Ropinirole 5mg tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

ropinirole 5mg tablets

phoenix healthcare distribution ltd - ropinirole hydrochloride - oral tablet - 5mg

Ropinirole 5mg tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

ropinirole 5mg tablets

mawdsley-brooks & company ltd - ropinirole hydrochloride - oral tablet - 5mg

ROPINIROLE tablet, film coated United States - English - NLM (National Library of Medicine)

ropinirole tablet, film coated

unit dose services - ropinirole hydrochloride (unii: d7zd41rzi9) (ropinirole - unii:030pyr8953) - ropinirole 1 mg - ropinirole tablets are indicated for the treatment of parkinson’s disease. ropinirole tablets are indicated for the treatment of moderate-to-severe primary restless legs syndrome (rls). ropinirole is contraindicated in patients known to have a hypersensitivity/allergic reaction (including urticaria, angioedema, rash, pruritus) to ropinirole or to any of the excipients. risk summary there are no adequate data on the developmental risk associated with the use of ropinirole in pregnant women. in animal studies, ropinirole had adverse effects on development when administered to pregnant rats at doses similar to (neurobehavioral impairment) or greater than (teratogenicity and embryolethality at >36 times) the maximum recommended human dose (mrhd) for parkinson’s disease. ropinirole doses associated with teratogenicity and embryolethality in pregnant rats were associated with maternal toxicity. in pregnant rabbits, ropinirole potentiated the teratogenic effects of l-dopa when these drugs were administered in combin