Does AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM Cause Condition aggravated? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Condition aggravated have been filed in association with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. This represents 64.1% of all adverse event reports for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM.
25
Reports of Condition aggravated with AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM
64.1%
of all AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM reports
20
Deaths
25
Hospitalizations
How Dangerous Is Condition aggravated From AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM?
Of the 25 reports, 20 (80.0%) resulted in death, 25 (100.0%) required hospitalization, and 4 (16.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMMONIUM\DIPHENHYDRAMINE\MENTHOL\SODIUM. However, 25 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)