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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does APIXABAN Cause Product storage error? 694 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 694 reports of Product storage error have been filed in association with APIXABAN (ELIQUIS). This represents 0.4% of all adverse event reports for APIXABAN.

694
Reports of Product storage error with APIXABAN
0.4%
of all APIXABAN reports
1
Deaths
16
Hospitalizations

How Dangerous Is Product storage error From APIXABAN?

Of the 694 reports, 1 (0.1%) resulted in death, 16 (2.3%) required hospitalization.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 694 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 storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which APIXABAN Alternatives Have Lower Product storage error Risk?

APIXABAN vs APOMORPHINE APIXABAN vs APRACLONIDINE APIXABAN vs APREMILAST APIXABAN vs APREPITANT APIXABAN vs APROTININ

Related Pages

APIXABAN Full Profile All Product storage error Reports All Drugs Causing Product storage error APIXABAN Demographics