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Alteplase

Recombinant tissue plasminogen activator (fibrinolytic) · Thrombolytic

START
Stroke: 0.9 mg/kg IV (10% bolus + 60-min infusion)
TYPICAL MAX
90 mg (stroke); 100 mg (STEMI/PE)
STOP IF
Any intracranial bleed signs, angioedema, or major haemorrhage
WATCH
Neuro status, BP <180/105, bleeding, airway (angioedema)
CDSCO approvedSchedule HATC B01AD02
Dose laddermg/d
50PE / mid90stroke max100STEMI/PE max
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo dose adjustment at any eGFR90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
3minONSET1hPEAK5min3hDURATION
ONSET
3min · fibrinolysis
PEAK
1h · end infusion
5min · t½ ~5 min
DURATION
3h · clotting recovery
EXCRETION
Hepatic proteolysis; rapid plasma clearance
route + CYP
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
Use only if life-threatening and benefit outweighs risk.
FDA category + note
Top interactionssee all 12
  • Tranexamic AcidContraindicatedDatabaseDDInter
  • BenazeprilSevereTextbookG&G 14e · p600
  • AbciximabSevereDatabaseDDInter
  • AcalabrutinibSevereDatabaseDDInter
Available in India

2 branded formulations. Look up specific brands in the Drugs workspace.

Mechanism

Recombinant human tPA that binds fibrin and converts entrapped plasminogen to plasmin, producing fibrin-selective clot lysis at the thrombus.

Indications

Acute ischaemic stroke (within 4.5 h)Acute STEMIAcute massive/submassive pulmonary embolismOccluded central venous catheters

Dosing

Adult
Ischaemic stroke: 0.9 mg/kg IV (max 90 mg) — 10% bolus, rest over 60 min. STEMI: accelerated weight-based ≤100 mg over 90 min. PE: 100 mg IV over 2 h.
Pediatric
Catheter clearance: 0.5–2 mg per lumen (specialist).
Renal adjustment
No dose adjustment.
Hepatic adjustment
No specific adjustment; bleeding risk in severe hepatic disease.
Geriatric
No dose change; higher ICH risk (assess carefully).
Max dose
90 mg (stroke); 100 mg (STEMI/PE)

Pharmacokinetics

Onset
Fibrinolysis within minutes
Peak effect
End of infusion
Duration
Fibrinolytic effect short; clotting recovers hours
Half-life
Initial ~4–5 min; terminal ~40 min
Bioavailability
IV 100%
Protein binding
Not applicable (protein)
Metabolism
Hepatic clearance (proteolysis)
Excretion
Hepatic metabolism; rapid plasma clearance

Contraindications

  • Active internal bleeding
  • Recent intracranial haemorrhage / known AVM / aneurysm / neoplasm
  • Recent intracranial or spinal surgery/trauma (<3 months)
  • Severe uncontrolled hypertension
  • Bleeding diathesis; (stroke) recent stroke or BP >185/110

Side effects

Common
Bleeding (puncture sites, GI, GU)HypotensionNauseaFever
Serious
  • Intracranial haemorrhage
  • Major systemic haemorrhage
  • Angioedema (orolingual, esp. with ACE inhibitors)
  • Reperfusion arrhythmias
  • Cholesterol embolisation

Pregnancy & lactation

Pregnancy

Use only if life-threatening and benefit outweighs risk.

Lactation

No data; short half-life — brief interruption reasonable.

Drug interactions

Tranexamic Acid
Contraindicated
Database

Tranexamic acid inhibits fibrinolysis, directly counteracting the thrombolytic effect of alteplase. This renders alteplase ineffective and may increase the risk of re-thrombosis.

Concomitant use is contraindicated. Tranexamic acid should not be administered with fibrinolytic agents.

Source: DDInter

Benazepril
Severe
Textbook

Increased risk of angioedema.

Avoid combination.

Source: G&G 14e · p600

Abciximab
Severe
Database

Clinical effect not specified

Source: DDInter

Acalabrutinib
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Anisindione
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Anticoagulants
Severe
Database

Additive bleeding

Strict protocol timing; monitor; weigh risk

Source: Kimi deep-research + Cla

Antiplatelets
Severe
Database

Additive bleeding

Per protocol; monitor closely

Source: Kimi deep-research + Cla

Apixaban
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Ardeparin
Severe
Database

Clinical effect not specified

Source: DDInter

Argatroban
Severe
Database

Clinical effect not specified

Source: DDInter

Avapritinib
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Betrixaban
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Related guidelines

Ask House about Alteplase

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, BNF·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20