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Antiviral treatment for influenza generally works as a complement to immunization, not as a substitute, for most patients.
People at high risk of serious complications from influenza who have not been vaccinated have the highest priority for prophylactic treatment, and such high-risk patients should also be treated if they become infected. Early diagnosis and prescribing are necessary when treating an infection because treatment is effective only when it is started within 2 days of an infection.
All four drug options appear to be effective for preventing disease in about 80% of patients, but drug-to-drug comparisons are lacking. Treatment may be more effective for alleviating symptoms in high-risk patients and severely ill patients with high fever. No drug has been shown to prevent serious influenza-related complications such as bacterial or viral pneumonia or exacerbation of chronic diseases.
Despite the higher cost of zanamivir and oseltamivir, either of these drugs is the treatment of choice for some experts because they cover both influenza strains, produce fewer side effects, and are less likely to lead to the emergence of drug-resistant viruses. Amantadine, the only generic option, or rimantadine may be the first choice for treatment when there are outbreaks of influenza A and when cost is particularly important. Distinguishing influenza A infection from influenza B infection requires attention to local epidemiologic trends, public health department findings, and laboratory results.
Oseltamivir, amantadine, and rimantadine are approved for influenza prophylaxis. Although they appear to prevent infection about half of the time, they also appear to prevent illness in approximately 70%-90% of people. Rimantadine and amantadine are preferred for prophylaxis against influenza A because of cost considerations; only oseltamivir protects against influenza B. The duration of prophylaxis differs from the duration of treatment for an acute infection.
When choosing a drug, dose, and duration of therapy consider the patient's age, weight, renal and hepatic function, the presence of other medical conditions, potential interactions with other medications, and whether the goal is prophylaxis or treatment of acute illness. All four drugs are in pregnancy category C and are not recommended for use during breast-feeding. No clinical studies have been conducted in pregnant women. Use the drugs during pregnancy only if the potential benefit justifies the potential risk. High doses of amantadine and rimantadine are teratogenic and embryotoxic in animals.
Drug Dosage Cost/Day (*)
oseltamivir 75 mg b.i.d. $11.90
(Tamiflu) (capsule)
zanamivir 10 mg b.i.d. $9.60
(Relenza)
rimantadine 100 mg b.i.d. $4.04
(Flumadine) (tablet)
amantadine 100 mg b.i.d. $0.82 (**)
(capsule)
Drug Comment (+)
oseltamivir Capsules and oral suspension available.
(Tamiflu) Listed dosage is for treatment of influenza;
prophylactic dosage is 75
mg/day. Reduce dosage to 75 mg/day
for treatment or 75 mg every 2 days for
prophylaxis in patients with
creatinine clearance of less than
30 mL/min. Adverse effects, occurring
in about 10% of patients, include
headache, nausea, and vomiting and
may be minimized if the drug is
given with food. May interact with other
drugs excreted by the anionic pathway
such as probenecid. Like zanamivir, a
neuraminidase inhibitor that's
effective against all strains of influenza
A and B. Reduces duration of symptoms
by about 1-1.5 days if begun
within 30-36 hours of infection. Despite
higher cost, zanamivir and oseltamivir
usually are the treatments of
choice because they cover both influenza
strains, produce fewer side effects, and
are less likely to lead to the
emergence of drug-resistant viruses.
Resistant virus has been seen, but the
rate is unknown. The biggest
difference between zanamivir and
oseltamivir is the route of delivery. Limit
treatment to 5 days. Some physicians
may treat severely ill patients for longer
than 5 days, despite a lack of data
showing that longer treatment boosts
efficacy. Treatment beyond 10-14
days probably gives no further benefit.
Prophylaxis is for the duration of
exposure, usually 6-8 weeks, or for
10-14 days after a known exposure.
zanamivir Used ...
Source: HighBeam Research, Drug update: Influenza.