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Alteplase

Published: July 26, 2026Updated: August 24, 2026

Alteplase is a thrombolytic medication, also known as a 'clot-busting' drug, used to dissolve dangerous blood clots in the body. It works by activating plasminogen to plasmin, which breaks down fibrin in clots. This medication is primarily used in emergency situations such as acute heart attacks, ischemic strokes, and pulmonary embolisms to restore blood flow and prevent tissue damage.

Quick summary

Alteplase is an emergency clot-dissolving medication used to treat life-threatening blood clots in the heart, brain, and lungs.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy

Key facts at a glance

ATC
B01AD02
RxNorm
8410
Generic
Alteplase
Class
atc-b01
Brands
Activase
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Dose significantly exceeding recommended therapeutic maximum (typically 90mg for stroke treatment) that may cause serious bleeding complications
Chronic overdose: Repeated administrations within 24 hours or cumulative dose exceeding 150mg increases risk of severe hemorrhage
Immediate actions
Discontinue infusion immediately, monitor vital signs, obtain CBC and coagulation studies, prepare for blood product transfusion
Antidote
No specific antidote available; treatment is supportive with cryoprecipitate, fresh frozen plasma, and platelet transfusion as needed(Supportive care effectiveness depends on prompt initiation and severity of bleeding)
Poison Control: 1-800-222-1222

Special Populations

9 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

pregnancy

second third trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use only when benefits clearly outweigh risks

Monitor

close maternal and fetal monitoring

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

temporarily discontinue breastfeeding for 24 hours after administration

Monitor

monitor infant for bleeding

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly 65 years
caution
FDA Category
N
Dose Adjustment

consider lower dose based on weight and indication

Key Recommendations

use with caution due to increased bleeding risk especially intracranial hemorrhage

Monitor

close neurological monitoring blood pressure monitoring

Use with caution and monitor for adverse effects.

?

pediatric_age

children under 18
unknown
FDA Category
N
Dose Adjustment

no standard pediatric dosing established

Key Recommendations

use only in life-threatening situations such as catheter clearance when benefits outweigh risks

Monitor

careful bleeding monitoring

⚠

renal_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

no dose adjustment typically required

Key Recommendations

use with caution due to increased bleeding risk

Monitor

monitor renal function and for signs of bleeding

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with extreme caution

Key Recommendations

weigh risks versus benefits carefully

Monitor

intensive bleeding monitoring

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

no specific dose adjustment but use cautiously

Key Recommendations

use with caution due to altered metabolism and bleeding risk

Monitor

monitor liver function and coagulation parameters

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

severe
unsafe
FDA Category
N
Dose Adjustment

avoid if possible

Key Recommendations

avoid use in severe hepatic impairment due to high bleeding risk

Monitor

close monitoring if use unavoidable

Use of this medication in this population requires careful consideration of risks and benefits.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1987

FDA approval for acute myocardial infarction

drug_classWHO
2023

Drug class

Value:Thrombolytic agent

Tissue-type plasminogen activator (tPA)

usageMedical guidelines
2023

Common uses

Value:Acute ischemic stroke, acute myocardial infarction, pulmonary embolism

Thrombolytic therapy for clot dissolution

mechanismFDA
2023

Mechanism of action

Value:Converts plasminogen to plasmin to dissolve fibrin clots

Fibrinolytic action

Treatment of acute myocardial infarction (heart attack), acute ischemic stroke (within 4.5 hours of symptom onset), acute massive pulmonary embolism, and acute peripheral arterial occlusion. It is used in hospital settings for time-sensitive clot-related emergencies.

Alteplase is a recombinant tissue plasminogen activator (tPA) that binds to fibrin in blood clots and converts plasminogen to plasmin. Plasmin then degrades fibrin, breaking down the clot and restoring blood flow to affected tissues.

Administered intravenously, typically within strict time windows depending on the condition. Major risk is bleeding, especially intracranial hemorrhage. Contraindicated in active bleeding, recent surgery, history of hemorrhagic stroke, or uncontrolled high blood pressure. Requires careful patient selection and monitoring. Efficacy depends on time from clot formation—earlier administration yields better outcomes.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 24, 2026. · Read our editorial policy