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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 REMIBRUTINIB Cause Condition aggravated? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Condition aggravated have been filed in association with REMIBRUTINIB (RHAPSIDO). This represents 71.4% of all adverse event reports for REMIBRUTINIB.

15
Reports of Condition aggravated with REMIBRUTINIB
71.4%
of all REMIBRUTINIB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Condition aggravated From REMIBRUTINIB?

Of the 15 reports.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REMIBRUTINIB. However, 15 reports have been filed with the FAERS database.

What Other Side Effects Does REMIBRUTINIB Cause?

Angioedema (16) Chronic spontaneous urticaria (15) Drug intolerance (15) Mental disorder due to a general medical condition (15) Treatment failure (15)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Related Pages

REMIBRUTINIB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated REMIBRUTINIB Demographics