Does DUPILUMAB Cause Intercepted product storage error? 325 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 325 reports of Intercepted product storage error have been filed in association with DUPILUMAB (Dupixent). This represents 0.1% of all adverse event reports for DUPILUMAB.
325
Reports of Intercepted product storage error with DUPILUMAB
0.1%
of all DUPILUMAB reports
1
Deaths
14
Hospitalizations
How Dangerous Is Intercepted product storage error From DUPILUMAB?
Of the 325 reports, 1 (0.3%) resulted in death, 14 (4.3%) required hospitalization.
Is Intercepted product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 325 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 Intercepted product storage error?
TOCILIZUMAB (381)
OMALIZUMAB (256)
ALTEPLASE (227)
INSULIN GLARGINE (129)
DORNASE ALFA (115)
BEVACIZUMAB (113)
RITUXIMAB (105)
OCRELIZUMAB (88)
PERTUZUMAB (84)
TRASTUZUMAB (75)
Which DUPILUMAB Alternatives Have Lower Intercepted product storage error Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE