Does DUPILUMAB Cause Incorrect product administration duration? 194 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 194 reports of Incorrect product administration duration have been filed in association with DUPILUMAB (Dupixent). This represents 0.1% of all adverse event reports for DUPILUMAB.
194
Reports of Incorrect product administration duration with DUPILUMAB
0.1%
of all DUPILUMAB reports
0
Deaths
7
Hospitalizations
How Dangerous Is Incorrect product administration duration From DUPILUMAB?
Of the 194 reports, 7 (3.6%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 194 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which DUPILUMAB Alternatives Have Lower Incorrect product administration duration Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE