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Bloxiverz (NEOSTIGMINE)

Fresenius Kabi · FDA-approved approved Small molecule Verified Quality 75/100

Bloxiverz works by blocking the enzyme acetylcholinesterase, allowing more acetylcholine to be available in the nervous system.

Bloxiverz (NEOSTIGMINE) is a small molecule cholinesterase inhibitor developed by ECLAT PHARMS LLC and currently owned by Fresenius Kabi Usa. It targets acetylcholinesterase to increase acetylcholine levels in the nervous system. Bloxiverz is FDA-approved for treating Myasthenia gravis, retention of urine, and reversal of neuromuscular blockade. The drug is off-patent with 16 generic manufacturers available. Key safety considerations include its short half-life of 1.3 hours and low bioavailability of 2%.

At a glance

Generic nameNEOSTIGMINE
SponsorFresenius Kabi
Drug classCholinesterase Inhibitor
TargetAcetylcholinesterase
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval2013

Mechanism of action

. Mechanism of Action. Neostigmine methylsulfate is competitive cholinesterase inhibitor. By reducing the breakdown of acetylcholine, neostigmine methylsulfate induces an increase in acetylcholine in the synaptic cleft which competes for the same binding site as nondepolarizing neuromuscular blocking agents, and reverses the neuromuscular blockade.

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

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