Introduction to
ZanamivirZanamivir, commonly marketed under the trade name Relenza, is an antiviral medication primarily used to treat and prevent influenza A and B. It is a
neuraminidase inhibitor, which targets the neuraminidase enzyme on the surface of the
influenza virus, essential for the virus's replication and spread. Zanamivir was developed by
GlaxoSmithKline (GSK) and received approval from the U.S. Food and Drug Administration (FDA) in 1999. It is specifically indicated for the treatment of acute, uncomplicated influenza in individuals who have been symptomatic for no more than two days. Additionally, it is approved for prophylactic use to prevent influenza infections in communities or family settings. Research and clinical trials have shown that zanamivir can help reduce the severity and duration of flu symptoms when administered promptly after the onset of illness.
Zanamivir Mechanism of Action
The mechanism of action of zanamivir revolves around its ability to inhibit the neuraminidase enzyme, a protein found on the surface of the influenza virus. Neuraminidase plays a crucial role in the release of newly formed viral particles from infected host cells. By cleaving sialic acid residues, neuraminidase facilitates the budding and release of progeny virions from the cell membrane. Zanamivir binds to the active site of neuraminidase, effectively blocking its activity. This inhibition prevents the virus from spreading to uninfected cells, thereby limiting the
infection's progression and aiding the immune system in controlling the viral load. By targeting this enzyme, zanamivir disrupts the virus's life cycle, curtailing its ability to propagate within the host.
How to Use Zanamivir
Zanamivir is administered via oral inhalation using a specially designed inhaler device known as the Diskhaler. This method ensures that the drug is delivered directly to the respiratory tract, where the influenza virus predominantly resides. The recommended dosage for treating influenza in adults and children aged seven years and older is two inhalations (each delivering 5 mg of zanamivir) twice daily for five days, totaling 20 mg per day. For prophylactic use, the dosage is generally two inhalations once daily for 10 days following close contact with an infected individual or for up to 28 days during a community outbreak.
The onset of action for zanamivir is relatively swift. Patients often begin to experience relief from influenza symptoms such as
fever,
cough,
sore throat, and
muscle aches within a day or two of starting treatment. However, it is crucial to initiate therapy within 48 hours of the first appearance of symptoms for maximum efficacy. The inhalation route offers the advantage of localized drug delivery to the respiratory tract, minimizing systemic absorption and potentially reducing the risk of side effects.
What is Zanamivir Side Effects
While zanamivir is generally well-tolerated, it is not without potential side effects. Common side effects include
headache,
dizziness,
nausea, and
diarrhea. These symptoms are typically mild and transient. However, some individuals may experience more severe reactions. Respiratory issues such as
bronchospasm (a sudden constriction of the muscles in the walls of the bronchioles) and worsening of underlying pulmonary conditions like
asthma or
chronic obstructive pulmonary disease (COPD) have been reported. Due to the risk of bronchospasm, zanamivir is contraindicated in individuals with a history of respiratory diseases that may exacerbate if inhalation triggers a bronchoconstrictive response.
Allergic reactions to zanamivir, though rare, can occur. Symptoms of an
allergic reaction may include
rash,
itching,
swelling (particularly of the face, tongue, or throat), severe dizziness, and
trouble breathing. Immediate medical attention is necessary if any signs of an allergic reaction are observed.
Furthermore, neuropsychiatric events such as
confusion,
delirium,
hallucinations, and abnormal behavior have been reported, particularly in pediatric patients. While a causal relationship has not been definitively established, it is advisable to monitor for unusual behavior changes, especially in children.
What Other Drugs Will Affect Zanamivir
Zanamivir is primarily administered via inhalation, resulting in limited systemic absorption. Consequently, the potential for drug interactions is relatively low compared to orally administered medications. However, certain factors should still be considered when using zanamivir.
Coadministration with other inhaled medications requires careful consideration. For example, individuals using bronchodilators for asthma or COPD should take their bronchodilator before using zanamivir to ensure optimal airway patency and drug delivery. Concurrent use of other antiviral medications, such as
oseltamivir (Tamiflu), may also be considered, although combining neuraminidase inhibitors is generally not recommended unless under medical supervision.
Since zanamivir is not extensively metabolized and is excreted unchanged in the urine, interactions with drugs affecting hepatic enzyme systems (such as
cytochrome P450) are unlikely. However, caution is advised when prescribing zanamivir to individuals with
renal impairment, as reduced renal function may affect drug clearance and increase the risk of side effects.
In summary, zanamivir is a valuable antiviral agent in the management of influenza. Its targeted mechanism of action, rapid onset of relief, and relatively low potential for drug interactions make it a beneficial option for treating and preventing influenza infections. However, awareness of potential side effects and contraindications is crucial to ensure safe and effective use. As with any medication, consultation with a healthcare provider is essential to determine the most appropriate treatment approach based on individual health status and medical history.
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