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Clopidogrel

Brand: Plavix (US/EU) / Clopitab (IN) / Clopivas (IN) / Clopid (BD)
Antiplatelet P2Y12 inhibitor (thienopyridine, prodrug)

Chemistry

Molecular Formula C16H16ClNO2S
PubChem CID: 60606
Open in PubChem
Structure
structure

Pharmacokinetics

Half-life 8 hours
Tmax 1 h
Protein Binding 98 %
Volume of Distribution 0.2 L/kg (approx)
Clearance Route hepatic
Active Metabolites yes
Notes Prodrug requiring CYP2C19 activation; reduced effect in poor metabolizers; consider alternative (ticagrelor/prasugrel) in loss-of-function alleles. | Updated 2025: CPIC and AHA guidelines recommend CYP2C19 genotyping before initiation. Poor metabolizers show reduced antiplatelet efficacy; consider prasugrel or ticagrelor instead. Avoid strong CYP2C19 inhibitors (omeprazole, esomeprazole). Reference: https://cpicpgx.org/guidelines/guideline-for-clopidogrel-and-cyp2c19/

⚠️ Safety & Warnings

Severity: Moderate

Adverse Effects:
Bleeding (GI/intracranial), dyspepsia, rash; RARE: thrombotic thrombocytopenic purpura (TTP), neutropenia

Contraindications:
Active pathological bleeding (e.g., intracranial hemorrhage, GI bleed), severe hepatic impairment, known hypersensitivity

Precautions:
Consider **Clopidogrel resistance test (CYP2C19)** in high-risk PCI or suspected poor response; avoid strong CYP2C19 inhibitors (e.g., omeprazole) if possible; stop 5–7 days before major surgery; use caution with concomitant anticoagulants/NSAIDs