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Pfizer MedicinesTherapy AreasExplore ContentEventsVideosMaterialsFeatured ArticlesLet’s ConnectSupplyAlliance HealthcareOff-contract claims

Adverse event reporting can be found at the bottom of the page
About DOSTINEXDosing & Administration  EfficacySafetySupport and Resources Materials Videos 

Dostinex (cabergoline) Prescribing Information (external link) Adverse event reporting information can be found at the bottom of the page 

Can offer a prolactin lowering effect with a single oral dose1

A snapshot of DOSTINEX 

Onset of action occurs within 3 hours.1 

Sustained action for 7 to 28 days in hyperprolactinaemia patients and up to 14 to 21 days in puerperal patients.1

Higher affinity for dopamine receptor–binding sites than bromocriptine.2,*

From a 2002 multivariate analysis of the binding profiles of 14 drugs at 21 native and cloned human receptor subtypes.  Control hyperprolactinaemia with DOSTINEX See how DOSTINEX works to lower prolactin levels in the body

DOSTINEX is a long-acting D2 dopamine agonist that directly stimulates receptors in the pituitary gland, decreasing the production of prolactin.



Our High Quality Manufacturing Process

Watch the short film (4 minutes) below celebrating 25 years of manufacture of DOSTINEX at Ascoli in Italy. 

References:Dostinex [summary of product characteristics]. Sandwich, Kent; Pfizer Limited; 2020.
Millan MJ, et al. Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. I. A multivariate analysis of the binding profiles of 14 drugs at 21 native and cloned human receptor subtypes. J Pharmacol Exp Ther 2002;303(2):791-804. Dosing and administration 

Learn more about the dosing for DOSTINEX

Learn moreLoading Efficacy 

View clinical trial data to show proven efficacy in hyperprolactinaemia & lactation suppression with DOSTINEX

Learn moreLoading Safety 

View the safety profile for DOSTINEX

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PP-DOS-GBR-0016. July 2023

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

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Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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