Zanamivir

DEA Class; Rx

Common Brand Names; Relenza

  • Antivirals, Influenza; 
  • Neuraminidase Inhibitors

Neuraminidase inhibitor given via oral inhalation
Used for the treatment and prophylaxis of influenza virus A and B infection
When used for treatment, most effective when started within 48 hours of symptom onset

Indicated for the treatment of uncomplicated acute influenza A virus infection or influenza B virus infection.

For seasonal influenza prophylaxis for infections due to influenza A or influenza B virus.
For the treatment of novel influenza A viruses associated with severe human disease, including avian influenza A virus infection.

Hypersensitivity to zanamivir or formulation, including milk proteins

  • Headache (13-24%)
  • Throat/tonsil pain (8-19%)
  • Cough ( 7-17%)
  • Viral infection (3-13%)
  • Dizziness (2%)
  • Nausea (3%)
  • Diarrhea (3% adults, 2% children)
  • Vomiting (1% adults, 2% children)
  • Sinusitis (3%)
  • Bronchitis (2%)
  • Infection (ear, nose, & throat; 2% adults, 5% children)

Administer only via the Diskhaler inhaler

Do not make into an extemporaneous solution for administration by nebulization or mechanical ventilation; fatality reports of hospitalized patients with influenza who received a solution made with Relenza Inhalation Powder administered by nebulization or mechanical ventilation; lactose in this formulation obstructs proper functioning of the equipment

Most effective when used within 24-48 hr of onset of symptoms

Not recommended for treatment or prophylaxis of influenza in individuals with underlying airway diseases (eg, asthma, COPD); serious cases of bronchospasm, including fatalities, have been reported during treatment

If use is considered for patient with underlying airway disease, carefully monitor respiratory function, closely observe patient, and have supportive therapy (ie, fast-acting bronchodilators) immediately available

Reports of abnormal behavior and delirium

Available data from published studies suggest that use during pregnancy is not associated with an increased risk of birth defects or adverse maternal or fetal outcomes

There are no data on presence of zanamivir in human milk or effects on milk production

Adults

10 mg (i.e., 2 oral inhalations of 5 mg) twice daily.

Geriatric

10 mg (i.e., 2 oral inhalations of 5 mg) twice daily.

Adolescents

10 mg (i.e., 2 oral inhalations of 5 mg) twice daily.

Children

7 to 12 years: 10 mg (i.e., 2 oral inhalations of 5 mg) twice daily.
5 to 6 years: 10 mg (i.e., 2 oral inhalations of 5 mg) once daily.
1 to 4 years: Safety and efficacy have not been established.

Infants

Safety and efficacy have not been established.

Neonates

Safety and efficacy have not been established.

Zanamivir

inhalation powder

  • 5mg (20 units per Rotadisk)

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