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S a result of this, the FDA removed pergolide from the U. market on March. 4 Since cabergoline is not approved in the U. for Parkinson's Disease, but for hyperprolactinemia, the cabergoline safety remains on the market.ince cabergoline exerts its cabergoline safety effect by direct stimulation of dopamine receptors, it should not be concurrently administered with drugs which have dopamine-antagonist activity such as phenothiazines, butyrophenones, thioxanthenes, metoclopramide since these might reduce the prolactin-lowering effect of cabergoline.
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In most cases, the condition is mild and resolves itself without treatment, but some women develop a cabergoline safety or severe form of OHSS, which requires hospitalisation.The side effects are considered mild when used for treatment of hyperprolactinemia and other endocrine cabergoline safeties or gynecologic cabergoline safeties where the typical dose is one hundredth to one tenth that for Parkinson's disease.
citation needed Cabergoline is considered the best tolerable option for hyperprolactinemia treatment although the newer and less tested quinagolide may offer similarly favourable side effect profile with quicker titration times.
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