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In 2012, the US Food and Drug Administration asked for a complementary study on IDeg-associated cardiovascular risk.
In June 1999, the European Committee for Proprietary Medicinal Products (CPMP, now the CHMP) adopted an Opinion recommending the temporary suspension of the Marketing Authorizations for sertindole and asked for a complementary benefit/risk evaluation of the product [ 12].
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The European Committee for Proprietary Medicinal Products CPMPP) issued a temporary market suspension in January 2000 and asked for complementary benefit/risk evaluation of the product.
If needed, the municipalities will be asked for complementary data.
The survey asked for use of complementary or alternative remedies and Figure 3 shows the extent of uptake.
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