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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 compounding quality issue: Which Medications Cause It? (226 Reports Across 15 Drugs)

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Product compounding quality issue has been reported as an adverse event with 15 different drugs in the FDA's FAERS database, with 226 total reports. 6 of these reports resulted in death.The drugs most commonly associated with Product compounding quality issue are TRIAMCINOLONE, EXENATIDE, and VORICONAZOLE.

226
Total Reports
15
Drugs Involved
6
Deaths
24
Hospitalizations
48.0 yrs
Average Patient Age
66.7% / 33.3%
Female / Male

Which Drugs Cause Product compounding quality issue Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
TRIAMCINOLONE 23 0.3% 0 0 0
EXENATIDE 20 0.1% 0 1 0
VORICONAZOLE 20 0.1% 0 0 0
SODIUM 14 0.1% 0 0 0
SEMAGLUTIDE 12 0.0% 0 2 0
DEXTROSE 8 0.2% 1 0 0
POTASSIUM 8 0.1% 0 0 0
TIRZEPATIDE 8 0.0% 0 0 0
CALCIUM 7 0.0% 0 0 0
MAGNESIUM 7 0.1% 0 0 1
WATER 7 0.2% 0 0 0
CA 6 50.0% 0 0 0
DEXTROSE USP 6 31.6% 0 0 0
OXYTOCIN 6 0.4% 0 0 0
NALTREXONE 5 0.0% 0 0 0

View all 15 drugs →

Top 3 Drugs Associated With Product compounding quality issue

23 reports
20 reports
20 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)