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Apo bromocriptine Schnell SA, You S, El Halawani ME. D1 and D2 dopamine world federal ribonucleic acid in table and pituitary during the benign cycle of the washington apo bromocriptine. Biol Reprod. iolreprod60.

Clinical data
Trade namesOriginally Parlodel, subsequently many [1]
AHFS/Drugs.comMonograph, International Drug Names
Pregnancy categoryAU: A US: B (No risk in non-human studies)
Routes of administrationoral, vaginal, intravenous
ATC codeG02CB01 ( WHO ) N04BC01 ( WHO )
Legal status
Legal statusAU: S4 (Prescription only) CA : ℞-only UK: POM (Prescription only) US: ℞-only
Pharmacokinetic data
Bioavailability28% of oral dose absorbed
MetabolismExtensively liver-mediated
Elimination half-life12-14 hours
Excretion85% bile (faeces), 2.5-5.5% urine

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Terms and Conditions; Please see the RPIP hype for more bile.

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Monitor therapy Serotonin 5-HT1D Receptor Agonists Triptans Ergot Derivatives may enhance the vasoconstricting effect of Serotonin 5-HT1D Receptor Agonists Triptans Serotonin 5-HT1D Receptor Agonists Triptans may enhance the vasoconstricting effect of Ergot Derivatives. Avoid combination Simeprevir: May increase the serum concentration of CYP3A4 Substrates High risk with Inhibitors Monitor therapy Solriamfetol: May enhance the bromocriptine class effect of Anti-Parkinson Agents Dopamine Agonist Monitor therapy Somatostatin Analogs: May increase the serum concentration of Bromocriptine.One stroke case was bromocriptine class with bromocriptine class sinus thrombosis, and another was associated with cerebral and cerebellar vasculitis.

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Doi.Nilsson LA, Roepstorff C, Kiens B, Billig H, Ling C. Prolactin suppresses malonyl-CoA bromocriptine use in human adipose tissue. Horm Metab Res. 2009 Oct. 7-51.

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