[Durgical](https://durgical.com/en/) › [DurgiPedia](https://durgical.com/en/durgipedia/) › [Pharmacology](https://durgical.com/en/pharmacology/) › [Antiplatelet drugs](https://durgical.com/en/pharmacology/classes/antiplatelet-drugs/) › Prasugrel

[Pharmacology](https://durgical.com/en/pharmacology/) · [Antiplatelet drugs](https://durgical.com/en/pharmacology/classes/antiplatelet-drugs/)

# Prasugrel

An oral thienopyridine that blocks P2Y12 irreversibly, more strongly than clopidogrel. Not used after a stroke or transient ischaemic attack.

Updated 2026-11-01

- Class: [Antiplatelet drugs](https://durgical.com/en/pharmacology/classes/antiplatelet-drugs/)
- Receptor: P2Y12 ADP receptor on platelets
- ATC code: B01AC22

◎**P2Y12 ADP receptor on platelets**Prasugrel

ⓘ The figure shows the human P2Y12 receptor with AZD1283, an experimental P2Y12 blocker. Prasugrel's active metabolite binds covalently and has no structure with the receptor.

**Target in 3D:** P2Y12 ADP receptor on platelets. PDB structure 4NTJ (RCSB PDB, public domain). [View the structure at RCSB PDB](https://www.rcsb.org/structure/4NTJ) · Drag to rotate · pinch to zoom

## Mechanism of action

Prasugrel is a prodrug. In the gut it is quickly hydrolysed to a thiolactone, which liver enzymes (mainly CYP3A4 and CYP2B6) turn into the active metabolite in a single step. The metabolite binds P2Y12 irreversibly, blocking ADP-driven activation and aggregation for the rest of the platelet's life. Because its activation is simpler, common CYP2C19 variants do not change its effect.

- Gut esterases turn prasugrel into a thiolactone
- One liver step (CYP3A4, CYP2B6) makes the active metabolite
- It binds P2Y12 irreversibly: platelets blocked for life

## Pharmacokinetics

**Absorption**
Rapid; prasugrel itself is not detected in plasma.

**Distribution**
The active metabolite is about 98% bound to albumin.

**Metabolism**
Intestinal hydrolysis, then one step mainly by CYP3A4 and CYP2B6; CYP2C19 genotype has no relevant effect.

**Half-life**
About 7 hours for the active metabolite (range 2 to 15).

**Onset and duration**
About 90% of patients reach at least 50% platelet inhibition within 1 hour of a loading dose.

## Indications

- Acute coronary syndrome (unstable angina, NSTEMI or STEMI) managed with percutaneous coronary intervention, together with aspirin. [Myocardial Infarction (Heart Attack) →](https://durgical.com/en/conditions/myocardial-infarction/)

## Adverse effects

### Common

- Bleeding, including nosebleeds and bruising
- Anaemia
- Headache, dizziness, back pain

### Serious (rare, important)

- Significant, sometimes fatal bleeding
- Bleeding related to coronary bypass surgery
- Thrombotic thrombocytopenic purpura (TTP)
- Allergic reactions, including angioedema

## Contraindications

- Active pathological bleeding
- Prior transient ischaemic attack or stroke
- Hypersensitivity to prasugrel

## Key interactions

**Warfarin, NSAIDs and other drugs that raise bleeding risk**
Increase the risk of bleeding.

**Opioids such as morphine**
Can delay and reduce platelet inhibition after the loading dose.

## What is monitored

- Signs of bleeding, especially after invasive procedures (suspect it with low blood pressure)
- Haemoglobin
- Platelet count and smear if TTP is suspected

## Administration and safety

- Oral, with or without food, together with aspirin
- Generally not recommended from age 75, except in high-risk patients (diabetes or prior MI); low body weight increases exposure
- Not started when urgent coronary bypass surgery is likely; stopped several days before surgery when possible, as planned by the team
- Not stopped early without the cardiology team

## Nursing care

- Ask about previous stroke or transient ischaemic attack before the first dose: it is a contraindication
- Note age and body weight, which change bleeding risk
- Watch for bleeding and low blood pressure after catheterisation
- Teach the patient to tell every dentist and surgeon and to report purple spots, fever or confusion

## Pregnancy and breastfeeding

There are no human data in pregnancy; animal studies showed no malformations. Bleeding at delivery is a concern.

## Memory aid

PRASugrel = PRoblem After Stroke: strong and irreversible, but not after stroke or TIA, and careful in the old and the light.

## Test yourself

Think of the answer, then tap the question to see it.

## Why does CYP2C19 genotype matter for clopidogrel but not for prasugrel?

Prasugrel becomes active through intestinal hydrolysis and one liver step, mainly CYP3A4 and CYP2B6; CYP2C19 variants have no relevant effect on its active metabolite.

## Which history contraindicates prasugrel?

A previous stroke or transient ischaemic attack, because of the higher risk of intracranial bleeding.

## In which patients is prasugrel generally not recommended because of bleeding?

People aged 75 or more (except high-risk cases such as diabetes or prior MI); low body weight also raises exposure and bleeding risk.

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## Related drugs

- [Clopidogrel](https://durgical.com/en/pharmacology/clopidogrel/)
- [Ticagrelor](https://durgical.com/en/pharmacology/ticagrelor/)
- [Acetylsalicylic acid](https://durgical.com/en/pharmacology/acetylsalicylic-acid/)

## Related conditions

- [Myocardial Infarction (Heart Attack)](https://durgical.com/en/conditions/myocardial-infarction/)

[← Back to the class: Antiplatelet drugs](https://durgical.com/en/pharmacology/classes/antiplatelet-drugs/)

Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: [DailyMed - PRASUGREL tablet, film coated](https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f51e64e0-f556-65d0-a876-fb709aaeefea) (DailyMed (U.S. National Library of Medicine), 2026); [Prasugrel: MedlinePlus Drug Information](https://medlineplus.gov/druginfo/meds/a609027.html) (MedlinePlus (U.S. National Library of Medicine), 2025); [4NTJ: Structure of the human P2Y12 receptor in complex with an antithrombotic drug](https://www.rcsb.org/structure/4NTJ) (RCSB Protein Data Bank, 2014).

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Representative model, for educational purposes only.

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