Does APIXABAN Cause Intentional product misuse? 881 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 881 reports of Intentional product misuse have been filed in association with APIXABAN (ELIQUIS). This represents 0.6% of all adverse event reports for APIXABAN.
881
Reports of Intentional product misuse with APIXABAN
0.6%
of all APIXABAN reports
13
Deaths
216
Hospitalizations
How Dangerous Is Intentional product misuse From APIXABAN?
Of the 881 reports, 13 (1.5%) resulted in death, 216 (24.5%) required hospitalization, and 103 (11.7%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 881 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which APIXABAN Alternatives Have Lower Intentional product misuse Risk?
APIXABAN vs APOMORPHINE
APIXABAN vs APRACLONIDINE
APIXABAN vs APREMILAST
APIXABAN vs APREPITANT
APIXABAN vs APROTININ