Drug intelligence / Profile preview

Ergocaff PB

Development stage
Discontinued
Lead developer
Centrix Pharmaceutical
Modality
Small Molecules
Administration
Rectal
01

Overview

Ergocaff PB is a combination small molecule medication formerly used for the treatment of migraine headaches, particularly in patients experiencing severe nausea and vomiting. It contains four active components: ergotamine tartrate, caffeine, pentobarbital, and belladonna alkaloids. Ergotamine acts as a vasoconstrictor by targeting serotonin receptors (5-HT1B/1D), while caffeine is included to enhance the absorption and efficacy of ergotamine. Pentobarbital serves as a sedative to address the agitation associated with migraines, and belladonna provides anticholinergic effects to mitigate nausea. Developed and manufactured by Centrix Pharmaceutical, the drug was available as a rectal suppository. In 2007, the FDA ordered the discontinuation of Ergocaff PB and similar unapproved ergotamine-containing products due to safety concerns regarding potential drug interactions and lack of formal approval.

Brand names
Ergocaff PB
02

Targets

HTR1B (5-Hydroxytryptamine Receptor 1B)HTR1D (5-hydroxytryptamine receptor 1D)ADOR (Adenosine receptors)

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