FDA MedWatch - Saphris (asenapine maleate): Drug Safety Communication: Serious Allergic Reactions

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Title: FDA MedWatch - Saphris (asenapine maleate): Drug Safety Communication: Serious Allergic Reactions
MedWatch logoMedWatch - The FDA Safety Information and Adverse Event Reporting Program

Saphris (asenapine maleate): Drug Safety Communication: Serious Allergic Reactions


AUDIENCE: Psychiatry, Patients

ISSUE: FDA notified healthcare professionals and patients that serious allergic reactions have been reported with the use of Saphris (asenapine maleate). The Contraindications, Warnings and Precautions, Adverse Reactions, and Patient Counseling Information sections have been revised to include information about type I hypersensitivity reactions which may include anaphylaxis, angioedema, low blood pressure, rapid heart rate, swollen tongue, difficulty breathing, wheezing, or rash. In several cases, these reactions occurred after the first dose.

BACKGROUND: Saphris (asenapine maleate) is used to treat symptoms of schizophrenia and bipolar disorder.

RECOMMENDATION: Healthcare professionals should be aware of the risk of hypersensitivity reactions with Saphris and counsel patients who are receiving the drug about how to recognize the signs and symptoms of a serious allergic reaction. Saphris should not be used in patients with a known hypersensitivity to the drug.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

Read the MedWatch safety alert, including links to the Drug Safety Communication with Data Summary,  and prescribing information, at:

http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm270600.htm

 

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