Storage
active substance: 1 ml of solution contains miramistin 0.1 mg;
excipient: purified water.
Pharmaceutical form Solution for external use.
Main physico-chemical properties: colorless or yellowish transparent liquid that foams when shaken.
Pharmacotherapeutic group Antiseptic and disinfectants.
Indication
Surgery, traumatology: local treatment of infected wounds of various localization and etiology; prevention of secondary infection of granulating wounds.
Combustiology: treatment of II and III A degree burns; preparation of burn wounds for dermatoplasty.
Obstetrics and gynecology: prevention and treatment of suppuration of postpartum wounds, postpartum infections, perineal and vaginal wounds; inflammatory diseases of the external genitalia and vagina (vulvovaginitis).
Dermatology: complex treatment of candidiasis of the skin and mucous membranes, mycosis of the feet and large folds.
Venereology: individual prevention of sexually transmitted diseases (syphilis, gonorrhea, genital herpes).
Otorhinolaryngology: complex treatment of acute and chronic otitis, sinusitis, tonsillitis.
Dentistry: treatment of periodontitis, stomatitis; hygienic processing of removable prostheses; prevention of microbial complications after surgical interventions on the mucous membrane of the oral cavity.
Contraindication
Individual sensitivity to miramistin.
Features of application
Venereology. After treatment with Miramistin® of the urinary canal, vagina, inner surfaces of the thighs, pubis and external genitalia, it is not recommended to urinate for 2 hours.
Use during pregnancy or breastfeeding.
Since there is practically no resorption of the drug, it is allowed to use Miramistin® during pregnancy or breastfeeding.
The ability to influence the speed of reaction when driving vehicles or other mechanisms.
The use of the drug is characterized by the lack of influence on the ability to drive vehicles and engage in other potentially dangerous activities that require increased concentration of attention and speed of psychomotor reactions.
Overdose Phenomena of overdose were not observed.
Adverse reactions
In some cases, a short-term burning sensation is possible, which disappears on its own after 15-20 seconds and does not require discontinuation of the drug.
Hypersensitivity reactions, including phenomena of local skin irritation: itching, hyperemia, burning sensation, dry skin.
The shelf life is 3 years.
Storage conditions Store in the original packaging at a temperature not higher than 30 °C.
Do not freeze. Keep out of the reach of children.
Packaging 50 ml in a bottle, 1 bottle with a urethral nozzle in a pack.
Release category Without a prescription.
Producer PJSC “Pharmaceutical firm “Darnytsia”.
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