Cerivastatin was voluntarily withdrawn from the market
worldwide in 2001, due to reports of fatal rhabdomyolysis.
During post-marketing surveillance, 52 deaths were reported
in patients using cerivastatin, mainly from rhabdomyolysis and its resultant renal
failure.
Risks were higher in patients using fibrates, mainly gemfibrozil (Lopid),
and in patients using the highest (0.8 mg/day) dose of cerivastatin. Bayer A.G.
added a contraindication for the concomitant use of cerivastatin and gemfibrozil to
the package 18 months after the drug interaction was found.
The frequency of deadly cases of rhabdomyolysis with
cerivastatin was 16 to 80 times higher than with other statins. Another 385
nonfatal cases of rhabdomyolysis were reported.
This put the risk of this (rare) complication at 5-10 times
that of the other statins.
Cerivastatin also
induced myopathy in a dose-dependent manner when administered as
monotherapy, but that was revealed only after Bayer was sued and unpublished
company documents were opened.
bron: wikipedia
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Commentaar
Ontwikkeld in dieren en op dieren getest alvorens toegelaten te worden als geneesmiddel.
En zo gaat het maar door.
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