Composition, form of production and packaging
? Suppositories vaginal white or white with a yellowish hue of color, torpedo-shaped, allowed marbling surface.
1 supp.
chlorhexidine bigluconate 8 mg
Excipients: polyethylene oxide base (polyethylene oxide 1500, polyethylene oxide 400).
5 pieces. - packings of cellular contour (1) - packs cardboard.
5 pieces. - packings cellular planimetric (2) - packs cardboard.
INSTRUCTION FOR THE SPECIALIST.
The product description was approved by the manufacturer for the 2009 print edition.
PHARMACHOLOGIC EFFECT
Antiseptic preparation for topical application.
It is active against Gram-positive and Gram-negative bacteria - Treponema pallidum, Chlamydia spp., Ureaplasma spp., Neisseria gonorrhoeae, Gardnerella vaginalis, Bacteroides fragilis; protozoa -Trichomonas vaginalis; viruses - Herpes simplex types 1 and 2.
The hexicon does not interfere with the functional activity of lactobacilli.
Keeps activity (albeit somewhat lowered) in the presence of blood, pus.
PHARMACOKINETICS
Virtually not absorbed from the digestive tract. After accidental ingestion, 300 mg of C max is reached after 30 minutes and is 0.206 Ојg / l. It is excreted mainly with feces (90%), less than 1% is excreted in urine.
INDICATIONS
- prevention of venereal diseases (including gonorrhea, syphilis, trichomoniasis, chlamydia, ureaplasmosis, genital herpes);
- prevention of infectious and inflammatory complications in obstetrics and gynecology (before operative treatment of gynecological diseases, before and after diathermocoagulation of the cervix, before intrauterine studies);
- Treatment of chronic exo- and endocervicitis, vaginitis (including nonspecific, mixed, trichomonas).
DOSING MODE
For the prevention of sexually transmitted diseases, one soup is prescribed once. The drug should be used not later than 2 hours after sexual intercourse.
For treatment appoint 1 soup. 2 times / day for 7-10 days. If necessary, prolongation of therapy is possible up to 20 days.
SIDE EFFECT
Possible: allergic reactions, itching, after the withdrawal of the drug.
CONTRAINDICATIONS
- hypersensitivity to the components of the drug;
- Allergic reactions.
PREGNANCY AND LACTATION
The drug is not contraindicated for use in pregnancy and lactation (breastfeeding).
SPECIAL INSTRUCTIONS
In childhood, it is recommended to use the drug Geksikon D.
OVERDOSE
At present, cases of overdose of the drug Hexicon D have not been reported.
DRUG INTERACTION
Hexicon D is not compatible with detergents containing an anionic group (saponins, sodium lauryl sulfate, sodium carboxymethylcellulose) and soaps. The presence of soap can inactivate chlorhexidine, so before using the drug, soap residues should be thoroughly rinsed off.
TERMS OF RELEASE FROM PHARMACY
The drug is approved for use as a means of OTC.
TERMS AND CONDITIONS OF STORAGE
The drug should be stored out of reach of children, protected from light at a temperature of no higher than 25 В° C. Shelf life - 2 years.
