznanjen s pravico do vpogleda, prepisa, kopiranja, dopolnitve, popravka, blokiranja in izbrisa njegovih/-nih osebnih podatkov, v skladu z odlocbami ZVOP-1.

Ce posameznik svojih podatkov, ki so v pristopni izjavi opredeljeni kot obvezni, ne zeli posredovati upravljavcu, ne more postati clan Fidikluba.

Posameznik lahko kadarkoli in brez navedbe razlogov preklice svoje privoljenje za obdelavo osebnih podatkov za namene statisticne obdelave, trzenjskih raziskav, itd. V tem primeru izgubi vse ugodnosti, ki mu pripadajo kot clanu Fidikluba.

Za vse spore, ki izhajajo iz clanstva Fidikluba in zgoraj napisanih splosnih pogojev in pravil, ki jih Pharmaswiss d. o.o. in clan Fidikluba ne bi mogla sporazumno resiti, je pristojno sodisce v Ljubljani.

Piromed, Piromed

Tag Archives: Piromed

Piroxicam (Feldene)

Piroxicam is a non-steroidal anti-inflammatory drug of the oxicam class used to relieve the symptoms of rheumatoid and osteoarthritis, primary dysmenorrhoea, postoperative pain; and act as an analgesic, especially where there is an inflammatory component. Piroxicam is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Feldene, of the chemical name Piroxicam, is utilised for treating the following:

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Piroxicam comes as a capsule to take by mouth. It is usually taken once or twice a day. Take piroxicam at around the same time(s) every day.

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Buy Clotrimin Clotrimazole Online Without Prescriptions, Clotrimanova

Mycelex-G (Clotrimazole) is an antifungal medication. It prevents fungus from growing.

Clotrimazole vaginal is used to treat vaginal candida (yeast) infections.

Clotrimazole vaginal may also be used for purposes other than those listed in this medication guide.

Use Mycelex-G exactly as directed by your doctor, or follow the directions that accompany the package. If you do not understand these instructions, ask your pharmacist, nurse, or doctor to explain them to you.

Wash your hands before and after using this medication.

Insert the tablet, suppository, or cream into the vagina using the applicator as directed.

Use this medication continuously for the prescribed amount of time, even during your menstrual period.

You can use a sanitary napkin to prevent the medication from staining your clothing but do not use a tampon.

If the infection does not clear up after you have finished one course of therapy, or if it appears to get worse, see your doctor. You may have another type of infection.

Avoid getting this medication in your eyes, nose, or mouth. Store clotrimazole vaginal at room temperature away from moisture and heat.

Active ingredient: Clotrimazole

Clotrimazole is an antifungal medication. It prevents fungus from growing.

Clotrimazole vaginal is used to treat vaginal candida (yeast) infections.

It also may be used for purposes other than those listed in this medication guide.

Do not use clotrimazole vaginal if you have ever had an allergic reaction to it.

If this is the first time that you have ever had symptoms of a vaginal yeast infection, consult your doctor before using this medication.

Do not use clotrimazole vaginal if you have a fever, abdominal pain, foul-smelling discharge, diabetes, HIV, or AIDS. Consult your doctor. Do not use this medication without first talking to your doctor if you are pregnant. Do not use clotrimazole vaginal without first talking to your doctor if you are breast-feeding a baby. Do not use this medication if you are younger than 12 years of age.

Important safety information

Use this medication for the full amount of time prescribed by your doctor or recommended in the package even if you begin to feel better. Your symptoms may improve before the infection is completely healed.

Avoid wearing tight-fitting, synthetic clothing (e. g. panty hose) that does not allow air circulation. Wear loose-fitting clothing made of cotton and other natural fibers until the infection is healed. Avoid getting this medication in your eyes, nose, or mouth.

Stop using clotrimazole vaginal and seek emergency medical attention if you experience an allergic reaction (shortness of breath; closing of your throat; swelling of your lips, face, or tongue; or hives).

Other, less serious side effects may be more likely to occur. These include burning, itching, irritation of the skin, and an increased need to urinate.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Avoid using other vaginal creams or douches at the same time as clotrimazole unless your doctor approves.

Drugs other than those listed here may also interact with clotrimazole vaginal. Talk to your doctor and pharmacist before taking any prescription or over the counter medicines.

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Diflucan $0.78 for pill Diflucan is used for treating and preventing certain yeast and fungal infections. More info Grifulvin V $0.38 for pill Grifulvin V is used for treating fungal infections of the scalp, body, foot (athlete's foot), nails, thigh (jock itch), or hair follicles (barber's itch). More info

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