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Eine Hoffnung weniger für übergewichtige Patienten: Sistierung der Zulassung von Rimonabant [Acomplia]

Posted on by by Posted in Behördliche Mitteilung, Gravierende Unerwünschte Nebenwirkung, Marktrückzug, Thasso Post, Theragenomische Medizin No Comments ↓

Aufgrund eines Entscheids des Ausschusses für Humanarzneimittel (CHMP) der 
Europäischen Arzneimittelagentur EMA wurde die Zulassung von Rimonabant [Acomplia] in der europäischen 
Union ab 23. Oktober 2008 bis auf weiteres sistiert. In der Folge wurde die Zulassung von Rimonabant [Acomplia] auch in der Schweiz sistiert.  Rimonabant [Acomplia] war in der Schweiz seit März 2007 zugelassen als Zusatztherapie zu einer leicht hypokalorischen Diät und zu einer Bewegungstherapie für die Behandlung von adiposen Patienten (BMI  >

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Gefährliche Schlankheitsmittel aus dem Internet: Alarmierende Analyse-Ergebnisse

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6. Juni 2011 – Neue Zahlen und  Alarmierende Analyse-Ergebnisse. Das Schweizerische Heilmittelinstitut (Swissmedic) hat heute die untenstehende Mitteilung  (im Originaltext wiedergegeben) veröffentlicht.

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Gefährliche Schlankheitsmittel aus dem Internet: neue Zahlen.

Swissmedic, das Schweizerische Heilmittelinstitut, hat 122 Proben beschlagnahmter Importe von Schlankheitsmitteln im Labor untersucht.

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