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P2Y12 Inhibitor Antiplatelet — ACS Pregnancy: As no clinical data on exposure during pregnancy are available, it is preferable not to use clopidogrel during pregnancy as a precautionary measure. Breast-feeding should not be continued during treatment.

Clopidogrel (Loading Dose)

Brand names: Plavix

Used in: Stroke & TIA

Clopidogrel is an antiplatelet (P2Y12 inhibitor) for acute coronary syndromes, after coronary stents, and in secondary prevention of vascular events.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Acute coronary syndrome (non-ST segment elevation ACS): initiate with a single 300 mg or 600 mg oral loading dose, then continue 75 mg once daily with acetylsalicylic acid (ASA) 75-325 mg daily (ASA dose recommended not to exceed 100 mg). A 600 mg loading dose may be considered in patients <75 years of age when percutaneous coronary intervention is intended.
Route: Oral (may be given with or without food)
Frequency: Single loading dose, then 75 mg once daily
Other regimens stated in SPC section 4.2: ST-segment elevation MI, medically treated and eligible for thrombolytic/fibrinolytic therapy - 75 mg once daily initiated with a 300 mg loading dose in combination with ASA, with or without thrombolytics; in patients over 75 years of age clopidogrel should be initiated WITHOUT a loading dose; combined therapy started as early as possible after symptom onset and continued for at least four weeks. When PCI is intended - 600 mg loading dose for primary PCI and for PCI more than 24 hours after fibrinolytic therapy (in patients >=75 years the 600 mg loading dose should be administered with caution); 300 mg loading dose for PCI within 24 hours of fibrinolytic therapy; then 75 mg once daily with ASA 75-100 mg daily, continued up to 12 months. Moderate-to-high-risk TIA (ABCD2 >=4) or minor ischaemic stroke (NIHSS <=3) - loading dose 300 mg then 75 mg once daily plus ASA 75-100 mg once daily, started within 24 hours of the event and continued for 21 days, followed by single antiplatelet therapy. Atrial fibrillation - 75 mg once daily with ASA 75-100 mg daily. Optimal duration of treatment in ACS has not been formally established; clinical trial data support use up to 12 months with maximum benefit at 3 months. Missed dose: if less than 12 hours after the scheduled time, take immediately then resume schedule; if more than 12 hours, take the next dose at the scheduled time and do not double the dose. Paediatric population - the SPC states clopidogrel should NOT be used in children because of efficacy concerns. Section 4.4 states the 600 mg loading dose is not recommended in patients with non-ST segment elevation ACS aged >=75 years due to increased bleeding risk, and that clopidogrel should be discontinued 7 days before elective surgery if antiplatelet effect is temporarily not desirable.

Dose adjustments

Renal

No dose adjustment stated; SPC section 4.2 states therapeutic experience is limited in patients with renal impairment (see section 4.4).

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

US labelling (FDA)

Reference — US labelling, may differ from UK

Acute coronary syndrome ( 2.1 ) – Initiate clopidogrel tablets with a single 300 mg oral loading dose and then continue at 75 mg once daily. – Initiating clopidogrel tablets without a loading dose will delay establishment of an antiplatelet effect by several days. Recent MI, recent stroke, or established peripheral arterial disease: 75 mg once daily orally without a loading dose. ( 2.2 ) 2.1 Acute Coronary Syndrome In patients who need an antiplatelet effect within hours, initiate clopidogrel tablets with a single 300 mg oral loading dose and then continue at 75 mg once daily. Initiating clopidogrel tablets without a loading dose will delay establishment of an antiplatelet effect by several …

Source: US FDA prescribing information (openFDA / DailyMed), label dated 2024-05-17. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.

Contraindications

  • Hypersensitivity to the active substance or to any of the excipients
  • Severe hepatic impairment
  • Active pathological bleeding such as peptic ulcer or intracranial haemorrhage

Side effects

  • Bleeding - the most common reaction, mostly reported during the first month of treatment (overall incidence of any bleeding 9.3% in CAPRIE)
  • Major bleeding, mainly extracranial and gastrointestinal, when combined with ASA (6.7% vs 4.3% for placebo + ASA in ACTIVE-A)
  • Intracranial bleeding (1.4% with clopidogrel + ASA vs 0.8% with placebo + ASA in ACTIVE-A)
  • Haematological adverse reactions - blood cell count determination should be considered if symptoms suggestive of bleeding arise (section 4.4)
  • Thrombotic thrombocytopenic purpura (TTP) - reported very rarely, sometimes after short exposure; potentially fatal, requires prompt treatment including plasmapheresis
  • Acquired haemophilia - reported following use of clopidogrel

Interactions

  • ASA, heparin, glycoprotein IIb/IIIa inhibitors, NSAIDs including COX-2 inhibitors, SSRIs, pentoxifylline - increased bleeding risk; use with caution (SPC section 4.4)
  • Oral anticoagulants - concomitant administration not recommended; may increase the intensity of bleeding (SPC section 4.4)
  • Triple antiplatelet therapy (clopidogrel + ASA + dipyridamole) for stroke secondary prevention - not recommended in acute non-cardioembolic ischaemic stroke or TIA due to increased haemorrhage risk (SPC section 4.4)
  • CYP2C19 strong inducers (e.g. rifampicin) - increase active metabolite levels and platelet inhibition; avoid concomitant use (SPC section 4.4; US label section 7.1)
  • CYP2C19 inhibitors omeprazole or esomeprazole - avoid concomitant use; both significantly reduce the antiplatelet activity of clopidogrel (US label sections 5.1 / 7.2)
  • Opioids - decreased exposure to clopidogrel; consider a parenteral antiplatelet agent (US label section 7.3)
  • Repaglinide (CYP2C8 substrates) - increased substrate plasma concentrations (US label section 7.8)

Clinical monograph

How it works

It is a pro-drug whose active metabolite irreversibly blocks the platelet P2Y12 ADP receptor, inhibiting aggregation for the platelet's lifespan.

Prescribing in practice

  • It requires CYP2C19 activation — omeprazole and esomeprazole reduce its effect, so use an alternative acid suppressant (e.g. lansoprazole or pantoprazole) if one is needed.
  • Bleeding risk rises when combined with other antithrombotics; stop it about 5–7 days before major surgery where appropriate.
  • Do not stop it prematurely after a stent without specialist advice (stent thrombosis risk).

Monitoring

Watch for bleeding and review antithrombotic combinations and acid-suppressant choice.

Counselling the patient

  • Don't stop it without advice, especially soon after a stent.
  • Report bleeding or bruising.
  • Tell clinicians you take it before surgery or dental work.

Evidence & guidelines

Established in ACS and secondary prevention (NICE guidance), often combined with aspirin for a defined period.

Reference: NICE NG185 (ACS); ESC ACS Guidelines 2023; MHRA Drug Safety Update (clopidogrel/PPI interaction); Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.

📚 MRCEM Revision

Featured in these MRCEM clinical pathways

Clopidogrel (Loading Dose) is a core drug in the following exam-focused workups on our sister siteReviseMRCEM.

MRCEM Primary / Intermediate / OSCE candidates: each pathway includes exam-style questions, RCEM/NICE citations, and FAQ summaries.