Active material: Lidokain, Fenazon
When ATH: S02DA30
CCF: Preparation with anti-inflammatory and mestnoanestezirutm effect for local application in ENT practice
ICD-10 codes (testimony): H60, H66
At KFU: 05.01.03.02
Manufacturer: S.C. ROMPHARM Company S.R.L. (Romania)
Ear Drops as a clear, colorless or slightly yellowish solution.
| 1 g | |
| fenazon | 40 mg |
| Lidocaine hydrochloride | 10 mg |
Excipients: Sodium Thiosulphate pentahydrate, ethanol 96%, glycerol, Sodium hydroxide (solution 1 m), Purified water.
15 ml (17.1 g) – флакон-капельницы полиэтиленовые (1) – пачки картонные.
Combination preparation for topical application. Provides mestnoanestezirutee and anti-inflammatory effect.
Феназон – анальгетик-антипиретик с противовоспалительным и анальгезирующим действием. Лидокаин – местный анестетик. The combination of Phenazone and lidocaine promotes more rapid onset of anaesthesia, as well as increases its intensity and duration.
The active substances are not absorbed into the bloodstream when an intact eardrum.
Local symptomatic treatment and pain relief in adults and children (including newborns) at:
-external otitis;
— in the treatment of otitis media with intact the eardrum;
— barotravmatičeskom otite.
Drops of fluid in the ear canal for 3-4 drops 2-3 times / day. Avoid contact of cold solution with auricle bottle before use, warm in your hands.
The course of treatment should not exceed 10 d.
Maybe: Local allergic reactions, irritation and hyperemia meatus, slight pain at the time of application.
-perforation of tympanic membrane;
- Hypersensitivity to the drug;
-hypersensitivity to derived pirazolona.
Pregnancy may only, when the intended benefits to the mother outweighs the potential risk to the fetus.
If necessary, use during lactation should decide the issue of termination of breastfeeding.
You must verify the integrity of the tympanic membrane before applying the product. In the case of drugs in a perforated eardrum, active substances can penetrate the bloodstream, that can lead to complications.
The duration of not more than Otirelaksa 10 days, then hold the assigned therapy correction.
If you are using the drug in combination with other Otirelaks ear drops must maintain a minimum interval 30 min between zakapyvaniâmi.
It will be appreciated, the drug contains an active component, who can give a positive test in a doping control.
The drug overdose Otirelaks not available.
Currently, information about drug interactions with other drugs Otirelaks are missing.
The drug is released under the prescription.
The drug should be stored in a dry, protected from light, inaccessible to children at temperature not exceeding 25 ° C. Shelf life - 3 year.
After opening the bottle the drug should be used within 6 months.
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