Does ELIQUIS Cause Adverse event? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Adverse event have been filed in association with ELIQUIS. This represents 2.8% of all adverse event reports for ELIQUIS.
40
Reports of Adverse event with ELIQUIS
2.8%
of all ELIQUIS reports
0
Deaths
11
Hospitalizations
How Dangerous Is Adverse event From ELIQUIS?
Of the 40 reports, 11 (27.5%) required hospitalization, and 2 (5.0%) 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 ELIQUIS. However, 40 reports have been filed with the FAERS database.
What Other Side Effects Does ELIQUIS Cause?
Haemorrhage (79)
Gastrointestinal haemorrhage (72)
Dizziness (65)
Rash (51)
Epistaxis (49)
Headache (49)
Dyspnoea (41)
Diarrhoea (37)
Contusion (34)
Drug dose omission (34)
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 ELIQUIS Alternatives Have Lower Adverse event Risk?
ELIQUIS vs ELOSULFASE ALFA
ELIQUIS vs ELOTUZUMAB
ELIQUIS vs ELOXATIN
ELIQUIS vs ELRANATAMAB
ELIQUIS vs ELRANATAMAB-BCMM