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Von Neuem: Valproat-haltige Arzneimittel und Schwangerschaft

10. Februar 2018 – Der Ausschuss für Risikobewertung (PRAC) der Europäischen Arzneimittelagentur (EMA) empfiehlt neue Einschränkungen, um eine Valproat-Exposition ungeborener Kinder im Mutterleib zu vermeiden; Eine

Valproat-Exposition ungeborener Kinder kann zu angeborenen Missbildungen und Entwicklungsstörungen führen.

Der PRAC untersuchte die zur Verfügung stehenden Daten und beriet sich umfassend mit Angehörigen der Heilberufe sowie Frauen und deren Kindern,

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Valproate: Verhindert denn eine Patientenkarte teratogene Schädigungen von Kindern?

14. Juli 2017 – Das deutsche Bundesinstitut für Arzneimittel und  Medizinprodukte (BfArM) hat soeben einen von den betroffenen pharmazeutischen Unternehmen verfassten Informationsbrief zur Einführung einer Patientenkarte für Arzneimittel, welche Valproat (Valproinsäaure) und verwandte Substanzen enthalten, zu Handen der Ärzte und Apotheker veröffentlicht.

Hintergrund dieses Informationsbriefes ist der Bescheid des BfArM vom 10.

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Riociguat (Adempas): Kontraindikation in PH-IIP

16. September 2016 – Riociguat (Adempas) ist ein Arzneimittel, welches zur Behandlung von zwei Formen der pulmonalen Hypertonie (PH), der chronisch thromboembolischen pulmonalen Hypertonie und der pulmonalarteriellen Hypertonie (PAH), eingesetzt wird. Der Wirkstoff Riociguat ist ein Stimulator der

löslichen Guanylatzyklase (sGC),

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Riociguat (Adempas): Kontraindikation für Patienten mit pulmonaler Hypertonie in Verbindung mit idiopathischen interstitiellen Pneumonien (PH-IIP)

06. Juli 2016 – In Übereinstimmung mit dem Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM) und der Europäischen Arzneimittel-Agentur (EMA) haben die Firmen Bayer AG und MSD Sharp & Dohme GmbH in Deutschland in einem Rote-Hand-Brief zu Riociguat (Adempas) soeben,

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Die Anwendung von Viekirax mit Exviera bei Child-Pugh-B und Child-Pugh-C Patienten kann zu fatalem Leberversagen führen

09. April 2016 – Gemäss einer sogenannten DHPC (Health Professional Communication) vom 8. April 2016 orientiert Swissmedic zusammen mit der Inhaberin der Zulassungsbewilligung (AbbVie) über ernsthafte und teilweise fatale Nebenwirkungen in einer Gruppe von Patientinnen / Patienten nach Hepatitis C CirrhosisBehandlung chronischer Hepatitis C  (CHC) mit Viekirax,

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