The following is a summary of adverse events for TASIGNA®(nilotinib) and GLIVEC® (imatinib). For additional information, please click here to view the European SMPCs.
TASIGNA®
The most common nonhematologic adverse events that have been reported by patients taking TASIGNA® are1:
- Rash
- Pruritus
- Nausea
- Fatigue
- Headache
- Constipation
- Diarrhea
Hematologic adverse events that have been reported by patients taking TASIGNA® are1:
- Thrombocytopenia
- Neutropenia
- Anemia
- Febrile neutropenia
- Pancytopenia
- Thrombocytosis
- Leukocytosis
GLIVEC®
The most common nonhematologic adverse events that have been reported by patients taking GLIVEC® are2:
- Fluid retention
- Nausea and vomiting
- Indigestion
- Diarrhea
- Itchy skin or rash
- Painful joints
- Muscle cramps
- Headache
Hematologic adverse events that have been reported by patients taking GLIVEC® are2:
- Neutropenia
- Thrombocytopenia
- Anemia
- Pancytopenia
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Note: Before prescribing, please read full European Summary of Product Characteristics.
References
- TASIGNA® (nilotinib) Summary of Product Characteristics. Basel, Switzerland: Novartis Pharma AG; September 2007.
- GLIVEC® (imatinib) Summary of Product Characteristics. West Sussex, UK: Novartis Europharm Limited; 2010.