Current issues of ACP Journal Club are published in Annals of Internal Medicine


Zanamivir speeds symptom relief in influenza


ACP J Club. 2000 May-June;132:92. doi:10.7326/ACPJC-2000-132-3-092

Related Content in this Issue
• Companion Abstract and Commentary: Oseltamivir once or twice daily safely prevented influenza

Source Citation

Monto AS, Fleming DM, Henry D, et al. Efficacy and safety of the neuraminidase inhibitor zanamivir in the treatment of influenza A and B virus infections. J Infect Dis. 1999 Aug;180:254-61. [PubMed ID: 10395837]



In patients with symptoms of influenza, what is the clinical efficacy and safety of zanamivir?


Randomized {allocation concealed*}†, blinded (clinicians and patients),* placebo-controlled trial with 21-day follow-up.


Clinical centers in North America and Europe.


1256 patients (mean age 35 y, 66% women) who presented with symptoms of influenza of ≤ 48 hours of duration during 1 influenza season: fever and ≥ 2 of myalgia, headache, cough, or sore throat. Exclusion criteria were unstable chronic illness, receipt of other antiviral agents in the previous 7 days, inability to use inhaler devices satisfactorily, known or suspected hypersensitivity to study medication, pregnancy, lactation, or potential for pregnancy. 1182 patients (94%) completed the study.


Patients were allocated to 5 days of treatment with zanamivir, 10 mg by oral inhalation and 6.4 mg by nasal spray 2 times/d (n = 419); zanamivir (same dosages and administration routes) 4 times/d (n = 415); or placebo (n = 422).

Main outcome measures

Time to alleviation of clinical symptoms, which had to be maintained for ≥ 24 hours. Secondary outcomes were mean symptom score, sleep disturbance, time to return to normal activities, and use of acetaminophen and dextromethorphan to relieve symptoms.

Main results

Analysis was by intention to treat. Both regimens of zanamivir reduced the time to alleviation of clinical symptoms by 1 day less than placebo (6 vs 7 d, P ≤ 0.014). The 2 drug groups did not differ (P = 0.77). In patients who entered the study within 30 hours of the onset of symptoms, symptom duration was reduced by 1 day with zanamivir 2 times/d (P = 0.015) and by 1.5 days with zanamivir 4 times/d (P = 0.001). Patients who were febrile at study entry (≥ 37.8 °C) had reduced symptom duration by 1.5 days with zanamivir 2 times/d (P = 0.049) and by 2 days with zanamivir 4 times/d (P = 0.032). In patients considered at high risk for developing complications (age ≥ 65 y or cardiovascular, respiratory, endocrine, or metabolic conditions), zanamivir 4 times/d reduced time to symptom relief by 2.8 days (P = 0.042), and both regimens were more effective than placebo in high-risk patients who had positive findings for influenza (P ≤ 0.016). Zanamivir was superior to placebo in all secondary clinical outcomes. The groups did not differ for adverse events.


In patients with symptoms of influenza, zanamivir given 2 or 4 times per day decreased the time to alleviation of symptoms by 1 to 1.5 days. Patients who presented early after onset of symptoms with fever ≥ 37.8 °C or who were at high risk for complications had the most benefit.

*See Glossary.

†Information provided by author.

Source of funding: GlaxoWellcome Research and Development.

For correspondence: Dr. A.S. Monto, University of Michigan, School of Public Health, Department of Epidemiology, 109 Observatory Street, Ann Arbor, MI 48109, USA. FAX 734-764-3192.


Influenza remains a major cause of morbidity and mortality each year. Although vaccination is the primary method for preventing influenza, antiviral agents play an important complementary role for preventing and treating the disease.

In 1999, zanamivir and oseltamivir were approved for the treatment of influenza A and B (1). Before 1999, amantadine and rimantadine were the only antiviral agents available and were active only against influenza A viruses. Their use has been limited by side effects (especially related to the central nervous system) and the rapid emergence of resistant viruses. The neuraminidase inhibitors appear to be much less likely to induce resistance. They are also generally well tolerated, as shown in these studies by Monto and Hayden and their colleagues, although zanamivir has been reported to induce bronchospasm and oseltamivir has been associated with gastrointestinal symptoms (1).

Zanamivir and oseltamivir are effective for the treatment of influenza A or B among adults when started within 2 days of onset of symptoms. Monto and colleagues administered zanamivir by nasal spray and in its currently available form of orally inhaled powder. Duration of influenza was reduced by about 1 day, with greater benefits for patients with more severe (e.g., febrile) illness and when started within 30 hours of onset of symptoms. 2 other trials reported similar findings: Zanamivir relieved symptoms 1 to 1.5 days earlier (2, 3). Oral oseltamivir also reduces the duration of influenza illness among healthy adults by about 30 hours when started within 1.5 days of the onset of symptoms (4).

Most of the available data on the efficacy of the neuraminidase inhibitors are from healthy adults < 65 years of age. 13% of participants in the study by Monto and colleagues were high risk (age ≥ 65 y or with stable chronic medical conditions). The study findings suggested that zanamivir was also effective in this subgroup, but the sample size was too small to detect a statistically significant benefit. More data are needed to define clearly the role of the neuraminidase inhibitors in high-risk groups.

Although not approved for prophylaxis, zanamivir and oseltamivir have also been shown to prevent influenza in healthy adults. Hayden and colleagues found oseltamivir given for 6 weeks was 74% effective in preventing influenza. Furthermore, a trial of a 4-week course of zanamivir in 1107 adults showed a 67% efficacy in preventing influenza and an 84% efficacy in preventing febrile influenza (5). Of note, Hayden and colleagues reported that 7 participants developed influenza within 2 weeks of completing the 6-week prophylaxis period, including 5 participants who had received oseltamivir. The neuraminidase inhibitors may protect against illness only for as long as the medication is actually taken. More data on the effectiveness of the neuraminidase inhibitors for the prevention of influenza among elderly persons, nursing-home residents, and other high-risk groups are needed.

How should the neuraminidase inhibitors be used? Immunization remains the mainstay of efforts for the prevention and control of influenza. However, antiviral agents, including the neuraminidase inhibitors, are important adjuncts to vaccination for prevention and treatment during interpandemic periods for persons who have not been vaccinated, who develop influenza even if they have been vaccinated, and who travel between May and September to areas of the world with influenza activity. Decisions about which antiviral agent to use should be based on the relative importance of spectrum of activity, side effects, risk for emergence of resistance, and cost. Given the need to start treatment within 2 days of the onset of symptoms, providers will have to develop efficient processes for accurate diagnosis and timely prescribing of these agents if they are to be used widely. The antirivals will also play an important role during the next pandemic, providing critical protection during times when sufficient supplies of vaccine may not be available.

Kristin L. Nichol, MD, MPH
Veterans Affairs Medical Center
Minneapolis, Minnesota, USA


1. Neuraminidase inhibitors for treatment of influenza A and B infections. MMWR Morb Mortal Wkly Rep. 1999;48(RR14):1-9.

2. Hayden FG, Osterhaus AD, Treanor JJ, et al. Efficacy and safety of the neuraminidase inhibitor zanamivir in the treatment of influenzavirus infections. GG167 Influenza Study Group. N Engl J Med. 1997;337:874-80.

3. The MIST (Management of Influenza in the Southern Hemisphere Trialists) Study Group. Randomised trial of efficacy and safety of inhaled zanamivir in treatment of influenza A and B virus infections. Lancet. 1998;352:1877-81.

4. Treanor JJ, Hayden FG, Vrooman PS, et al. Efficacy and safety of the oral neuraminidase inhibitor oseltamivir in treating acute influenza. A randomized controlled trial. JAMA. 2000;283:1016-24.

5. Monto AS, Robinson DP, Herlocher ML, et al. Zanamivir in the prevention of influenza among healthy adults: a randomized controlled trial. JAMA. 1999;282:31-5.