Wirkstoffe & Arzneimittelsicherheit

Nebenwirkungen · Pramipexole Teva

Pramipexole Teva 0.088 mg tablets Pramipexole Teva 0.18 mg tablets Pramipexole Teva 0.35 mg tablets Pramipexole Teva 0.7 mg tablets · Abschnitt 4.8 · PDF-Seite 8–9

HOS-119869 · Präparat HOS-095037

8  Nervous somnolence headache sudden onset of system dizziness sleep disorders dyskinesia amnesia hyperkinesia syncope Eye disorders visual impairment including diplopia vision blurred visual acuity reduced Cardiac cardiac failure1 disorders Vascular hypotension disorders Respiratory, dyspnoea thoracic, and hiccups mediastinal disorders Gastrointestinal nausea constipation disorders vomiting Skin and hypersensitivity subcutaneous pruritus tissue disorders rash Reproductive spontaneous system and penile breast disorders erection General fatigue dopamine disorders and peripheral agonist administration oedema withdrawal site conditions syndrome including apathy, anxiety, depression, fatigue, sweating and pain. Investigations weight decrease weight increase including decreased appetite 1 This side effect has been observed in post-marketing experience. With 95 % certainty, the frequency category is not greater than uncommon, but might be lower. A precise frequency estimation is not possible as the side effect did not occur in a clinical trial database of 2 762 patients with Parkinson’s Disease treated with pramipexole.

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