Does APIXABAN Cause Product prescribing error? 287 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 287 reports of Product prescribing error have been filed in association with APIXABAN (ELIQUIS). This represents 0.2% of all adverse event reports for APIXABAN.
287
Reports of Product prescribing error with APIXABAN
0.2%
of all APIXABAN reports
7
Deaths
127
Hospitalizations
How Dangerous Is Product prescribing error From APIXABAN?
Of the 287 reports, 7 (2.4%) resulted in death, 127 (44.3%) required hospitalization, and 11 (3.8%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 287 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which APIXABAN Alternatives Have Lower Product prescribing error Risk?
APIXABAN vs APOMORPHINE
APIXABAN vs APRACLONIDINE
APIXABAN vs APREMILAST
APIXABAN vs APREPITANT
APIXABAN vs APROTININ