Does BRILINTA Cause Adverse event? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Adverse event have been filed in association with BRILINTA. This represents 2.1% of all adverse event reports for BRILINTA.
12
Reports of Adverse event with BRILINTA
2.1%
of all BRILINTA reports
3
Deaths
2
Hospitalizations
How Dangerous Is Adverse event From BRILINTA?
Of the 12 reports, 3 (25.0%) resulted in death, 2 (16.7%) required hospitalization, and 2 (16.7%) 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 BRILINTA. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does BRILINTA Cause?
Dyspnoea (97)
Thrombosis in device (50)
Myocardial infarction (49)
Death (40)
Off label use (40)
Coronary artery occlusion (37)
Gastrointestinal haemorrhage (30)
Acute myocardial infarction (23)
Fatigue (23)
Weight decreased (23)
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 BRILINTA Alternatives Have Lower Adverse event Risk?
BRILINTA vs BRILIQUE
BRILINTA vs BRIMONIDINE
BRILINTA vs BRIMONIDINE\BRINZOLAMIDE
BRILINTA vs BRIMONIDINE\TIMOLOL
BRILINTA vs BRINTELLIX