Does DUPILUMAB Cause Product prescribing error? 725 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 725 reports of Product prescribing error have been filed in association with DUPILUMAB (Dupixent). This represents 0.2% of all adverse event reports for DUPILUMAB.
725
Reports of Product prescribing error with DUPILUMAB
0.2%
of all DUPILUMAB reports
1
Deaths
17
Hospitalizations
How Dangerous Is Product prescribing error From DUPILUMAB?
Of the 725 reports, 1 (0.1%) resulted in death, 17 (2.3%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 725 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
RAMIPRIL (322)
Which DUPILUMAB Alternatives Have Lower Product prescribing error Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE