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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 reconstitution quality issue: Which Medications Cause It? (759 Reports Across 29 Drugs)

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Product reconstitution quality issue has been reported as an adverse event with 29 different drugs in the FDA's FAERS database, with 759 total reports. 5 of these reports resulted in death.The drugs most commonly associated with Product reconstitution quality issue are SOMATROPIN, LEUPROLIDE, and RISPERIDONE.

759
Total Reports
29
Drugs Involved
5
Deaths
44
Hospitalizations
41.6 yrs
Average Patient Age
39.7% / 60.3%
Female / Male

Which Drugs Cause Product reconstitution quality issue Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
SOMATROPIN 149 0.2% 0 2 0
LEUPROLIDE 108 0.2% 1 0 0
RISPERIDONE 34 0.0% 1 1 0
TRIPTORELIN 28 0.5% 0 1 0
SULFUR HEXAFLUORIDE 23 1.6% 0 0 0
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT 20 0.2% 0 5 0
HUMAN C1-ESTERASE INHIBITOR 20 0.1% 0 4 1
AZACITIDINE 17 0.1% 0 0 0
ONABOTULINUMTOXINA 16 0.0% 0 0 0
NALTREXONE 15 0.1% 0 0 0
TEDUGLUTIDE 15 0.2% 1 11 0
WATER 14 0.3% 0 0 0
ARIPIPRAZOLE 13 0.0% 0 2 0
DEVICE 12 0.1% 0 1 0
HUMAN IMMUNOGLOBULIN G 12 0.0% 0 4 0
OCTREOTIDE 12 0.1% 1 1 1
ABATACEPT 11 0.0% 0 0 0
CHORIOGONADOTROPIN ALFA 11 0.4% 0 0 0
VEDOLIZUMAB 11 0.0% 0 1 0
VON WILLEBRAND FACTOR 10 4.4% 0 0 0

View all 29 drugs →

Top 3 Drugs Associated With Product reconstitution quality issue

149 reports
108 reports
34 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)