Oprymea Европска Унија - Енглески - EMA (European Medicines Agency)

oprymea

krka, d.d., novo mesto - pramipexole dihydrochloride monohydrate - parkinson disease - anti-parkinson drugs - oprymea is indicated for treatment of the signs and symptoms of idiopathic parkinson's disease, alone (without levodopa) or in combination with levodopa, i.e. over the course of the disease, through to late stages when the effect of levodopa wears off or becomes inconsistent and fluctuations of the therapeutic effect occur (end of dose or "on off" fluctuations).oprymea is indicated in adults for symptomatic treatment of moderate to severe idiopathic restless legs syndrome in doses up to 0.54 mg of base (0.75 mg of salt) (see section 4.2).

Oprymea 0.26mg modified-release tablets Велика Британија - Енглески - MHRA (Medicines & Healthcare Products Regulatory Agency)

oprymea 0.26mg modified-release tablets

consilient health ltd - pramipexole dihydrochloride monohydrate - modified-release tablet - 260microgram

Oprymea 0.52mg modified-release tablets Велика Британија - Енглески - MHRA (Medicines & Healthcare Products Regulatory Agency)

oprymea 0.52mg modified-release tablets

consilient health ltd - pramipexole dihydrochloride monohydrate - modified-release tablet - 520microgram