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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 Fibrin d dimer increased? 35 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Fibrin d dimer increased have been filed in association with BARICITINIB (Olumiant). This represents 0.4% of all adverse event reports for BARICITINIB.

35
Reports of Fibrin d dimer increased with BARICITINIB
0.4%
of all BARICITINIB reports
4
Deaths
10
Hospitalizations

How Dangerous Is Fibrin d dimer increased From BARICITINIB?

Of the 35 reports, 4 (11.4%) resulted in death, 10 (28.6%) required hospitalization, and 17 (48.6%) were considered life-threatening.

Is Fibrin d dimer increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BARICITINIB. However, 35 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 Fibrin d dimer increased?

ADALIMUMAB (97) RIVAROXABAN (91) PREDNISONE (69) RITUXIMAB (63) APIXABAN (59) ASPIRIN (54) ACETAMINOPHEN (53) LENALIDOMIDE (53) METHOTREXATE (52) BAMLANIVIMAB (49)

Which BARICITINIB Alternatives Have Lower Fibrin d dimer increased 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 Fibrin d dimer increased Reports All Drugs Causing Fibrin d dimer increased BARICITINIB Demographics