Does AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM Cause Off label use? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Off label use have been filed in association with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. This represents 71.8% of all adverse event reports for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM.
28
Reports of Off label use with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM
71.8%
of all AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM reports
20
Deaths
25
Hospitalizations
How Dangerous Is Off label use From AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM?
Of the 28 reports, 20 (71.4%) resulted in death, 25 (89.3%) required hospitalization, and 4 (14.3%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM Cause?
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)
Mobility decreased (26)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)