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Antiplatelet (P2Y12 Inhibitor)

Clopidogrel (Stroke/TIA Secondary Prevention)

Brand names: Plavix

This page covers clopidogrel used for secondary prevention after ischaemic stroke or transient ischaemic attack, where it is an established oral antiplatelet option.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

Clopidogrel is a prodrug whose active metabolite irreversibly blocks the platelet P2Y12 ADP receptor, inhibiting platelet aggregation for the lifespan of the platelet.

Prescribing in practice

  • The principal hazard is bleeding, so assess bleeding risk and avoid unnecessary combination with other antiplatelets or anticoagulants beyond any defined short dual-therapy window.
  • Proton pump inhibitors that strongly inhibit CYP2C19, particularly omeprazole and esomeprazole, may reduce its antiplatelet effect, so an alternative acid-suppressant is preferred if one is needed.
  • As a prodrug requiring CYP2C19 activation, response may be reduced in poor metabolisers, a relevant consideration if recurrent events occur on treatment.

Monitoring

No routine platelet-function monitoring is required; review clinically for bleeding and recurrent vascular events at follow-up.

Counselling the patient

  • Take once daily and do not stop without medical advice, as stopping increases stroke risk.
  • Report unusual bruising, prolonged bleeding, black stools or blood in urine.
  • Tell any dentist or surgeon you take an antiplatelet before procedures.

Evidence & guidelines

Long-term single-agent clopidogrel is recommended by NICE for secondary prevention after ischaemic stroke or TIA, with short-term dual antiplatelet therapy supported by trials such as POINT and CHANCE in the acute phase.

Reference: CAPRIE Trial (Lancet 1996); CHANCE Trial (Wang et al, NEJM 2013); NICE NG128; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.