Does BELUMOSUDIL Cause Product dose omission in error? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product dose omission in error have been filed in association with BELUMOSUDIL (Rezurock). This represents 0.9% of all adverse event reports for BELUMOSUDIL.
24
Reports of Product dose omission in error with BELUMOSUDIL
0.9%
of all BELUMOSUDIL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission in error From BELUMOSUDIL?
Of the 24 reports, 2 (8.3%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELUMOSUDIL. However, 24 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)
Condition aggravated (127)
Off label use (124)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which BELUMOSUDIL Alternatives Have Lower Product dose omission in error Risk?
BELUMOSUDIL vs BELVIQ
BELUMOSUDIL vs BELZUTIFAN
BELUMOSUDIL vs BEMPEDOIC ACID
BELUMOSUDIL vs BEMPEDOIC ACID\EZETIMIBE
BELUMOSUDIL vs BEMPEGALDESLEUKIN