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Zanamivir

Published: July 26, 2026Updated: August 20, 2026

Zanamivir is an antiviral medication classified as a neuraminidase inhibitor, used specifically for the treatment and prevention of influenza A and B virus infections in adults and children. It is administered via oral inhalation using a specialized device (Diskhaler) and works by inhibiting viral replication, thereby reducing the severity and duration of flu symptoms when treatment begins within 48 hours of symptom onset.

Quick summary

Zanamivir is an inhaled antiviral medication used to treat and prevent influenza A and B infections.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ATC
J05AH01
RxNorm
69722
Generic
Zanamivir
Class
atc-j05
Brands
Relenza
Availability
rx
Lactation
unknown
Routes
—
Forms
inhaler
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 inhalation dose that may cause toxicity
Chronic overdose: Not typically applicable due to poor systemic absorption; prolonged excessive use may lead to respiratory irritation
Immediate actions
Monitor respiratory function, provide supportive care, administer bronchodilators if needed
Antidote
No specific antidote available(Supportive care is mainstay of treatment)
Poison Control: 1-800-222-1222

Special Populations

11 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh potential risks to fetus

Monitor

regular prenatal care and fetal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use when benefits outweigh risks; influenza can be more severe in pregnant women

Monitor

standard prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use as needed

Key Recommendations

recommended if exposed to or infected with influenza; benefits outweigh risks

Monitor

standard prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

lactation

nursing mothers
caution
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

use with caution; minimal systemic absorption may result in low milk transfer

Monitor

monitor infant for any adverse effects

Use with caution and monitor for adverse effects.

✓

pediatric_age

children 5 12 years
safe
FDA Category
N
Dose Adjustment

adult dose - 2 inhalations twice daily

Key Recommendations

approved for treatment and prophylaxis in children 5 years and older

Monitor

monitor for bronchospasm especially in patients with asthma

⚠

pediatric_age

children under 5 years
caution
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not approved for children under 5; limited safety and efficacy data

Monitor

close monitoring if used off-label

Use with caution and monitor for adverse effects.

✓

geriatric

elderly 65 years and older
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

use standard adult dosing; no dose adjustment required for age alone

Monitor

monitor for bronchospasm and respiratory function

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

no dose adjustment required due to minimal systemic absorption

Monitor

standard monitoring

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

limited data available; use only if benefits outweigh risks

Monitor

monitor renal function

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

no dose adjustment required; drug is not significantly metabolized by hepatic enzymes

Monitor

standard monitoring

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

limited data available; use only if benefits outweigh risks

Monitor

monitor liver function

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1999

FDA approval year for Zanamivir (Relenza)

drug_classWHO
2023

Drug class

Value:Neuraminidase inhibitor (Antiviral)

Pharmacological classification

usageCDC
2023

Common uses

Value:Treatment and prevention of influenza A and B

Therapeutic indications

administrationFDA
2023

Route of administration

Value:Inhaled (oral inhalation)

Delivery method

Treatment and prevention of uncomplicated influenza A and B virus infections in adults and children aged 5 years and older. It is particularly useful for patients at high risk of complications or those who cannot use other antiviral medications.

Zanamivir inhibits the neuraminidase enzyme on the surface of influenza viruses. Neuraminidase is essential for cleaving sialic acid residues, which allows newly formed viral particles to be released from infected host cells. By blocking this enzyme, the drug prevents viral spread to uninfected cells.

Most effective when started within 48 hours of symptom onset; not a substitute for annual flu vaccination. Should be used with caution in patients with asthma or COPD due to risk of bronchospasm. Common side effects include headache, throat pain, and nasal discomfort. Resistance is uncommon but has been reported.

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 20, 2026. · Read our editorial policy