Does DICHLORPHENAMIDE Cause Intentional product use issue? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Intentional product use issue have been filed in association with DICHLORPHENAMIDE (Dichlorphenamide). This represents 2.6% of all adverse event reports for DICHLORPHENAMIDE.
42
Reports of Intentional product use issue with DICHLORPHENAMIDE
2.6%
of all DICHLORPHENAMIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From DICHLORPHENAMIDE?
Of the 42 reports, 1 (2.4%) required hospitalization, and 1 (2.4%) 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 DICHLORPHENAMIDE. However, 42 reports have been filed with the FAERS database.
What Other Side Effects Does DICHLORPHENAMIDE Cause?
Paraesthesia (295)
Fatigue (219)
Disease recurrence (173)
Muscular weakness (159)
Feeling abnormal (157)
Wrong technique in product usage process (151)
Asthenia (130)
Confusional state (123)
Dizziness (108)
Nausea (107)
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)
Which DICHLORPHENAMIDE Alternatives Have Lower Intentional product use issue Risk?
DICHLORPHENAMIDE vs DICLOFENAC
DICHLORPHENAMIDE vs DICLOFENAC DIETHYLAMINE
DICHLORPHENAMIDE vs DICLOFENAC EPOLAMINE
DICHLORPHENAMIDE vs DICLOFENAC\DICLOFENAC
DICHLORPHENAMIDE vs DICLOFENAC\MISOPROSTOL