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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 ELIQUIS Cause Drug administration error? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Drug administration error have been filed in association with ELIQUIS. This represents 1.7% of all adverse event reports for ELIQUIS.

24
Reports of Drug administration error with ELIQUIS
1.7%
of all ELIQUIS reports
0
Deaths
3
Hospitalizations

How Dangerous Is Drug administration error From ELIQUIS?

Of the 24 reports, 3 (12.5%) required hospitalization, and 1 (4.2%) were considered life-threatening.

Is Drug administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ELIQUIS. However, 24 reports have been filed with the FAERS database.

What Other Side Effects Does ELIQUIS Cause?

Haemorrhage (79) Gastrointestinal haemorrhage (72) Dizziness (65) Rash (51) Epistaxis (49) Headache (49) Dyspnoea (41) Adverse event (40) Diarrhoea (37) Contusion (34)

What Other Drugs Cause Drug administration error?

INSULIN GLARGINE (1,189) ACETAMINOPHEN (980) FLUTICASONE\SALMETEROL (732) DOCOSANOL (721) ASPIRIN (542) METHYLPHENIDATE (526) NICOTINE (492) ALBUTEROL (418) FLUTICASONE (292) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (257)

Which ELIQUIS Alternatives Have Lower Drug administration error Risk?

ELIQUIS vs ELOSULFASE ALFA ELIQUIS vs ELOTUZUMAB ELIQUIS vs ELOXATIN ELIQUIS vs ELRANATAMAB ELIQUIS vs ELRANATAMAB-BCMM

Related Pages

ELIQUIS Full Profile All Drug administration error Reports All Drugs Causing Drug administration error ELIQUIS Demographics