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Fights the flu at the primary
site of infection.
Often perceived as a systemic
disease, influenza is actually an acute respiratory infection
primarily restricted to the lungs and airways. It's onset is
initially characterized by fever and upper respiratory symptoms,
e.g. sore throat and cough.
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Cytokines--the
culprits of “systemic” symptomatology
- Cytokine release causes
systemic symptoms, e.g., high fever, myalgia/arthralgia,
and loss of appetite
- Host defences lead to
mucosal inflammation
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| Common
Symptoms |
Cold |
Flu |
| Fatigue |
No |
Yes |
| Muscle
ache |
No |
100°
- 104°F |
| Joint
pain |
No |
Yes |
| Loss
of appetite |
No |
Yes |
| Headache |
No |
Yes |
| Cough |
Yes |
Yes |
| Stuffy
nose |
Yes |
No |
| Diarrhea/Vomiting |
No |
No |
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Antiviral action
helps shorten the misery of the flu
- Reduces the duration of
influenza A & B for adults and adolescents 12 and older*
- In North American
phase II and III studies, RELENZA shortened the course of flu
by up to a median of 1 day
- In a Southern Hemisphere phase
III study, a 1.5-day difference in median time to symptom
improvement was observed
- Additional evidence of
efficacy was provided by a phase III European study
For maximum benefit,
therapy with RELENZA should be initiated as soon as possible
and within 2 days of symptom onset. There are no data on the
effectiveness of treatment with RELENZA when initiated more
than 2 days after the onset of signs or symptoms.
* Across all phase III
studies, 89% of patients had influenza A and 11% had influenza
B.
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Favourable safety
profile
- Side effects comparable to
placebo with no adverse events >3% in over 2,500 patients
- The most commonly reported
side effects vs. placebo were diarrhoea (3% vs. 4%), nausea
(3% vs. 3%), and sinusitis (3% vs. 2%)
- CNS, gastrointestinal, and
other systemic effects are comparable to placebo
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RELENZA also has a
well-defined product profile
- No clinically significant drug
interactions expected, based on data from in vitro studies
- Pharmacokinetic studies
indicate that approximately 4% to 17% of the inhaled dose is
systemically absorbed
- Not metabolised, no
interference with P450 liver enzymes
- Limited plasma protein binding
(<10%)
- No interference with the
antibody response to the influenza vaccine
The safety and efficacy of
RELENZA have not been established in patients with high-risk
underlying medical conditions and may cause bronchospasm
and/or a decline in lung function in patients with severe or
decompensated COPD or asthma. These patients should have
fast-acting inhaled bronchodilators available.
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Appropriate for a
wide age range
- Indicated for treatment of
uncomplicated acute illness due to influenza virus in adults
and adolescents 12 years and older
- Breath-activated, nonaerosol
oral DISKHALER®
- Two inhalations (2 x 5 mg)
twice daily--approximately 12 hours apart--5 days
Patients should be instructed in
the use of the delivery system, including a demonstration whenever
possible.
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In Summary
Relenza is not indicated for
pregnant women, breastfeeding mothers or children below the age of
12. It should be used with caution in patients with asthma or
other chronic lung conditions.
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available throughout this website is for your general knowledge
only and is NOT a substitute for medical advice or treatment.
Should you need medical assistance, always seek professional help
and consult a physician. PPMS.net shall not be held liable for any
situation that may result directly or indirectly from use or
misuse of this information.
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www.ppms.net
2002 -:- info@ppms.net
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