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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 Haemoglobin decreased? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Haemoglobin decreased have been filed in association with BARICITINIB (Olumiant). This represents 0.5% of all adverse event reports for BARICITINIB.

40
Reports of Haemoglobin decreased with BARICITINIB
0.5%
of all BARICITINIB reports
8
Deaths
20
Hospitalizations

How Dangerous Is Haemoglobin decreased From BARICITINIB?

Of the 40 reports, 8 (20.0%) resulted in death, 20 (50.0%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BARICITINIB. However, 40 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 Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which BARICITINIB Alternatives Have Lower Haemoglobin decreased 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 Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased BARICITINIB Demographics