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Pralidoxime Chloride (Autoinjector) (PRALIDOXIME)

Baxter · FDA-approved approved Small molecule Verified Quality 75/100

Pralidoxime Chloride works by reactivating the enzyme acetylcholinesterase, which is inhibited by organophosphate poisoning.

Pralidoxime Chloride (Autoinjector) (PRALIDOXIME) is a cholinesterase reactivator developed by Baxter Healthcare Corp. It targets acetylcholinesterase to treat cholinesterase inhibitors toxicity, organophosphate poisoning, and organophosphorous overdose. Originally approved by the FDA in 1964, it remains off-patent with no active Orange Book patents. The autoinjector modality provides a convenient treatment option for emergency situations. Key safety considerations include its short half-life of 1.4 hours.

At a glance

Generic namePRALIDOXIME
SponsorBaxter
Drug classCholinesterase Reactivator
TargetAcetylcholinesterase
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1964

Mechanism of action

Imagine your body's 'off' switch for a chemical called acetylcholine. When you're poisoned with something like nerve gas, this switch gets stuck in the 'on' position, causing problems. Pralidoxime Chloride helps flip the switch back to 'off' by reactivating the enzyme that normally turns it off.

Approved indications

Common side effects

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