Skip to content
Influenza

Relenza (Zanamivir)

Dowiedz się o Relenza (Zanamivir) inhaled antiviral for flu A and B. Must start within 48 hours. Ocenione przez lekarzy zarejestrowanych w UE za pośrednictwe...

2026-04-12 Zanamivir

From €49.99

Obejmuje opiate platformowa, ocene lekarza i oplaty za realizacje w zaleznosci od sciezki.

Kontynuuj sciezka recepty papierowej

Dawki i rodzaje

Otrzymaj powiadomienie o dostepnosci

Apteki partnerskie nie maja obecnie tej dawki/rodzaju w ofercie. Rozpoczecie ankiety dla realizacji przez apteke partnerska jest wstrzymane dla tej opcji.

Kontynuuj sciezka recepty papierowej

Sciezka recepty papierowej oznacza, ze niezalezny lekarz moze wystawic recepte, z ktora mozna udac sie do lokalnej apteki. Realizacja podlega wewnetrznym zasadom kazdej apteki.

Czym jest Relenza?

Relenza (zanamivir) is an inhaled antiviral medicine approved by the Europejska Agencja Leków (EMA) for the treatment and prevention of influenza A and B. It belongs to the neuraminidase inhibitor class of antiviral drugs — the same class as Tamiflu (oseltamivir), though it is delivered by inhalation rather than orally.

Relenza is delivered directly to the respiratory tract — the primary site of influenza infection — via a breath-activated inhaler device called the Diskhaler. This targeted delivery means that systemic absorption is low (approximately 10–20% of the inhaled dose reaches the bloodstream), which reduces the likelihood of systemic side effects but also means Relenza is not suitable for patients who cannot inhale effectively.

Jak działa Relenza work?

Grypa viruses are coated with two surface proteins: haemagglutinin (H) and neuraminidase (N). Haemagglutinin allows the virus to attach to and enter host cells. Neuraminidase allows newly formed virus particles to detach from infected cells and spread to infect additional cells throughout the respiratory tract.

Zanamivir is a neuraminidase inhibitor: it binds directly and selectively to the neuraminidase enzyme on the surface of influenza A and B viruses, blocking its activity. By blocking neuraminidase, zanamivir:

  • Prevents newly formed viral particles from detaching from infected cells
  • Limits the spread of the virus to additional respiratory cells
  • Reduces the total viral load in the respiratory tract

This mechanism is most effective when started early — ideally within the first 24 hours, and no later than 48 hours after symptoms begin — because viral replication is most active in this early phase.

Dla kogo jest Relenza for?

Relenza is indicated for:

Treatment:

  • Adults and children aged 5 years and over with symptomatic influenza A or B, when symptoms began within the past 48 hours
  • Patients in groups at higher risk of complications (elderly, immunocompromised, those with chronic medical conditions), where antiviral treatment is particularly warranted

Prevention (post-exposure prophylaxis):

  • Adults and adolescents (aged 12 and over) who have been exposed to influenza and require preventive treatment in certain circumstances, such as during outbreaks

Relenza is generally NOT recommended for:

  • Patients with asthma or COPD (significant risk of bronchospasm)
  • Patients who cannot use inhaler devices correctly
  • Patients under 5 years of age
  • People who have not started treatment within 48 hours of symptom onset (limited benefit)

Dawkowanie

Relenza is inhaled using the Diskhaler device. Each blister of the Diskhaler contains 5 mg of zanamivir powder.

IndicationDoseFrequencyDuration
Treatment (adults and children ≥5 years)10 mg (2 inhalations of 5 mg)Twice daily5 days
Prevention (post-exposure)10 mg (2 inhalations of 5 mg)Once daily10 days
Prevention (seasonal / outbreak)10 mg (2 inhalations of 5 mg)Once dailyUp to 28 days

The two inhalations for each dose should be taken one after the other. Patients with asthma or COPD who are prescribed Relenza despite the risk (in exceptional circumstances) should have a fast-acting bronchodilator available to use before each Relenza dose.

Skutki uboczne

Częste skutki uboczne

  • Bronchospasm: The most clinically important risk — sudden tightening of the airways. Particularly dangerous in patients with underlying respiratory disease.
  • Headache
  • Dizziness
  • Throat or nasal irritation
  • Nausea

Serious risks

  • Severe bronchospasm: Some cases have been fatal, particularly in patients with known asthma or COPD. Relenza should be discontinued immediately if bronchospasm occurs and appropriate medical care sought.
  • Neuropsychiatric events: Confusion, abnormal behaviour, delirium, and hallucinations have been reported in some patients receiving neuraminidase inhibitors, particularly children. Whether these are caused by zanamivir or are a manifestation of influenza itself is unclear.
  • Anaphylaxis and allergic reactions: Rare but reported; discontinue immediately if severe hypersensitivity occurs.

Relenza vs Tamiflu

FeatureRelenza (Zanamivir)Tamiflu (Oseltamivir)
Active ingredientZanamivirOseltamivir
RouteInhaled (Diskhaler)Oral (capsule or suspension)
Systemic absorptionLow (~10–20%)High (~80%)
Suitable for asthma/COPDNot recommendedPreferred in respiratory disease
Starting age (treatment)5 years and over1 year and over
Side effect profileBronchospasm riskMainly GI (nausea, vomiting)

Tamiflu is generally preferred in patients with underlying respiratory disease or those who cannot use inhaler devices. Relenza may be preferred in patients who tolerate it and for whom systemic exposure should be minimised.

Jak uzyskać dostęp do influenza treatment online w Europie

Relenza is a lek wydawany na receptę in most państwach członkowskich UE. Prescrivia operates as a technology intermediary, connecting patients with independent EU-registered doctors for online health assessments. We do not prescribe medicines, employ doctors, or sell medicines directly.

Note on timing: Given that antiviral treatment for influenza must be started within 48 hours of symptom onset to be effective, prompt medical consultation is critical. If you are experiencing flu symptoms, seek medical assessment as soon as possible.

Important: Prescrivia nie gwarantuje that a prescription will be issued. All clinical decisions are made independently by qualified medical professionals.

Ważne informacje dotyczące bezpieczeństwa

Nie stosować Relenza if you:

  • Have asthma or chronic obstructive pulmonary disease (COPD)
  • Cannot use inhaler devices effectively
  • Are allergic to zanamivir or any excipient in Relenza

Stop Relenza and natychmiast zasięgnij pomocy medycznej if you:

  • Experience difficulty breathing, wheezing, or chest tightness after inhalation (bronchospasm)
  • Develop severe allergic symptoms

Vaccinate: Annual influenza vaccination remains the most important preventive measure against influenza and its complications, per WHO recommendations.

Źródła

Medical information on this page is based on the following sources:

  • Europejska Agencja Leków (EMA). Relenza (zanamivir) — Summary of Product Characteristics. ema.europa.eu
  • Światowa Organizacja Zdrowia (WHO). Grypa (Seasonal) — Fact sheet. who.int
  • Światowa Organizacja Zdrowia (WHO). WHO guidelines for pharmacological management of pandemic and seasonal influenza. 2010. who.int

This content is reviewed periodically to reflect updated clinical guidance. It is provided for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional for advice relevant to your individual health circumstances.

Frequently asked questions

Czym jest Relenza used for?
Relenza (zanamivir) is an inhaled antiviral medicine used to treat influenza A and B in adults and children aged 5 years and over when they are showing flu symptoms. It is also used to prevent influenza in adults and adolescents in certain circumstances. Relenza must be started within 48 hours of the first appearance of flu symptoms to be effective.
Why must Relenza be started within 48 hours?
Grypa viruses replicate most rapidly in the first 24–48 hours of infection. Zanamivir works by blocking neuraminidase — an enzyme the virus uses to release copies of itself from infected cells and spread to new cells. Starting treatment early, when viral replication is still active, significantly limits the extent of infection and shortens the duration of illness. Starting after 48 hours has passed provides little clinical benefit.
How is Relenza taken?
Relenza is inhaled using a breath-activated inhaler device called a Diskhaler. Each dose consists of two inhalations (2 x 5 mg = 10 mg per dose), taken twice daily for 5 days. The Diskhaler contains a blister pack of powdered zanamivir and requires the patient to breathe in through the device to deliver the medication to the airways.
Can people with asthma or COPD use Relenza?
Caution is required. Relenza is inhaled as a powder, and has been associated with bronchospasm (sudden narrowing of the airways) in patients with underlying respiratory conditions such as asthma or COPD. Some patients have experienced severe and even fatal bronchospasm shortly after inhaling zanamivir. Relenza should generally not be used in patients with asthma or COPD; Tamiflu (oseltamivir) oral capsules are typically preferred in this group.
Is Relenza the same as Tamiflu?
Both Relenza (zanamivir) and Tamiflu (oseltamivir) are neuraminidase inhibitor antivirals used to treat influenza, and they have a similar mechanism of action. The key differences are the route of administration (Relenza is inhaled; Tamiflu is taken orally), their side effect profiles, and their suitability for patients with respiratory conditions. A doctor can advise which is most appropriate for individual patients.

Prescrivia jest wyłącznie platformą pośredniczącą. Nie świadczymy usług medycznych, nie przepisujemy leków ani nie wydajemy leków. Wszystkie decyzje medyczne podejmowane są przez niezależnych lekarzy zarejestrowanych w UE. Wszystkie leki wydawane są przez licencjonowane apteki w UE. Platforma ta ułatwia kontakt między pacjentami a podmiotami świadczącymi opiekę zdrowotną.

Written by Prescrivia Editorial. Medical information sourced from European Medicines Agency (EMA), World Health Organization (WHO), and published clinical data.

This content is informational only and does not constitute medical advice.

Last updated:

Gotowy, aby zacząć?

Wypełnij poufną ocenę zdrowotną w około 3 minuty.