Universal reference book for medicines
Product name: FEMILEX ® (FEMILEX)

Active substance: lactic acid

Type: The drug regulating the balance of the microflora of the vagina

Manufacturer: NIZHFARM (Russia)
Composition, form of production and packaging
?
Suppositories vaginal white or white with a yellowish hue of color, torpedo-shaped; Marble surface is allowed.
1 supp.

lactic acid 100 mg

Auxiliary substances: the suppository base is sufficient for obtaining a suppository with a mass of 3 g (macrogol 400 (polyethylene oxide 400) - 8-2%, macrogol 1500 (polyethylene oxide 1500) - 92-98%).

5 pieces.
- packings of cellular contour (1) - packs cardboard.
5 pieces.
- packings cellular planimetric (2) - packs cardboard.
INSTRUCTION FOR THE SPECIALIST.

Description of the drug approved by the manufacturer for the printed edition of 2014.

PHARMACHOLOGIC EFFECT

Lactic acid is a natural product of the vital activity of lactic acid bacteria of the vagina, provides a pH of the vaginal secretion in the range 3.5-4.5.
Suppositories with lactic acid help restore and maintain normal pH and flora of the vagina, suppress the growth of acid-sensitive pathogenic and conditionally pathogenic flora.
Lactic acid creates an acid reserve to correct the shift of pH observed in vaginal infections to the alkaline side.
Promotes increased natural protection of the vagina from genital infections.
PHARMACOKINETICS

There is no information on pharmacokinetics.

INDICATIONS

- normalization of the disturbed microflora and pH of the vagina, incl.
with bacterial vaginosis (as part of complex therapy).
DOSING MODE

Intravaginal.
Before use, the suppository is freed from the contoured package. One vaginal suppository is inserted into the vagina (lying on the back with slightly bent legs) 1 time / day. The course of treatment is 10 days.
SIDE EFFECT

There may be allergic reactions, itching, in rare cases - burning in the vagina, after the drug is withdrawn.

CONTRAINDICATIONS

Candidiasis vulvovaginitis;

- Pregnancy;

- the period of breastfeeding;

- Children's age (up to 18 years);

- Hypersensitivity to the components of the drug.

PREGNANCY AND LACTATION

Use during pregnancy is contraindicated, because.
clinical studies in pregnant women have not been conducted.
There is no information on the penetration into breast milk.
Application in the period of breastfeeding.
APPLICATION FOR CHILDREN

Contraindicated in children under 18 years.

SPECIAL INSTRUCTIONS

If burning and itching occurs, it is recommended that a check be done to exclude the fungal infection of the vagina.

OVERDOSE

No cases of drug overdose have been reported.

DRUG INTERACTION

There is no information.

TERMS OF RELEASE FROM PHARMACY

The drug is released by prescription.

TERMS AND CONDITIONS OF STORAGE

The drug should be stored out of the reach of children, at a temperature of no higher than 25 ° C.
Shelf life - 2 years.
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