Active ingredient: Each tablet contains 0.003*q affinity-purified antibodies against prostate-specific antigen.
Benign hyperplasia of the prostate gland, stages I and II. It is prescribed as part of complex therapy for acute and chronic prostatitis, as an anti-inflammatory and analgesic agent. Dysuric disorders (including nocturia, difficulty during urination, pain in the perineal area, and/or frequent urination), including those accompanying benign hyperplasia of the prostate gland, stages I and II; acute and chronic prostatitis.
High sensitivity to any component of the product. Since there is insufficient information regarding efficacy and safety in this age group, use in patients under 18 years of age is not recommended.
The Afala product is not intended for use in women.
Afala does not affect the ability to drive vehicles and operate other potentially dangerous machinery.
For oral use. 2 tablets are prescribed per dose (kept in the mouth until fully dissolved, but not during food intake). The product is taken 2 times a day, in the morning and in the evening (before and after bedtime). The recommended duration of use is 16 weeks.
In cases of pronounced pain and dysuric disorders, during the first 2–3 weeks of therapy, taking the product is indicated 4 times per day. If necessary, with the doctor’s advice, it is possible to repeat the treatment course after 1–4 months.
Product Filters | ||
|---|---|---|
| Supplier Product Code | : | 111-18191 |