Does CLOBETASONE Cause Product prescribing issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product prescribing issue have been filed in association with CLOBETASONE. This represents 2.2% of all adverse event reports for CLOBETASONE.
7
Reports of Product prescribing issue with CLOBETASONE
2.2%
of all CLOBETASONE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product prescribing issue From CLOBETASONE?
Of the 7 reports, 6 (85.7%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOBETASONE. However, 7 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 Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which CLOBETASONE Alternatives Have Lower Product prescribing issue Risk?
CLOBETASONE vs CLODRONATE
CLOBETASONE vs CLOFARABINE
CLOBETASONE vs CLOFAZIMINE
CLOBETASONE vs CLOMETHIAZOLE
CLOBETASONE vs CLOMIPHENE