Does APIXABAN Cause Product use issue? 999 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 999 reports of Product use issue have been filed in association with APIXABAN (ELIQUIS). This represents 0.6% of all adverse event reports for APIXABAN.
999
Reports of Product use issue with APIXABAN
0.6%
of all APIXABAN reports
23
Deaths
191
Hospitalizations
How Dangerous Is Product use issue From APIXABAN?
Of the 999 reports, 23 (2.3%) resulted in death, 191 (19.1%) required hospitalization, and 21 (2.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 999 reports have been filed with the FAERS database.
What Other Side Effects Does APIXABAN Cause?
Death (18,501)
Cerebrovascular accident (7,237)
Atrial fibrillation (5,690)
Off label use (5,590)
Thrombosis (5,298)
Fall (5,063)
Cardiac disorder (4,917)
Haemorrhage (4,770)
Dyspnoea (4,379)
Gastrointestinal haemorrhage (4,030)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which APIXABAN Alternatives Have Lower Product use issue Risk?
APIXABAN vs APOMORPHINE
APIXABAN vs APRACLONIDINE
APIXABAN vs APREMILAST
APIXABAN vs APREPITANT
APIXABAN vs APROTININ