Propolis suppositories 0.1 g blister No. 10

Instructions Propolis suppositories 0.1 g blister No. 10

Composition

active ingredient: phenolic hydrophobic propolis preparation;

1 suppository contains phenolic hydrophobic propolis preparation (calculated as 50% content of the sum of phenolic compounds) 0.1 g (100 mg);

excipients: dimethyl sulfoxide, propylene glycol, solid fat.

Dosage form

Suppositories.

Main physicochemical properties: suppositories from light brown to dark brown in color, spherical in shape, with a specific odor. The presence of a coating and non-uniformity of color in the form of inclusions and marbling is allowed.

Pharmacotherapeutic group

Preparations for the treatment of hemorrhoids and anal fissures for topical use. ATX code C05A X.

Pharmacological properties

Pharmacodynamics.

Phenolic hydrophobic preparation of propolis provides anti-inflammatory, reparative and antimicrobial effects. The presence of dimexide in the composition of suppositories complements the spectrum of activity of the drug with analgesic properties, increases the resorption of pharmacological substances through the mucous membrane.

Propylene glycol and the base create conditions for the implementation of the therapeutic effects of the active ingredients of suppositories.

Pharmacokinetics.

No data.

Indication

Proctitis, anal fissures, postoperative wounds of the distal rectum.

Contraindication

Hypersensitivity to the components of the drug, allergic reactions to beekeeping products.

Interaction with other medicinal products and other types of interactions

Can be used in combination with other drugs intended for the treatment of concomitant diseases. Simultaneous use with other beekeeping products is not recommended.

Application features

Before using the suppository, you must:

tear off one suppository from the primary packaging along the perforation line of the blister pack;

Next, you need to pull the edges of the film, tearing it in different directions, and release the suppository from the primary packaging.

Use during pregnancy or breastfeeding

During pregnancy or breastfeeding, the use of the drug is possible as prescribed by a doctor in cases where the expected benefit to the woman outweighs the potential risk to the fetus/child.

The ability to influence the reaction speed when driving or working with other mechanisms

There is no data on the effect of the drug on the ability to drive a car or operate other mechanisms.

Method of administration and doses

Adults and children over 7 years of age – 1 suppository 3 times a day after bowel movement. The duration of treatment is determined by the doctor depending on the severity of the disease. The course of treatment can be from 8–10 days to 14–21 days.

Children

The drug is not used to treat children under 7 years of age.

Overdose

Not installed.

Side effects

Allergic reactions are possible.

Expiration date

2 years.

Storage conditions

Store at a temperature not exceeding 25 °C.

Keep out of reach of children.

Packaging

5 suppositories in a blister, 1 or 2 blisters in a pack.

Leave category.

Without a prescription.

Vacation category

Without a prescription.

Producer

Private Joint-Stock Company "Lekhim-Kharkiv".

Address

Ukraine, 61115, Kharkiv region, Kharkiv city, Severyna Pototskoho street, building 36.