Does DUPILUMAB Cause Intentional dose omission? 2,269 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,269 reports of Intentional dose omission have been filed in association with DUPILUMAB (Dupixent). This represents 0.6% of all adverse event reports for DUPILUMAB.
2,269
Reports of Intentional dose omission with DUPILUMAB
0.6%
of all DUPILUMAB reports
3
Deaths
84
Hospitalizations
How Dangerous Is Intentional dose omission From DUPILUMAB?
Of the 2,269 reports, 3 (0.1%) resulted in death, 84 (3.7%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 2,269 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 Intentional dose omission?
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
SOFOSBUVIR\VELPATASVIR (474)
Which DUPILUMAB Alternatives Have Lower Intentional dose omission Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE