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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 BARICITINIB Cause Intentional dose omission? 22 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Intentional dose omission have been filed in association with BARICITINIB (Olumiant). This represents 0.3% of all adverse event reports for BARICITINIB.

22
Reports of Intentional dose omission with BARICITINIB
0.3%
of all BARICITINIB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Intentional dose omission From BARICITINIB?

Of the 22 reports.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BARICITINIB. However, 22 reports have been filed with the FAERS database.

What Other Side Effects Does BARICITINIB Cause?

Drug ineffective (569) Off label use (479) Covid-19 (347) Pulmonary embolism (288) Rheumatoid arthritis (284) Headache (216) Herpes zoster (216) Pneumonia (216) Death (206) Deep vein thrombosis (201)

What Other Drugs Cause Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which BARICITINIB Alternatives Have Lower Intentional dose omission Risk?

BARICITINIB vs BARIUM BARICITINIB vs BARNIDIPINE BARICITINIB vs BASILIXIMAB BARICITINIB vs BAYER GENUINE ASPIRIN ORIGINAL STRENGTH BARICITINIB vs BAZEDOXIFENE\ESTROGENS, CONJUGATED

Related Pages

BARICITINIB Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission BARICITINIB Demographics