Does DUPILUMAB Cause Product dose omission? 2,729 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,729 reports of Product dose omission have been filed in association with DUPILUMAB (Dupixent). This represents 0.7% of all adverse event reports for DUPILUMAB.
2,729
Reports of Product dose omission with DUPILUMAB
0.7%
of all DUPILUMAB reports
6
Deaths
72
Hospitalizations
How Dangerous Is Product dose omission From DUPILUMAB?
Of the 2,729 reports, 6 (0.2%) resulted in death, 72 (2.6%) required hospitalization, and 2 (0.1%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 2,729 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 Product dose omission?
APREMILAST (4,567)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
TOFACITINIB (1,104)
Which DUPILUMAB Alternatives Have Lower Product dose omission Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE