Choline salicylate
Otinum is a medicine used for the short-term treatment of inflammatory conditions of the external ear canal characterized by pain, itching, and redness.
Otinum is also recommended for softening earwax before ear irrigation.
The active substance of Otinum ear drops, solution is a salicylic acid derivative - choline salicylate.
Choline salicylate has local analgesic and anti-inflammatory properties when applied topically. This reduces pain and inflammation in the external ear canal. The glycerol in the medicine softens earwax, making it easier to remove. After local application to the ear, the medicine does not have a systemic effect.
Signs of eardrum perforation may include: severe ear pain (gradually decreasing), ringing in the ears (which may indicate damage to deeper ear structures), hearing loss, dizziness, and/or discharge from the ear. Causes of eardrum damage (perforation) include infections, injuries (e.g., after improper ear cleaning with cotton swabs), and medical procedures (e.g., ear irrigation due to earwax).
Any ear pain is a reason to consult a doctor.
Otinum can be used for the short-term treatment of external ear canal inflammation without consulting a doctor, but not for more than 3 days. If there is no improvement or if symptoms worsen despite using Otinum for 3 days as recommended, consult a doctor.
If additional symptoms occur, indicating a developing disease process (e.g., fever, malaise, weakness, dizziness, discharge from the ear), consult a doctor.
In case of recurrence of the disease, the use of Otinum should be decided by a doctor.
Otinum may mask symptoms of other ear diseases and hinder or delay their proper diagnosis.
Inform your doctor about using Otinum.
Otinum contains a preservative - chlorobutanol hemihydrate.
Do not use Otinum contrary to the indications listed in the leaflet or by a different route of administration (e.g., orally, on open wounds, especially in the ear canal or in the eyes).
Tell your doctor or pharmacist about all medicines you are taking, have recently taken, or might take, including those obtained without a prescription.
The medicine is used locally and does not have a systemic effect.
Concomitant use with non-steroidal anti-inflammatory drugs (e.g., aspirin, ibuprofen) may enhance local effects.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.
The medicine does not affect the ability to drive or use machines.
Always use this medicine exactly as described in the patient leaflet or as directed by your doctor or pharmacist. If you are not sure, talk to a doctor or pharmacist.
Otinum is for local use in the ear only. Otinum is intended for use in adults.
If you feel that the effect of Otinum is too strong or too weak, talk to a doctor.
Usually 3 to 4 drops into the external ear canal every 6 to 8 hours.
Without a doctor's recommendation, do not use Otinum for more than 3 days.
Elderly:
No dose adjustment is necessary.
Patients with liver or kidney function disorders:
No dose adjustment is necessary.
It is not possible to overdose on the medicine by administering it into the ear. Symptoms of overdose, which may occur after accidental oral ingestion of the medicine, include: disorientation, dizziness, excessive sweating, vomiting, ringing in the ears, and rapid breathing (hyperventilation). In case of oral ingestion of very large doses of the medicine, central nervous system disorders may occur, including breathing and circulation problems. If you have taken the medicine orally, seek medical help immediately.
If you miss a dose, use it as soon as you remember. However, if it is almost time for your next dose, skip the missed dose. Do not use a double dose to make up for a missed dose.
Like all medicines, Otinum can cause side effects, although not everybody gets them.
The frequency of the following side effects is unknown (cannot be estimated from the available data).
Local hypersensitivity reactions (redness and itching of the skin).
In patients with eardrum perforation during treatment, hearing loss may occur.
If you get any side effects, talk to a doctor, pharmacist, or nurse. This includes any possible side effects not listed in the leaflet. You can also report side effects directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309,
website: https://smz.ezdrowie.gov.pl
By reporting side effects, you can help provide more information on the safety of this medicine.
Do not store above 25°C.
Store in the original package.
Keep the medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The packaging is a LDPE bottle with a dropper and a screw cap with a tamper-evident ring, in a cardboard box. The pack contains 10 g of the medicine.
For more detailed information, contact the marketing authorization holder or the parallel importer:
SIA Meda Pharma, Mūkusalas 101, Riga LV-1004, Latvia
ICN Polfa Rzeszów S.A.
ul. Przemysłowa 2
35-959 Rzeszów
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź
Lithuanian, the country of export, authorization number: LT/1/94/1929/001
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