Betadine vaginal suppositories

Betadine vaginal suppositories

Composition:  Active ingredient: 200 mg of povidone-iodine (corresponding to 18-24 mg of active iodine) in each vaginal suppository.

EXCIPIENTS:  Macrogol 1000 2800 mg. Description: Torpedo-like homogeneous suppositories of dark brown color.

DOSAGE FORMS:

Vaginal suppositories

PHARMACOLOGICAL PROPERTIES: Pharmacodynamics Has antiseptic, disinfectant, antifungal and antiprotozoal effect. It blocks amino groups of cellular proteins. Has a wide spectrum of antimicrobial action.).

Pharmacokinetics: With topical application, there is almost no reabsorption of iodine from the mucous membrane.

INDICATIONS:  Acute or chronic vaginitis (mixed, nonspecific infection), bacterial vaginosis (caused by Gardnerella vaginalis), candidiasis, infection of Trichomonas vaginalis. Infections of the vagina after treatment with antibiotics or steroid preparations.

CONTRAINDICATIONS: Hypersensitivity to iodine and other constituents of the drug; dysfunction of the thyroid gland (nodular colloid goiter, endemic goiter and Hashimoto's tiroiditis, hyperthyroidism); adenoma of the thyroid gland; herpetiform dermatitis of Dühring; simultaneous application of radioactive iodine; children under 8 years old. With caution: pregnancy and lactation.

PREGNANCY AND LACTATION

The betadine should not be given from the 3rd month of pregnancy. If needed then at that time the treatment should  be given under medical supervision.

METHOD OF USE AND DOSES

For insertion into the vagina. It is compulsary  to moisten the suppository with water and inject it  into the vagina  before going to bed.

For 1 suppository to enter deep into the vagina: with acute vaginitis 1-2 times a day for 7 days, with chronic and subacute vaginitis - 1 time per day before bedtime for 14 days (possibly longer).

It is also recommended to use hygienic pads during the course of treatment. Do not stop using suppositories during menstruation.

SIDE EFFECTS

Reactions of hypersensitivity to the drug, hyperemia, pruritus. In rare cases, it can cause hypersensitivity reactions,

 for example, contact dermatitis with the formation of psoriasis-like red small bullous elements. Prolonged application of povidone-iodine can lead to absorption of significant amounts of iodine.

OVERDOSE

If over dose, the following symptoms are typical: burning sensation or pain in the mouth or throat. Irritation and swelling of the eyes; skin reactions; gastrointestinal disorders and diarrhea; impaired renal function and anuria; circulatory insufficiency; edema of the larynx with secondary asphyxia, pulmonary edema, metabolic acidosis, hypernatremia.

SPECIAL INSTRUCTIONS

Due to the oxidative properties of povidone-iodine, its traces can lead to false-positive results of some types of studies for the detection of latent blood in feces, as well as blood or glucose in the urine. In case of thyroid dysfunction, the drug can be used only as directed by a physician. If symptoms of hyperthyroidism occur during the course of treatment, the function of the thyroid gland should be checked.

The use of povidone iodine is allowed from the newborn period, but taking into account the form of release - vaginal suppositories, the drug is not recommended for use before 8 years and be careful when introducing virgins.

Coloring on the skin and tissues is easily washed off with water. During the use of suppositories can recommend the use of sanitary napkins.

FORM OF ISSUE

Vaginal suppositories 200 mg. For 7 vaginal suppositories in the blister of PVC / PE film. For 1 or 2 blisters in a cardboard box together with instructions for use. SHELF LIFE 5 years.

 STORAGE CONDITIONS

 Store in a dry place at a temperature of 5 to 15 oC. Keep out of the reach of children.