Does DESONIDE Cause Intentional product use issue? 11 Reports in FDA Database
Visibly Younger Skin in Weeks
Synevra Lift & Lock — Swiss peptide serum + nutrients. 60-day money-back guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Intentional product use issue have been filed in association with DESONIDE (Desonide). This represents 0.8% of all adverse event reports for DESONIDE.
11
Reports of Intentional product use issue with DESONIDE
0.8%
of all DESONIDE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From DESONIDE?
Of the 11 reports, 1 (9.1%) resulted in death, 1 (9.1%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESONIDE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does DESONIDE Cause?
Drug ineffective (931)
Macular degeneration (752)
Off label use (230)
Therapeutic product effect incomplete (226)
Pain (217)
Erythema (212)
Chronic sinusitis (203)
Pyrexia (199)
Malaise (196)
Nausea (193)
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 DESONIDE Alternatives Have Lower Intentional product use issue Risk?
DESONIDE vs DESOXIMETASONE
DESONIDE vs DESVENLAFAXINE
DESONIDE vs DETROL
DESONIDE vs DEUCRAVACITINIB
DESONIDE vs DEUTETRABENAZINE