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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 in error: Which Medications Cause It? (22,148 Reports Across 368 Drugs)

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Product dose omission in error has been reported as an adverse event with 368 different drugs in the FDA's FAERS database, with 22,148 total reports. 128 of these reports resulted in death.The drugs most commonly associated with Product dose omission in error are DUPILUMAB, TOFACITINIB, and LENALIDOMIDE.

22,148
Total Reports
368
Drugs Involved
128
Deaths
2,094
Hospitalizations
50.4 yrs
Average Patient Age
65.4% / 34.6%
Female / Male

Which Drugs Cause Product dose omission in error Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
DUPILUMAB 7,586 2.0% 5 269 1
TOFACITINIB 2,461 1.6% 8 189 1
LENALIDOMIDE 618 0.2% 2 37 0
PALBOCICLIB 592 0.7% 11 60 3
DIROXIMEL 481 4.5% 0 24 0
ABALOPARATIDE 457 2.0% 0 12 0
NIRAPARIB 428 2.0% 6 66 3
RUXOLITINIB 425 0.6% 1 53 0
TERIFLUNOMIDE 371 0.9% 1 25 0
DIMETHYL 308 0.3% 0 30 0
RELUGOLIX 293 1.4% 1 26 0
SACUBITRIL\VALSARTAN 279 0.3% 1 32 2
DOLUTEGRAVIR\LAMIVUDINE 234 7.4% 0 2 0
CERTOLIZUMAB PEGOL 226 0.2% 0 21 0
PIMAVANSERIN 180 0.4% 7 12 0
HUMAN IMMUNOGLOBULIN G 166 0.2% 1 57 1
SOFOSBUVIR\VELPATASVIR 161 0.9% 0 10 0
PIRFENIDONE 159 0.4% 1 10 0
SARILUMAB 155 0.7% 1 6 0
HUMAN C1-ESTERASE INHIBITOR 153 1.1% 1 34 5

View all 368 drugs →

Top 3 Drugs Associated With Product dose omission in error

7,586 reports
2,461 reports
618 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)