Joint pain (arthralgia), Atopic dermatitis, EczemaProphylaxis and treatment (as part of the complex therapy) of influenza and acute respiratory infections. Prevention and treatment (as part of complex therapy) of influenza H5N1 and H1N1.
Human recombinant interferon gamma
How to take, the dosage
Intranasally. The contents of the bottle must be dissolved in 5 ml of water for injection.
In case of the first signs of flu, SARS, 2 drops in each nostril after clearing the nasal passages 5 times a day for 5 – 7 days.
One course of therapy requires two bottles of the drug.
To prevent SARS and flu in case of contact with a patient and/or hypothermia
2-3 drops in each nasal passage every day 30 minutes before breakfast for 10 days.
In case of a single contact, one shot is enough.
One bottle of the drug is enough for one course of prevention of Acute Respiratory Influenza and Flu.
If necessary, the preventive courses are repeated.
After application, it is recommended that the patient rub the nasal wings with his/her fingers for several minutes to evenly distribute the product in the nasal cavity.
If at the end of a course of prevention or treatment, there is no improvement, or if symptoms get worse or new symptoms develop, you should talk to your doctor.
Please only use the product according to the indication, route of administration and dosage listed in the instructions.
Instructions for preparing the drug solution
- Gently pull the plastic nozzle on the glass bottle in the direction of the arrows on the aluminum shield.
- The plastic cap along with the part of the aluminum guard comes off.
- Circle the remaining part of the aluminum guard. Remove the rubber stopper from the glass vial.
- Open the ampoule of water for injection by breaking off its upper part.
- Pour 5 ml of water for injection into the glass vial with the dry substance.
- Remove the dropper cap from the package, and secure it to the neck of the vial. Shake well before use.
In order to store the active ingredient in a full vacuum, the aluminum cap needs to be airtight and secure. Slowly remove the aluminum protection of the vial and avoid cuts. If the cap has come off while you are removing it, you can use scissors to remove the rest of the metal cap.
Pharmaceutical interactions: Ingaron® lyophilisate or ready-made solution for intranasal administration must not be mixed with other powders, solutions or solvents (except water for injection) in the same vial to avoid loss of activity of the active substance. If you use other medicinal products (including over-the-counter ones), consult your doctor before using Ingaron® .
Do not exceed the maximum recommended doses if using the drug alone. In case of absence of reduction or aggravation of symptoms it is recommended to consult a physician.
Influence of the drug on the ability to drive vehicles, mechanisms
Special clinical trials of the drug effect on the ability to drive vehicles, mechanisms have not been conducted. The effect of the drug on the ability to perform activities requiring concentration and quick psychomotor functions is unlikely.
Individual intolerance to interferon gamma or any other drug component. Pregnancy. Childhood (under 7 years).
Not noted. If you notice any side effects not listed in the instructions, tell your doctor or the manufacturer.
There are no known cases of overdose.
Preclinical studies showed no teratogenic or fetotoxic effects, but the safety of the drug in pregnant women and nursing mothers has not been established, therefore, the use during pregnancy and breastfeeding is contraindicated.
2 years. After preparation of the solution for 10 days. Do not use after the expiration date.
|Conditions of storage|
Store the drug in a dry place protected from light at a temperature not higher than +25o C. Store the drug solution not more than 10 days in refrigerator (do not freeze). Keep out of reach of children.
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