Adverse reactions are classified according to the medical vocabulary for regulatory legal activity MedDRA and systematized according to the frequency of development in accordance with the WHO Classification: very frequent - 1/10 appointments (≥ 10%);
frequent - 1/100 appointments (≥ 1%, but <10%);
infrequent - 1/1000 appointments (≥ 0.1%, but <1%);
rare - 1/10000 prescriptions (≥ 0.01%, but <0.1%);
very rare - less than 1 / 10,000 appointments (<0.01%).
Disturbances from the nervous system: often - headache.
Violations with hand gastro-intestinal tract: often - abdominal pain; infrequently - nausea.
Violations with hand liver and bile ducts: infrequently - an increase in the activity of gamma-glutamyl transferase, an increase activity of transaminases.
Disturbances from the skin and subcutaneous tissues: infrequently - rash.
Violations of the genitals and breast: infrequently - gynecomastia (reversible after discontinuation of treatment).
Allergic Reagents: frequency is unknown (can not be estimated from available data) - edema.
If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, inform the doctor about it.