Afala tab. blister, 100

Storage:

active substance:

1 tablet contains affinity-purified antibodies to prostate-specific antigen: a mixture of homeopathic dilutions C12, C30 and C200 – 3 mg;

excipients: lactose monohydrate, microcrystalline cellulose, magnesium stearate.

Medicinal form. Tablets.

Main physico-chemical properties: flat-cylindrical tablets, with a line and chamfer, from white to almost white in color. One flat side has a dash, the other flat side has AFALA written on it.

Pharmacotherapeutic group. Homeopathic drug.
Clinical characteristics.

Indication.

Benign prostatic hyperplasia of stage I and II.

As part of the complex therapy of acute and chronic prostatitis.

Dysuric disorders (frequent urges to urinate, including at night, complications during urination, pain or discomfort in the perineum), which, among other things, accompany benign prostatic hyperplasia of the I and II stages, acute and chronic prostatitis.

Contraindication.

Increased individual sensitivity to the drug.

Contraindicated for children (under the age of 18).

Interaction with other medicinal products and other types of interactions.

Cases of incompatibility with other medicinal products have not been registered.

Method of application and dosage.

Take the drug internally. Use 2 tablets per reception (do not use the drug together with food). Keep the tablets in your mouth (preferably without chewing or swallowing) until completely dissolved. Take the drug twice a day, in the evening and in the morning (before and after bedtime). The recommended duration of the treatment course is 16 weeks.

With pronounced pain syndrome and dysuric disorders in the first 2-3 weeks of therapy, take the drug up to 4 times a day.

If necessary, it is possible to carry out a repeated course of treatment after 1-4 months.

Children.

The drug is contraindicated for children (under 18 years of age).

Overdose.

In case of an accidental overdose, dyspeptic manifestations caused by the components included in the composition of the drug are possible. Treatment of dyspeptic manifestations is symptomatic.

Adverse reactions.

Reactions of increased individual sensitivity to the components of the drug are possible.

Expiration date.

3 years.

Do not use the drug after the expiration date indicated on the package.

Storage conditions.

Store at a temperature not higher than 25 °C.

Keep out of the reach of children.

Packaging.

20 tablets in a blister; 5 blisters in a cardboard box.

Leave category.

Without a prescription.

Producer.

Santonika CJSC.

The location of the manufacturer and its address of the place of business.

St. Waveryu 134B, Kaunas, Kaunas sam., LT-46353, Lithuania.

The applicant

“Materia Medica-Ukraine” LLC.
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