F. Hoffmann-La Roche Brand: F. Hoffmann-La Roche

Ex Tax: $32.99


  • influenza treatment: the preparation is indicated for adults and children from one year of age who have symptoms of influenza during the circulation of the influenza virus (effectiveness was demonstrated when treatment was started within 2 days after the first onset of symptoms);
  • flu prevention:
  • prevention of influenza in adults and children over one year of age after contact with a person with clinically diagnosed influenza during the circulation of the influenza virus;
  • the appropriate use of the preparation for the prevention of influenza must be determined on a case-by-case basis, taking into account the circumstances and taking into account the group of patients who need protection; in exceptional situations (for example, in the event of a disagreement between the circulating influenza virus and the influenza virus against which vaccination was carried out, and during a pandemic) seasonal prophylaxis can be carried out in persons aged one year or older.


Active substance: oseltamivir;
1 capsule contains oseltamivir 75.00 mg in the form of oseltamivir phosphate 98.50 mg;
Excipients: corn starch, talc, povidone K30, sodium croscarmellose, sodium stearyl fumarate;
Capsule shell:
  • cap: titanium dioxide (E 171), iron oxide yellow (E172), iron oxide red (E172), gelatin, printing ink;
  • body: titanium dioxide (E 171), black iron oxide (E172), gelatin, printing ink.


Hypersensitivity to oseltamivir phosphate or to any component of the preparation.

Mode of application

For oral administration.
Patients who cannot swallow the capsule can receive appropriate doses of Tamiflu® powder for oral suspension.

Application features

If necessary, the use of Tamiflu during pregnancy can be considered taking into account the available information on the safety and benefits, as well as the pathogenicity of the circulating strain of the influenza virus.
Applied to children aged 1 year and older weighing more than 40 kg, who are able to swallow the capsule.
The preparation does not affect the reaction rate when driving vehicles or other mechanisms.


Overdose reports were received during clinical trials and during post-marketing use of the preparation. In most of the recorded cases of overdose, no adverse reactions were reported.
The adverse reactions reported in overdose were similar in nature and type to those observed with therapeutic doses of the preparation.
There is no specific antidote.
Overdose has been reported more frequently in children than in adults and adolescents. Caution should be exercised when using the preparation in children.

Side effects

In adults / adolescents, when taking the preparation for the treatment of influenza, frequent adverse events were nausea and vomiting, for the prevention of influenza - nausea. They were transient and usually appeared on the first or second day of treatment and disappeared after 1-2 days. Vomiting was the most common adverse event in children. In most cases, adverse reactions did not lead to preparation withdrawal.


With the simultaneous administration of oseltamivir and probenecid for patients with normal renal function, dose adjustment is not required. Concomitant administration of probenecid, which is a potent inhibitor of the anionic pathway of renal tubular secretion, approximately doubles the exposure to the active metabolite of oseltamivir.

Storage conditions

Keep out of the reach of children.
Store at a temperature not exceeding 25 ° C.
The shelf life is 10 years.

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