0.1 mg/ml, solution for intraocular administration
Carbachol chloride
Miostat is a medicine used by a doctor during eye surgery when immediate and complete constriction of the pupil is desired. Maximum constriction of the pupil usually occurs within a few minutes of administration. Miostat is used only during eye surgery.
Before starting treatment with Miostat, discuss it with your doctor. Be particularly cautious and inform your doctor if the patient has any of the following conditions:
Tell your doctor or pharmacist about all medicines the patient is taking, has recently taken, or plans to take. Large doses of medicines like Miostat (strong cholinergic agonists) may enhance the effects of cardiac glycosides (such as digoxin) or alter the effects of certain muscle relaxants used during anesthesia.
If the patient is pregnant, breastfeeding, or thinks they may be pregnant, they should consult their doctor or pharmacist before using this medicine.
Miostat may cause blurred vision and sensitivity to light. Do not drive or operate machinery until these symptoms have resolved.
The bottle stopper contains natural rubber (latex), which may cause severe allergic reactions.
The medicine contains less than 1 mmol (23 mg) of sodium per 1.5 ml vial, which means it is considered "sodium-free". The medicine contains less than 1 mmol (39 mg) of potassium per dose, which means it is considered "potassium-free".
About 0.5 ml of Miostat is injected into the anterior chamber of the eye during surgery. The effect of Miostat may last up to 24 hours after eye surgery.
If a larger dose of Miostat is administered than recommended, the doctor may need to inject an anticholinergic medicine to counteract the symptoms of overdose. These symptoms may include: headache, increased salivation, fainting, slow heart rate, decreased blood pressure, abdominal cramps, vomiting, asthma, and diarrhea. If there are any further doubts about using this medicine, consult a doctor or pharmacist.
Like all medicines, Miostat can cause side effects, although not everybody gets them. The following side effects have been observed with Miostat:
Uncommon side effects (may affect up to 1 in 100 people)
Additionally, the following side effects have been reported after the medicine was placed on the market, and their frequency cannot be estimated from the available data:
The following side effects may also occur:
Eye disorders:
Rarely:retinal detachment
Skin and subcutaneous tissue disorders:
Uncommon:excessive sweating
Renal and urinary disorders:
Uncommon:urinary urgency
If any side effects occur, including any not listed in this leaflet, inform a doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Post-Marketing Surveillance of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: 22 49-21-301, fax: 22 49-21-309, website: https://smz.ezdrowie.gov.pl. Reporting side effects will help gather more information on the safety of the medicine.
Keep the medicine out of sight and reach of children. Store at a temperature below 30°C. Do not use this medicine after the expiry date stated on the carton and vial after: EXP. The expiry date refers to the last day of the month. Medicines should not be disposed of via wastewater or household waste. Ask a pharmacist how to dispose of unused medicines. This will help protect the environment.
The active substance of Miostat is carbachol. 1 ml of solution contains 0.1 mg of carbachol (as carbachol chloride). The other ingredients are: sodium chloride, potassium chloride, calcium chloride dihydrate, magnesium chloride hexahydrate, sodium acetate trihydrate, sodium citrate dihydrate, sodium hydroxide, and (or) hydrochloric acid to adjust the pH, and water for injections.
Miostat is available in PVC blister packs containing glass vials with a rubber stopper and aluminum cap, each containing 1.5 ml of a clear, colorless solution for intraocular administration.
Marketing authorization holder:
Alcon Polska Sp. z o.o.
ul. Marynarska 15
02-674 Warsaw
Importer, where the batch is released:
Alcon Laboratories Belgium
Lichterveld 3
2870 Puurs-Sint-Amands
Belgium
To obtain more detailed information, contact the local representative of the marketing authorization holder:
Alcon Polska Sp. z o.o.
ul. Marynarska 15
02-674 Warsaw
tel.: 22 820 34 50
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