Pharma’s Cutting Edge

Pharma’s Cutting Edge

Pharmaceutical and biotech science and business

 
 
 
 

Archive for Drug Safety

Wyeth v Levine #2: Implications for drug manufacturers

Yesterday, I presented my overview of the US Supreme Court decision in Wyeth v Levine, to join the thousands of other overviews published online in the last couple of days.  Many of those commenting are focusing on the implications of the decision for consumers and lawyers.  You will find less commentary on the likely business [...]

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The Future Food Shortage
Adjusting, Adjusting, and Adjusting
Read more on Drug Manufacturers, Food & Beverage at Wikinvest

Reading Wyeth v Levine: Preemption narrowly interpreted

When I reported on the implications of Riegel v Medtronic for device manufacturers in February of last year, I indicated that the related Wyeth v Levine case would have potentially farther reaching implications for the pharmaceutical industry.  Yesterday, the US Supreme Court issued its 6-3 opinion in the case.  Let’s have a look at the [...]

FDA finally admits need for large safety studies premarketing

For the last few years, I have held an opinion contrary to most of my colleagues in the industry–that sponsors should be required to conduct large (simple) safety studies prior to marketing authorization for drugs intended to be used chronically in large, especially elderly, populations.  Such studies would have as their primary goal a safety evaluation including [...]

Consumers Union’s misguided approach to improving drug safety surveillance

Consumers Union Petition

Petition for Better Reporting of Drug Side Effects
I support requiring all drug ads to include a 1-800 number and website so citizens can report drug side effects (petition docket 2008P-0012/CP1).

All too often, drug advertisements fail to present the benefits and risks of using prescription drugs in an accurate and balanced way. It is [...]

Grassley seeks GAO input into use of surrogates and postmarketing followup by FDA

S. Sen. Grassley: Secures independent review of FDA approvals based on narrow health benefits - FierceBiotech
In his letter to the GAO, Sen. Grassley asks for an investigation into FDA’s use of surrogates for product approval and whether FDA has appropriately followed up drugs approved initially based on surrogate markers.  He cites recent examples of [...]

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Funding on the Trail
Sen. Isakson Goes Off the Deep End
Heart Attacks and Tax Codes
Read more on SEMCO Energy, GlaxoSmithKline, Cardiac Disease at Wikinvest

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