Editorial
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When the quest for profitability jeopardises the level of evidence through multiple statistical analyses and a lack of comparative trials.
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Marketing Authorisations
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An advance in rare urea cycle disorders
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A third-line option in chronic hepatitis B
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In certain age-related macular degeneration: too little evidence
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No place in multiple sclerosis
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A real advance in severe Scedosporium infection. Invasive aspergillosis: benefits to be confirmed
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Corneal herpes: valaciclovir is now the reference oral treatment
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Kidney transplantation in children: basiliximab is still the reference drug
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No better than other betalactam agents
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Adverse Effects
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Bupropion, benfluorex, ephedrine derivatives, methylphenidate
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Several drugs that are not marketed as appetite suppressants nonetheless have amphetamine-like properties; these include amfebutamone (bupropion) for smoking withdrawal; benfluorex for adjuvant treatment of hypertriglyceridemia and diabetes with overweight; ephedrine derivatives for "ENT decongestion"; and methylphenidate for narcolepsy and attention deficit-hyperactivity disorder in children.
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Reviews
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Modest practical merits
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Paracetamol, nonsteroidal antiinflammatory drugs (NSAIDs) and aspirin are first-line drugs for mild to moderate pain. The paracetamol + codeine combination barely augments the analgesic effect of paracetamol but carries a higher risk of adverse effects. Combinations of paracetamol with dextropropoxyphene or tramadol are even less interesting.
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All amphetamine derivatives marketed as appetite suppressants in the late 1990s were withdrawn from the French market, owing to life-threatening cardiovascular adverse effects such as pulmonary hypertension and valve disease. Sibutramine, marketed in France since 2001, is a closely related drug.
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Antiviral agents moderately effective
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Few data, no known specific hazard
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Fewer deaths and complications
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The generally quoted costs of pharmaceutical research and development were calculated by an institute that is largely funded by the industry itself, based on confidential data provided by drug companies. Closer scrutiny shows that the costs are vastly overestimated. By accepting these data at face value, the health authorities are ignoring the ground rules of good management.
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On the basis of purely legal arguments, five appetite suppressants whose licences had been withdrawn may find their way back on to the market.
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If we are to pay for real therapeutic progress, and not for simple commercial novelties, negotiations must be conducted on a transparent basis.
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