Press Release: European Medicines Agency recommends changes in use of leukaemia medicine Iclusig (ponatinib) in order to minimise risk of blood clots

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Series Details EMA/716841/2013 (22.11.13)
Publication Date 22/11/2013
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Iclusig is an anticancer medicine that contains the active substance ponatinib. It is used to treat adults with the certain types of leukaemia (cancer of the white blood cells).

The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP), in November 2013, made a number of recommendations to help minimise the risk of blood clots obstructing arteries or veins in patients taking Iclusig.

Source Link Link to Main Source http://www.ema.europa.eu/ema/index.jsp?curl=pages/news_and_events/news/2013/11/news_detail_001968.jsp&mid=WC0b01ac058004d5c1
Related Links
EMA: Press Release: EMA/716841/2013 (22.11.13): European Medicines Agency recommends changes in use of leukaemia medicine Iclusig (ponatinib) in order to minimise risk of blood clots http://www.ema.europa.eu/docs/en_GB/document_library/Press_release/2013/11/WC500155451.pdf
EMA: Press Release: EMA/745969/2013 (06.12.13): Further review of Iclusig started http://www.ema.europa.eu/ema/index.jsp?curl=pages/news_and_events/news/2013/12/news_detail_001986.jsp&mid=WC0b01ac058004d5c1

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