Exjade receives black box warning
Written by Sadaka Associates
Sunday, 07 March 2010 23:48
Novartis Oncology and FDA notified healthcare professionals about recent changes in the Prescribing Information (PI) for Exjade, indicated for the treatment of chronic iron overload due to blood transfusions in patients 2 years of age and older. New language was added to the Contraindications, Warnings and Precautions, and Drug Interactions sections of the PI, including a Boxed Warning, that the product may cause:
- renal impairment, including failure
- hepatic impairment, including failure
- gastrointestinal hemorrhage
In some reported cases, these reactions were fatal. These reactions were more frequently observed in patients with advanced age, high risk myelodysplastic syndromes, underlying renal or hepatic impairment or low platelet counts. Exjade therapy requires close patient monitoring, including measurement of serum creatinine and/or creatinine clearance as specified in the PI and serum transaminases and bilirubin as specified in the PI.
Click here to see the “Dear Healthcare Professional Letter”
Liver Failure Associated with Exjade
Written by Sadaka Associates
Wednesday, 09 April 2008 10:12
Exjade is a medicine used to treat chronic iron overload caused by blood transfusions in patients 2 years of age and older. Recent adverse event reports to the FDA indicates that the drug may be associated with liver failure.
If you or a loved one has been injured by Exjade, please fill out our free case evaluation form and someone will call you within 24 hours.
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