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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 Therapy non-responder? 49 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Therapy non-responder have been filed in association with BARICITINIB (Olumiant). This represents 0.6% of all adverse event reports for BARICITINIB.

49
Reports of Therapy non-responder with BARICITINIB
0.6%
of all BARICITINIB reports
7
Deaths
9
Hospitalizations

How Dangerous Is Therapy non-responder From BARICITINIB?

Of the 49 reports, 7 (14.3%) resulted in death, 9 (18.4%) required hospitalization, and 8 (16.3%) were considered life-threatening.

Is Therapy non-responder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BARICITINIB. However, 49 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 Therapy non-responder?

ETANERCEPT (3,472) APREMILAST (3,360) METHOTREXATE (2,965) RITUXIMAB (2,731) ADALIMUMAB (2,595) PREDNISONE (2,563) TREPROSTINIL (2,289) INFLIXIMAB (2,122) TOCILIZUMAB (1,775) HYDROXYCHLOROQUINE (1,699)

Which BARICITINIB Alternatives Have Lower Therapy non-responder 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 Therapy non-responder Reports All Drugs Causing Therapy non-responder BARICITINIB Demographics