Does AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM Cause Adverse event? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Adverse event have been filed in association with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. This represents 41.0% of all adverse event reports for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM.
16
Reports of Adverse event with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM
41.0%
of all AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM reports
13
Deaths
16
Hospitalizations
How Dangerous Is Adverse event From AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM?
Of the 16 reports, 13 (81.3%) resulted in death, 16 (100.0%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. However, 16 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)