Last reviewed · How we verify

néfopam

University Hospital, Bordeaux · FDA-approved active Small molecule

Nefopam is a non-opioid analgesic that inhibits the reuptake of monoamines (norepinephrine, dopamine, and serotonin) in the central nervous system to produce analgesia.

Nefopam is a non-opioid analgesic that inhibits the reuptake of monoamines (norepinephrine, dopamine, and serotonin) in the central nervous system to produce analgesia. Used for Moderate acute and postoperative pain, Chronic pain conditions.

At a glance

Generic namenéfopam
SponsorUniversity Hospital, Bordeaux
Drug classNon-opioid analgesic; monoamine reuptake inhibitor
TargetNorepinephrine transporter (NET); dopamine transporter (DAT); serotonin transporter (SERT)
ModalitySmall molecule
Therapeutic areaPain Management
PhaseFDA-approved

Mechanism of action

Nefopam works primarily by blocking the reuptake of norepinephrine and dopamine at presynaptic terminals, increasing their synaptic concentrations and enhancing pain modulation pathways. Unlike opioids, it does not bind to opioid receptors and has a distinct mechanism that makes it useful as a non-opioid alternative for moderate pain relief. It also has mild anticholinergic and sympathomimetic properties that contribute to its analgesic effects.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: