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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 label issue? 50 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Product label issue have been filed in association with APIXABAN (ELIQUIS). This represents 0.0% of all adverse event reports for APIXABAN.

50
Reports of Product label issue with APIXABAN
0.0%
of all APIXABAN reports
1
Deaths
4
Hospitalizations

How Dangerous Is Product label issue From APIXABAN?

Of the 50 reports, 1 (2.0%) resulted in death, 4 (8.0%) required hospitalization, and 1 (2.0%) were considered life-threatening.

Is Product label issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 50 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 label issue?

RIVAROXABAN (379) ACETAMINOPHEN (276) GUSELKUMAB (177) USTEKINUMAB (164) DIMETHICONE\LOPERAMIDE (154) CETIRIZINE (138) IBUPROFEN (99) GOLIMUMAB (76) POLYETHYLENE GLYCOL 3350 (76) FENTANYL (72)

Which APIXABAN Alternatives Have Lower Product label issue Risk?

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

Related Pages

APIXABAN Full Profile All Product label issue Reports All Drugs Causing Product label issue APIXABAN Demographics