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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Product dose omission issue: Which Medications Cause It? (238,187 Reports Across 1,313 Drugs)

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Product dose omission issue has been reported as an adverse event with 1,313 different drugs in the FDA's FAERS database, with 238,187 total reports. 3,243 of these reports resulted in death.The drugs most commonly associated with Product dose omission issue are DUPILUMAB, USTEKINUMAB, and GUSELKUMAB.

238,187
Total Reports
1,313
Drugs Involved
3,243
Deaths
31,038
Hospitalizations
51.9 yrs
Average Patient Age
63.3% / 36.7%
Female / Male

Which Drugs Cause Product dose omission issue Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
DUPILUMAB 18,189 4.8% 21 598 10
USTEKINUMAB 9,405 11.0% 5 214 15
GUSELKUMAB 9,267 33.1% 2 78 1
LENALIDOMIDE 8,145 2.3% 24 691 12
MEPOLIZUMAB 5,873 13.7% 88 957 24
TOFACITINIB 5,646 3.6% 34 538 5
VOXELOTOR 5,122 23.4% 10 2,362 3
BELIMUMAB 4,671 17.5% 11 358 2
SECUKINUMAB 4,572 3.0% 22 319 31
APREMILAST 4,460 3.3% 2 81 3
GOLIMUMAB 4,216 6.1% 10 260 6
PIMAVANSERIN 3,808 8.2% 655 928 6
CERTOLIZUMAB PEGOL 3,630 3.7% 9 315 5
TIRZEPATIDE 3,211 3.2% 0 47 4
VEDOLIZUMAB 3,078 4.2% 47 859 9
ALBUTEROL 2,714 2.8% 68 396 47
SACUBITRIL\VALSARTAN 2,548 2.3% 30 318 33
HUMAN IMMUNOGLOBULIN G 2,267 3.2% 100 1,061 14
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE 2,235 8.6% 18 209 16
PALBOCICLIB 2,143 2.4% 62 266 3

View all 1,313 drugs →

Top 3 Drugs Associated With Product dose omission issue

18,189 reports
9,405 reports
9,267 reports

Related Side Effects

Drug ineffective (1,049,718) Off label use (762,782) Death (660,423) Fatigue (599,248) Nausea (562,301) Diarrhoea (491,550) Pain (471,975) Headache (460,069) Dyspnoea (409,496) Dizziness (352,922)