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Bupivacaine-adrenaline

University of Aarhus · FDA-approved active Small molecule

Bupivacaine is a local anesthetic that blocks sodium channels in nerve fibers, while adrenaline (epinephrine) causes vasoconstriction to prolong anesthetic duration and reduce systemic toxicity.

Bupivacaine is a local anesthetic that blocks sodium channels in nerve fibers, while adrenaline (epinephrine) causes vasoconstriction to prolong anesthetic duration and reduce systemic toxicity. Used for Local and regional anesthesia for surgical procedures, Infiltration anesthesia, Nerve blocks.

At a glance

Generic nameBupivacaine-adrenaline
Also known asMarcain-adrenalin
SponsorUniversity of Aarhus
Drug classLocal anesthetic with vasopressor
TargetVoltage-gated sodium channels; alpha-1 adrenergic receptors (adrenaline component)
ModalitySmall molecule
Therapeutic areaAnesthesia/Pain Management
PhaseFDA-approved

Mechanism of action

Bupivacaine penetrates nerve cell membranes and reversibly inhibits sodium influx, preventing depolarization and action potential propagation in sensory and motor nerves. The addition of adrenaline causes local vasoconstriction, which slows systemic absorption of the anesthetic, extends its duration of action, and reduces peak plasma concentrations and associated toxicity risks.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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