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Iclusig® (ponatinib) REMS

ICLUSIG REMS ( R. A REMS is a program required by the Food and Drug Administration (FDA) to manage known or potential serious risks associated with a drug product. The purpose of the Iclusig REMS is to inform Healthcare Providers about the indications and the serious risks of Iclusig. Safety information about risks of arterial occlusion and venous thromboembolism. The indications are limited to:. UPDATED RISKS OF ARTERIAL OCCLUSION AND VENOUS THROMBOEMBOLISM. Iclusig can cause fatal and life-threatening ...

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Iclusig® (ponatinib) REMS | iclusigrems.com Reviews
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ICLUSIG REMS ( R. A REMS is a program required by the Food and Drug Administration (FDA) to manage known or potential serious risks associated with a drug product. The purpose of the Iclusig REMS is to inform Healthcare Providers about the indications and the serious risks of Iclusig. Safety information about risks of arterial occlusion and venous thromboembolism. The indications are limited to:. UPDATED RISKS OF ARTERIAL OCCLUSION AND VENOUS THROMBOEMBOLISM. Iclusig can cause fatal and life-threatening ...
<META>
KEYWORDS
1 prescribing information
2 medication guide
3 iclusig
4 ponatinib rems
5 isk e
6 valuation and m
7 itigation s
8 trategy
9 safety updates include
10 indications
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KEYWORDS ON
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prescribing information,medication guide,iclusig,ponatinib rems,isk e,valuation and m,itigation s,trategy,safety updates include,indications,dosing considerations,limitations of use,in boxed warning,events observed included,fatal myocardial infarction
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Iclusig® (ponatinib) REMS | iclusigrems.com Reviews

https://iclusigrems.com

ICLUSIG REMS ( R. A REMS is a program required by the Food and Drug Administration (FDA) to manage known or potential serious risks associated with a drug product. The purpose of the Iclusig REMS is to inform Healthcare Providers about the indications and the serious risks of Iclusig. Safety information about risks of arterial occlusion and venous thromboembolism. The indications are limited to:. UPDATED RISKS OF ARTERIAL OCCLUSION AND VENOUS THROMBOEMBOLISM. Iclusig can cause fatal and life-threatening ...

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Iclusig® (ponatinib)

http://iclusig.com/hcp

This site is for United States residents. 18 years of age or older. Iclusig (ponatinib) is a kinase inhibitor indicated for the:. Treatment of adult patients with T315I-positive chronic myeloid leukemia (CML) (chronic phase, accelerated phase, or blast phase) or T315I-positive Philadelphia chromosome positive acute lymphoblastic leukemia (Ph ALL). These indications are based upon response rate. There are no trials verifying an improvement in disease-related symptoms or increased survival with Iclusig.

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ICLUSIG® (ponatinib)

This site is for United States residents 18 years of age or older. Ponatinib) is a prescription medicine used to treat adults who have:. Chronic phase, accelerated phase, or blast phase chronic myeloid leukemia (CML) or Philadelphia chromosome positive acute lymphoblastic leukemia (Ph ALL) who cannot receive any other tyrosine kinase inhibitor (TKI) medicines. A specific type of abnormal gene (T315I-positive) chronic phase, accelerated phase, or blast phase CML, or T315I-positive Ph ALL. Ponatinib) is a ...

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Iclusig® (ponatinib) REMS

ICLUSIG REMS ( R. A REMS is a program required by the Food and Drug Administration (FDA) to manage known or potential serious risks associated with a drug product. The purpose of the Iclusig REMS is to inform Healthcare Providers about the indications and the serious risks of Iclusig. Safety information about risks of arterial occlusion and venous thromboembolism. The indications are limited to:. UPDATED RISKS OF ARTERIAL OCCLUSION AND VENOUS THROMBOEMBOLISM. Iclusig can cause fatal and life-threatening ...

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