Does CLOBETASONE Cause Incorrect product administration duration? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Incorrect product administration duration have been filed in association with CLOBETASONE. This represents 3.8% of all adverse event reports for CLOBETASONE.
12
Reports of Incorrect product administration duration with CLOBETASONE
3.8%
of all CLOBETASONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From CLOBETASONE?
Of the 12 reports, 3 (25.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOBETASONE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does CLOBETASONE Cause?
Skin exfoliation (154)
Erythema (144)
Insomnia (129)
Skin weeping (129)
Pruritus (120)
Skin burning sensation (116)
Steroid withdrawal syndrome (104)
Medication error (81)
Alopecia (74)
Neuralgia (59)
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 CLOBETASONE Alternatives Have Lower Incorrect product administration duration Risk?
CLOBETASONE vs CLODRONATE
CLOBETASONE vs CLOFARABINE
CLOBETASONE vs CLOFAZIMINE
CLOBETASONE vs CLOMETHIAZOLE
CLOBETASONE vs CLOMIPHENE