| Subject: | FDA Issues Notice about CellCept (mycophenolate mofetil); FDA Issues Notice about Products Approved for the Treatment of ADHD |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 26 Feb 2007 - 12:00 am |
| CellCept:
The FDA and Roche Pharmaceuticals have notified cardiac transplant healthcare practitioners about a clinical study (Heart Spare The Nephron) that was terminated due to an observed increased incidence of grade IIIA acute rejection in heart transplant patients switched from calcineurin inhibitor and CellCept to Rapamune (sirolimus) and CellCept at 12 weeks post heart transplantation. The safety and efficacy of CellCept in combination with sirolimus following withdrawal of initial... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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