Does DUPILUMAB Cause Condition aggravated? 16,459 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16,459 reports of Condition aggravated have been filed in association with DUPILUMAB (Dupixent). This represents 4.3% of all adverse event reports for DUPILUMAB.
16,459
Reports of Condition aggravated with DUPILUMAB
4.3%
of all DUPILUMAB reports
34
Deaths
652
Hospitalizations
How Dangerous Is Condition aggravated From DUPILUMAB?
Of the 16,459 reports, 34 (0.2%) resulted in death, 652 (4.0%) required hospitalization, and 13 (0.1%) 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 DUPILUMAB. However, 16,459 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)
Arthralgia (15,176)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
TOCILIZUMAB (8,471)
Which DUPILUMAB Alternatives Have Lower Condition aggravated Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE