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Description
This peptide provides a standardized research format that supports consistency across experimental protocols and facilitates administration within laboratory settings
J Am Acad Dermatol 1996
Adverse Reactions (n (%))* During the 4-Week, Double-Blind, Placebo-Controlled Trial in Hyperprolactinemic Females In the 8-week, double-blind period of the comparative trial with bromocriptine, 2% (4/221) of DOSTINEXtreated patients (0.5 mg twice weekly) discontinued treatment because of an adverse event and 6% (14/231) of bromocriptine-treated patients (at a dose of 2.5 mg twice daily) discontinued treatment because of an adverse event
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