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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 container issue: Which Medications Cause It? (7,315 Reports Across 197 Drugs)

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Product container issue has been reported as an adverse event with 197 different drugs in the FDA's FAERS database, with 7,315 total reports. 43 of these reports resulted in death.The drugs most commonly associated with Product container issue are CYCLOSPORINE, MINOXIDIL, and MOMETASONE FUROATE.

7,315
Total Reports
197
Drugs Involved
43
Deaths
346
Hospitalizations
60.6 yrs
Average Patient Age
71.7% / 28.3%
Female / Male

Which Drugs Cause Product container issue Most Often?

Drug Reports % of Drug Reports Deaths Hosp. Life-Threat.
CYCLOSPORINE 910 1.3% 0 4 0
MINOXIDIL 556 0.9% 0 0 0
MOMETASONE FUROATE 450 3.9% 0 6 0
FORMOTEROL\MOMETASONE FUROATE 375 4.6% 0 9 0
LIFITEGRAST 244 1.8% 0 0 0
ALBUTEROL 192 0.2% 1 5 1
LATANOPROST 158 1.0% 0 4 0
CARBOXYMETHYLCELLULOSE\GLYCERIN 123 5.5% 0 1 0
BRIMONIDINE 121 1.0% 0 0 0
ACETAMINOPHEN 118 0.1% 0 2 0
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM 102 0.1% 3 27 1
BIMATOPROST 92 0.6% 0 0 0
RISPERIDONE 90 0.1% 0 0 1
DORZOLAMIDE\TIMOLOL 80 1.7% 0 0 0
BRIMONIDINE\TIMOLOL 78 3.1% 0 0 0
TIMOLOL 76 1.0% 0 2 0
TRAVOPROST 67 1.0% 0 0 0
INFLIXIMAB 62 0.0% 2 4 1
INSULIN ASPART 61 0.3% 1 46 4
CLOBETASOL 57 0.7% 0 0 0

View all 197 drugs →

Top 3 Drugs Associated With Product container issue

910 reports
556 reports
450 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)