Does APIXABAN Cause Product dispensing error? 299 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 299 reports of Product dispensing error have been filed in association with APIXABAN (ELIQUIS). This represents 0.2% of all adverse event reports for APIXABAN.
299
Reports of Product dispensing error with APIXABAN
0.2%
of all APIXABAN reports
3
Deaths
30
Hospitalizations
How Dangerous Is Product dispensing error From APIXABAN?
Of the 299 reports, 3 (1.0%) resulted in death, 30 (10.0%) required hospitalization, and 2 (0.7%) were considered life-threatening.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 299 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 dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
PALBOCICLIB (299)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (296)
Which APIXABAN Alternatives Have Lower Product dispensing error Risk?
APIXABAN vs APOMORPHINE
APIXABAN vs APRACLONIDINE
APIXABAN vs APREMILAST
APIXABAN vs APREPITANT
APIXABAN vs APROTININ