Does REVUMENIB Cause Product use complaint? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use complaint have been filed in association with REVUMENIB (Revuforj). This represents 1.4% of all adverse event reports for REVUMENIB.
5
Reports of Product use complaint with REVUMENIB
1.4%
of all REVUMENIB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product use complaint From REVUMENIB?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REVUMENIB. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does REVUMENIB Cause?
Off label use (57)
Platelet count decreased (50)
Nausea (49)
Product dose omission issue (40)
Death (38)
Vomiting (26)
Fatigue (24)
Pyrexia (22)
Differentiation syndrome (16)
Haemoglobin decreased (16)
What Other Drugs Cause Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which REVUMENIB Alternatives Have Lower Product use complaint Risk?
REVUMENIB vs REYATAZ
REVUMENIB vs REZAFUNGIN
REVUMENIB vs RIBASPHERE
REVUMENIB vs RIBAVIRIN
REVUMENIB vs RIBOCICLIB