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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 administration error: Which Medications Cause It? (18,035 Reports Across 744 Drugs)

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Product administration error has been reported as an adverse event with 744 different drugs in the FDA's FAERS database, with 18,035 total reports. 725 of these reports resulted in death.The drugs most commonly associated with Product administration error are HYDROXYPROGESTERONE CAPROATE, ACETAMINOPHEN, and CENEGERMIN-BKBJ.

18,035
Total Reports
744
Drugs Involved
725
Deaths
3,981
Hospitalizations
52.0 yrs
Average Patient Age
61.3% / 38.7%
Female / Male

Which Drugs Cause Product administration error Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
HYDROXYPROGESTERONE CAPROATE 972 4.3% 0 64 0
ACETAMINOPHEN 666 0.5% 128 252 36
CENEGERMIN-BKBJ 613 5.1% 1 41 0
LEUPROLIDE 595 0.8% 4 7 0
EVOLOCUMAB 565 0.4% 0 11 1
ADALIMUMAB 543 0.1% 1 32 0
METHYLPHENIDATE 414 1.3% 1 12 4
OLMESARTAN MEDOXOMIL 314 2.6% 8 231 1
ASPIRIN 241 0.3% 54 152 29
SECUKINUMAB 225 0.2% 1 5 1
HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL 222 3.8% 5 168 1
IBUPROFEN 211 0.2% 19 129 19
NALTREXONE 211 0.8% 3 21 0
CLOZAPINE 197 0.2% 14 141 20
RISPERIDONE 189 0.2% 2 128 18
DICLOFENAC 188 0.2% 12 55 12
MEDROXYPROGESTERONE 187 2.2% 0 2 1
QUETIAPINE 174 0.2% 4 117 13
LEVETIRACETAM 170 0.3% 3 144 4
METFORMIN 160 0.2% 12 113 20

View all 744 drugs →

Top 3 Drugs Associated With Product administration error

666 reports
613 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)