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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 Dyspnoea? 124 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 124 reports of Dyspnoea have been filed in association with BARICITINIB (Olumiant). This represents 1.5% of all adverse event reports for BARICITINIB.

124
Reports of Dyspnoea with BARICITINIB
1.5%
of all BARICITINIB reports
13
Deaths
71
Hospitalizations

How Dangerous Is Dyspnoea From BARICITINIB?

Of the 124 reports, 13 (10.5%) resulted in death, 71 (57.3%) required hospitalization, and 12 (9.7%) were considered life-threatening.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BARICITINIB. However, 124 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 Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

Which BARICITINIB Alternatives Have Lower Dyspnoea 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 Dyspnoea Reports All Drugs Causing Dyspnoea BARICITINIB Demographics