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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 Poor quality product administered? 45 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Poor quality product administered have been filed in association with APIXABAN (ELIQUIS). This represents 0.0% of all adverse event reports for APIXABAN.

45
Reports of Poor quality product administered with APIXABAN
0.0%
of all APIXABAN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Poor quality product administered From APIXABAN?

Of the 45 reports, 1 (2.2%) required hospitalization.

Is Poor quality product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 45 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 Poor quality product administered?

ONABOTULINUMTOXINA (495) ICOSAPENT ETHYL (452) MINOXIDIL (428) TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376) ADALIMUMAB (239) TESTOSTERONE CYPIONATE (235) SOMATROPIN (234) POLYETHYLENE GLYCOL 3350 (223) IBUPROFEN (222) INSULIN GLARGINE (133)

Which APIXABAN Alternatives Have Lower Poor quality product administered Risk?

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

Related Pages

APIXABAN Full Profile All Poor quality product administered Reports All Drugs Causing Poor quality product administered APIXABAN Demographics