Does DUPILUMAB Cause Unevaluable event? 1,410 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,410 reports of Unevaluable event have been filed in association with DUPILUMAB (Dupixent). This represents 0.4% of all adverse event reports for DUPILUMAB.
1,410
Reports of Unevaluable event with DUPILUMAB
0.4%
of all DUPILUMAB reports
4
Deaths
104
Hospitalizations
How Dangerous Is Unevaluable event From DUPILUMAB?
Of the 1,410 reports, 4 (0.3%) resulted in death, 104 (7.4%) required hospitalization, and 2 (0.1%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 1,410 reports have been filed with the FAERS database.
What Other Side Effects Does DUPILUMAB Cause?
Pruritus (44,279)
Dermatitis atopic (33,670)
Product use in unapproved indication (33,452)
Rash (30,895)
Injection site pain (27,799)
Drug ineffective (23,712)
Dry skin (20,239)
Eczema (20,020)
Product dose omission issue (18,189)
Condition aggravated (16,459)
What Other Drugs Cause Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
HYDROMORPHONE (1,118)
Which DUPILUMAB Alternatives Have Lower Unevaluable event Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE