Xumadol

Xumadol 1 g 20 sobres

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1. What is Xumadol - Xumadol belongs to the group of drugs called analgesics (medications to treat pain and antipyretics (medicines to treat fever) anilines. - This medicine is used for the relief of moderate pain and fever.

2. Before you start taking Xumadol Check with your doctor before taking Xumadol if: - If you are allergic (hypersensitive) to paracetamol or any of the other ingredients of this medicine (listed in section 6). - If you have liver disease.

Warnings and Precautions Consult your doctor or pharmacist before you start taking this medicine. - If you have kidney disease, the interval between two doses must be at least 8 hours. - If you have heart disease or lung disease or anemia (low hemoglobin in the blood, or because of a decrease in red blood cells, you should consult your doctor before taking this medicine. - In chronic alcoholics should be careful not to take more than 2 g / day of paracetamol. - Caution is advised in patients sensitive to aspirin (aspirin) asthma. - Do not exceed the recommended dose in paragraph 3. How to take Xumadol. If the pain persists for more than 5 days, fever more than 3 days or pain or fever worsen or other symptoms, consult a doctor and re-evaluate the clinical situation.

Children and adolescents: In children and adolescents under 15 consult your doctor or pharmacist as there are other presentations at doses that cater to this group of patients.

Interference with laboratory tests: If you are going to perform analytical testing (including blood, urine, etc. ) inform the doctor that you are taking this medicine because it can alter the results of those tests.

Xumadol use with other medicines Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Paracetamol can interact with the following medications: - Antibiotics (chloramphenicol) - Oral anticoagulants (used for the treatment of thromboembolic diseases). - Antiepileptics (used for the treatment of epileptic seizures). - Contraceptives. - Diuretics (used to increase urine output). - Isoniazid (used for the treatment of tuberculosis). - Lamotrigine (used for the treatment of epilepsy). - Probenecid (used to treat gout). - Propranolol (used for the treatment of hypertension, cardiac arrhythmias). - Rifampicin (used for the treatment of tuberculosis). - Anticholinergics (used to relieve spasms or contractions of the stomach, intestines and bladder). - Zidovudine (used for the treatment of HIV infections). - Colestiramida (used to lower blood cholesterol levels). Do not use with other analgesics (medications that reduce pain) without consulting a doctor.

Taking Xumadol with food, drink and alcohol The use of paracetamol in patients who consume alcohol regularly (three or more alcoholic drinks a day) can cause liver damage.

Pregnancy and lactation If you are pregnant or breast feeding, or think you might be pregnant or planning to become pregnant, ask your doctor or pharmacist before using this medicine. Acetaminophen passes into breast milk so women breastfeeding should consult their doctor or pharmacist before using this medicine.

Driving and using machines The influence of paracetamol on the ability to drive and use machines or negligible.

Xumadol contains aspartame. This medicine may be harmful for people with phenylketonuria because it contains aspartame, a source of phenylalanine. Xumadol contains sodium. Patients with sodium diet should be aware that this medicine contains 91.34 mg (3.97 mmol) of sodium per sachet.

3. How to take Xumadol Follow the instructions exactly this medicine provided by your doctor or pharmacist. If in doubt, refer back to your doctor or pharmacist. This drug is given orally, by dissolving the contents of the envelope in a glass of water. Do not take until effervescence ceases completely. The recommended dose is: - Adults and adolescents over 15 years: 1 about every 4-6 hours, not to exceed 4 grams (4 sachets) of paracetamol in 24 hours. - Elderly patients should consult their doctor as it may recommend a dose reduction. - In case of severe kidney failure, the interval between two doses should be at least 8 hours. Always take the lowest possible dose required for symptom relief. Taking this medicine is subject to the occurrence of painful symptoms or fever. As this medication may disappear should be discontinued. If symptoms worsen or do not improve after 5 days, you should consult with your doctor.

If you take more than you should Xumadol You should immediately consult your doctor or your pharmacist. In case of overdose or accidental ingestion, immediately seek medical center or call the Information Service Toxicological +34 91 562 04 20, indicating the medicine and the amount taken. If swallowed an overdose, you should quickly go immediately to a medical center even if no symptoms because they often do not appear until after 3 days from the ingestion of overdose, even in cases of severe poisoning. Symptoms of overdose may include: dizziness, vomiting, loss of appetite, yellowing of the skin and eyes (jaundice) and abdominal pain. Treatment of overdose is most effective if started within 4 hours after ingestion of the drug. Patients treated with barbiturates or chronic alcoholics, may be more susceptible toxicity of acetaminophen overdose.

If you forget to take Xumadol Do not take a double dose to make up for missed doses.

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Co Norfloxacin, Co Norfloxacin

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CO Norfloxacin

CO NORFLOXACIN 400 MG Tablet

How does this medication work? What will it do for me?

Norfloxacin is an antibiotic that belongs to the class of medications called quinolones . It is used to treat infections caused by certain types of bacteria. It is most commonly used to treat urinary tract (bladder) infections. Norfloxacin works by killing some types of bacteria that can cause these infections.

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

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

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

How should I use this medication?

The usual recommended adult dose is 400 mg twice daily, taken with a glass of water at least one hour before or 2 hours after a meal or milk. You should drink plenty of liquids (water or juice) every day unless your doctor has told you otherwise. Norfloxacin should not be taken within 2 hours of taking iron, zinc supplements, or multivitamins containing them. The dose of norfloxacin can vary depending on the circumstances and the condition being treated.

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

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

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

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

What form(s) does this medication come in?

Each white, coated, oval, convex tablet, embossed with “N” breakline “O” on one side and a symbol on the other side, contains norfloxacin 400 mg. Nonmedicinal ingredients: croscarmellose sodium, magnesium stearate, and microcrystalline cellulose; film coating: polyvinyl alcohol, soya lecithin, talc, titanium dioxide, and xanthan gum.

Who should NOT take this medication?

Do not take norfloxacin if you are allergic to norfloxacin, other quinolones (e. g. ciprofloxacin, nalidixic acid), or any other ingredients of the medication.

What side effects are possible with this medication?

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

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

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

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

diarrhea (mild)

dizziness or lightheadedness

headache

heartburn

increased skin sensitivity to the sun

loss of appetite

nausea

trouble sleeping

vomiting

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

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

blistering of skin

increasing muscle weakness

joint or muscle pain

mood changes such as anxiety or depression

pain, swelling, or rupture of a tendon

sensation of skin burning

skin itching, rash, redness, or swelling

symptoms of high blood sugar (e. g. frequent urination, increased thirst, excessive eating, unexplained weight loss, poor wound healing, infections, fruity breath odour)

symptoms of low blood sugar (e. g. cold sweat, cool pale skin, headache, fast heart beat, weakness)

vision changes

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

diarrhea (watery and severe or bloody)

seizures

signs of a serious allergic reaction (swelling of face or throat, hives, or difficulty breathing)

signs of a severe skin reaction (e. g. blistering, peeling, a rash covering a large area of the body, a rash that spreads quickly, or a rash combined with fever or discomfort)

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

Are there any other precautions or warnings for this medication?

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

Blood sugar levels: Norfloxacin may cause a loss of control of blood sugar levels and glucose tolerance may change. People with diabetes may find it necessary to monitor their blood sugar more frequently while using this medication. People without diabetes have also been known to experience high or low blood sugars while taking norfloxacin.

If you have diabetes or are at risk for developing diabetes, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.

If you experience signs of high blood sugar (fruity breath odour, weight loss, increased thirst, or increased need to urinate) or low blood sugar (cold sweat, cool pale skin, headache, or weakness) contact your doctor.

Diarrhea: People taking this medication may develop diarrhea caused by an infection with the bacteria C. difficile. If you have loose, watery and bloody bowel movements, with or without fever or stomach cramps, after taking norfloxacin, get medical attention as soon as possible. Diarrhea caused by C. difficile infection can lead to serious health problems if it is not properly treated.

Kidney: Norfloxacin is passed from the body mostly by the kidney. If you have reduced kidney function, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.

Neuromuscular disorders: Norfloxacin may cause increased muscle weakness for people with myasthenia gravis (an autoimmune disorder that causes muscle weakness). If you have myasthenia gravis, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.

Seizures: Rarely, seizures have been reported with this medication. If you have a history of epilepsy or medical conditions that increase the risk of seizures, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed. If you have a seizure while taking this medication, stop taking it and get immediate medical attention.

Sunburn: People who take norfloxacin are more likely to suffer from sunburn. Avoid exposure to excessive sunlight, including sunlamps and tanning beds, and use sunblock with minimum SPF 15. Stop taking the medication if sun sensitivity occurs.

Tendons: Rarely, people taking norfloxacin have experienced tendonitis and/or tendon rupture, especially if they were also taking corticosteroids. If you experience any joint or tendon pain or swelling, contact your doctor as soon as possible.

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

Breast-feeding: Norfloxacin may pass into breast milk. If you are a breast-feeding mother and are taking this medication, it may affect your baby. Talk to your doctor about whether you should continue breast-feeding.

Children: The safety and effectiveness of using this medication have not been established for children under 16 years of age.

What other drugs could interact with this medication?

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

aminophylline

amiodarone

antacids containing aluminum, calcium or magnesium (do not take within 2 hours of norfloxacin)

antipsychotics (e. g. chlorpromazine, clozapine, haloperidol, olanzapine, quetiapine, risperidone)

BCG

caffeine

calcium supplements and multivitamins containing calcium (do not take within 2 hours of norfloxacin)

chloroquine

colchicine

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

cyclosporine

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

didanosine (do not take within 2 hours of norfloxacin)

disopyramide

dofetilide

domperidone

dronedarone

eplerenone

fentanyl

iron supplements, such as ferrous sulfate, or multivitamins containing iron (do not take within 2 hours of norfloxacin)

lopinavir

macrolide antibiotics (e. g. clarithromycin, erythromycin)

methadone

mifepristone

multivitamins with minerals

mycophenolate

nilotinib

nitrofurantoin

nonsteroidal anti-inflammatory medications (e. g. diclofenac, ibuprofen, ketoprofen, naproxen)

pazopanib

porfimer

primaquine

probenecid

procainamide

quinapril

quinidine

quinine

saquinavir

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

serotonin antagonists (anti-emetic medications; e. g. granisetron, ondansetron)

sevelamer

sodium picosulfate

sotalol

sucralfate (do not take within 2 hours of norfloxacin)

tetrabenazine

theophylline

tizanidine

typhoid vaccine

varenicline

warfarin

zinc supplements or multivitamins containing zinc (do not take within 2 hours of norfloxacin)

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

stop taking one of the medications,

change one of the medications to another,

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

leave everything as is.

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

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

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

Virden, Il Real Estate - Homes For Sale Near You, Virfen

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Find Virden, IL homes for sale and other Virden real estate on realtor. com®. Search Virden houses, condos, townhomes and single-family homes by price and location. Our extensive database of real estate listings provide the most comprehensive property details like home values, features and local school and neighborhood info so you can be sure that you have nearly all the facts you need upfront. Search realtor. com® today! Want a closer look at what other Virden properties are available? Also search our listings for Virden Open Houses. Newest Virden Listings and Virden Homes with Price Reductions now.

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Eanox, Eanox

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I'd like to take a minute to offer the very highest praise for Engine & Transmission World. I initially ordered a motor, finding that they had the best value/lowest mileage engines available from all the quotes (and there were many quotes I received, at least 15, ranging from $1500 for a motor with well over 100,000 miles on it, to $400 with 80,000 miles). I finally decided to go with the offer from ETW, which was $500 for a 51,000 mile motor. The motor was here in 7 days, well within the range promised. Unfortunately, the motor had an oil pressure problem, and after a quick email to them, everything was settled. Despite the fact that under the terms of the warranty, I could have been out significant shipping costs for a replacement, they took care of me. As I recall, the salesperson's exact words were: "We are going to do whatever it takes to make this right". The replacement motor arrived 3 days later, was installed, and performs as if it were factory new. I can't offer any higher recommendation or praise for this company. If you are in the market for parts, have no fear that you will receive what you need, very quickly, and if there turns out to be a problem (which, let's face it. things happen), this company will go above and beyond to make things right. I intend to call Engine & Transmission World first in the future for any part requirements I may have.

My new engine is flawless! It drives like a new car. Dealing with E T W. was effortless. My sales rep was kind and helpful. The delivery was on time. I recommended you to my mechanic, he was impressed as well. The cost was better than all of the estimates I researched. ETW has a good thing going. Thank you so much.

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

Ortoton

Ortoton review

Ortoton is a brand name for methocarbamol. and is a muscle relaxant. It is used to relax certain muscles in the body, relieving stiffness, discomfort, and pain and to treat spasms. Ortoton is not to be used in the place or other treatments, such as rest, exercise, physical therapy, or any other course of treatment that your doctor recommends. It acts on the central nervous system. which in turn signals to the muscles the desired effect. It is administered in tablets.

Ortoton can cause several side effects, including fainting, runny or stuffy nose. fast or slow heartbeat, burning eyes, fever. skin rash with itching or redness, swelling on face, eyelids. mouth. lips. or tongue. shortness of breath or other breathing difficulties, tightness in chest or wheezing. You might also experience the rare side effects of blood in your urine, jaundiced eyes or skin, blood or black stools, vomiting of blood or of material that looks like coffee grounds, cough. unusual bruising or bleeding, hoarseness, unusual tiredness or weakness, lower back or side pain, swollen or painful glands, sore throat, fever, irregular breathing, pain, tenderness or swelling over a vein, red spots on the skin, puffiness or swelling around the eyes, sores, ulcers or white spots on the lips, or painful or difficult urination. Other rare side effects can include stomach cramps, unsteadiness, confusion. constipation. trouble sleeping, trembling, diarrhea. seizures, memory problems, excitement or nervousness, nausea or vomiting, flushing, heartburn. headache. hiccups. or muscle weakness. In addition to the above rare effects, Ortoton might turn your urine orange, purple, black, brown or green. This is a harmless effect that should soon fade. More common side effects include blurred or double vision, or any change in vision, drowsiness, or dizziness.

Because of the common side effects of drowsiness and dizziness, you should be careful to ascertain whether Ortoton does indeed cause these effects when you are taking it. If it does, you should avoid driving, operating machinery, or any other exercise that requires mental or physical alertness. In addition, because Ortoton depresses the central nervous system, you should also be very careful about using alcohol or other substances that depress the central nervous system. You should also let your doctor know if you are taking Mestinon. Aricept, Reminyl. Exelon. or Cognex, as these medications can react badly with Ortoton and may need to be adjusted. You should also not start a new medication, either prescription or over-the-counter, without consulting your doctor.

Orton is in Pregnancy Category C, which means it is not known whether it will cause harm to a pregnancy or to a developing fetus, but no studies on humans have been done. Therefore, you should be very careful in taking Ortoton if you are pregnant, and make sure that the benefits outweigh any possible risks. Ortoton is known to pass into breast milk, and has been shown to cause drowsiness and upset stomach in nursing babies. Ortoton has not been tested in children under 16, and is not recommended for pediatric use.

Ortoton has the following structural formula:

• Molecular formula of ortoton is C11H15NO5 • Chemical IUPAC Name is [2-hydroxy-3-(2-methoxyphenoxy)-propyl] aminoformate • Molecular weight is 241.241 g/mol • Ortoton available. 750mg tablets

Generic name: Methocarbamol

Brand name(s): Avetil, Delaxin, Etroflex, Forbaxin, Glycerylguaiacolate carbamate, Guaiphenesin carbamate, Guaiphenesine carbamate, Lumirelax, Methocal, Metocarbamol, Metocarbamolo, Metofenia, Metofenina, Miolaxene, Miorilas, Miowas, Myolaxene, Neuraxin, Parabaxin, Perilax, Reflexyn, Relax, Relestrid, Robamol, Robaxan, Robaxin. Robaxine, Robaxon, Robinax, Romethocarb, Surquetil, Traumacut, Tresortil

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Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Stop Blushing - With Medicines - The Blushers Manual, Lopranol

Stop blushing - With medicines

Recommended medicines Here is a list of medicines that are used for treating facial blushing and social phobia. Always consult your doctor before using any medicine. The medical cures for facial blushing/social phobia can be divided into three categories.

1.) Anxiolytic - (Benzodiazepines.) A drug used in the treatment of anxiety and muscle spasms. Should not be used by people with a drinking problem. May help persons with social phobia to talk in front of a group of people. Benzodiazepines slow down the nervous system. They should not be taken to overcome the stress of everyday life. They may be habit-forming, causing mental or physical dependence. Valium, Xanax, Lorazepam and other benzodiazapine medications can be very effective for controlling the anxiety that results in facial blushing.

2.) Adrenergic Beta Blocker - Beta-Adrenergic Blockers or “Beta Blockers” are a family of drugs used to treat high blood pressure, angina, heart arrhythmia, tremors, alcohol withdrawal, glaucoma, and other conditions. They are also used to prevent migraine headaches, stage fright, and second heart attacks. Beta blockers help the heart rate from racing and can reduce anxiety associated with public speaking.

3.) Antidepressant medicine - This category work for people with social phobia and depression. The time of treatment should be long and the initial dose should be low. Moklobemid treatment (marketed under the names Moklobemid and Aurorix are helpful to help the patient to brake his/hers social isolation. SSRI's (selective serotonin reuptake inhibitors) such as Paxil, Zoloft and Prozac can be helpful to reduce anxiety that causes the flushing.

The first name after the number (in the list below) is the generic name. Names with the ® symbol are the trade name of the drugs.

1.) Anxiolytic (Benzodiazepines.) Most medicines in this category are highly addictive, don't use daily. Alprazolam (Xanax®) Bromazepam (Lexotan®) Chlordiazepoxide (Librium®) Clonazepam (Klonopin®) Clorazepate (Tranxene®) Diazepam (Valium®, Xanax®) Estazolam (ProSom®) Flunitrazepam (RoHypnol®)

2.) Adrenergic Beta Blocker Acebutalol (Sectral®) Atenolol (Atenolol®,Tenormin®) Bisoprolol (Emcor®, Monocor®) Carvedilol (Carvedilol®,Eucardic®) Celiprolol (Celectol®) Clonidine (Catapresan®) Metoprolol (Betaloc®, Lopresor®) Oxprenolol (Slow-Trasicor®, Trasicor®) Propranolol (Adrexan®, Angilol®, Apo-Propranolol®, Avlocardyl®, Bedranol®, Betachron ER®, Betadur®, Cardinal®, Detensol®, Hemipralon®, Inderal®, Lopranol®, Novopranol®, Propranololum®, Syprol®) Sotalol (Beta-Cardone®, Sotacor®) ZOK (metoprolol CR/XL) (Seloken®

3.) Antidepressant Medicine Moklobemid (Aurorix®) Paroxetin (Seroxat®, Paxil®) Escitalopram (Cipralx®) Venlafaxine (Effexor®) Sertraline (Zoloft®) Clomipramine (Ofepramin®) Moclobemide (Aurorix®) Clomipramine (Anafranil®) Fluvoxamine (Luvox®) Fluoxetine (Prozac®) Citalopram (Celexa®)

Recommendations I asked two doctors for a general recommendations and I was suggested to take Paxil 20 mg/day Zoloft 50 mg/day, and by the other doctor only Paxil. I was also told that Paxil should be taken at least for some months maybe 6-12 months depending on the symptoms. Some people take 50 mg of Atenolol, and 5 mg of Xanax before a performance situation. (Warning don’t take Xanax or any other benzodiazepines regularly because it’s highly addictive.) Remember that medicines are very individual, for one person Paxil may work, but for some other person Efexor makes a better job and so on.

A study of Atenolol and Nardil (Phenelzine) in social phobia A patient should be told that the role of medication is to alleviate their social or performance anxiety in social situations. Increasing exposure to such situations is therefore crucial to overcoming their condition. Seventy-four patients meeting DSM-III criteria for social phobia completed 4 or more weeks of double-blind, randomized treatment with the monoamine oxidase inhibitor phenelzine, the cardioselective beta-adrenergic blocker Atenolol, or placebo.

Sixty-four percent of the patients on phenelzine demonstrated moderate or marked improvement, compared to 30 percent on Atenolol and 23 percent on placebo. Phenelzine was significantly more effective than Atenolol or placebo, whereas the efficacy of Atenolol and placebo did not differ significantly. Patients were also prospectively divided into generalized and discrete subtypes of social phobia. Phenelzine appeared to be a particularly effective treatment for the generalized form of social phobia. Atenolol may be useful for discrete forms of social phobia such as performance anxiety.

Naproxen - Side Effects, Dosage, Interactions, Naprozen

Naproxen

Naproxen sodium is the generic ingredient in Aleve and several other brands of pain medication.

Naproxen is in a class of drugs called non-steroidal anti-inflammatory drugs (NSAIDs), which work by blocking the production of prostaglandins, substances in the body that play a role in pain and inflammation.

Naproxen has been used in the United States since 1980. It is available generically and under many brand names.

After 14 years as a prescription-only medication, in 1994 naproxen was approved by the Food & Drug Administration (FDA) as an over-the-counter (OTC) drug.

The best-known brand name for OTC naproxen is Aleve, which is made by the Bayer Healthcare.

Other brand names for naproxen include Anaprox DS, Naprelan, Anaprox, EC-Naprosyn, and Naprosyn.

As a prescription-strength drug, naproxen comes in the form of tablets or as a liquid.

Tablets may be coated to protect your stomach, or they may be extended-release tablets that you need to take only once a day.

Prescription-strength naproxen is often used to treat joint pain, menstrual pain, rheumatoid arthritis. gout, ankylosing spondylitis. juvenile arthritis, tendonitis, and bursitis.

Nonprescription naproxen is commonly used to relieve pain, swelling, fever, cold and flu symptoms, and headaches.

Naproxen Warnings

Naproxen may raise your risk for heart attacks and stroke .

Heart and stroke risk is greater if you have a history of or risk factors for heart disease.

Naproxen may cause ulcers and bleeding in your gastrointestinal (GI) tract. Ulcer and bleeding risk is higher if you are elderly.

Because elderly people are more likely to have side effects, you should take the lowest possible effective dose if you are over age 65.

This drug is not recommended for children younger than 2 years.

Always tell your doctor if you are taking naproxen before having any surgical procedure, including dental surgery.

Before you take naproxen, it is important to tell your doctor or pharmacist about any allergies to NSAIDs.

In addition to stroke, heart disease, and gastrointestinal bleeding, other conditions also carry warnings related to naproxen use, so tell your doctor or pharmacist if you have any of these conditions:

High blood pressure

Fluid retention

Kidney disease

Liver disease

Anemia

Asthma

Nasal congestion or nasal polyps

Stomach ulcer

Inflammatory bowel disease (IBD)

Naproxen and Pregnancy

Naproxen may cause harm to a developing fetus, and should not be used in the later stages of pregnancy.

There's some evidence that naproxen can cause problems for developing babies and increase the risk for maternal bleeding during delivery.

Naproxen and Breastfeeding

Studies of naproxen use by women who are breastfeeding are inconsistent.

Some evidence suggests that naproxen is safe for a breastfeeding mother to use in moderate doses if her infant is at least one month old.

However, the American Academy of Family Physicians warns that naproxen can accumulate in an infant if a breastfeeding mother uses the drug for an extended period of time.

Ask your doctor if it's safe to use naproxen while breastfeeding. There may be safer alternatives for you and your nursing baby.

Q: When my husband had outpatient surgery on his back (lumbar discectomy), we were told that he should not take naproxen (500 mg) because it hinders the healing process. Yet my foot doctor gave me a prescription for naproxen (500 mg) to ease the swelling I experienced after foot surgery. So we are confused. Does Naproxen hinder the healing process? In both of our surgeries, we had bones that needed to heal.

A: Non-steroidal anti-inflammatory drugs like naproxen are powerful and effective drugs. They are routinely used in orthopedic conditions and in the perioperative setting. They are however associated with potentially serious side effects, and it is important to evaluate the risk versus benefit prior to medication use. There is evidence suggesting that these drugs adversely affect bone formation, and this has implications for their use in patients with fractures and other pathologies that involve bone remodelling. Similarly, other data suggest that nonsteroidal anti-inflammatory drugs significantly inhibit spinal fusion at doses typically used for postoperative pain control.

Q: Can Naproxen 500 mg or high blood pressure medications cause weight gain?

A: Naproxen does not appear to cause weight gain in patients taking the medication. High blood pressure medications do not generally cause weight gain, but if you are experiencing a sudden weight change you should consult your physician to rule out fluid retention.

Q: Can Naproxen 500 mg or high blood pressure medications cause weight gain?

A: Naproxen does not appear to cause weight gain in patients taking the medication. High blood pressure medications do not generally cause weight gain, but if you are experiencing a sudden weight change you should consult your physician to rule out fluid retention.

Q: I've been taking naproxen 500 mg twice a day for a year now for arthritis and bursitis pain. What are the long-term effects? Is it safe to continue?

A: According to the medication guide for naproxen, you should not stop taking this medication with out first consulting your health care provider. Naproxen is in a group of drugs called non-steroidal anti-inflammatory drugs (NSAIDs). NSAID medicines may increase the chance of a heart attack or stroke that can lead to death. This chance increases with longer use of NSAID medicines in people who have heart disease. NSAID medicines can cause ulcers and bleeding in the stomach and intestines at any time during treatment. Ulcers and bleeding can happen without warning symptoms and may cause death. NSAID medicines should only be used exactly as prescribed at the lowest dose possible for your treatment for the shortest time needed. Do not take an NSAID medicine if you had an asthma attack, hives, or other allergic reaction with aspirin or any other NSAID medicine for pain right before or after heart bypass surgery. Tell your health care provider about all of your medical conditions and all of the medicines you take. NSAIDs and some other medicines can interact with each other and cause serious side effects. These are not all the side effects with NSAID medicines. Talk to your health care provider for more information about NSAID medicines.

Q: What is the effect of naproxen sodium on the kidneys?

A: Depending on the individual, naproxen can have a effect on kidneys. As long as you have good kidney function and no liver disease, you can use naproxen. Your health care provider should monitor your kidney functions as long as you are on this medication. The following are kidney conditions are listed in the literature: glomerular nephritis, hematuria, interstitial nephritis, nephrotic syndrome, nephropathy and tubular necrosis. Be sure to discuss your concerns with your health care provider. I have included a site with more information for you. http://www. everydayhealth. com/drugs/naproxen Gerald R. Levy, RPh

Q: I'm a type 2 diabetic and have started spilling phosphorus into my urine, A1C 6.4. Could naproxen be the culprit?

A: According to the FDA, the use of drugs like naproxen (Brand: Aleve), which are called NSAIDs, have been reported to cause kidney damage especially with long-term use and at high doses. Patients with impaired kidney function (which diabetes can cause over time) should avoid NSAIDs all together if possible. If while taking an NSAID, you develop sudden weight gain or fluid retention (for example, you notice swelling in your legs), notify your doctor right away. NSAIDs such as naproxen can also cause a change in blood sugar and decrease the effectiveness of oral diabetes medications. Check with your doctor before using NSAIDs, if you have diabetes. You may still be able to use them, but you may need to follow your blood sugars closely and, with the help of your doctor, adjust your diabetes medications appropriately. The elderly are at increased risk for side effects such as kidney damage and peptic ulcers from NSAIDs even at low doses. Consult with your doctor for an evaluation of your kidney function, to discuss your concerns about phosphorous in you urine, and for an appropriate course of action regarding the use of Naproxen. http://www. everydayhealth. com/drugs/naproxen http://www. everydayhealth. com/diabetes/type2/understanding. aspx

Q: If I take 500 mg of naproxen twice a day for 5 days as prescribed, can I get a hole in my stomach? Or is that only a long-term side effect? Can it happen in a few days?

A: Studies suggest that this is usually a long-term effect over the course of many months. But if a patient has existing stomach problems or if on multiple medications such as aspirin, other NSAIDs (Motrin, Advil, Aleve, etc.) stomach problems can be severe. Sometimes if physicians suspect stomach problems, they prescribe other medications to protect against it. Please consult with your physician prior to starting any new medications. Beena Thomas, PharmD

Q: I used to take Darvocet because I have sciatica pain and the doctor took me off of it and put me on Naproxen 500 mg twice daily. Now I am having shortness of breath and so tired I can hardly walk. I have been on this for one month. Could this medicine be causing me shortness of breath and the feeling of passing out?

A: Naproxen is a non-steroidal anti-inflammatory drug (or NSAID) that is used to treat pain and inflammation. The most common side effects of naproxen are heartburn, abdominal pain, nausea, constipation, headache, dizziness, drowsiness, itching, skin rashes, ringing of the ears, swelling, and shortness of breath. Naproxen, like other NSAIDs, may cause serious cardiovascular side effects, such as heart attack or stroke. Although serious cardiovascular events can occur without warning symptoms, patients should be aware of the signs and symptoms of chest pain, shortness of breath, weakness, slurring of speech, and should contact their health care provider if any of these occur. Michelle McDermott, PharmD

Q: What health effects does naproxen have on the kidneys?

A: As long as you have good kidney function and no liver disease, you can use naproxen. Your doctor should monitor your kidney function as long as you are on naproxen, however. The literature cites effects such as glomerular nephritis, hematuria, interstitial nephritis, nephrotic syndrome, nephropathy, and tubular necrosis. Since your doctor knows your medical condition, discuss any concerns you have about naproxen with him or her. For more information about naproxen, go to http://www. everydayhealth. com/drugs/naproxen. Gerald S. Levy, RPh

Q: I have rheumatoid arthritis and have been on Naproxen 500 mg once a day as a part of my treatment along with Enbrel 50 mg injection once a week and methotrexate 20 mg once a week. I've been stable on this protocol for the last four years. Recently, I've been having an increase in swelling of the feet/ankles that does not seem to resolve with decreasing salt intake or remaining in a cooler environment. I get a regular CBC and liver panel every three months and all is normal. Could the Naproxen be causing the swelling?

A: Naproxen is a medication used to treat pain and inflammation and is part of a class called nonsteroidal anti-inflammatory drugs (NSAIDs). It works by blocking a hormone, called prostaglandin, that contributes to inflammation in the body. According to the prescribing information on Naproxen the most common side effects of this medication are: heartburn, nausea, constipation, headache, ringing in the ears, and fluid retention. These effects were seen in up to 3 percent of patients taking the medication during clinical trials. For more information on naproxen, visit http://www. everydayhealth. com/drugs/naproxen. If you feel you are experiencing fluid retention due to this medication, it would be best to consult with your physician to be sure that no other underlying condition is contributing to the problem. He or she will help you come up with a plan to deal with this issue. For more information on rheumatoid arthritis, visit http://www. everydayhealth. com/arthritis/rheumatoid-arthritis/index. aspx. For more specific information, consult with your doctor or pharmacist for guidance based on your health status and current medications, particularly before taking any action. Lori Poulin, PharmD

Q: What is the difference between naproxen and Aleve? Is it true that you can't take both together?

A: Aleve is a brand name of naproxen, so they are the same. Naproxen is in a class of drugs called non-steroidal anti-inflammatory drugs (NSAIDs). NSAIDs work by reducing hormones that cause inflammation and pain in the body. Naproxen is used to treat pain or inflammation caused by conditions such as arthritis, ankylosing spondylitis, tendonitis, bursitis, gout, or menstrual cramps. Common side effects of naproxen include upset stomach, mild heartburn, stomach pain, diarrhea, constipation, bloating, gas, dizziness, headache, nervousness, blurred vision, and ringing in the ears. This is not a complete list of side effects that can occur with naproxen. Using NSAIDs can increase the risk of serious side effects, such as heart attack, stroke, and bleeding from the digestive tract. The risk of heart attack and stroke increase with long-term use of NSAIDS. Seek emergency medical attention if you experience chest pain, weakness, shortness of breath, slurred speech, or problems with vision or balance. Bleeding from the digestive tract can happen at any time during treatment with an NSAID. Contact your doctor right away if you have any symptoms of bleeding from the digestive tract, such as black, bloody, or tarry stools, or coughing up blood or vomit that looks like coffee grounds. Always read and follow the complete directions and warnings on over-the-counter medicines and discuss their use with your health care provider before taking them. For more specific information, consult with your doctor or local pharmacist for guidance based on your health status and current medications. Sarah Lewis, PharmD

Q: Can naproxen be used for inflammation of the tooth?

A: Naprosyn (naproxen) is anti-inflammatory medication commonly used to treat mild to moderate pain, osteoarthritis, rheumatoid arthritis, headaches, and fever. Naprosyn (naproxen) could be used to relieve dental pain caused by inflammation and swelling. Common side effects of Naprosyn (naproxen) are constipation, diarrhea, abdominal pain, nausea, vomiting, heartburn, headache, dizziness, and drowsiness. This is not a complete list of possible side effects for Naprosyn (naproxen). Naprosyn (naproxen) should be taken with milk or food as prescribed by your physician. Naprosyn (naproxen) should not be taken with any other blood thinners (e. g. Coumadin) or other anti-inflammatory medication (e. g. Advil, Motrin, ibuprofen, or Aleve) unless directed by a physician. When your doctor prescribes a new medication, be sure to discuss all your prescription and over-the-counter drugs, including dietary supplements, vitamins, botanicals, minerals, and herbals, as well as the foods you eat. Always keep a current list of the drugs and supplements you take and review it with your health care providers and your pharmacist. If possible, use one pharmacy for all your prescription medications and over-the-counter products. This allows your pharmacist to keep a complete record of all your prescription drugs and to advise you about drug interactions and side effects. For more specific information, consult with your doctor or pharmacist for guidance based on your health status and current medications, particularly before taking any action. Jennifer Carey, PharmD

Q: I've recently started suffering from osteoarthritis and have discovered that taking naproxen every day seems to keep the pain in check. What are the short - and long-term risks involved in taking naproxen every day?

A: Naproxen is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). It works by reducing hormones that cause inflammation and pain in the body and is used to treat conditions such as arthritis. Common side effects of naproxen include dizziness, drowsiness, stomach upset, mild heartburn, and rash. All NSAIDS can increase the risk of life-threatening heart or circulation problems, including heart attack or stroke. This risk will increase the longer you use naproxen. Don't use this medicine just before or after having heart bypass surgery. Seek emergency medical help if you have symptoms of heart or circulation problems, such as chest pain, weakness, shortness of breath, slurred speech, or problems with vision or balance. NSAIDS can also increase the risk of serious effects on the stomach or intestines, including bleeding or perforation. These conditions can be fatal, and gastrointestinal effects can occur without warning at any time while you are taking naproxen. Older adults may have greater risk of these serious gastrointestinal side effects. Call your doctor at once if you have symptoms of bleeding in your stomach or intestines. This includes black, bloody, or tarry stools, or coughing up blood or vomit that looks like coffee grounds. Consult your health care provider for any specific concerns you have about using naproxen. For more information about this medication, go to http://www. everydayhealth. com/drugs/naproxen. Sarah Lewis, PharmD

Q: Does Naprelan have a generic equivalent?

A: Your question regards if Naprelan (naproxen) http://www. everydayhealth. com/drugs/naprelan-500 has a generic equivalent. To the best of my knowledge, there is no generic equivalent available for Naprelan. However, the active medication in Naprelan is naproxen. The medication Naprosyn http://www. everydayhealth. com/drugs/naprosyn also has naproxen as the active ingredient and that product is available in a generic. The medications have a different release into the body. Naprelan is usually dosed once daily, and it is a controlled release tablet while Naprosyn is dosed more often. As always, talk with your health care provider about questions you have about your medications. Jen Marsico, RPh

Q: Naproxen upsets my stomach. What else can I take for pain?

A: Over-the-counter medications for pain include non-steroidal anti-inflammatory drugs (NSAIDs) and the analgesic Tylenol (acetaminophen). Ibuprofen (Motrin, Advil) is an NSAID used for pain and inflammation. Doses of 200 to 400 mg every 4 to 6 hours or 1200 mg daily can be used over the counter. Naproxen (Aleve) is another over the counter NSAID. Naproxen can be taken at doses of 200 mg every 12 hours. NSAIDs should be avoided in patients with kidney or liver disease, patients with heart disease or a history of stomach ulcer or bleeding. Aspirin can also be considered an NSAID, but it should not be used in doses high enough to treat pain without the direction of a physician due to bleeding risks. Tylenol is an analgesic used to treat mild to moderate pain and fever. The maximum daily dose of Tylenol is 4000 mg (4 grams) daily. It is important to note that some prescription pain medications or cough and cold medications also contain acetaminophen. It is important to not take more than 4 grams of acetaminophen a day from all sources. Tylenol can affect the liver, so patients who already have liver damage should avoid taking Tylenol. Patients who drink more than 3 alcoholic drinks a day should also avoid taking Tylenol due to the increased risk of liver damage. Tylenol typically does not upset the stomach the way NSAIDs, such as naproxen, can. There are also many prescription pain medications available for moderate to severe pain that cannot be treated with an over-the-counter medication. If you have chronic pain or short term pain that is not relieved by over-the-counter medications, it is best to see your doctor who may evaluate your pain and decide to prescribe a pain medication. For more specific information, consult with your doctor or pharmacist for guidance based on your health status and current medications, particularly before taking any action. Laura Cable, PharmD

Q: I've been taking naproxen for about 5 weeks. My doctor wants to give me a lower dose and have me take it one day on and two days off. His concern is that it will burn out my stomach. I have not had any adverse abdominal problems to date. The lower dose does not relieve enough of the pain to be worth it to me. Is this the best approach? Is there a test to check if there is a problem developing?

A: Naproxen (Naprosyn) is a non-steroidal anti-inflammatory drug (NSAID) that blocks substances in the body that normally cause pain and inflammation. Naproxen is indicated for pain associated with headache, cramps, and other pain. Naproxen is also used for pain and inflammation associated with arthritis and used as a fever reducer. Some of the common side effects associated with naproxen include constipation, diarrhea, headache, nausea, and stomach upset. According to the prescribing information, there are warnings associated with the use of naproxen. Long-term used of naproxen can increase the risk of serious cardiovascular events such as strokes and heart attacks. The risk of a serious adverse event can increase with the duration of treatment with naproxen. Naproxen should not be used just before or after coronary artery surgery. People with cardiovascular risk factors, those who are 60 years of age or older, have stomach ulcers or bleeding problems, take blood thinners or drink alcoholic drinks while taking naproxen are at a greater risk of a complication. Naproxen can increase the risk of serious stomach and intestine problems including bleeding or forming a hole (perforation). Talk to the doctor if signs and symptoms of bleeding occur. These symptoms include black, tarry or bloody stools or coughing up blood or vomit that looks like coffee grounds. Alcohol can increase the risk of stomach bleeding caused by naproxen. Avoid prolonged exposure to sunlight. Naproxen can worsen existing hypertension (high blood pressure), so talk to your doctor if you have hypertension. The lowest dose and shortest duration of treatment with NSAIDs for effective therapy is usually recommended. However, talk to your doctor if naproxen is not relieving the pain. Do not stop taking naproxen or take more medicine than what is prescribed. For more specific information and guidance on your current treatment based on your medical condition, consult with your healthcare provider. Kimberly Hotz, PharmD

Q: Does naproxen cause anemia?

A: Naproxen (Aleve, Naprosyn) belongs to a class of drugs called non-steroidal anti-inflammatory drugs (NSAIDs). NSAIDs work by blocking substances in the body that cause pain and inflammation. Naproxen is used to treat fever, pain, and inflammation caused by a wide variety of conditions, including arthritis, bursitis, gout, headache, ankylosing spondylitis, tendonitis, menstrual cramps, and minor injuries. Common side effects of naproxen include nausea, stomach upset, heartburn, bloating, gas, diarrhea, constipation, dizziness, drowsiness, blurred vision, and ringing in the ears. A search of a drug database shows that anemia can occur in up to 10 percent of patients taking NSAIDs, including naproxen. This would be considered a frequent or common side effect. Consult with your doctor if you are concerned about anemia or if you are experiencing symptoms of anemia, such as fatigue, pale skin, coldness, or dizziness. This is not a complete list of risks or side effects that can occur with naproxen or any other NSAID. For more specific information, consult with your doctor or local pharmacist for guidance based on your health status and current medications, particularly before taking any action. Sarah Lewis, PharmD

Q: Does naproxen affect bowel movements?

A: Naproxen (Aleve, Naprosyn) is a nonsteroidal anti-inflammatory drug (NSAID) that is used to reduce pain and inflammation in a variety of conditions, including arthritis and gout. Naproxen and other NSAIDs can be irritating to the stomach, causing inflammation, bleeding, ulceration, and perforation of the stomach, small intestine, or large intestine. To reduce the risk of gastrointestinal side effects, patients should receive the lowest effective dose of naproxen for the shortest period of time to adequately relieve symptoms. Other gastrointestinal side effects include nausea, diarrhea, constipation, and abdominal pain. If you think you are experiencing a side effect from your medication, talk to your doctor. Do not stop or change your medication unless your doctor directs you to do so. For more specific information, consult with your doctor or pharmacist for guidance based on your health status and current medications, particularly before taking any action. Michelle McDermott, PharmD

By Chris Iliades, MD | Medically Reviewed by Pat F. Bass III, MD

Diclosal - Gel, Diclosal

Medicament OTC – se vinde fara reteta

Denumirea comerciala: DICLOSAL 10mg/g Denumirea comuna internationala: DICLOFENACUM Forma farmaceutica: gel Bucati: 1 gel Doza (concentratia): 10mg/g Forma de prezentare: cutie cu 1 tub x 25 g gel Firma: SLAVIA Tara: Romania

Cod ATC: M02AA15 M – sistemul muscular-scheletic M02 – preparate topice pentru leziuni si algii musculare M02AA – antiinflamatoare nesteroidiene de uz topic

Acest pret este PRET mediu de RAFT al medicamentului DICLOSAL 10mg/g gel (pret necompensat)

PRET DICLOSAL 10mg/g gel: VEZI PRET

VEZI AICI pretul medicamentului si al inlocuitorilor

Vezi pret medicamente care contin aceeasi substanta activa:

Atentie! Informatiile privind medicamantul DICLOSAL 10mg/g gel au caracter informativ. Nu folositi informatiile prezentate in scopul diagnosticarii sau tratarii unei probleme de sanatate.

Nasair, Nasair

Hajj and Umrah Travel Information

flynas Guests holding Umrah Visas, and planning to travel to Saudi Arabia to perform Umrah, can book their tickets through flynas. com. Umrah season restarts on 1 November 2016 (1 Safar 1438)

Umrah Visa Holders are not allowed to perform Hajj

flynas guests holding Hajj Visas and planning to visit Saudi Arabia to perform Hajj are not allowed to book tickets on flynas. com and are advised to contact the nearest flynas office or certified travel agency by Saudi Hajj ministry

Hajj passenger should hold a valid passport with a valid Hajj Visa attached

Hajj visa holders will enter and depart from Hajj terminal

For pilgrims coming from the GCC countries during Hajj period, it is obligatory to get a Hajj permit to perform Hajj. Whomever performs Ihram during the flight to perform Hajj without having Hajj permit, will be returned to his/her home country according to the guidelines set by the Saudi authorities

During the Hajj period from 10 Dhu Alqedah 1437H (13 August 2016) to 10 Dhu Alhijja 1437H (11 September 2016), all flynas guests holding Visit Visa are permitted to enter Saudi Arabia via King Khalid International Airport in Riyadh or King Fahd International Airport in Dammam

flynas guests holding Visit Visa and arriving at King Abdulaziz International Airport in Jeddah or Prince Mohammad Bin Abdulaziz International Airport in Madinah during the Hajj season have to check with the embassies and consulates of Saudi Arabia in their countries to make sure that the instructions and directives issued by the official authorities in Saudi Arabia allow them to enter the country during the Hajj season

flynas will not assume liability in the event of refusal of your travel based on the instructions issued by the official authorities in Saudi Arabia

Departure phase of Hajj flights

Departure of Domestic flights starts from 15 September 2016

Departure of GCC Countries starts from 16 September 2016

Departure of Other Countries starts from 17 September 2016

For further details about Hajj and Umrah, click here: (http://www. haj. gov. sa )

All flynas domestic flights to/from KKIA Riyadh are now operating from Terminal 5.

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Naproxen Side Effects In Detail, Diproxen

Naproxen Side Effects

For the Consumer

Applies to naproxen: oral capsule liquid filled, oral suspension, oral tablet, oral tablet enteric coated, oral tablet extended release

As well as its needed effects, naproxen may cause unwanted side effects that require medical attention.

Major Side Effects

If any of the following side effects occur while taking naproxen, check with your doctor immediately:

More common:

Belching

bruising

difficult or labored breathing

feeling of indigestion

headache

itching skin

large, flat, blue, or purplish patches in the skin

pain in the chest below the breastbone

shortness of breath

skin eruptions

stomach pain

swelling

tightness in the chest

wheezing

Less common:

Bloating

bloody or black, tarry stools

blurred or loss of vision

burning upper abdominal or stomach pain

cloudy urine

constipation

decrease in urine output or decrease in urine-concentrating ability

disturbed color perception

double vision

fast, irregular, pounding, or racing heartbeat or pulse

halos around lights

indigestion

loss of appetite

nausea or vomiting

night blindness

overbright appearance of lights

pale skin

pinpoint red or purple spots on the skin

severe and continuing nausea

severe stomach burning, cramping, or pain

skin rash

swelling or inflammation of the mouth

troubled breathing with exertion

tunnel vision

unusual bleeding or bruising

unusual tiredness or weakness

vomiting of material that looks like coffee grounds

weight loss

Rare

Anxiety

back or leg pains

bleeding gums

blindness

blistering, peeling, or loosening of the skin

blood in the urine or stools

blue lips and fingernails

canker sores

change in the ability to see colors, especially blue or yellow

chest pain or discomfort

clay-colored stools

cold sweats

coma

confusion

cool, pale skin

cough or hoarseness

coughing that sometimes produces a pink frothy sputum

cracks in the skin

darkened urine

decreased vision

depression

diarrhea

difficult, burning, or painful urination

difficult, fast, or noisy breathing

difficulty with swallowing

dilated neck veins

dizziness

dry cough

dry mouth

early appearance of redness, or swelling of the skin

excess air or gas in the stomach

extreme fatigue

eye pain

fainting

fever with or without chills

fluid-filled skin blisters

flushed, dry skin

frequent urination

fruit-like breath odor

greatly decreased frequency of urination or amount of urine

hair loss

high fever

hives

increased hunger

increased sensitivity of the skin to sunlight

increased sweating

increased thirst

increased urination

increased volume of pale, dilute urine

irregular breathing

joint or muscle pain

large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs

late appearance of rash with or without weeping blisters that become crusted, especially in sun-exposed areas of skin, may extend to unexposed areas

light-colored stools

lightheadedness

loss of heat from the body

lower back or side pain

nervousness

nightmares

no blood pressure

no breathing

no pulse

nosebleeds

numbness or tingling in the hands, feet, or lips

pain in the ankles or knees

pain or burning in the throat

pain or discomfort in the arms, jaw, back, or neck

painful, red lumps under the skin, mostly on the legs

pains in the stomach, side, or abdomen, possibly radiating to the back

pale or blue lips, fingernails, or skin

pounding in the ears

puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

rapid, shallow breathing

red, irritated eyes

red skin lesions, often with a purple center

red-green color blindness

redness or other discoloration of the skin

redness, swelling, or soreness of the tongue

scaly skin

seizures

severe sunburn

shakiness

skin thinness

slurred speech

sneezing

sore throat

sores, ulcers, or white spots on the lips or tongue or inside the mouth

sores, welting, or blisters

spots on your skin resembling a blister or pimple

stiff neck or back

stomach cramps or tenderness

stomach upset

swelling in the legs and ankles

swelling of the face, fingers, feet, or lower legs

swollen, painful, or tender lymph glands in the neck, armpit, or groin

tiny bumps on the inner lining of the eyelid

unexplained weight loss

unpleasant breath odor

watery or bloody diarrhea

weakness or heaviness of the legs

weight gain

yellow eyes or skin

If any of the following symptoms of overdose occur while taking naproxen, get emergency help immediately:

Symptoms of overdose:

Bleeding under the skin

confusion about identity, place, and time

muscle tremors

restlessness

sleepiness

Minor Side Effects

Some naproxen side effects may not need any medical attention. As your body gets used to the medicine these side effects may disappear. Your health care professional may be able to help you prevent or reduce these side effects, but do check with them if any of the following side effects continue, or if you are concerned about them:

More common:

Continuing ringing or buzzing or other unexplained noise in the ears

hearing loss

Less common:

Acid or sour stomach

change in hearing

feeling of constant movement of self or surroundings

passing gas

sensation of spinning

stomach soreness or discomfort

Rare

Appetite changes

burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings

burning, dry, or itching eyes

difficulty with moving

discharge, excessive tearing

general feeling of discomfort or illness

lack or loss of strength

menstrual changes

muscle aching, cramping, stiffness, or weakness

not able to concentrate

redness, pain, or swelling of the eye, eyelid, or inner lining of the eyelid

seeing, hearing, or feeling things that are not there

shakiness in the legs, arms, hands, or feet

sleeplessness

swollen joints

trembling or shaking of the hands or feet

trouble getting pregnant

trouble performing routine tasks

trouble sleeping

unable to sleep

unusual drowsiness, dullness, or feeling of sluggishness

For Healthcare Professionals

Applies to naproxen: compounding powder, oral capsule, oral delayed release tablet, oral suspension, oral tablet, oral tablet extended release, oral and topical kit

Gastrointestinal

Very common (10% or more): Dyspepsia (14%), heartburn, nausea, constipation Common (1% to 10%): Diarrhea, abdominal pain Very rare (less than 0.01%): Pancreatitis Frequency not reported: Flatulence, gastritis, vomiting, dysphagia, stomatitis, abdomen enlarged, eructation, GI hemorrhage, rectal hemorrhage, aphthous, mouth ulcer, stomach ulcer, cardiospasm, colitis, esophagitis, gastroenteritis, GI disorder, rectal disorder, tooth disorder, melena esophageal ulcer, hematemesis, non-peptic GI ulceration, ulcerative stomatitis, sialadenitis, colitis Postmarketing reports: Inflammation, bleeding, ulceration, perforation, obstruction, exacerbation of inflammatory bowel disease [Ref ]

Hepatic

Rare (less than 0.1%): Hepatitis, jaundice Frequency not reported: Cholecystitis, cholelithiasis, hepatosplenomegaly, liver function abnormality, SGOT increased, SGPT increased, elevated liver enzymes [Ref ]

Nervous system

Very common (10% or more): Headache (15%) Common (1% to 10%): Drowsiness, dizziness Uncommon (0.1% to 1%): Cognitive dysfunction, poor concentration Very rare (less than 0.01%): Convulsions, stroke Frequency not reported: Paresthesia, lightheadedness, migraine, syncope, hypertonia, neuralgia, neuritis, amnesia, paralysis [Ref ]

Renal

Very rare (less than 0.01%): Glomerular nephritis, interstitial nephritis, nephrotic syndrome, renal papillary necrosis Frequency not reported: Kidney function abnormality, pyelonephritis, creatinine increased, glucosuria, albuminuria, BUN increased, renal failure, renal disease, kidney pain, nephrosclerosis, kidney failure, kidney calculus, nephropathy [Ref ]

Cardiovascular

Uncommon (0.1% to 1%): Palpitations Rare (0.01% to 0.1%): Vasculitis Very rare (less than 0.01%): Arterial thrombotic events, myocardial infarction Frequency not reported: Hypertension, angina pectoris, coronary artery disease, deep thrombophlebitis, vasodilation, vascular anomaly, arrhythmia, bundle branch block, abnormal ECG, right heart failure, hemorrhage, aortic stenosis, tachycardia, congestive heart failure Postmarketing reports: Cardiac failure [Ref ]

Hematologic

Rare (0.01% to 0.1%): Hemolytic anemia Very rare (less than 0.01%): Granulocytopenia, thrombocytopenia, agranulocytosis Frequency not reported: Anemia, aplastic anemia, leukopenia, bleeding time increased, eosinophilia, abnormal RBC, abnormal WBC, neutropenia, pancytopenia [Ref ]

Hypersensitivity

Rare (less than 0.1%): Allergic reaction, anaphylactoid/anaphylaxis reaction, hypersensitivity reaction [Ref ]

Dermatologic

Common (1% to 10%): Ecchymosis, rash, skin eruptions, pruritus, purpura Uncommon (0.1% to 1%): Urticaria, photosensitivity Rare (0.01% to 0.1%): Alopecia, pseudo-porphyria Very rare (less than 0.01%): Toxic epidermal necrolysis, erythema multiforme, Stevens-Johnson syndrome, epidermolysis bullosa Frequency not reported: Angioneurotic edema/angioedema, angiodermatitis, dry skin, sweating, skin ulcer, acne, contact dermatitis, eczema, skin necrosis, subcutaneous nodule, photosensitive dermatitis, porphyria cutaneous tarda, nail disorder, epidermal necrosis, exfoliative dermatoses, bullous dermatoses, lichen planus Postmarketing reports: Erythema nodosum, fixed drug eruption, pustular reaction, bullous reactions [Ref ]

Respiratory

Common (1% to 10%): Pharyngitis, rhinitis, dyspnea Rare (less than 0.1%): Aggravated asthma, eosinophilic pneumonitis Frequency not reported: Bronchitis, cough increased, asthma, pulmonary edema, laryngitis, lung disorder, epistaxis, pneumonia, respiratory distress, respiratory disorder, bronchospasm, sore throat [Ref ]

Other

Very common (10% or more): Influenza-like syndrome (10%) Common (1% to 10%): Infection, edema, tinnitus, fatigue Rare (0.01% to 0.1%): Hearing impairment Very rare (less than 0.01%): Aseptic meningitis Frequency not reported: Fever, accidental injury, asthenia, chest pain, peripheral edema, hearing disturbances, thirst, abscess, cellulitis, malaise, mucous membrane disorder, periodontal abscess, necrosis, aseptic meningitis, chills, weight increased, otitis media, deafness, ear disorder, herpes simplex, herpes zoster, vertigo, subdural hematoma, exacerbation of Parkinson's disease [Ref ]

Metabolic

Rare (less than 0.1%): Hyperkalemia Frequency not reported: Hyperglycemia, anorexia, hypoglycemia, hypercholesteremia, alkalosis, dehydration, glucose tolerance increase, hyperuricemia, hypokalemia [Ref ]

Endocrine

Postmarketing reports: Infertility [Ref ]

General

The most frequently reported adverse events were headache, dyspepsia, nausea, constipation, heartburn, abdominal pain, and influenza-like syndrome. [Ref ]

Genitourinary

Common (1% to 10%): Urinary tract infection Very rare (less than 0.01%): Hematuria Frequency not reported: Cystitis, monilia, pelvic pain, dysmenorrhea, dysuria, nocturia, prostate disorder, urinary incontinence, menorrhagia, menstrual disorders, vaginitis, uterine spasm, urinary retention, urinary frequency, abnormal urine, pyuria, metrorrhagia [Ref ]

Musculoskeletal

Common (1% to 10%): Back pain Rare (less than 0.1%): Myalgia, muscle weakness Frequency not reported: Leg cramps, arthralgia, joint disorder, tendon disorder, neck rigid/pain, LE syndrome, myasthenia, bone disorder, spontaneous bone fracture, fibrotendinitis, bone pain, spasm, bursitis Postmarketing reports: Systemic lupus erythematosus [Ref ]

Ocular

Common (1% to 10%): Visual disturbances Frequency not reported: Ptosis, amblyopia, scleritis, cataract, conjunctivitis, keratoconjunctivitis, lacrimation disorder, eye pain, diplopia, retrobulbar optic neuritis Postmarketing reports: Corneal opacity, papillitis, papilledema [Ref ]

Oncologic

Frequency not reported: Carcinoma, breast carcinoma, breast neoplasm, skin neoplasm [Ref ]

Psychiatric

Common (1% to 10%): Confusion Uncommon (0.1% to 1%): Depression, dream abnormalities, mood alterations Frequency not reported: Insomnia, anxiety, nervousness, emotional lability, hallucinations [Ref ]

References

1. "Product Information. Anaprox (naproxen)." Roche Laboratories, Nutley, NJ.

2. MHRA. Medicines and Health Regulatory Agency "MHRA Drug Safety Update. Available from: URL: http://www. mhra. gov. uk/Safetyinformation/DrugSafetyUpdate."

3. "Product Information. Naprelan 375 (naproxen)." Shionogi USA Inc, Florham Park, NJ.

4. Cerner Multum, Inc. "Australian Product Information." O 0

5. Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0

6. "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc, Palo Alto, CA.

It is possible that some side effects of naproxen may not have been reported. These can be reported to the FDA here. Always consult a healthcare professional for medical advice.

More about naproxen

Consumer resources

Professional resources

Related treatment guides

Disclaimer: 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. In addition, the drug information contained herein may be time sensitive and should not be utilized as a reference resource beyond the date hereof. This material does not endorse drugs, diagnose patients, or recommend therapy. This information is a reference resource designed as supplement to, and not a substitute for, the expertise, skill. knowledge, and judgement of healthcare practitioners in patient care. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate safety, effectiveness, or appropriateness for any given patient. Drugs. com does not assume any responsibility for any aspect of healthcare administered with the aid of materials provided. 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 substances you are taking, check with your doctor, nurse, or pharmacist.

Drug Status

Betaprol Questions We Have Answers At Healthsofa, Betaprol

Betaprol is a non selective beta blocker which is used in the treatment of hypertension. It may be used alone or with a diuretic to adequately treat hypertension or high blood pressure. Betaprol can also treat other circulatory diseases such as atrial fibrillation, angina pectoris and acute myocardial infarction or heart attack. It is also used in the treatment of migraine headaches, essential tremors, hyperoptic sub aortic stenosis, and phenocromocytoma.

Recent Forum Posts

Side Effects

nausea / constipation / chest pain / dizziness / vomiting / lightheadedness / insomnia / diarrhea / pharyngitis / bradycardia / anorexia / fatigue / somnolence / hyperlipidemia / rash / weakness / paresthesia / hypotension / urticaria / pruritus / bronchospasm / alopecia / pulmonary edema / fever /

Pregnancy

Pregnancy and Betaprol Embryo and Betaprol Fetal Weaning and Betaprol Breastfeeding and Betaprol

Dosage

How to Properly Take propranolol? What is the children dosage for Betaprol What is the adult dosage for Betaprol How often should Betaprol be taken? What is the dosage for Betaprol?

Usage

Storage

Interactions

Biological Half-life

How long does it take Betaprol to leave the system?

Nursing responsibilities for Betaprol

ATC CODE: C07AA05 ATC CODE: C07AA05

Other medications containing propranolol

Manufacturer: Hoechst Marion Roussel propranolol is the active ingredient in Betaprol

Drafen War Band - Compendium Caidis, Drafen

Drafen War Band

Gules, a raven-headed wyvern displayed counter-ermine.

Drafn is a warband in the SCA, in the kingdom of Caid, in the barony of Calafia (San Diego, California). "Drafen War Band" is the registered name of the group, however they prefer to use the spelling "Drafn".

Drafn was formed in 1979 and specializes in recreating the Norse culture. Its goals are to promote the SCA, to provide the kingdom with a well-equipped fighting unit composed of gentle persons, to provide a lively and interesting picture of the Varangian Guard and Norse culture, to promote the art of Rattando, to sustain a period encampment of the Viking Age, and to have parties.

Drafn is a contraction of the old Norse words "dreki" and "rafn" (dragon and raven). Lady Chloe designed the wyvern-like emblem that we carry on our shields. At least two Medieval towns, one on the Oslo Fjord in Norway and another on the banks of the Volga River in Russia were named Drafn. The names mean something like "place where driftwood washes up on the shore."

Drafn is not a secret society or an exclusive social clique. Membership is open to anyone of good character who shares the group's interests. Drafn also publishes a monthly newsletter with articles of interest to its membership, "Runestones."

The Drafn Warband was awarded the Crossed Swords in 05/31/1986 and 05/23/2003.

More Information

3 Ways To Make A Heart On Facebook, Sylmes

How to Make a Heart on Facebook

Making a heart on Facebook is a fun way to express your undying love and affection - whether it's for your significant other, best friend, or just a picture of a really cute puppy. There are several easy ways to make this universal symbol of care and romance, all of which take approximately two seconds! See Step 1 below to get started.

Steps Edit

Method One of Three: Simple Pink Heart Edit

Write <3. Then press enter. Once published, your <3 will be replaced with a pink colored ¦.

Use heart-shaped emoji. Not everyone will believe it, but the icons you see in Step 2 below are actually hidden heart-shaped emoji.

If you're a Chrome user, you will see plain black squares, and if you're a Firefox, IE or Safari user, you will see plain black hearts.

All you need to do is copy the square/heart you want and paste it into a Facebook post or comment.

Once you post your comment, it will magically turn into one of the hearts described below.

Copy and paste a pre-typed heart. You can use one of the following:

Beating Heart--??

Broken Heart-- ??

Sparkling Heart--??

Growing Heart--??

Heart with Arrow/ Fall in Love--??

Blue Heart--??

Green Heart--??

Yellow Heart--??

Red Heart--??

Purple Heart --??

Heart with Ribbon--??

Method Three of Three: Old-School Techniques Edit

Use the Character Map on a PC. This will give you access to a wide array of symbols, hearts, skulls, and much more. Simply open Character Map, and click on the desired symbol.

You can open character map on Windows XP, Windows 7 or Windows 8 by going to the start menu and looking under All Programs > Accessories > System Tools > Character Map.

Use Character Viewer on a Mac. Click on the Character Viewer icon on the menubar, and pick a character set from the left-hand sidebar.

For example, pictographs contain the heart symbol in both black and white. Click on either, and a list of variations will appear on the right.

Right-click on the desired heart variation and copy to the clipboard.

Paste into Facebook, and delete the extra font information, leaving only the heart.

Use the Alt-codes on a PC. This technique will work on most computers running Windows. Simply hold the Alt key + 3, and when you post your status or chat, the heart symbol appears.

Try Shift + Ins. For some computers, another combination will work. Press down Shift and Ins at the same time, which will make the ¦ symbol.

About Neovisc? For Tribute Pharmaceuticals Canada Inc, Neovisc

Stellar Pharmaceut Inc (SLXCF)

SLXCF » Topics » About NeoVisc?

This excerpt taken from the SLXCF 8-K filed Jun 18, 2009.

NeoVisc is a viscosupplement that when injected into the effected joints, offers patients a drug-free method to treat the pain of osteoarthritis ("OA"). NeoVisc is available in Canada, Europe, Asia, Middle East and the Caribbean as a three injection product administered over a two-week period. The 3 dose NeoVisc has been shown to provide symptomatic relief of OA pain for an average of 6-12 months. There are certain situations however, where administering the 3 dose treatment is difficult to schedule for certain patients in a busy practice. NeoVisc Single Dose provides physicians and patients the convenience of a single injection treatment. This single injection provides symptomatic relief but usually over a shorter duration than the 3 dose NeoVisc. Both the NeoVisc Single Dose and 3 dose NeoVisc use a natural, linear hyaluronan derived from a fermentation process, unlike competitors that use an altered, cross-linked hyaluronan.

This excerpt taken from the SLXCF 10-K filed Apr 10, 2009.

NeoVisc is a 2 mL pre-filled syringe of sterile 1.0% sodium hyaluronate solution used for the temporary replacement of synovial fluid in osteoarthritic joints. NeoVisc is classified in Canada by the TPD as a “medical device” under the Medical Devices Regulations of the Food and Drugs Act (Canada). NeoVisc is packaged, sold and marketed as a three injection therapy. The product is administered weekly by injection directly into the affected joint. This type of injection is called an intra-articular injection.

This type of treatment, referred to as viscosupplementation, is a relatively new therapy for the treatment of osteoarthritis, having gained Canadian approval in 1992 and United States approval in 1997. However, viscosupplementation has been used since the mid 1980s in many European markets. Replacing or supplementing the joint fluid provides symptomatic relief from the pain of osteoarthritis for up to 6 to 8 months before a repeat set of injections is required.

Osteoarthritis and Treatment Options . Osteoarthritis is a degenerative disease associated with long-term wear on weight bearing joints. With no known cure, it is estimated that OA affects an estimated 33% of persons over 45 years of age, and approximately 85% over the age of 70. The Canadian Arthritis Association estimates that 3 million Canadians suffer from the “osteo” form of arthritis. Stellar estimates the number of OA sufferers in American to be over 30 million. The aggregate number of patients with OA is expected to grow significantly as the average age of the population increases.

Current OA remedies focus on symptomatic relief and postponement of surgical intervention. These remedies include:

Pain killers such as aspirin, acetaminophen and other non-steroidal anti-inflammatory drugs (NSAID), such as naproxen and diclofenac, as well as new COX/2 Inhibitors;

Corticosteroids are also used to treat the inflammation associated with the disease; and

Surgical replacement with artificial joints.

Products such as NeoVisc have added a fourth non-pharmacological option in obtaining symptomatic improvements by supplementing the synovial fluid in the affected joint. NeoVisc can also be used in conjunction with drug treatments like NSAIDs, thereby reducing the overall cost of treatment, increasing clinical benefits and delaying or avoiding steroid use and joint replacement.

Role of Hyaluronate . The active ingredient in NeoVisc is hyaluronate, also referred to as hyaluronic acid or HA. HA is a naturally occurring polysaccharide found throughout the human body, which has been shown to play an important role in such biological processes as cell differentiation, tissue hydration and proteoglycans organization. Injected HA also provides an anti-inflammatory and analgesic effect. HA also plays a fundamental role in human joints, where by virtue of its viscosity, elasticity and other rheological properties, acts as a lubricating and shock absorbing component in joint fluids, and as an ocular lubricant. HA products are currently being used in eye surgery, wound healing, intra-articular injections and as an adjunct to certain grafting procedures.

Marketing Strategy . Purchase decisions in the prescription pharmaceutical market are influenced by the prescribing physician, pharmacist and end use patient/customer. State and private health care plans and patient user groups may also play a role in product/therapy selection, especially where the cost of therapy is high. In treating OA, it is typically the physician that decides which therapeutic option is best for the patient and which related products to use.

Stellar’s marketing and sales strategy focuses on those physicians currently prescribing HA viscosupplements. Stellar has created a database focused on orthopaedic surgeons, rheumatologists, sports medicine specialists and select general practitioners in Canada. Direct marketing to the physicians in this database has been, and will continue to be, effective in persuading treating physicians and specialists already using viscosupplementation to convert to NeoVisc or recommend it to their patients. Management of the Company believes that NeoVisc is at least as effective as any other competitive product and is the lowest cost intra-articular therapy currently on the market. Stellar’s strategy is to demonstrate that NeoVisc is the most cost-effective viscosupplement therapy available.

Competitive Analysis . The major competitive product to NeoVisc in Canada and the United States is Synvisc®, which is manufactured and sold by Genzyme Corp. Synvisc is a three injection dosage regime, which has been available in Canada since 1992 and in the United States since 1997. Synvisc is the dominant product in the viscosupplementation market. Management of Stellar estimates Synvisc’s market share at over 60% in the United States and 50% in Canada.

If approved for sale in the United States, NeoVisc would also compete with Fidia, SpA’s product, marketed under the trade name “Hyalgan®” by Sanofi-Synthelabo Inc. and Seikagaku’s product “Supartz®” marketed by Smith and Nephew, Orthovisc®, manufactured by Anika Therapeutics, Inc. and marketed by Johnson & Johnson. In Canada, NeoVisc also competes with Suplasyn®, manufactured by Bioniche Life Sciences Inc. With little to differentiate these HA products for use in the treatment of degenerative joint disease, management of the Company believes that Stellar’s lower patient cost and high quality will allow NeoVisc to effectively further penetrate the market and obtain a significant share in Canada and, if approved for sale, the United States.

As stated above, the Company has signed the following agreements for NeoVisc;

in June 2003, Stellar entered into a distribution agreement with BurnsAdler Pharmaceuticals (located in Charlotte, North Carolina), to distribute NeoVisc in Latin America and the Caribbean;

in June 2004, Stellar entered into a distribution agreement with Triptibumus Sdn Bhd. for sale of NeoVisc in Malaysia, Singapore and Brunei;

in August 2005, the Company signed a distribution agreement with Technimed for the sale of NeoVisc in Lebanon;

in July 2006, a distribution agreement was signed with Bio-Technic Romania SRL for NeoVisc® in Romania; and

in November of 2007, the Company signed a licensing agreement with Torrex Chiesi Pharma GmbH, based in Vienna, Austria for the distribution and sale of NeoVisc in Eastern Europe. The territory covers a number of countries, including Austria, Czech Republic, Slovakia, Croatia, Serbia, Montenegro, Macedonia, Bosnia, Herzegovina, Poland, Hungary, Russia and the Commonwealth of Independent States.

This excerpt taken from the SLXCF 8-K filed Mar 19, 2008.

NeoVisc is a 2 mL pre-filled syringe of sterile 1.0% sodium hyaluronate solution used for the temporary replacement of synovial fluid in osteoarthritic joints. NeoVisc is packaged, sold and marketed as a three injection therapy that has been shown to provide symptomatic relief of the pain of osteoarthritis for an average of 6-12 months. The product is administered in three weekly injections directly into the affected joint.

EXCERPTS ON THIS PAGE:

Lisinopril - Blood Pressure, Zovanta-40

Lisinopril is used to treat high blood pressure (hypertension) in adults and children 6 years and older, including renovascular, acute myocardial infarction in clinically stable condition of the patients, heart failure (adjuvant treatment), diabetic nephropathy. The principle of this drug is to relax blood vessels, causing them to expand, it can lead to prevention of occurrence of strokes, heart attacks and kidney problems. Lisinopril is also used after acute myocardial recovery, and is used with other drugs (eg, "water pills" / diuretics, digoxin) to treat heart failure. This drug belongs to a class of medications called ACE inhibitors.

Dosage and direction Take medicine for adults 1 time a day. The dose is determined individually, depending on the evidence, the state of renal function and concomitant therapy. Typically, the initial dose is 2,5-5 mg, the average maintenance dose - 5-20 mg, the maximum daily - 80 mg.

Precautions Treatment is carried out under regular medical supervision (water-electrolyte balance). The process of treatment requires monitoring of blood pressure, protein level and plasma potassium, urea nitrogen, creatinine, renal function, blood picture, body weight and dieting. You have to be careful during surgery (including dental), especially when using general anesthetics that have a hypotensive effect.

Hypersensitivity, pregnancy, breast-feeding.

Possible side effects You can feel headache, dizziness, nervousness, fainting, drowsiness, insomnia, tremors, convulsions, visual disturbances, palpitations, chest pain, hypotension, arrhythmia, dry cough and malignant tumors of the lung, hemoptysis, pain when breathing, bronchitis, dry mouth, indigestion, heartburn, vomiting, diarrhea / constipation, bloating, abdominal pain, renal failure, weakening of libido, impotence, arthritis, neck pain, back pain, rash, urticaria, and syndrome of Stevens - Johnson.

Drug interactions List of the drugs that can interact with Lisinopril: gold injections to treat arthritis, lithium (Lithobid, Eskalith), a potassium supplement such as K-Dur, Klor-Con, salt substitutes that contain potassium, insulin or diabetes medication you take by mouth, aspirin or other NSAIDs (non-steroidal anti-inflammatory drugs) such as ibuprofen (Motrin, Advil), diclofenac (Voltaren), etodolac (Lodine), indomethacin (Indocin), ketoprofen (Orudis), naproxen (Aleve, Naprosyn), and others, or a diuretic (water pill).

Missed dose Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Overdose Seek emergency medical attention if you think you have used too much of this medicine. Lisinopril overdose symptoms may include feeling extremely dizzy or light-headed, or fainting.

Storage Store Lisinopril at room temperature away from moisture and heat.

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

Lisinopril is used to treat high blood pressure (hypertension) in adults and children 6 years and older, including renovascular, acute myocardial infarction in clinically stable condition of the patients, heart failure (adjuvant treatment), diabetic nephropathy. The principle of this drug is to relax blood vessels, causing them to expand, it can lead to prevention of occurrence of strokes, heart attacks and kidney problems. Lisinopril is also used after acute myocardial recovery, and is used with other drugs (eg, "water pills" / diuretics, digoxin) to treat heart failure. This drug belongs to a class of medications called ACE inhibitors.

Dosage and direction Take medicine for adults 1 time a day. The dose is determined individually, depending on the evidence, the state of renal function and concomitant therapy. Typically, the initial dose is 2,5-5 mg, the average maintenance dose - 5-20 mg, the maximum daily - 80 mg.

Precautions Treatment is carried out under regular medical supervision (water-electrolyte balance). The process of treatment requires monitoring of blood pressure, protein level and plasma potassium, urea nitrogen, creatinine, renal function, blood picture, body weight and dieting. You have to be careful during surgery (including dental), especially when using general anesthetics that have a hypotensive effect.

Hypersensitivity, pregnancy, breast-feeding.

Possible side effects You can feel headache, dizziness, nervousness, fainting, drowsiness, insomnia, tremors, convulsions, visual disturbances, palpitations, chest pain, hypotension, arrhythmia, dry cough and malignant tumors of the lung, hemoptysis, pain when breathing, bronchitis, dry mouth, indigestion, heartburn, vomiting, diarrhea / constipation, bloating, abdominal pain, renal failure, weakening of libido, impotence, arthritis, neck pain, back pain, rash, urticaria, and syndrome of Stevens - Johnson.

Drug interactions List of the drugs that can interact with Lisinopril: gold injections to treat arthritis, lithium (Lithobid, Eskalith), a potassium supplement such as K-Dur, Klor-Con, salt substitutes that contain potassium, insulin or diabetes medication you take by mouth, aspirin or other NSAIDs (non-steroidal anti-inflammatory drugs) such as ibuprofen (Motrin, Advil), diclofenac (Voltaren), etodolac (Lodine), indomethacin (Indocin), ketoprofen (Orudis), naproxen (Aleve, Naprosyn), and others, or a diuretic (water pill).

Missed dose Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Overdose Seek emergency medical attention if you think you have used too much of this medicine. Lisinopril overdose symptoms may include feeling extremely dizzy or light-headed, or fainting.

Storage Store Lisinopril at room temperature away from moisture and heat.

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

Thyrohormone, Thyrohormone

?????? ? ??????? ?. ?????????? ?????????????? MD, Phd, ???????? ????????????? ?????? www. familywellness. gr

?????? ?????????, ???? ???? ?????? ????????? ??? ??? 2 ????? ??? 2 ????? 5 ???????? ???????. ???? ?? ?????? ? ????????. ?? ????????? ??????? ??????? ??????????? ????, ????? ???? ?? ???????????? ?????, ??????? ?? ?? ????? ????? ??? ????? ?? ?????????? (TSH, T4, T3 ???). ?????????????? ??? ????????? ?? ???? ?? thyrohormone 1/2 ??? ????? 6 ????? ??? ???????? ??? ??? ???????? ?????, ??? ?????? ????????? ?? 1 ???? ??? ?????.

?????? ? ????? ??? ????? ??? ????? ??????? ?? ???? ???? ?? ???? ??? ?? ????????? ??????? ???? ??? ????? ????? ????????????; ??????? ?????? ???? ??????????? ???????????? ??? ????? ?? ?????????? ??? ?? ??? ???????????? ??????? ?? ????????????;

????????? ?? ??? ????????.

?? ?????? ?? ???????? ??? ????? ??? ?????? ?? ????????? ??? ?????? ?? ?????????? ???? ?????????? ????? ??????????? ???????? ??????? ???????? (???????? ??? ??????? ???????). ??????????? ???????? ?????? ?? ????? ????? ? ???? ?? ?????????? ???? ???????????.

??????, ???? ??? ?????? ?? ???????? ???? ???????? ???? ??????? ??? ????????? ???? ?????? ??? ??????? (?. ?. ?? ????? ??? ???????????? ??????? ????? ???? ??? ????? ??? ????? ?? ??????????, ??? ????? ???????????? – ?????? ?? ?? ?????!).

???? ?????????? ????????? ???????? ??? ????? ??????? ??? ??? ????? ???????????? ?? ???????? ?? ???????, ??? ???? ??? ?????????? ????? ??? ???? ???????. ?? ??? ??????? ???????? ???????, ???? ??????? ??? ?????????? ?? ???????. ????? ???? ????!

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Thyrohormone (Levothyroxine)

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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.

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Buy Brolukat - Montelukast - Online Without Prescriptions, Brolukat

Singulair (Brolukat)

Singulair is used for prevention and long-term treatment of asthma. It is also used in certain patients to relieve runny nose caused by allergies and to prevent asthma attacks caused by exercise. Singulair is a leukotriene receptor antagonist. It works by blocking a substance called leukotriene, which helps to decrease certain asthma and allergy symptoms.

Use Singulair as directed by your doctor.

Take Singulair by mouth with or without food.

Continue to use Singulair even if you feel well. Do not miss any doses.

If you miss a dose of Singulair, 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 Singulair.

Store Singulair 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 Singulair out of the reach of children and away from pets.

Active Ingredient: Montelukast sodium.

Do NOT use Singulair if:

you are allergic to any ingredient in Singulair.

Contact your doctor right away if any of these apply to you.

Some medical conditions may interact with Singulair. 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 liver problems

if you have a history of mental or mood problems, or suicidal thoughts or actions.

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

Certain anticonvulsants (eg, phenobarbital) or rifampin because they may decrease Singulair's effectiveness.

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

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

Singulair will not stop an asthma attack once one has started. Be sure you always carry appropriate medicine (eg, bronchodilator inhalers) with you in case of an asthma attack.

Contact your doctor promptly if your short-acting inhaler use increases or if use exceeds the 24-hour maximum prescribed by your doctor. Contact your doctor if your asthma worsens.

Do not decrease your dose or stop using Singulair or other asthma medicines without first checking with your doctor.

If your asthma is sensitive to aspirin or nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen), continue to avoid those medicines as directed by your doctor.

Some patients taking Singulair have developed mental or mood changes, including suicidal thoughts or actions. Contact your doctor immediately if you experience symptoms such as agitation, aggression, hostility, anxiety, depression, strange dreams, trouble sleeping, sleepwalking, tremor, hallucinations, restlessness, irritability, or any unusual change in mood or behavior. Contact your doctor immediately if any signs of suicidal thoughts or actions occur.

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

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

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

Cough; dizziness; headache; indigestion; nausea; stomach upset or pain; stuffy nose; tiredness; trouble sleeping; weakness.

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); aggressive behavior; agitation; chest pain; dark urine; fever; flu-like symptoms; hallucinations; irregular heartbeat; mental or mood changes; new or worsening wheezing or other breathing problems; numbness or tingling of the hands or feet; seizures; severe or persistent stomach pain; severe sinus inflammation; suicidal thoughts or actions; swelling; tremor; unusual bruising or bleeding; upper respiratory tract infection; 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.

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Wymox Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Wymox

Wymox

Uses

Amoxicillin is used to treat a wide variety of bacterial infections. This medication is a penicillin - type antibiotic. It works by stopping the growth of bacteria.

This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold. flu ). Unnecessary use or misuse of any antibiotic can lead to its decreased effectiveness.

Amoxicillin is also used with other medications to treat stomach /intestinal ulcers caused by the bacteria H. pylori and to prevent the ulcers from returning.

OTHER USES: This section contains uses of this drug that are not listed in the approved US 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 drug may also be used by people with certain heart problems (such as heart valve disease) before medical/dental procedures (such as tooth /gum procedures) to prevent heart infection.

How to use Wymox

Take this medication by mouth with or without food as directed by your doctor, usually every 8 or 12 hours. The dosage is based on your medical condition and response to treatment.

Drink plenty of fluids while using this medication unless your doctor tells you otherwise.

Antibiotics work best when the amount of medicine in your body is kept at a constant level. Therefore, take this drug at evenly spaced intervals. To help you remember, take it at the same times each day.

Continue to take this medication until the full prescribed amount is finished, even if symptoms disappear after a few days. Stopping the medication too early may allow bacteria to continue to grow, which may result in a return of the infection.

Tell your doctor if your condition persists or worsens.

Side Effects

Nausea. vomiting. or diarrhea may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

Use of this medication for prolonged or repeated periods may result in oral thrush or a new vaginal yeast infection (oral or vaginal fungal infection). Contact your doctor if you notice white patches in your mouth. a change in vaginal discharge or other new symptoms.

Tell your doctor right away if any of these rare but serious side effects occur: dark urine, persistent nausea or vomiting, stomach /abdominal pain. yellowing eyes or skin. easy bruising or bleeding, persistent sore throat or fever.

This medication may rarely cause a severe intestinal condition (Clostridium difficile - associated diarrhea) due to a type of resistant bacteria. This condition may occur during treatment or weeks to months after treatment has stopped. Do not use anti-diarrhea products or narcotic pain medications if you have the following symptoms because these products may make them worse. Tell your doctor right away if you develop: persistent diarrhea, abdominal or stomach pain/cramping, blood /mucus in your stool.

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

Amoxicillin can commonly cause a mild rash that is usually not serious. However, you may not be able to tell it apart from a rare rash that could be a sign of a severe allergic reaction. Therefore, get medical help right away if you develop any rash.

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

Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney disease. a certain type of viral infection (infectious mononucleosis ).

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

During pregnancy. this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor.

Amoxicillin passes into breast milk. Consult your doctor before breast - feeding.

Interactions

The effects of some drugs can change if you take other drugs or herbal products at the same time. This can increase your risk for serious side effects or may cause your medications not to work correctly. These drug interactions are possible, but do not always occur. Your doctor or pharmacist can often prevent or manage interactions by changing how you use your medications or by close monitoring.

To help your doctor and pharmacist give you the best care, be sure to tell your doctor and pharmacist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products) before starting treatment with this product. While using this product, do not start, stop, or change the dosage of any other medicines you are using without your doctor's approval.

Some products that may interact with this drug include: live bacterial vaccines. methotrexate .

Although most antibiotics are unlikely to affect hormonal birth control such as pills, patch, or ring, a few antibiotics (such as rifampin, rifabutin ) can decrease their effectiveness. This could result in pregnancy. If you use hormonal birth control. ask your doctor or pharmacist for more details.

Amoxicillin may cause false positive results with certain diabetic urine testing products (cupric sulfate-type). This drug may also affect the results of certain lab tests. Make sure laboratory personnel and your doctors know you use this drug.

This document does not contain all possible drug interactions. Keep a list of all the products you use. Share this list with your doctor and pharmacist to lessen your risk for serious medication problems.

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 vomiting, persistent diarrhea, a severe decrease in the amount of urine, or seizures.

Notes

Do not share this medication with others.

This medication has been prescribed for your current condition only. Do not use it later for another infection unless your doctor directs you to do so. A different medication may be necessary in that case.

With prolonged treatment, laboratory and/or medical tests (such as kidney and liver function, complete blood counts) may be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

Missed Dose

If you miss a dose, use 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 according to the product labeling, away from light and moisture. Different brands of this medication have different storage needs. Check the product package for instructions on how to store your brand, or ask your pharmacist. 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 for more details about how to safely discard your product.

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

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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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Carvedilol Uses, Dosage - Side Effects, Cardival

Carvedilol

What is carvedilol?

Carvedilol is a beta-blocker. Beta-blockers affect the heart and circulation (blood flow through arteries and veins).

Carvedilol is used to treat heart failure and hypertension (high blood pressure). It is also used after a heart attack that has caused your heart not to pump as well.

Carvedilol may also be used for purposes not listed in this medication guide.

Important information

You should not take carvedilol if you have asthma, bronchitis, emphysema, severe liver disease, or a serious heart condition such as heart block, "sick sinus syndrome," or slow heart rate (unless you have a pacemaker).

Avoid drinking alcohol within 2 hours before or after taking extended-release carvedilol (Coreg CR). Also avoid taking medicines or other products that might contain alcohol. Alcohol may cause the carvedilol in Coreg CR to be released too quickly into the body.

If you are being treated for high blood pressure, keep using carvedilol even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.

Before taking this medicine

You should not take carvedilol if you are allergic to it, or if you have:

asthma, bronchitis, emphysema;

severe liver disease; or

a serious heart condition such as heart block, "sick sinus syndrome," or slow heart rate (unless you have a pacemaker).

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

diabetes (taking carvedilol can make it harder for you to tell when you have low blood sugar);

angina (chest pain);

liver or kidney disease;

a thyroid disorder;

pheochromocytoma (tumor of the adrenal gland);

circulation problems (such as Raynaud's syndrome); or

a history of allergies.

FDA pregnancy category C. It is not known whether carvedilol will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.

It is not known whether carvedilol passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are taking carvedilol.

How should I take carvedilol?

Take carvedilol exactly as prescribed by your doctor. Follow all directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Carvedilol works best if you take it with food.

You may open the carvedilol capsule and sprinkle the medicine into a spoonful of pudding or applesauce to make swallowing easier. Swallow right away without chewing. Do not save the mixture for later use. Discard the empty capsule.

Take carvedilol at the same time every day. Do not skip doses or stop taking carvedilol without first talking to your doctor. Stopping suddenly may make your condition worse.

If you are switched from carvedilol tablets to carvedilol extended-release capsules (Coreg CR), your daily total dose of this medicine may be higher or lower than before. Older adults may be more likely to become dizzy or feel faint when switching from tablets to extended-release capsules. Follow your doctor's instructions.

Your blood pressure will need to be checked often.

If you are being treated for high blood pressure, keep using this medication even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.

If you need surgery, tell the surgeon ahead of time that you are using carvedilol. You may need to stop using the medicine for a short time.

You should not stop using carvedilol suddenly. Stopping suddenly may make your condition worse.

Carvedilol can affect your pupils during cataract surgery. Tell your eye surgeon ahead of time that you are using this medication. Do not stop using carvedilol before surgery unless your surgeon tells you to.

Carvedilol is only part of a complete program of treatment for hypertension that may also include diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely if you are being treated for hypertension.

Store at room temperature away from moisture and heat.

What happens if I miss a dose?

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

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include uneven heartbeats, shortness of breath, bluish-colored fingernails, dizziness, weakness, fainting, and seizure (convulsions).

What should I avoid while taking carvedilol?

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

Drinking alcohol can further lower your blood pressure and may increase certain side effects of carvedilol. You should especially avoid drinking alcohol within 2 hours before or after taking extended-release carvedilol (Coreg CR).

Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall.

Carvedilol side effects

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

Call your doctor at once if you have a serious side effect such as:

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

slow or uneven heartbeats;

swelling, rapid weight gain, feeling short of breath (even with mild exertion);

cold feeling or numbness in your fingers or toes;

chest pain, dry cough, wheezing, chest tightness, trouble breathing; or

high blood sugar (increased thirst, increased urination, hunger, dry mouth, fruity breath odor, drowsiness, dry skin, blurred vision, weight loss).

Common carvedilol side effects may include:

tired feeling; 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.

Carvedilol dosing information

Usual Adult Dose for Angina Pectoris:

Immediate-release tablets: Initial dose: 6.25 mg orally twice a day with food Maintenance dose: 6.25 mg to 25 mg orally twice a day with food Maximum dose: 50 mg per day

Usual Adult Dose for Congestive Heart Failure:

Immediate-release tablets: Initial dose: 3.125 mg orally twice a day for 2 weeks. If tolerated, increase dosage to 6.25 mg orally twice a day.

Dosage should then be doubled every 2 weeks to the highest level tolerated by the patient.

Maximum dose: 50 mg orally twice a day in patients weighing 85 kg or greater and 25 mg orally twice a day in patients weighing 85 kg or less

Extended-release capsules: Initial dose: 10 mg orally once a day for 2 weeks. If tolerated, increase dosage to 20 mg, 40 mg, and 80 mg over successive intervals of at least 2 weeks.

Usual Adult Dose for Hypertension:

Immediate-release tablets: Initial dose: 6.25 mg orally twice a day with food Maintenance dose: 6.25 mg to 25 mg orally twice a day with food Maximum dose: 50 mg per day

Extended-release capsules: Initial dose: 20 mg orally once a day for 7 to 14 days. If tolerated, may increase dosage to 40 mg orally once a day, then again to 80 mg orally once a day after 7 to 14 days.

Maximum dose: 80 mg per day

Usual Adult Dose for Left Ventricular Dysfunction:

Immediate-release tablets: Initial dose: 6.25 mg orally twice a day (an initial dosage of 3.25 mg twice daily can be given to patients unable to tolerate the initial dosage).

Maintenance dose: If tolerated, the initial dosage may be titrated to 12.5 mg twice a day after 3 to 10 days to a target dose of 25 mg twice a day.

Extended-release capsules: Initial dose: 20 mg orally once a day (an initial dosage of 10 mg once daily can be given to patients unable to tolerate the initial dosage). If tolerated, may increase dosage to 40 mg after 3 to 10 days, then again to 80 mg orally once a day.

What other drugs will affect carvedilol?

Other drugs may interact with carvedilol, 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 carvedilol

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about carvedilol.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use carvedilol 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 1996-2016 Cerner Multum, Inc. Version: 15.01. Revision Date: 2014-01-20, 8:29:33 AM.

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Danaren Dental Laboratories, Dnaren

Danaren is an independent, full-service dental lab located in Seneca Falls, NY. Our highly skilled technicians produce top-quality restorations at affordable prices. We’re in business to save you money and help you succeed.

As the practical alternative to labs that outsource dentists’ casework offshore, all of our highly esthetic restorations are made of safe, FDA-approved materials right here in the USA. Danaren offers a variety of low-cost options when patient care is regimented by Medicaid and other low-reimbursement insurance plans.

We deliver cases to dentists in all 50 states with absolutely NO COST for shipping and handling. With the added benefits of our incredibly FAST turnaround times, FREE rush cases, and CASH-BACK programs, Danaren can make your practice become more profitable .

Danaren announces the introduction of its Z•One Full Contour Zirconia crowns.

Danaren announces the introduction of its Z•One Full Contour Zirconia crowns.

Z•One Full Contour Zirconia crowns are made from monolithic solid zirconia, giving patients the strength they need while still obtaining natural-looking esthetics. More »

Z•One Full Contour Zirconia crowns are made from monolithic solid zirconia, giving patients the strength they need while still obtaining natural-looking esthetics. Z•One Full Contour Zirconia crowns are precision milled using CAD/CAM technology and hand finished by Danaren's highly specialized technicians. Just like all of Danaren's restorations, Z•One Full Contour Zirconia crowns are 100% American Made, ensuring the use of safe FDA-approved materials and guaranteeing consistent quality with every restoration. Perfect for posterior crowns and short-span bridges, and ideally suited for bruxers and grinders, Z•One Full Contour Zirconia crowns offer an esthetic alternative to full-cast crowns at a price of only $109 with free shipping both ways. Unyielding strength, effortless insertions, and an economic price tag means Z•One puts patient satisfaction and your profitability in total focus. Get in the ZONE today and Discover the Danaren Difference with Z•One Full Contour Zirconia crowns.

Santa and Mrs. Claus show up to the BonaDent Children's Christmas Party!

Santa and Mrs. Claus show up to the BonaDent Children's Christmas Party! With gifts!

Santa Claus was generous enough to clear time in his busy holiday schedule to swing through BonaDent's Children's Christmas Party this Sunday. More »

Santa Claus was generous enough to clear time in his busy holiday schedule to swing through BonaDent's Children's Christmas Party this Sunday. Bearing gifts and spreading holiday cheer to all, ol' St. Nick was even joined by Mrs. Claus, who helped distribute gifts to the children of BonaDent and Danaren employees.

A holiday tradition at BonaDent for years, the Children's Christmas Party always brings magic to the holiday season for the little ones. Stay tuned for photos of the BonaDent Christmas Party (for grown-ups), where by party's end, Santa Claus typically has made clear determinations about who's been naughty and who's been nice…

Grow Your Partial Business, Let Danaren Build Your Partial Frameworks

Grow Your Partial Business, Let Danaren Build Your Partial Frameworks

Capitalize on Danaren’s artistry and craftsmanship, and let our technology team build beautiful and durable cast partial frameworks for your lab. More »

Capitalize on Danaren’s artistry and craftsmanship, and let our technology team build beautiful and durable cast partial frameworks for your lab. Consistent, accurate and highly uniform, our frameworks are designed to instill complete confidence in your product.

Simplify your workflow, make your job easier and achieve superior results. Our dedicated team of technicians will ensure proper fits, and deliver esthetic, delicate, yet durable castings. We offer more than high-quality frameworks; enjoy quicker turnaround times, super-reliable communication, and competitive pricing.

We sweat the details so you don’t have to. We’ll also provide all shipping materials and handle all pick-ups and deliveries for your lab. Partner with Danaren and satisfy even your most demanding accounts. Let us help you grow your cast partial business to its full potential!

Contact Erin Bonafiglia by email or call 866.326.2736 with any questions.

Lab Day a Hit at Danaren

Lab Day a Hit at Danaren

Lab Day is when we open our doors to welcome our team members and our valued technical partners. More »

Now an annual event, Lab Day is when we open our doors to welcome team members from across the organization and our valued technical partners in the dental industry (such as Jensen, Dentsply, Captek, CMP Industries, SensAble, among others) to come together under one roof for a day of continuing education.

BonaDent supports the professional development of our entire staff, and Lab Day — now an annual event — presents an ideal opportunity for colleagues to come together through education, skill-building, and camaraderie, all of which takes place in-house on Lab Day. The lab at Seneca Falls was specifically designed for in-house training, featuring an 84-seat auditorium and a state-of-the-art hands-on training center, which is equipped with operatories and dental simulators.

BonaDent Department Managers typically offer up technical training and workshops for BonaDent employees from all departments. In addition, each of BonaDent’s technical partners offer informative training on time-tested and newly developed products to the laboratory team. Typically, there are also a few non-technical offerings, including customer-service and administrative development courses for our office teams.

The afternoon usually culminates with all participants catching up and sharing a delicious and substantial late lunch together. After only the second go-around, Lab Day has already proven itself to be a highlight of the BonaDent experience.

When: Saturday, June 11th 2011

Times: 7:30am - Continental Breakfast; 11:10-12:20 - Lunch

Course Time: 8:30 – 4:30 PM

A delicious breakfast and lunch at Angelo's Cafe are included.

E-mail Tina Rook or call 800.732.6222 for registration information.

Tensol, Tensol

TENSOL-3-A/B

Our Pledge:

Subject to your instructions, we undertake to supply you with p/n TENSOL-3-A/B in good order and on time and with all the mandatory certification of both the manufacturer and our own. We shall advise you of expiry date of p/n TENSOL-3-A/B and do our utmost to meet your expectations in getting your material to you as rapidly as possible.

We not only stock p/n TENSOL-3-A/B but also thousands of other parts and materials for Airbus, Boeing, McDonald Douglas, Embraer, ATR, Fokker and Bombardier. Our globally-respected company serves over 400 airlines and MRO's in 5 continents. We do so around the clock 24 hours a day, 365 days a year and have done so for the last 20 years. Our motto is "Material should wait for the aircraft and not aircraft for the material" and we look forward to being at your service.

Shipping:

Our shipping partner FedEx (Federal Express), the preferred carrier which handles hazardous materials, will ensure that your chosen product TENSOL-3-A/B reaches you in the fastest and safest possible way. Check shipping for TENSOL-3-A/B via FedEx Check shipping for TENSOL-3-A/B via UPS

The information provided with TENSOL-3-A/B:

We undertake to provide MSDS & TDS with TENSOL-3-A/B . provided on availability.

Victrix, Victrix

victrix

References Edit

victrix in Charlton T. Lewis & Charles Short (1879) A Latin Dictionary. Oxford: Clarendon Press

victrix in Charlton T. Lewis (1891) An Elementary Latin Dictionary. New York: Harper & Brothers

victrix in Felix Gaffiot ( 1934 ), Dictionnaire Illustre Latin-Francais . Paris: Hachette.

victrix in Harry Thurston Peck, editor (1898) Harper's Dictionary of Classical Antiquities. New York: Harper & Brothers

victrix in William Smith, editor (1848) A Dictionary of Greek Biography and Mythology. London: John Murray

Wiktionary ®

Welcome To The Clipper Group S Home Page, Clipper

Established in 1993 in Wellesley, Mass. and since 2010 in Rye, NH, we are technology acquisition consultants, strategic advisors, and Internet publishers on enterprise-class information technology and infrastructure. We specialize in large servers (including mainframes , Linux , UNIX . and Windows ); enterprise storage solutions (including SAN, NAS, virtualization, tape, archiving, object management, software-defined storage management, and storage appliances); and enterprise software (applications, database management systems, and middleware), whether deployed in an enterprise or mid-sized data center or in the cloud.

We are independent consultants and do not sell information technology products (hardware, software, etc.). We serve two client sets, to the betterment of both:

Helping mid-sized and large enterprises make the best information technology procurement decisions, in terms of identified business objectives, by focusing on each client's specific situation and critical business requirements

Helping information technology vendors resolve strategic product and marketing issues by better understanding the business needs of the marketplace

The Clipper Group concentrates on critical issues and decisions for information technology buyers, vendors and investors. Our portfolio of services combines technology assessment with business process expertise, specializing in the following:

Technologies

Enterprise servers and systems

z Systems, Linux, UNIX, and Windows

Enterprise storage solutions

Network-Attached Storage (NAS)

Storage-Area Networks (SAN)

Storage management and virtualization

Tape solutions, including virtual tape

Object storage and archiving

Applications and Solutions

Enterprise business modeling

Data warehousing and data marts

Database management systems

E-commerce and e-business

Data center management

Enterprise systems/network management & security

Finance and banking systems

End User and Buyer Services

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Investors and investment advisors receive our insight into the marketplace and products of selected high-tech companies.

The Clipper Group's full-time consultants average more than 25 years of experience in solving business issues and technology problems for users and vendors of complex technology. Our capabilities are augmented by a team of staff consultants with significant experience across a broad spectrum of applications and environments.

Note: We do not do Clipper programming and are not associated with the Clipper software product, which is owned by Computer Associates .

The Clipper Group's commitment to customer satisfaction is second to none. If you need a down-to-earth consulting firm to help you make the best information technology decisions, please contact Mike Kahn, Managing Director, in strictest confidence:

Or Call 781-235-0085 Ext. 121 (Dial "121" when you hear the automated attendant.)

The Clipper Group is always looking for talented, self-motivated enterprise systems and solutions analysts and consultants to join the team, either fulltime or parttime. We are an equal opportunity employer.

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Oestraclin, Oestraclin

How Do I Use EstroGel?

Managing Estrogen Levels After Menopause

Today’s women are smart, well informed, and deserve to be the best they can be. And if the symptoms of menopause are negatively affecting your life, you have the choice to address them. Fortunately, there are many treatment options for you and your healthcare provider to consider—from lifestyle changes to hormone therapy (HT), including EstroGel 0.06% (estradiol gel).

EstroGel is an FDA-approved, bioidentical estrogen therapy (ET) gel, which means the estrogen in EstroGel is similar to the estrogen your body produces naturally. 1,2

EstroGel is the only non-patch transdermal  estrogen therapy  that provides relief of both moderate to severe hot flashes due to menopause  and  moderate to severe vaginal dryness, itching, and burning after menopause. 1

EstroGel delivers a consistent, effective dose which helps a woman manage some of her menopausal symptoms more easily, day in and day out.

Maybe that is why EstroGel is the #1 prescribed estrogen product in Europe and the #1 prescribed transdermal estrogen product in Canada. 3

Talk with your healthcare provider today about estrogen therapy and if a prescription for EstroGel is right for you. 

EstroGel ®  0.06% is approved by the FDA for use after menopause to reduce moderate to severe hot flashes and to treat moderate to severe menopausal changes in and around the vagina. If you use EstroGel only to treat your menopausal changes in and around your vagina, talk with your healthcare provider about whether a topical vaginal product would be better for you.

External Promotional Message

WHAT IS THE MOST IMPORTANT RISK INFORMATION I SHOULD KNOW ABOUT EstroGel ® (AN ESTROGEN HORMONE)?

Using estrogen-alone may increase your chance of getting cancer of the uterus (womb). Report any unusual vaginal bleeding right away while you are using EstroGel.  Vaginal bleeding after menopause may be a warning sign of cancer of the uterus (womb).  Your healthcare provider should check any unusual vaginal bleeding to find out the cause.

Do not use estrogen-alone to prevent heart disease, heart attacks, strokes or dementia (decline in brain function).

Using estrogen-alone may increase your chances of getting strokes and blood clots.

Using estrogen-alone may increase your chance of getting dementia, based on a study of women 65 years of age or older.

Do not use estrogens with progestins to prevent heart disease, heart attack, strokes or dementia.

Using estrogens with progestins may increase your chances of getting heart attacks, strokes, breast cancer, or blood clots.

Using estrogens with progestins may increase your chance of getting dementia, based on a study of women 65 years of age or older.

You and your healthcare provider should talk regularly about whether you still need treatment with EstroGel.

Do not start using EstroGel if you have unusual vaginal bleeding, currently have or have had certain cancers, had a stroke or heart attack, currently have or have had blood clots, currently have or have had liver problems, have been diagnosed with a bleeding disorder, are allergic to EstroGel or any of its ingredients, or think you may be pregnant.

Tell your healthcare provider if you have any unusual vaginal bleeding, have any other medical conditions, are going to have surgery or will be on bed rest, are breastfeeding, and about all the medicines you take.

Serious but less common side effects include heart attack, stroke, blood clots, dementia, breast cancer, cancer of the lining of the uterus (womb), cancer of the ovary, high blood pressure, high blood glucose, gallbladder disease, liver problems, changes in your thyroid hormone levels, and enlargement of benign tumors (“fibroids”).

Common side effects of estrogens include headache, breast pain, stomach or abdominal cramps, bloating, nausea and vomiting, hair loss, fluid retention, and vaginal yeast infection.

If you would like more information, talk with your healthcare provider.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www. fda. gov/medwatch, or call 1-800-FDA-1088.

Estrogen Therapy has evolved

References

EstroGel 0.06% (estradiol gel) [package insert]. Herndon, VA: ASCEND Therapeutics; 2014.

Files JA, Ko MG, Pruthi S. Bioidentical hormone therapy. Mayo Clin Proc . 2011;86(7):673-680.

Data on file, ASCEND Therapeutics.

Estradiol

Click for further information on drug naming conventions and International Nonproprietary Names .

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Norsic And Son, Inc, Norsic

About Us

Emil Norsic & Son was created in 1932 because a local trash collector was not picking up trash from Southampton estates. Emil Norsic saw the need for a reliable garbage collector and created a company based on exceptional service. More than 80 years later, the company continues to "go the extra mile" when providing service to its clients.

Emil Norsic & Son is now a full-service sanitation company, offering rubbish removal, dumpsters, and cesspool pumping and repairs. Phones are answered during business hours and emergency lines are monitored during evenings and weekends. Norsic understands that sanitation emergencies do not always happen during office hours and that customers want problems resolved quickly.

Norsic provides portable rental toilets for construction sites, sporting events, parties, horse shows, fairs, carnivals, benefits and galas. Norsic's Special Events Coordinator guides customers through the rental process and helps determine the amount of equipment that is needed, as well as the power and water supply requirements. Norsic also provides on-site monitoring to take care of any problems that may arise.

Some of Norsic's most challenging work is with film production companies. Norsic currently provides mobile luxury restrooms, showers and dressing rooms for more than 15 film production companies. Production companies have tight deadlines and ever-changing schedules based on script changes and weather conditions. In these cases, Norsic staff are on standby to make sure that trailers arrive on schedule. Norsic assigns a dedicated liaison to meet the needs of each production company.

Norsic staff have many stories about customer service. Skip Norsic recalls a client who dropped a precious ring – containing 22 diamonds, 22 sapphires and 22 rubies – down her sink. He was asked to locate the ring, which required climbing into the cesspool and sifting through liquid waste with a pool skimmer. In the end, Skip found the ring. Despite being covered in sewage, the ring's owner gave him a big hug!

"We are a service business," says Skip Norsic. "We try our best to get things right the first time. If we don't, I want to hear about it and fix it. We've earned the reputation of delivering to our customers, especially under difficult circumstances or tight deadlines. I think about my father and grandfather every day, and am proud to continue their legacy."

Garbage / Rubbish Removal Service / Dumpster Service for The Hamptons and Long Island, New York.

Any way you say it, it's garbage, and ever since 1932, folks on the East End of Long Island have turned to Emil Norsic & Son for a reliable, professional, and worry free way to dispose of that garbage. We haven't disappointed them because we have consistently delivered just that kind of service and we feel it's why we've been around longer than any other sanitation company in the area.

But we're also constantly looking for ways to improve our garbage removal service by offering flexible programs to accommodate our customers' specific needs, by keeping abreast of the latest technologies and equipment, and investing in a vigorous training program for our employees.

So if you are a year 'round resident, a seasonal resident, a small or a large business, a school district or other institution, Norsic has a trash removal program and the right equipment to take care of your sanitation requirements.

Call us for more information about pricing, pick up scheduling and of course, recycling. For your convenience, you may opt to have your monthly service fees charged directly to a credit card.

Special Offer for Norsic Customers

Rugged, 98 gal. capacity Tip Cart is the easy and efficient way to deal with household rubbish. Made of high-impact, stain resistant polyvinyl, the unit holds more than 3 times as much material as standard trashcans. The large sturdy wheels make easy work of relocating the Tipster, even when full.

Large mouth and fully articulated lid allows for larger trash bags to be disposed of easily. Each unit is heat stamped with a permanent, antitheft serial number.

Tipsters are available to Norsic customers at a special low price or even as a "loaner" for long-term contract customers. Call for details: 283-0604

Cipramil 20 - Mg Tablets, Cipramil

SCHEDULING STATUS: S5

PROPRIETARY NAME: (and dosage form)

CIPRAMIL 20 mg Tablets

COMPOSITION: Each tablet contains citalopram hydrobromide corresponding to 20 mg citalopram.

PHARMACOLOGICAL CLASSIFICATION: A 1.2 Psychoanaleptics (antidepressants)

PHARMACOLOGICAL ACTION: Citalopram is a bicyclic phthalane derivative with antidepressant effect. The substance is a racemate, in which one of the enantiomers is responsible for the effect. The pharmacodynamic effect is specifically related to a selective inhibition of serotonin (5-HT) uptake. Citalopram has no effect on the uptake of noradrenaline, dopamine or GABA. Moreover neither citalopram nor its metabolites have antidopaminergic, antiadrenergic, antiserotoninergic, antihistaminergic or anticholinergic (antimuscarinic) properties. After prolonged treatment, the 5-HT - uptake inhibitory efficacy is unchanged and citalopram does not induce changes in the density of neurotransmitter receptors at the recommended dosages. Citalopram has no effect on the cardiac conduction system, blood pressure or blood picture. Pharmacokinetic data are based on the racemate. The oral bioavailability is high (>80%). Maximum plasma levels are reached within 4 hours (interval 1 - 6 hours) after administration. A linear relationship has been demonstrated between steady-state plasma levels and administered dose and varies four-fold between individuals treated with the same dose. Steady state levels are reached within 1 - 2 weeks. The volume of distribution is about 14 L/kg. The protein binding is about 80%. Unchanged citalopram is a predominant compound in plasma. The metabolites have the same pharmacological effect as citalopram, but are less potent. It is not known whether the kinetics of the active enantiomer differs in patients, who are slow metabolisers of spartein/debrisoquine or mephenytoin. The biological half-life is about 36 hours (interval 28 - 42 hours). The systemic plasma clearance is about 0.4 L/min. Longer half-lives and decreased clearance value due to a reduced rate of metabolism have been demonstrated in elderly patients, and therefore these patients should be given a lower dose. Patients with reduced liver function have a slower elimination. Patients with reduced kidney function have a decreased elimination, especially by low creatinine clearance. The excretion proceeds with the urine. In steady-state about 30% of the administered dose is identified in the urine, 12% as unchanged substance. Citalopram is a weak inhibitor of the cytochrome P450 IID6 metabolic pathway with a consequent reduction in potential for adverse events and interactions.

INDICATIONS: Treatment of depression and prevention of relapse. Treatment of panic disorder with or without agoraphobia. Treatment of obsessive compulsive disorder (OCD).

CONTRA-INDICATIONS: Hypersensitivity to CIPRAMIL. Severely impaired renal function (creatinine clearance less than 20 mL/min). Safety in pregnancy and lactation has not been established.

WARNINGS: CIPRAMIL should not be given to patients receiving Monoamine Oxidase Inhibitors (MAOIs), or for 14 days after their discontinuation. MAOIs should not be introduced for seven days after discontinuation of CIPRAMIL . CIPRAMIL should be discontinued if the patient enters a manic phase. There is little clinical experience of concurrent use of CIPRAMIL and electroconvulsive treatment. CIPRAMILdoes not impair intellectual function or psychomotor performance. Nevertheless, patients who are depressed and require treatment may have an impaired ability to drive or operate machinery. They should be warned of the possibility and advised to avoid such tasks if so affected.

DOSAGE AND DIRECTIONS FOR USE: Adults: Treating Depression

CIPRAMIL should be administered as a single oral dose of 20 mg daily. Dependent on individual patient response this may be increased to a maximum of 60 mg daily. The dose may be taken in the morning or evening, not necessarily with food.

Duration of treatment The antidepressant effect usually sets in after 2 to 4 weeks. Treatment with antidepressants is symptomatic and must therefore be continued for an appropriate length of time, usually up to 6 months after recovery in order to prevent relapse. Treating Panic Disorder A single dose of 10 mg is recommended for the first week before increasing the dose to 20 mg daily. The dose may be further increased, up to a maximum of 60 mg daily, dependent on individual patient response. Treating OCD An initial dose of 20 mg is recommended. Although the dose effect has not been demonstrated this dose can be increased in increments of 20 mg to 60 mg daily, if necessary, based on clinical judgement. Duration of Treatment The onset of action in treating OCD is 2-4 weeks with further improvement over time. Elderly: The recommended daily dose is 20 mg. Dependent on individual patient response this may be increased to a maximum of 30 mg daily. Children up to the age of 18 years: Not recommended, as safety and efficacy have not been established in this population. Reduced hepatic function: Dosage should be halved. Reduced renal function: Dosage adjustment is not necessary in cases of mild or moderate renal impairment. Duration of treatment:

A treatment period of at least six months is usually necessary to minimise potential for relapse.

When stopping therapy the drug should be gradually withdrawn during a couple of weeks.

SIDE-EFFECTS AND SPECIAL PRECAUTIONS: The most commonly observed adverse events associated with the use of CIPRAMIL and not seen at an equal incidence among placebo-treated patients were: sweating, somnolence, nausea, tremor, dry mouth and asthenia. Adverse events usually decrease in intensity and frequency as the depressive state improves. Clinical evidence shows that citalopram is not associated with tachycardia or postural hypotension. A decrease in pulse rate has been reported. Common: Generally:

headache, sweating, asthenia/fatigue, tremor, weight loss/weight gain, dizziness

Circulation: palpitations Central nervous system: sleep disturbances, paraethesia, restlessness Gastro-intestinal . nausea, constipation, diarrhoea, dyspepsia, dry mouth Urogenital: micturition disorder Eyes: accommodation disturbances Less common: Generally: malaise, yawning Central nervous system: agitation, confusion, impaired concentration, decreased libido, ejaculation disorder, mania. Gastro-intestinal: salivation Skin: rash Respiratory system: nose congestion Eyes: mydriasis Very rare: Convulsions, hepatitis, serotonin syndrome, neuroleptic malignant syndrome. Interactions: Simultaneous administration of MAOIs (see Warnings). There was no interaction with lithium. Citalopram interacts with imipramine, moclobemide, selegiline and sumatriptan. The weak inhibition of the sparteine metabolism will have only a minor effect on the elimination of agents which are dependent on the sparteine oxygenase. No pharmacodynamic interactions have been found in clinical studies in which citalopram has been given concomitantly with benzodiazepines, neuroleptics, analgesics, lithium, antihistamines, antihypertensive agents, betablockers and other cardiovascular agents. In animal studies cimetidine had little or no influence on citalopram kinetics. Plasma protein binding of citalopram is 80%. The potential for interactions with agents which are highly protein bound is thought to be minimal.

KNOWN SYMPTOMS OF OVERDOSAGE AND PARTICULARS OF ITS TREATMENT: Overdosage may give rise to tiredness, weakness, sedation, dizziness, tremor, nausea and somnolence. Treatment is symptomatic and supportive. Gastric lavage should be carried out as soon as possible after oral ingestion. Medical surveillance for about 24 hours is advisable.

IDENTIFICATION: Oval (8 x 5.5 mm), white, scored, film-coated and marked “C”and “N”symmetrically around the score.

PRESENTATION: Blister packs containing 28 tablets.

STORAGE INSTRUCTIONS: Store below 25°C. Keep out of reach of children.

REGISTRATION NUMBER: 29/1.2/0232

NAME AND BUSINESS ADDRESS OF THE APPLICANT: H. Lundbeck (Pty) Ltd 372 Oak Avenue Ferndale RANDBURG

DATE OF PUBLICATION OF THIS PACKAGE INSERT: 17 November 2001

Updated on this site: February 2004 Current: December 2004 Source: Community Pharmacy SAEPI HOME PAGE TRADE NAME INDEX GENERIC NAME INDEX FEEDBACK Information presented by Malahyde Information Systems © Copyright 1996-2004

Dermoph Llc, Lipostop

A reduction in the circumference of treated areas of more than 3 cm after 60 days during certification testing; the sample expressed 100% satisfaction with results.

LIPOSTOP CREAM Specific cream treatment to deal with fatty tissues and cellulite. The exclusive patented Fito Kylip® phytocomplex effectively solves and prevents problems caused by localized build-up of fatty tissues, plus intense sculpturing, draining and toning action. Good vasodilating action: your skin becomes red and hot for a short period due to the physiological increase in the micro-circulation to encourage the consumption of fat reserves. The result: Long-lasting effective reduction in the circumference of the treated area; a better, slimmer and more harmonious figure in just a short period; smoother, more supple skin.

LIPOSTOP GEL A fast absorbing, non-greasy gel treatment. No vasodilating effect. Especially suited to sensitive, delicate skin. The exclusive patented Fito Kylip® phytocomplex effectively solves problems caused by localized fatty tissues, encouraging the metabolism of built-up fat. Synephrine, Ginkgo Biloba phytosomes, Vitamin E and Grape (Vitis Vinifera) polyphenols stimulate the micro-circulation and guarantee more compact and firmer skin. The result: Long-lasting effective reduction in the circumference of the treated area; an immediately better sculpted, slimmer and firmer silhouette.

LIPOSNELL dietary supplement Liposnell is a dietary supplement based on plant extracts and nutrients to encourage your body's metabolism. Ideal for use as part of a slimming diet. Carnitine encourages the production of energy for cells, carrying fatty acids to the areas where these are then metabolized.

Lipostop Fast Patch Slimming patch with targeted action against localized problems caused by fatty tissues. Thanks to the exclusive patented Fitokilip® complex and Phosphate Dil Colina, this patch acts constantly and continuously on localized fat, also preventing its build-up. Discrete to wear, it guarantees that the active principles are released within just 40 minutes from application. For progressive and persistent results. The exclusive Dermophisiologique formulation is 100% paraben/preservative free. No counter-indications. Certified slimming action.

Use: Apply to dry skin for at least 40 minutes.

Cefpodoxime - Side Effects, Dosage, Interactions, Cefpodoximum

Cefpodoxime

Cefpodoxime is in a group of drugs called cephalosporin (SEF a low spor in) antibiotics. It works by fighting bacteria in your body.

Cefpodoxime is used to treat many different types of infections caused by bacteria.

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

Do not take this medication if you are allergic to cefpodoxime, or to similar antibiotics, such as Ceftin, Cefzil, Keflex, Omnicef, and others.

Before taking this medication, tell your doctor if you are allergic to any drugs (especially penicillin). Also tell your doctor if you have kidney disease or a history of intestinal problems.

Take this medication for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Cefpodoxime will not treat a viral infection such as the common cold or flu.

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or has blood in it, call your doctor. Do not use any medicine to stop the diarrhea unless your doctor has told you to.

Do not take this medication if you are allergic to cefpodoxime or to other cephalosporin antibiotics, such as:

cefaclor (Raniclor);

cefadroxil (Duricef);

cefazolin (Ancef);

cefdinir (Omnicef);

cefditoren (Spectracef);

cefixime (Suprax);

cefprozil (Cefzil);

ceftibuten (Cedax);

cefuroxime (Ceftin);

cephalexin (Keflex); or

cephradine (Velosef); and others.

Before taking cefpodoxime, tell your doctor if you are allergic to any drugs (especially penicillins) or if you have:

kidney disease (or if you are on dialysis); or

a history of intestinal problems, such as colitis.

If you have any of these conditions, you may need a dose adjustment or special tests to safely take this medication.

FDA pregnancy category B. This medication is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment.

Cefpodoxime passes into breast milk and could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Cefpodoxime Side Effects

Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Take this medicine with a full glass of water.

The cefpodoxime tablet should be taken with food.

Cefpodoxime oral suspension (liquid) can be taken with or without food.

Shake the liquid well just before you measure a dose. To be sure you get the correct dose, measure the liquid with a marked measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

This medication can cause you to have false results with certain medical tests, including urine glucose (sugar) tests. Tell any doctor who treats you that you are using cefpodoxime.

Take cefpodoxime for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Cefpodoxime will not treat a viral infection such as the common cold or flu.

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

Store cefpodoxime oral liquid in the refrigerator. Do not allow it to freeze. Throw away any unused medication that is older than 14 days.

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

Overdose symptoms may include nausea, vomiting, stomach pain, and diarrhea.

Take the medication as soon as you remember the missed dose. If it is almost time for your next dose, skip the missed dose and use the medicine at your next regularly scheduled time. Do not use extra medicine to make up the missed dose.

Copyright 1996-2016 Cerner Multum, Inc.

Latest Update: 9/3/2016, Version: 5.03

Navixen Plus 600 Mg, Navixen Plus

NAVIXEN PLUS 600 mg/12,5 mg COMPRIMIDOS RECUBIERTOS CON PELICULA

QUE ES NAVIXEN plus Y PARA QUE SE UTILIZA

NAVIXEN plus es un medicamento que se utiliza para el tratamiento de la tension arterial elevada. Contiene una asociacion de dos principios activos, eprosartan e hidroclorotiazida (HCTZ). Eprosartan y HCTZ disminuyen la tension arterial, tanto conjuntamente como por separado. Eprosartan pertenece a un grupo de farmacos denominados “antagonistas de los receptores de la angiotensina II”. La angiotensina II es una sustancia que se produce en el organismo y provoca la constriccion de los vasos sanguineos. Esto dificulta el flujo de sangre a traves de los vasos sanguineos, con el consiguiente aumento de la tension arterial. Eprosartan bloquea la accion de la angiotensina II, de manera que los vasos sanguineos se relajan y la tension arterial disminuye. El segundo principio activo, HCTZ, pertenece a un grupo de farmacos denominados “diureticos tiazidicos”. HCTZ incrementa la excrecion urinaria, disminuyendo asi tambien la tension arterial. NAVIXEN plus se utiliza: para el tratamiento de la tension arterial elevada no organica (hipertension esencial). Este producto de asociacion se utiliza en pacientes cuya tension arterial no disminuye suficientemente con eprosartan solo. 2.

ANTES DE TOMAR NAVIXEN plus

No tome NAVIXEN plus - si es alergico (hipersensible) a eprosartan, HCTZ y otras sulfonamidas o a cualquiera de los demas componentes de NAVIXEN plus - si esta embarazada de mas de 3 meses (es tambien mejor evitar NAVIXEN Plus al inicio del embarazo – ver la seccion de embarazo) - si tiene enfermedad del higado o del rinon grave - si tiene niveles altos de calcio o bajos de potasio o sodio que no han respondido al tratamiento - si tiene cualquier tipo de obstruccion de la vesicula biliar o de las vias biliares, como por ejemplo calculos biliares. - si tiene gota u otros sintomas de aumento de acido urico en sangre Consulte a su medico si no esta seguro de encontrarse en alguno de estos casos. Tenga especial cuidado con NAVIXEN plus - si tiene estrechamiento de las arterias renales, enfermedad renal o le han hecho un transplante de rinon. Puede ser necesario que su medico le analice los niveles de potasio, creatinina y acido urico en sangre. - si esta tomando medicinas que aumentan el nivel de potasio en sangre - si tiene un defecto cardiaco, como p. ej. estrechamiento de las valvulas cardiacas o trastornos del musculo cardiaco - si tiene una enfermedad del higado - si tiene lupus eritematoso sistemico - si tiene diabetes. Puede ser necesario adaptar la dosis de su tratamiento antidiabetico - si tiene una produccion excesiva de aldosterona - si usted es de raza negra (en este caso, el farmaco es aparentemente menos eficaz) - si tiene antecedentes de alergia o asma bronquial. Informe a su medico si piensa que esta embarazada (o planea estarlo). NAVIXEN Plus no esta recomendado al inicio de la gestacion y no debe tomarse si esta de mas de 3 meses de gestacion, ya que puede causar graves danos al bebe si se encuentra en esta fase (ver seccion de embarazo). Signos tales como una sed excesiva, sequedad de boca, debilidad general, somnolencia, dolor muscular o calambres, nauseas, vomitos y diarrea, o una frecuencia cardiaca anormalmente rapida indican, a veces, un efecto excesivo del principio activo HCTZ de NAVIXEN plus. Si usted presenta cualquiera de estos sintomas, debe consultar a su medico. Es posible que este le analice los niveles de electrolitos en sangre. En caso de que usted este siguiendo una dieta baja en sal, tome altas dosis de diureticos o tenga vomitos o diarrea, su volumen sanguineo o sus niveles de sodio en sangre podrian haber descendido. Esta situacion se debe corregir antes de comenzar el tratamiento con NAVIXEN plus. El tratamiento con NAVIXEN plus se debe interrumpir antes de realizar una prueba de la funcion paratiroidea. Consulte con su medico si se encuentra en este caso. HCTZ puede producir un resultado positivo en una prueba del dopaje. Uso de otros medicamentos Informe a su medico o farmaceutico si esta utilizando o ha utilizado recientemente otros medicamentos, incluso los adquiridos sin receta. Los medicamentos que contengan litio no se deben tomar con NAVIXEN plus excepto si su medico lo considera necesario y monitoriza cuidadosamente el nivel de litio en sangre. No se recomienda el uso simultaneo de NAVIXEN plus con medicamentos que puedan afectar los niveles de potasio en sangre. Pueden ser necesarias medidas especiales de precaucion (p. ej. analisis de sangre) si usted tiene que tomar suplementos de potasio, sustitutos de la sal que contengan potasio o medicamentos ahorradores de potasio, medicamentos que incrementen los niveles sericos de potasio (p. ej. heparina, inhibidores de la ECA), laxantes, medicamentos para la gota (p. ej. probenecida, sulfinpirazona), medicamentos para la diabetes (medicamentos orales como la metformina; insulina), medicamentos para controlar el ritmo del. corazon, algunos antipsicoticos, sales de calcio, esteroides, algunos antibioticos (tetraciclinas). Dependiendo del resultado de dichas medidas, puede que sea necesario adaptar el tratamiento previo. El uso concomitante de NAVIXEN plus con glicosidos cardiacos (p. ej. digitalis) puede favorecer la aparicion de irregularidades en el ritmo cardiaco. El efecto de disminucion de la tension arterial de NAVIXEN plus puede ser potenciado por ciertos medicamentos inductores del sueno, sedantes, narcoticos, el alcohol, algunos farmacos utilizados para tratar la enfermedad de Parkinson, relajantes musculares (p. ej. baclofeno), medicamentos protectores celulares (p. ej. amifostina), atropina u otros medicamentos que tambien poseen un efecto de disminucion de la tension arterial. El efecto de disminucion de la tension arterial de NAVIXEN plus puede ser atenuado por los calmantes para el dolor, algunos antiinflamatorios (p. ej. AINEs como el acido acetilsalicilico (> 3 g/dia)) o algunos medicamentos que actuan contra el exceso de grasa en la sangre (p. ej. colestipol, colestiramina). Si usted toma NAVIXEN plus junto con beta-bloqueantes o diazoxido, le puede aumentar el nivel de azucar en sangre. El efecto de las aminas presoras (p. ej. noradrenalina) puede disminuir. Pueden potenciarse los efectos adversos de los medicamentos utilizados para tratar el cancer (p. ej. ciclofosfamida, metotrexato), asi como del virostatico y antiparkinsoniano amantadina. Toma de NAVIXEN plus con los alimentos y bebidas Los comprimidos pueden tomarse con o sin comida. El consumo de alcohol puede reducir la tension arterial y hacer que usted se sienta cansado o mareado. Debe informar a su medico en caso de que este siguiendo una dieta baja en sal. Embarazo y lactancia Consulte a su medico o farmaceutico antes de tomar cualquier medicamento. Embarazo Informe a su medico si piensa que esta embarazada (o planea estarlo). Su medico normalmente le avisara de que deje el tratamiento con NAVIXEN Plus antes de quedar en estado o tan pronto como usted sepa que esta embarazada y le avisara de que tome otro medicamento en lugar de NAVIXEN Plus. NAVIXEN Plus no esta recomendado al inicio del embarazo, y no debe tomarse con mas de 3 meses de gestacion, ya que puede causar graves danos a su bebe si se usa despues del tercer mes de gestacion. Lactancia Informe a su medico si esta en periodo de lactancia o a punto de iniciar la lactancia. NAVIXEN Plus no esta recomendado a las madres que estan en periodo de lactancia, y su medico puede escoger otro tratamiento para usted si usted desea lactar, en particular si su bebe es recien nacido o prematuro. Conduccion y uso de maquinas No es probable que NAVIXEN plus afecte su capacidad para conducir o utilizar maquinas. Sin embargo, en ocasiones se puede sentir cansancio o mareos durante el tratamiento de la tension arterial alta. Si usted padece estos sintomas, debe consultar a su medico antes de conducir o utilizar maquinas. Informacion importante sobre algunos de los componentes de NAVIXEN plus. Este medicamento contiene lactosa. Si su medico le ha comunicado que usted tiene intolerancia a algunos azucares, consulte con el antes de tomar este medicamento. 3.

COMO TOMAR NAVIXEN plus

Siga exactamente las instrucciones de administracion de NAVIXEN plus de su medico. Consulte a su medico o farmaceutico si tiene dudas. La dosis normal es de un comprimido, una vez al dia, por la manana. Ingiera los comprimidos con una cantidad suficiente de agua. Intente tomar siempre los comprimidos a la misma hora. Es importante que siga tomando los comprimidos hasta que su medico le indique lo contrario. NAVIXEN plus no debe administrarse a ninos y adolescentes menores de 18 anos. Si usted toma mas NAVIXEN plus del que debiera Consulte inmediatamente con su medico o acuda a urgencias del hospital mas cercano si se toma accidentalmente demasiados comprimidos o un nino se traga algun comprimido. En caso de sobredosis o ingestion accidental, consultar al Servicio de Informacion Toxicologica. Telefono: 91.562.04.20. Si olvido tomar NAVIXEN plus Si olvida tomar algun comprimido, tomelo tan pronto como pueda y reanude el tratamiento de forma habitual. Si olvida tomar un comprimido un dia, espere al dia siguiente, a la hora habitual, para tomar su dosis. No tome una dosis doble para compensar las dosis olvidadas. Si interrumpe el tratamiento con NAVIXEN plus No interrumpa el tratamiento con NAVIXEN plus usted mismo. Consulte con su medico si no esta satisfecho con el efecto de NAVIXEN plus.4.

POSIBLES EFECTOS ADVERSOS

Al igual que todos los medicamentos, NAVIXEN plus puede tener efectos adversos, aunque no todas las personas los sufran. En la lista siguiente de posibles reacciones adversas, se indica cual es la probabilidad de que usted presente dichas reacciones adversas: muy frecuente: mas de 1 entre 10 pacientes pueden experimentar ese efecto adverso frecuente: menos de 1 entre 10 pero mas de 1 entre 100 pacientes pueden experimentar ese efecto adverso poco frecuente: menos de 1 entre 100 pero mas de 1 entre 1.000 pacientes pueden experimentar ese efecto adverso raro: menos de 1 entre 1.000 pero mas de 1 entre 10.000 pacientes pueden experimentar ese efecto adverso muy raro: menos de 1 entre 10.000 pacientes pueden experimentar ese efecto adverso. Trastornos del sistema nervioso: Frecuentes: mareos, dolor de cabeza, neuralgia (dolor en el trayecto de los nervios), sensacion de. hormigueo, insomnio, fatiga, intranquilidad, depresion Poco frecuentes: ansiedad, nerviosismo Trastornos cardiacos: Poco frecuentes: alteraciones del ritmo cardiaco Trastornos vasculares: Muy raros: reduccion de la tension arterial (hipotension) o mareo al levantarse Trastornos del tracto respiratorio superior: Frecuentes: bronquitis Poco frecuentes: tos, hemorragia nasal, dolor de garganta, molestia nasal, infeccion del tracto respiratorio superior Trastornos gastrointestinales: Frecuentes: dolor del abdomen Poco frecuentes: gastroenteritis (inflamacion del estomago y del intestino delgado), nauseas Trastornos de la piel: Poco frecuentes: erupcion Muy raros: picor Trastornos musculares y de los huesos: Frecuentes: enfermedad degenerativa de las articulaciones, dolor de espalda Poco frecuentes: dolor de articulaciones, artritis Trastornos urinarios: Frecuentes: excrecion de proteina por la orina, infecciones del tracto urinario Otros trastornos: Poco frecuentes: hinchazon de los tobillos, fiebre, sequedad de boca, sudoracion Pruebas de laboratorio: Frecuentes: enzimas hepaticos aumentados, niveles de potasio aumentados, niveles de azucar aumentados, recuento de leucocitos en sangre aumentado Los pacientes que tomaron solo eprosartan, presentaron ademas las siguientes reacciones adversas: Frecuentes: dolor del pecho, palpitaciones (latidos rapidos del corazon) Poco frecuentes: problemas en la respiracion, aumento de grasas (trigliceridos) en sangre Raros: incremento de urea en sangre, urticaria Muy raros: reacciones alergicas (p. ej. hinchazon de la cara, inflamacion de la piel y membranas mucosas, lengua o faringe, con dificultad para tragar o respirar). Si usted cree que le esta ocurriendo alguna de estas reacciones, acuda al medico inmediatamente. Los pacientes que tomaron solo HCTZ, mayoritariamente a dosis superiores a las que se encuentra en NAVIXEN plus, presentaron las siguientes reacciones adversas no mencionadas anteriormente: Perdida de apetito, irritacion gastrica, vomitos, calambres en el estomago, diarrea, estrenimiento, ictericia (coloracion amarillenta de la piel o de los ojos), inflamacion del pancreas, somnolencia, trastornos de la vision, alteraciones de las celulas de la sangre: disminucion de los leucocitos de la sangre, granulocitos y plaquetas, alteraciones de la formacion de los globulos rojos de la sangre; niveles disminuidos de sodio. potasio, magnesio y cloruro en la sangre, niveles aumentados de acido urico, calcio y colesterol (grasas) en sangre, gota, trastornos del rinon, inflamacion del rinon, insuficiencia renal aguda, inflamacion de los pulmones, edema pulmonar, sensibilidad a la luz, inflamacion de las paredes de los vasos sanguineos, formacion de ampollas en la piel que contienen celulas muertas de la piel (necrolisis epidermica toxica), lupus eritematoso sistemico, calambres musculares, debilidad, disfuncion sexual y/o cambios en la libido, reacciones alergicas. Si considera que alguno de los efectos que sufre es grave o si aprecia cualquier efecto adverso no mencionado en este prospecto o si sufre uno de los efectos adversos descritos de forma grave, informe a su medico o farmaceutico.5.

CONSERVACION DE NAVIXEN plus

Mantenga NAVIXEN plus fuera del alcance y de la vista de los ninos. No use NAVIXEN plus despues de la fecha de caducidad que aparece en la caja y en el blister. Los medicamentos no se deben tirar a las aguas residuales o a la basura. Pregunte a su farmaceutico como deshacerse de los medicamentos que no necesita. De esta forma ayudara a proteger el medio ambiente.6.

INFORMACION ADICIONAL

?Que contiene NAVIXEN plus? - Los principios activos son 600 mg de eprosartan (en forma de mesilato) y 12,5 mg de hidroclorotiazida por comprimido. - Los demas componentes son: Nucleo del comprimido: lactosa monohidrato, celulosa microcristalina, almidon pregelatinizado (de maiz), crospovidona, estearato de magnesio y agua purificada. Recubrimiento: alcohol polivinilico, talco, dioxido de titanio (E 171), macrogol 3350, oxido de hierro amarillo (E 172) y oxido de hierro negro (E 172). Aspecto del producto y tamano del envase Comprimidos recubiertos blanco-amarillentos, con forma de capsula. Los comprimidos tienen la inscripcion “5147” en una de las caras. NAVIXEN plus esta envasado en blisters que contienen 28 comprimidos. Titular de la autorizacion de comercializacion y responsable de la fabricacion El titular del medicamento es: FERRER INTERNACIONAL, S. A. Gran Via Carlos III, 94 08028 Barcelona - Espana El responsable de la fabricacion del medicamento es: Abbott Healthcare S. A.S. Route de Belleville Lieu dit Maillard F - 01400 Chatillon-sur-Chalaronne, Francia.

Este prospecto ha sido aprobado en junio de 2010

ABDOMEN . Es la cavidad delimitada, por arriba, por el diafragma por abajo, por los huesos y musculos de la pelvis: por detras, por la columna vertebral y sus musculos y por los lados y por delante, por los musculos que se tienden entre las costillas, la pelvis y la columna vertebral.

EDEMA . Es la tumefaccion de los tejidos debido a un aumento del liquido existente en ellos y suele aparecer tras una lesion.

GASTROENTERITIS . Es la inflamacion del estomago (gastritis) y del intestino (enteritis).

ICTERICIA . Es la pigmentacion amarilla del blanco de los ojos o de la piel, provocada por un exceso de bilirrubina en la sangre que acaba depositandose en los tejidos.

NEURALGIA . Termino que se utiliza para describir las distintas formas de dolorprovocadas por la presion sobre un nervio o por una alteracion funcional.

PALPITACIONES . Este termino significa que la persona percibe el latido de su corazon, lo que ocurre a menudo durante la quietud de la noche.

SANGRE . El organismo contiene alrededor de 7 litros de sangre, compuesta en un 50% por plasma y en otro 50% por celulas.

URTICARIA . Existen multiples causas de la urticaria, pero la erupcion se caracteriza siempre por ronchas rojas pruriginosas.

Opiniones

Retirides, Retirides

Retirides

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Lisinopril - Blood Pressure, Eupril

Lisinopril is used to treat high blood pressure (hypertension) in adults and children 6 years and older, including renovascular, acute myocardial infarction in clinically stable condition of the patients, heart failure (adjuvant treatment), diabetic nephropathy. The principle of this drug is to relax blood vessels, causing them to expand, it can lead to prevention of occurrence of strokes, heart attacks and kidney problems. Lisinopril is also used after acute myocardial recovery, and is used with other drugs (eg, "water pills" / diuretics, digoxin) to treat heart failure. This drug belongs to a class of medications called ACE inhibitors.

Dosage and direction Take medicine for adults 1 time a day. The dose is determined individually, depending on the evidence, the state of renal function and concomitant therapy. Typically, the initial dose is 2,5-5 mg, the average maintenance dose - 5-20 mg, the maximum daily - 80 mg.

Precautions Treatment is carried out under regular medical supervision (water-electrolyte balance). The process of treatment requires monitoring of blood pressure, protein level and plasma potassium, urea nitrogen, creatinine, renal function, blood picture, body weight and dieting. You have to be careful during surgery (including dental), especially when using general anesthetics that have a hypotensive effect.

Hypersensitivity, pregnancy, breast-feeding.

Possible side effects You can feel headache, dizziness, nervousness, fainting, drowsiness, insomnia, tremors, convulsions, visual disturbances, palpitations, chest pain, hypotension, arrhythmia, dry cough and malignant tumors of the lung, hemoptysis, pain when breathing, bronchitis, dry mouth, indigestion, heartburn, vomiting, diarrhea / constipation, bloating, abdominal pain, renal failure, weakening of libido, impotence, arthritis, neck pain, back pain, rash, urticaria, and syndrome of Stevens - Johnson.

Drug interactions List of the drugs that can interact with Lisinopril: gold injections to treat arthritis, lithium (Lithobid, Eskalith), a potassium supplement such as K-Dur, Klor-Con, salt substitutes that contain potassium, insulin or diabetes medication you take by mouth, aspirin or other NSAIDs (non-steroidal anti-inflammatory drugs) such as ibuprofen (Motrin, Advil), diclofenac (Voltaren), etodolac (Lodine), indomethacin (Indocin), ketoprofen (Orudis), naproxen (Aleve, Naprosyn), and others, or a diuretic (water pill).

Missed dose Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Overdose Seek emergency medical attention if you think you have used too much of this medicine. Lisinopril overdose symptoms may include feeling extremely dizzy or light-headed, or fainting.

Storage Store Lisinopril at room temperature away from moisture and heat.

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

Lisinopril is used to treat high blood pressure (hypertension) in adults and children 6 years and older, including renovascular, acute myocardial infarction in clinically stable condition of the patients, heart failure (adjuvant treatment), diabetic nephropathy. The principle of this drug is to relax blood vessels, causing them to expand, it can lead to prevention of occurrence of strokes, heart attacks and kidney problems. Lisinopril is also used after acute myocardial recovery, and is used with other drugs (eg, "water pills" / diuretics, digoxin) to treat heart failure. This drug belongs to a class of medications called ACE inhibitors.

Dosage and direction Take medicine for adults 1 time a day. The dose is determined individually, depending on the evidence, the state of renal function and concomitant therapy. Typically, the initial dose is 2,5-5 mg, the average maintenance dose - 5-20 mg, the maximum daily - 80 mg.

Precautions Treatment is carried out under regular medical supervision (water-electrolyte balance). The process of treatment requires monitoring of blood pressure, protein level and plasma potassium, urea nitrogen, creatinine, renal function, blood picture, body weight and dieting. You have to be careful during surgery (including dental), especially when using general anesthetics that have a hypotensive effect.

Hypersensitivity, pregnancy, breast-feeding.

Possible side effects You can feel headache, dizziness, nervousness, fainting, drowsiness, insomnia, tremors, convulsions, visual disturbances, palpitations, chest pain, hypotension, arrhythmia, dry cough and malignant tumors of the lung, hemoptysis, pain when breathing, bronchitis, dry mouth, indigestion, heartburn, vomiting, diarrhea / constipation, bloating, abdominal pain, renal failure, weakening of libido, impotence, arthritis, neck pain, back pain, rash, urticaria, and syndrome of Stevens - Johnson.

Drug interactions List of the drugs that can interact with Lisinopril: gold injections to treat arthritis, lithium (Lithobid, Eskalith), a potassium supplement such as K-Dur, Klor-Con, salt substitutes that contain potassium, insulin or diabetes medication you take by mouth, aspirin or other NSAIDs (non-steroidal anti-inflammatory drugs) such as ibuprofen (Motrin, Advil), diclofenac (Voltaren), etodolac (Lodine), indomethacin (Indocin), ketoprofen (Orudis), naproxen (Aleve, Naprosyn), and others, or a diuretic (water pill).

Missed dose Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Overdose Seek emergency medical attention if you think you have used too much of this medicine. Lisinopril overdose symptoms may include feeling extremely dizzy or light-headed, or fainting.

Storage Store Lisinopril at room temperature away from moisture and heat.

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

Lisinopril is used to treat high blood pressure (hypertension) in adults and children 6 years and older, including renovascular, acute myocardial infarction in clinically stable condition of the patients, heart failure (adjuvant treatment), diabetic nephropathy. The principle of this drug is to relax blood vessels, causing them to expand, it can lead to prevention of occurrence of strokes, heart attacks and kidney problems. Lisinopril is also used after acute myocardial recovery, and is used with other drugs (eg, "water pills" / diuretics, digoxin) to treat heart failure. This drug belongs to a class of medications called ACE inhibitors.

Dosage and direction Take medicine for adults 1 time a day. The dose is determined individually, depending on the evidence, the state of renal function and concomitant therapy. Typically, the initial dose is 2,5-5 mg, the average maintenance dose - 5-20 mg, the maximum daily - 80 mg.

Precautions Treatment is carried out under regular medical supervision (water-electrolyte balance). The process of treatment requires monitoring of blood pressure, protein level and plasma potassium, urea nitrogen, creatinine, renal function, blood picture, body weight and dieting. You have to be careful during surgery (including dental), especially when using general anesthetics that have a hypotensive effect.

Hypersensitivity, pregnancy, breast-feeding.

Possible side effects You can feel headache, dizziness, nervousness, fainting, drowsiness, insomnia, tremors, convulsions, visual disturbances, palpitations, chest pain, hypotension, arrhythmia, dry cough and malignant tumors of the lung, hemoptysis, pain when breathing, bronchitis, dry mouth, indigestion, heartburn, vomiting, diarrhea / constipation, bloating, abdominal pain, renal failure, weakening of libido, impotence, arthritis, neck pain, back pain, rash, urticaria, and syndrome of Stevens - Johnson.

Drug interactions List of the drugs that can interact with Lisinopril: gold injections to treat arthritis, lithium (Lithobid, Eskalith), a potassium supplement such as K-Dur, Klor-Con, salt substitutes that contain potassium, insulin or diabetes medication you take by mouth, aspirin or other NSAIDs (non-steroidal anti-inflammatory drugs) such as ibuprofen (Motrin, Advil), diclofenac (Voltaren), etodolac (Lodine), indomethacin (Indocin), ketoprofen (Orudis), naproxen (Aleve, Naprosyn), and others, or a diuretic (water pill).

Missed dose Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Overdose Seek emergency medical attention if you think you have used too much of this medicine. Lisinopril overdose symptoms may include feeling extremely dizzy or light-headed, or fainting.

Storage Store Lisinopril at room temperature away from moisture and heat.

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

Kopen Clactirel (Biaxin) Zonder Recept, Clactirel

Clactirel (Biaxin) Kopen Online Zonder Recept

Clactirel (Biaxin) Toelichting

Clactirel wordt gebruikt om te gaan met verschillende soorten transmissies beinvloeden van uw huid en de ademhaling. Clactirel kan ook worden gebruikt samen met andere geneesmiddelen te behandelen buik zweren veroorzaakt door Helicobacter pylori.

Clactirel arguements ziektekiemen in je lichaam.

Clactirel kan ook worden aangeduid als Claritromycine, Maclar, Klaricid, Klacid, Clarimac, Claribid.

Algemeen Titel geassocieerd met Clactirel is eigenlijk Claritromycine.

Merken geassocieerd met Clactirel neiging om Clactirel, Clactirel XL, Clactirel XL-Pak zijn.

Clactirel (Biaxin) Dosis

Clactirel komt in:

250mg lagere dosis frictiemateriaal

500mg normale dosis frictiemateriaal

Clactirel komt in pillen, evenals tandheelkundige vertraging, pauze.

Get Clactirel via de mond.

Get Clactirel samen met complete kop in verband met het drinken van water.

Get Clactirel zonder of met maaltijden.

Meestal niet te malen, kauwen, of zelfs barsten de feitelijke Clactirel pil. Consumeer de pil hele.

Beeft de werkelijke Clactirel tandheelkundige vertraging, enige tijd wachten voordat het berekenen van de dosering. Bereken de werkelijke Clactirel tandheelkundige vertraging, pauzeren met een merkbare berekenen plaats of zelfs medicatie mok.

Get Clactirel met betrekking tot met betrekking tot de zeven, om de twee weken.

De werkelijke dosis en ook type geneesmiddel afhankelijk van de conditie en de aanbevolen therapie.

Meestal niet stoppen met behulp van Clactirel ineens.

Clactirel (Biaxin) ontbreekt in verband met de dosering

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

Clactirel (Biaxin) Overdose

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

Clactirel (Biaxin) Opslagruimte

Shop in de ruimte een temperatuur tussen twintig en vijfentwintig niveaus D (68 en zevenenzeventig niveaus F) tegen vocht en temperatuur. Handhaaf tekstvak stevig dicht. Beschermen door middel van verlichting. Versterken elke vorm van ongerepte medicatie na het verstrijken dag. Handhaven van het bereiken van kinderen.

Clactirel (Biaxin) Negatieve effecten

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

matige buik ongemak frictiemateriaal

misselijkheid of braken frictiemateriaal

het gooien van frictiemateriaal

diarree frictiemateriaal

geergerd buik frictiemateriaal

ongebruikelijk of zelfs ongemakkelijk smaak op je tanden frictiemateriaal

verkleuring frictiemateriaal

vermoeidheid frictiemateriaal

hoofdpijn frictiemateriaal

angstgevoelens frictiemateriaal

misverstanden frictiemateriaal

de porien en de huid allergie frictiemateriaal

genitale jeuk of zelfs frictiemateriaal

Veel minder typische en ernstige nadelige gevolgen voor de hele behulp Clactirel los:

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

ongelijke hartslagen; frictiemateriaal

hartproblemen frictiemateriaal

gebrek geassocieerd met ademhaling frictiemateriaal

sproeisysteem of zelfs zwakkeling uitwerpselen frictiemateriaal

buik ongemak wrijving materiaal

lagere temperatuur frictiemateriaal

gebrek aan honger frictiemateriaal

geelzucht frictiemateriaal

temperatuur frictiemateriaal

pijnlijke amandelen frictiemateriaal

hoofdpijn met een ernstige verzengende frictiemateriaal

rood-gekleurde huid allergie frictiemateriaal

problemen met het luisteren naar frictiemateriaal

Negatieve effecten indicaties worden afhankelijk van medicijnen die u zou kunnen gebruiken, maar bovendien rekenen op uw welzijn conditie en andere aspecten

Clactirel (Biaxin) Contra-indicaties

Meestal doen Clactirel niet te gebruiken in het geval dat u gevoelig bent om Clactirel elementen of claritromycine of vergelijkbare medicijnen bijvoorbeeld azitromycine (Zithromax), dirithromycin (Dynabac), erytromycine (E. Electronic. H. E-mycin, Ery-Tab, Erythrocin), troleandomycine (Tao).

Word voorzichtig als u op een andere manier je van plan bent om een ??kind te bezitten verwacht worden, anders wordt je echt een medische moeder.

Meestal niet gebruiken Clactirel voor astemizol (Hismanal), cisapride (Propulsid), ergot medicatie bijvoorbeeld ergotamine (Ergomar, Ergostat, Cafergot, Ercaf, Wigraine), of zelfs dihydroergotamine (D. Ze zouden. Elektronisch. vijfenveertig, Migranal neusspray), pimozide (Orap), terfenadine (Seldane).

speelt de rol van voorzichtig met Clactirel gebruik bij om ziekten in de lever, nier ziekte, myasthenia gravis, porfyrie; individu of zelfs genealogie geassocieerd met "Lange QT-syndroom".

Speel de rol van voorzichtige, samen met Clactirel gebruik moet u gebruik maken van elke vorm van voorgeschreven arts of zelfs nonprescription medicijnen, natuurlijke voorbereiding, of zelfs aan te vullen.

Voorkom alcoholische dranken.

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

Clactirel (Biaxin) Veelgestelde vragen

Queen: Wat is Clactirel precies?

De: Clactirel is echt een medicijn geassocieerd met macrolide anti-biotica team. Clactirel arguements ziektekiemen in je body. A

Queen: Precies wat met betrekking tot echt Clactirel benut?

De: Clactirel wordt gebruikt om te gaan met verschillende soorten transmissies beinvloeden van uw huid en de ademhaling. Clactirel kan ook worden gebruikt samen met andere geneesmiddelen te behandelen buik zweren veroorzaakt door Helicobacter pylori. A

Queen: Zeer beste algemene titel verbonden Clactirel?

De: General titel is eigenlijk Clarithromycin. A

Queen: Wat zijn de andere merken dan Clactirel?

De: Brands neiging om Clactirel, Clactirel XL, Clactirel XL-Pak. A zijn

Queen: Over welke soorten is eigenlijk Clactirel toegankelijk?

De: Clactirel komt in pillen, evenals tandheelkundige vertraging, pause. A

Queen: Precies wat moet ik fag situatie als gevolg van gebrek aan de werkelijke dosering?

De: In het geval van de dosering ontbreekt moet je om de pil zo snel mogelijk. Meestal geen dubbele dosis krijgen. En als het echt meest gelukkige tijd voor de dosis die u nodig hebt om te dragen op je eigen normale routine geassocieerd met Clactirel using. A

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Brief Info About Medicine

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

1 Why Is it Used ?

CLARITHROMYCIN :

Adult: PO Resp tract infections; Skin and soft tissue infections; Susceptible infections 250 mg twice daily, up to 500 mg twice daily for severe infections, for 7-14 days. Mycobacterium avium complex infections W/ other antimycobacterials: 500 mg twice daily. Leprosy As part of multidrug therapy: 500 mg/day. H. pylori infection W/ another antibacterial and either a proton pump inhibitor or H2 antagonist: 500 mg twice daily for 7-14 days. IV Resp tract infections; Skin and soft tissue infections; Susceptible infections 500 mg twice daily for 2-5 days.

2 What are the Side Effects ?

CLARITHROMYCIN :

GI upset, glossitis, stomatitis, altered taste; headache, dizziness, hallucinations, insomnia, other CNS effects; rash; hepatic dysfunction, Potentially Fatal: Pseudomembranous colitis, anaphylaxis, Stevens-Johnson syndrome.

3 What Precautions should be taken ?

CLARITHROMYCIN :

Renal and hepatic impairment; macrolide cross-resistance; lactation, children.

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

CLARITHROMYCIN :

Hypersensitivity. Patients receiving terfenadine, astemizole, pimozide, cisapride and ergot derivatives. Pregnancy; history of acute porphyria.

5 Interaction with other medicines.

CLARITHROMYCIN :

May potentiate oral anticoagulant action. May elevate serum-digoxin concentration. Potentially Fatal: Increases plasma concentrations of terfenadine or astemizole. Increases the risk of ventricular arrhythmias in patients with preexisting cardiac diseases.

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Amoxycare (Amoxicillin Trihydrate) - United Pharmacies, Amoxycare

Amoxycare

Description

Amoxycare (Amoxicillin Trihydrate) is a type of penicillin antibiotic used for feline and canine infections caused by bacteria. Its mechanism of action is interfering with bacterial cell wall synthesis. This medicine is able to work against many different strains of microorganisms, including both gram negative and gram positive. E. coli, Pasteurella spp. streptococci and many others which are considered susceptible to it.

Veterinarians often use it to treat cystitis and urethritis, as well as upper and lower respiratory infections such as sinusitis, pharyngitis and bronchitis. This semi-synthetic penicillin acts on the bacteria and it irreversibly damages the cell wall peptidoglycan (the amino acids which form the cell walls of the bacteria), which causes the cell walls to fall apart. As a result of this, the bacteria are unable to survive and the symptoms of the infection can be treated.

Dosage and Administration

Amoxycare (Amoxicillin Trihydrate) is provided in the form of 200mg strength tablets which are intended for administration to the pet by mouth. Owners may either give the tablet directly to their animal or else mix it in with the food. Veterinarians generally calculate the correct dosage based on the animal`s weight at a rate of 10mg per kilogram (equal to one 200mg tablet per 20 kilogram), administered twice per day for a period of 7 days. As the dosage can vary for each animal, it will be necessary to follow the instructions given by the veterinarian.

Use of Amoxycare (Amoxicillin Trihydrate) in pets might lead to side effects in some cases, however this is not considered extremely common. Observe your animal carefully and take it to the veterinarian if it appears to be suffering from side effects.

Amoxycare (Amoxicillin Trihydrate) is a veterinary product which is approved for use in animals only. It is not to be taken by humans.

If your animal does not get better after treatment, the veterinarian may recommend other treatment options.

Tamoxifen - Woman S Health, Bioxifeno

Tamoxifen is used for treating breast cancer that has spread to other sites in the body. It is also used along with other medicines to treat other types of breast cancer. It is used in women who are at high risk of breast cancer and in women with DCIS (after surgery and radiation) to decrease the risk of developing breast cancer. It may also be used for other conditions as determined by your doctor.

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

Tamoxifen comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Tamoxifen refilled.

Tamoxifen may be taken by mouth with or without food.

Take Tamoxifen with water or another nonalcoholic liquid.

Swallow this medication whole. Do not break, crush, or chew before swallowing.

Continue taking Tamoxifen even if you feel well. Do not miss any doses. Take Tamoxifen at the same time each day.

Drug Class and Mechanism

Tamoxifen is an antiestrogen. It works by blocking the effect of estrogen on certain tumors. This may prevent the growth of tumors that are activated by estrogen.

If you miss a dose of Tamoxifen, 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 Tamoxifen between 68 and 77 degrees F (20 and 25 degrees C) in a tightly closed, light-resistant container. Store away from moisture, heat, and light. Do not store in the bathroom. Do not take tablets after the expiration date printed on the label. Keep Tamoxifen out of the reach of children and away from pets.

Do NOT use Tamoxifen if: you are allergic to any ingredient in Tamoxifen you are using Tamoxifen to reduce your risk of breast cancer and you have a history of blood clots in the lung or leg you are using Tamoxifen to reduce your risk of breast cancer and you also take certain anticoagulants (eg, warfarin) you are taking anastrozole Some medical conditions may interact with Tamoxifen. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have a history of blood clots in the legs or lungs if you have high levels of calcium in your blood, a weakened immune system, or low levels of white blood cells or platelets in your blood if you have high cholesterol or lipid levels if you have cataracts or other vision problems if you are using cytotoxic cancer medicines if you are confined to a bed or chair

Possible Side Effects

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:

bone pain; constipation; coughing; hot flashes; muscle pain; nausea; tiredness; vaginal discharge; weight loss.

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; unexplained hoarseness); abnormal menstrual periods; abnormal vaginal bleeding or bloody discharge; chest pain; coughing up blood; dark urine; decreased sexual desire or ability; depression; fever, chills, or persistent sore throat; groin or pelvic pain or pressure; loss of appetite; loss of balance or coordination; missed menstrual period; new or increased breast tumor or pain; new or unusual lumps; one-sided weakness; pain or swelling in one or both legs; red, swollen, blistered, or peeling skin; severe or persistent tiredness or weakness; shortness of breath; skin changes; stomach pain; sudden severe headache; swelling of the arms or the legs; unusual bleeding or bruising; vision or speech problems; yellowing of the eyes or skin.

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

Naprelan (Naproxen Sodium) Side Effects, Interactions, Warning, Dosage & Uses, Naprelan

RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS

Cardiovascular Thrombotic Events

Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use [see WARNINGS AND PRECAUTIONS ].

NAPRELAN is contraindicated in the setting of coronary artery bypass graft (CABG) surgery [see CONTRAINDICATIONS and WARNINGS AND PRECAUTIONS ].

Gastrointestinal Bleeding, Ulceration, and Perforation

NSAIDs cause an increased risk of serious gastrointestinal (GI) adverse events including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. These events can occur at any time during use and without warning symptoms. Elderly patients and patients with a prior history of peptic ulcer disease and/or GI bleeding are at greater risk for serious GI events [see WARNINGS AND PRECAUTIONS ].

DRUG DESCRIPTION

NAPRELAN (naproxen sodium) Controlled-Release Tablets is a nonsteroidal anti-inflammatory drug, available as controlled-release tablets in 375 mg, 500 mg, and 750 mg strengths for oral administration. The chemical name is 2-naphthaleneacetic acid, 6-methoxy-α-methyl-sodium salt, (S)-. The molecular weight is 252.24. Its molecular formula is C 14 H 13 NaO 3 . and it has the following chemical structure.

Naproxen sodium is an odorless crystalline powder, white to creamy in color. It is soluble in methanol and water. NAPRELAN Tablets contain 412.5 mg, 550 mg, or 825 mg of naproxen sodium, equivalent to 375 mg, 500 mg, and 750 mg of naproxen, and 37.5 mg, 50 mg, and 75 mg sodium respectively. Each NAPRELAN Tablet also contains the following inactive ingredients: ammoniomethacrylate copolymer Type A, ammoniomethacrylate copolymer Type B, citric acid, crospovidone, magnesium stearate, methacrylic acid copolymer Type A, microcrystalline cellulose, povidone, and talc. The tablet coating contains hydroxypropyl methylcellulose, polyethylene glycol, and titanium dioxide.

Last reviewed on RxList: 6/7/2016 This monograph has been modified to include the generic and brand name in many instances.

Desmedipham (Betanex) Nys Dec Letter - Specific Exemption Request For Use On Red Beets 1, Betanex

Desmedipham (Betanex) NYS DEC Letter - Specific Exemption Request for Use on Red Beets 1/03

New York State Department of Environmental Conservation Division of Solid and Hazardous Materials Bureau of Pesticides Management, 9th Floor 625 Broadway, Albany, New York 12233-7254 Phone: (518) 402-8788 FAX: (518) 402-9024 Website: www. dec. state. ny. us

January 15, 2003

Mr. Dan Rosenblatt Acting Team Leader USEPA / Office of Pesticide Programs Emergency Response Team (7505C) Document Processing Desk Crystal Mall 2-- 2nd Floor 1921 Jefferson Davis Hwy. Arlington, Virginia 22202

Dear Mr. Rosenblatt:

Re: Specific Exemption Request for Use of Desmedipham (Betanex 1.3 EC, EPA Reg. No. 45639-86) for Postemergence Control of Broadleaf Weeds in Red Beets in 2003

The New York State Department of Environmental Conservation (Department), as the State lead agency for pesticide matters, hereby requests approval of the referenced application (see enclosure) under Section 18 of the Federal Insecticide, Fungicide and Rodenticide Act, as amended. The enclosed application includes the information required in 40 CFR, Part 166, Subpart B (166.20). Also enclosed is the use report from the 2002 Section 18 use.

The one currently registered postemergence herbicide, Spin-Aid, is only effective against early growth of some broadleaf weeds and is not effective against pigweed or hairy galinsoga. Other postemergent herbicides, such as Stinger, are only registered for use on sugar beets. Growers still have no other postemergence herbicide weed control options available to them. Registered pre-emergence herbicides often fail to provide adequate control of troublesome broadleaf weeds due to their dependency on rainfall for activation. The lack of control, coupled with the inability to eliminate in-row weeds with cultivation, results in the majority of beets requiring expensive chopping at harvest to remove weeds.

Studies have consistently shown that Betanex provides good to excellent control of many important broadleaf weeds (Appendix B). With Betanex, growers are able to control in-row weeds without costly hand weeding or yield losses due to competition. Betanex can be used on an as-needed basis when soil-applied, rainfall-dependent herbicides fail to adequately control weeds. This form of selective application will enable growers to practice integrated pest management to a greater extent than they now do.

The use of up to three applications of Betanex per season is requested. The first application will be made at 0.125 to 0.25 lbs. ai/acre when the red beets are in the cotyledon to 2-leaf stage (i. e. late cotyledon stage, not fully expanded 2-leaf stage), followed by 0.25 to 0.38 and 0.25 to 0.50 lbs ai/acre in the 2 to 4- and 4 to 6-leaf stages, respectively. The final application will not be made later than 75 days prior to harvest. It is estimated that greater than 50% of the 2500 acres of red beets expected to be grown in New York State in 2003 may need to be treated with the requested material.

The Department is aware that this is the eighth year that we are requesting desmedipham (Betanex 1.3 EC, EPA Reg. No. 45639-86) for emergency use to control broadleaf weeds in the major red beet production areas of New York State. The 2002 exemption, file # 02-NY-01, discussed the United States Environmental Protection Agency's (USEPA) concerns about progress toward a Section 3 registration, due to the fact that desmedipham is an aryl carbamate. However, the time-limited tolerance originally established in 1998 does not expire until December 31, 2003, well past the end of the next anticipated use season. Because this tolerance is already in place, we are requesting that one more season of the emergency exemption be granted.

Aventis Crop Science (Bayer), the manufacturer of Betanex 1.3 EC, fully supports our efforts to obtain an emergency exemption for the use of Betanex on red beets in New York State. The National Interregional Research Project No. 4, IR-4, continues to work to establish a tolerance for desmedipham on red beets as soon as possible and needs only for the USEPA to include the project in their work plan (see Appendix C of enclosure).

Processing red beets are planted from May 1 to June 30, emerging from the soil in 7 to 14 days, and are ready to harvest 90 to 110 days later. The anticipated use season for desmedipham in New York State is from May 15 to August 15.

Please contact Robin Hackett, of our Pesticide Product Registration Section, at (518) 402-8768 if you require further assistance on this request.

Maureen P. Serafini Director, Bureau of Pesticides Management Division of Solid & Hazardous Materials

Enclosure cc: w/enc. - A. Enache, EPA Region II cc: w/o enc. - G. GoodW. Smith, Cornell University, PMEP R. ZimmermanR. Mungari, New York State Dept. Of Ag & Mkts.

Finarid, Finarid

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Also, be sure to see these pages on FinAid:

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The difference between the cost of your education and your family's expected contribution is how much financial aid you'll need.

Step Two: Consider Your Options

Student Loans describes low interest loans available for your education.

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Scholarships are offered for everything from academic merit and athletic prowess to particular fields of study.

Other Sources of Aid provides additional options, from national service and military reserve programs to tuition payment plans and other government aid.

Step Three: Apply for Financial Aid

Submit the Free Application for Federal Student Aid (FAFSA) even if you don't think you're eligible for financial aid -- you may be surprised. Remember, you'll need to submit a new FAFSA application each year.

If you are a man between the ages of 18 and 26, you may be required to register with Selective Service. If you fail to register with Selective Service by your 26th birthday you will be ineligible for Federal and state student loans and grants. You can register using the FAFSA form.

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If your parents refuse to help you financially, read the section on tips for students who are living on their own.

Generally, scholarships and fellowships are reserved for students with special qualifications, such as academic, athletic or artistic talent. Awards are also available for students who are interested in particular fields of study, who are members of underrepresented groups, who live in certain areas of the country or who demonstrate financial need.

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Students who are awarded scholarships often need additional financial assistance. See the Loans section for information on student and parent loans. To find out about contest, grants and other aid options, visit the section discussing Other Types of Aid. Businesses and philanthropists who are thinking about sponsoring a new scholarship may find the Scholarship Design & Management section helpful.

Copyright © 2016 by FinAid Page, LLC. All rights reserved. Mark Kantrowitz, Founder www. FinAid. org

Klazidem, Klazidem

Product Description Common use Biaxin belongs to a group of macrolide antibiotics, which inhibit bacterial synthesis of protein. This action is mainly bacteriostatic, but can also be bactericidal. Macrolides tend to accumulate within leukocytes, and are transported into the site of infection. Biaxin is effective against Haemophilus influenzae, Streptococcus pneumoniae, Mycoplasma pneumoniae, Staphylococcus aureus, mycobacterium avium, and many others so it is used to treat many kinds of bacterial infections of skin and respiratory system, stomach ulcers caused by Helicobacter pylori.

Dosage and directions Biaxin tablets should be taken with or without food with a big glass of water. Swallow the pill whole. Do not take more of the medication than it was recommended to you. Continue to take the drug even if symptoms of your illness became less pronounced and you feel fine. Biaxin is usually given from 7 to 14 days or longer when stomach ulcers are treated.

Precautions Do not use this drug if you are allergic to erythromycin and any of its derivatives or related macrolide antibiotics. If you have diseases of liver or kidneys, mineral dis-balance (low levels of potassium or magnesium), certain heart disease, arrhythmias, discuss it with your doctor before taking Bizxin. This mediation is not recommended during pregnancy or breastfeeding.

Contraindications Biaxin cannot be administered in patients with a known hypersensitivity to clarithromycin, erythromycin, or any of the macrolide antibiotics.

Possible side effects If you have such signs of allergic reaction as hives, difficulty breathing, swelling of your face, lips, tongue, or throat or more serious signs of poor health as uneven heartbeats, chest pain, nausea, stomach pain, low fever, problems with hearing contact your doctor or pharmacist or seek for immediate medical help.

Biaxin may interact with cisapride, pimozide, ergot medicines and result in life-threatening heart rhythm disorders.

Never take a double dose of this medication. If it is almost time for the next dose just skip the missed portion and continue to take the medicine according to the schedule.

Signs of overdose may be: nausea, vomiting, diarrhea, and abdominal discomfort. If you suppose that you took too much of Biaxin contact your doctor for help.

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

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 advisor or doctor in charge of the case. We disclaim all responsibility for the reliability of this information. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Biaxin belongs to a group of macrolide antibiotics, which inhibit bacterial synthesis of protein. This action is mainly bacteriostatic, but can also be bactericidal. Macrolides tend to accumulate within leukocytes, and are transported into the site of infection. Biaxin is effective against Haemophilus influenzae, Streptococcus pneumoniae, Mycoplasma pneumoniae, Staphylococcus aureus, mycobacterium avium, and many others so it is used to treat many kinds of bacterial infections of skin and respiratory system, stomach ulcers caused by Helicobacter pylori.

Dosage and directions Biaxin tablets should be taken with or without food with a big glass of water. Swallow the pill whole. Do not take more of the medication than it was recommended to you. Continue to take the drug even if symptoms of your illness became less pronounced and you feel fine. Biaxin is usually given from 7 to 14 days or longer when stomach ulcers are treated.

Precautions Do not use this drug if you are allergic to erythromycin and any of its derivatives or related macrolide antibiotics. If you have diseases of liver or kidneys, mineral dis-balance (low levels of potassium or magnesium), certain heart disease, arrhythmias, discuss it with your doctor before taking Bizxin. This mediation is not recommended during pregnancy or breastfeeding.

Contraindications Biaxin cannot be administered in patients with a known hypersensitivity to clarithromycin, erythromycin, or any of the macrolide antibiotics.

Possible side effects If you have such signs of allergic reaction as hives, difficulty breathing, swelling of your face, lips, tongue, or throat or more serious signs of poor health as uneven heartbeats, chest pain, nausea, stomach pain, low fever, problems with hearing contact your doctor or pharmacist or seek for immediate medical help.

Biaxin may interact with cisapride, pimozide, ergot medicines and result in life-threatening heart rhythm disorders.

Never take a double dose of this medication. If it is almost time for the next dose just skip the missed portion and continue to take the medicine according to the schedule.

Signs of overdose may be: nausea, vomiting, diarrhea, and abdominal discomfort. If you suppose that you took too much of Biaxin contact your doctor for help.

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

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 advisor or doctor in charge of the case. We disclaim all responsibility for the reliability of this information. 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.

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