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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 Device power source issue? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device power source issue have been filed in association with APIXABAN (ELIQUIS). This represents 0.0% of all adverse event reports for APIXABAN.

7
Reports of Device power source issue with APIXABAN
0.0%
of all APIXABAN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device power source issue From APIXABAN?

Of the 7 reports, 1 (14.3%) required hospitalization.

Is Device power source issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APIXABAN. However, 7 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 Device power source issue?

SOMATROPIN (1,219) PEGFILGRASTIM (486) TREPROSTINIL (299) CARBIDOPA\LEVODOPA (62) ETANERCEPT (54) BACLOFEN (50) GLYCOPYRROLATE (39) DEVICE (20) FOSCARBIDOPA\FOSLEVODOPA (14) INTERFERON BETA-1B (13)

Which APIXABAN Alternatives Have Lower Device power source issue Risk?

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

Related Pages

APIXABAN Full Profile All Device power source issue Reports All Drugs Causing Device power source issue APIXABAN Demographics