Drug Uses

Tamiflu is used for the treatment of uncomplicated acute illness due to influenza infection.

How Taken

You may take Tamiflu with or without food. However, when taken with food, your tolerability to Tamiflu may be enhanced. The recommended oral dose of Tamiflu is 75 mg twice daily for 5 days. You should begin treatment within 2 days of onset of symptoms of influenza.

Warnings/Precautions

Tamiflu is not a substitute for a flu vaccination. You should continue receiving an annual flu vaccination. It is not known whether this medicine is excreted in human milk. You should therefore, use this drug only if the potential benefit justifies the potential risk to the breast-fed infant.

Missed Dose

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

Possible Side Effects

You may experience some common, less serious side effects: nausea (without vomiting), vomiting, diarrhea, abdominal pain, dizziness, headache, cough, insomnia, fatigue.

Storage

Store Tamiflu under refrigeration at 36º to 46ºF (2º to 8ºC). Do not freeze.

Overdose

Symptoms of a Tamiflu overdose are nausea and/or vomiting. Seek medical attention if an overdose is suspected.

More Information

You should begin treatment with Tamiflu as soon as possible from the first appearance of flu symptoms. Similarly, prevention should begin as soon as possible after exposure, at the recommendation of a physician.

Disclaimer

This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.

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F.A.Q

Q: What is your cancellation policy for Tamiflu?
A: The only time possible to cancel your order for a Tamiflu product is before the order has shipped or been approved by the doctor. If that is not the time, meaning the order was shipped or approved, we cannot cancel your order. You can read more referring to the current cancellation policy in the terms & conditions section of our order page.

What are the differences between Tamiflu brand-name drugs and Tamiflu generic drugs?
You probably know that pharmaceutical companies carry out extensive research and clinical testing to win approval from the Food and Drug Administration for new drugs. The new drug is then protected by patent for at least 10 years. Hence, a brand-name drug. When the patent expires another drug company can "copy the recipe" for the brand drug. This "copy" is called a generic drug. The FDA requires that generic Tamiflu have the same active chemical composition, be dispensed in the same dosage form such as a tablet or capsule and be taken in the same dosage as the brand-name drug.
Paylessforgeneric.com recommends the use of a generic drug only when it is "A" rated, the highest bioequivalent rating by the FDA.
Generic Tamiflu cost less and competitive pricing by the different manufacturers further reduces the prices. Occasionally, generic drugs may look different from their brand-name versions because the inactive ingredients such as fillers and dyes can be different. However, these ingredients do not affect the safety or performance (efficacy) of the drug.

More Highlights

Different definition / meanings for the word "drug abuse":
The use of a drug for a purpose other than that for which it is normally prescribed or recommended.

Definition for pharmacy discount
Pharmacies have to grant a discount to the NHS. According to law, since 1997, the 66.65% of the selling price of a drug (after VAT) is due to the manufacturer, the 6.65% is due to the wholesaler while the 26.7% is due to the pharmacist.

Different definition / meanings for the word "new drug application":
An application requesting FDA approval to market a new drug for human use in interstate commerce. The application must contain, among other things, data from specific technical viewpoints for FDA review--including chemistry, pharmacology, medical, biopharmaceutics, statistics, and, for anti-infectives, microbiology.

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