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Antabuse (DISULFIRAM)

Teva Womens · FDA-approved approved Small molecule Quality 50/100

Antabuse (Disulfiram) is a small molecule aldehyde dehydrogenase inhibitor, originally developed and currently owned by Teva Women's, that targets lysyl oxidase homolog 4. It was FDA-approved in 1951 for the treatment of alcoholism. As an off-patent medication, it is available from multiple generic manufacturers. Key safety considerations include the risk of severe reactions when combined with alcohol. Antabuse works by inhibiting the enzyme responsible for breaking down acetaldehyde, a toxic byproduct of alcohol metabolism.

At a glance

Generic nameDISULFIRAM
SponsorTeva Womens
Drug classAldehyde Dehydrogenase Inhibitor [EPC]
TargetLysyl oxidase homolog 4
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved
First approval1951

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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