Does DESONIDE Cause Incorrect product administration duration? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Incorrect product administration duration have been filed in association with DESONIDE (Desonide). This represents 1.2% of all adverse event reports for DESONIDE.
16
Reports of Incorrect product administration duration with DESONIDE
1.2%
of all DESONIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From DESONIDE?
Of the 16 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESONIDE. However, 16 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which DESONIDE Alternatives Have Lower Incorrect product administration duration Risk?
DESONIDE vs DESOXIMETASONE
DESONIDE vs DESVENLAFAXINE
DESONIDE vs DETROL
DESONIDE vs DEUCRAVACITINIB
DESONIDE vs DEUTETRABENAZINE