Does AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM Cause Product use issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use issue have been filed in association with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. This represents 18.0% of all adverse event reports for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM.
7
Reports of Product use issue with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM
18.0%
of all AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM reports
2
Deaths
7
Hospitalizations
How Dangerous Is Product use issue From AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM?
Of the 7 reports, 2 (28.6%) resulted in death, 7 (100.0%) required hospitalization, and 3 (42.9%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM Cause?
Off label use (28)
General physical health deterioration (27)
Infusion related reaction (27)
Intentional product use issue (27)
Abdominal discomfort (26)
Alopecia (26)
Arthralgia (26)
Decreased appetite (26)
Fatigue (26)
Hypertension (26)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)