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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 dose omission? 34 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Drug dose omission have been filed in association with ELIQUIS. This represents 2.4% of all adverse event reports for ELIQUIS.

34
Reports of Drug dose omission with ELIQUIS
2.4%
of all ELIQUIS reports
0
Deaths
2
Hospitalizations

How Dangerous Is Drug dose omission From ELIQUIS?

Of the 34 reports, 2 (5.9%) required hospitalization.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ELIQUIS. However, 34 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 dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) GOLIMUMAB (2,652) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153)

Which ELIQUIS Alternatives Have Lower Drug dose omission 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 dose omission Reports All Drugs Causing Drug dose omission ELIQUIS Demographics