Does AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM Cause Intentional product use issue? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Intentional product use issue have been filed in association with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. This represents 69.2% of all adverse event reports for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM.
27
Reports of Intentional product use issue with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM
69.2%
of all AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM reports
20
Deaths
24
Hospitalizations
How Dangerous Is Intentional product use issue From AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM?
Of the 27 reports, 20 (74.1%) resulted in death, 24 (88.9%) required hospitalization, and 3 (11.1%) were considered life-threatening.
Is Intentional 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, 27 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)
Abdominal discomfort (26)
Alopecia (26)
Arthralgia (26)
Decreased appetite (26)
Fatigue (26)
Hypertension (26)
Mobility decreased (26)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)