Does BELUMOSUDIL Cause Condition aggravated? 127 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 127 reports of Condition aggravated have been filed in association with BELUMOSUDIL (Rezurock). This represents 4.9% of all adverse event reports for BELUMOSUDIL.
127
Reports of Condition aggravated with BELUMOSUDIL
4.9%
of all BELUMOSUDIL reports
2
Deaths
30
Hospitalizations
How Dangerous Is Condition aggravated From BELUMOSUDIL?
Of the 127 reports, 2 (1.6%) resulted in death, 30 (23.6%) required hospitalization, and 1 (0.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELUMOSUDIL. However, 127 reports have been filed with the FAERS database.
What Other Side Effects Does BELUMOSUDIL Cause?
Inappropriate schedule of product administration (377)
Product use in unapproved indication (340)
Fatigue (246)
Nausea (154)
Product dose omission issue (143)
Drug ineffective (141)
Diarrhoea (136)
Death (135)
Off label use (124)
Dyspnoea (114)
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)
Which BELUMOSUDIL Alternatives Have Lower Condition aggravated Risk?
BELUMOSUDIL vs BELVIQ
BELUMOSUDIL vs BELZUTIFAN
BELUMOSUDIL vs BEMPEDOIC ACID
BELUMOSUDIL vs BEMPEDOIC ACID\EZETIMIBE
BELUMOSUDIL vs BEMPEGALDESLEUKIN