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Ropivacaine Ketorolac

University of Aarhus · FDA-approved active Small molecule

Ropivacaine provides local anesthesia by blocking sodium channels in nerve fibers, while ketorolac provides anti-inflammatory and analgesic effects by inhibiting cyclooxygenase enzymes.

Ropivacaine provides local anesthesia by blocking sodium channels in nerve fibers, while ketorolac provides anti-inflammatory and analgesic effects by inhibiting cyclooxygenase enzymes. Used for Perioperative pain management and anesthesia.

At a glance

Generic nameRopivacaine Ketorolac
SponsorUniversity of Aarhus
Drug classLocal anesthetic + NSAID combination
TargetVoltage-gated sodium channels (ropivacaine); COX-1/COX-2 (ketorolac)
ModalitySmall molecule
Therapeutic areaPain Management / Anesthesia
PhaseFDA-approved

Mechanism of action

This is a combination product where ropivacaine, a long-acting amide local anesthetic, reversibly blocks voltage-gated sodium channels to prevent nerve impulse transmission in localized tissues. Ketorolac, a nonsteroidal anti-inflammatory drug (NSAID), inhibits COX-1 and COX-2 enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain. Together, they provide both local anesthetic and systemic analgesic/anti-inflammatory effects for perioperative pain management.

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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