Irreversible COX-1 inhibitor

Acetylsalicylic acid

Trombyl · Aspirin

Irreversibly acetylates COX-1, eliminating thromboxane synthesis in platelets for their entire lifespan. This is why a low once-daily dose is sufficient, and why the effect persists for 7–10 days after discontinuation.

BOXED WARNING

Gastrointestinal bleeding, particularly in combination with NSAIDs, anticoagulants, or corticosteroids. Do not give to children with viral infections — Reye's syndrome.

Dosing in adults

By indicationuppdaterad 2026-08-19
IndicationRegimenComment
Acute coronary syndrome, loading dose300–500 mg orally, chewedadminister immediately on suspicion
Secondary prevention75 mg orally once dailylifelong in established atherosclerotic disease
After PCI, dual antiplatelet therapy75 mg daily together with P2Y12 inhibitorduration based on bleeding risk
Preeclampsia prophylaxis75–150 mg at night from week 12in high-risk patients
Renal impairment

Avoid as analgesic at eGFR < 30; low cardiovascular doses can often be maintained.

Hepatic impairment

Avoid in severe hepatic failure and coagulopathy.

Children

Not given as analgesic or antipyretic to children. Exception: Kawasaki disease.

Pitfall

Primary prevention in individuals without known atherosclerotic disease now offers limited benefit relative to bleeding risk — reassess ongoing treatment when there is no clear indication.

Pharmacokinetics

BIOAVAIL.
50–75 %
Vd
0,15 l/kg
15–20 min (effect is irreversible)
PROTEIN BINDING
90 %
METABOLISM
Hydrolysis to salicylate
EXCRETION
Renal
EFFECT DURATION
7–10 days
ONSET
20 min (chewed)

Adverse effects by frequency

≥ 10 %
Dyspepsia, bruising, prolonged bleeding time
1–10 %
Peptic ulcer, iron deficiency anaemia, urticaria
< 1 %
Gastrointestinal bleeding, intracranial haemorrhage, bronchospasm in aspirin intolerance