Does FOSTAMATINIB Cause Adverse event? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Adverse event have been filed in association with FOSTAMATINIB (TAVALISSE). This represents 1.1% of all adverse event reports for FOSTAMATINIB.
71
Reports of Adverse event with FOSTAMATINIB
1.1%
of all FOSTAMATINIB reports
6
Deaths
6
Hospitalizations
How Dangerous Is Adverse event From FOSTAMATINIB?
Of the 71 reports, 6 (8.5%) resulted in death, 6 (8.5%) required hospitalization, and 1 (1.4%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOSTAMATINIB. However, 71 reports have been filed with the FAERS database.
What Other Side Effects Does FOSTAMATINIB Cause?
Diarrhoea (904)
Platelet count decreased (804)
Product dose omission issue (711)
Off label use (680)
Hospitalisation (403)
Platelet count (375)
Drug ineffective (340)
Fatigue (332)
Blood pressure increased (314)
Death (307)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which FOSTAMATINIB Alternatives Have Lower Adverse event Risk?
FOSTAMATINIB vs FOSTEMSAVIR TROMETHAMINE
FOSTAMATINIB vs FOTEMUSTINE
FOSTAMATINIB vs FRAMYCETIN
FOSTAMATINIB vs FREMANEZUMAB
FOSTAMATINIB vs FREMANEZUMAB-VFRM