DESOXIMETASONE
Generic: DESOXIMETASONE
Padagis Israel Pharmaceuticals LtdManufacturer
TOPICALRoute
DESOXIMETASONEActive Substance
2015-04-20Original Approval
DESOXIMETASONE is FDA application ANDA077770, sponsored by PADAGIS ISRAEL. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Recalls
Class II2016-09-13
Desoximetasone Cream USP, 0.25% 100 g, Rx only, mfd. by Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T 1C1, DisFailed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Modera
Class II2016-09-13
Desoximetasone Cream USP, 0.05% 100 g, Rx only, mfd. by Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T 1C1, DisFailed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Modera
Top Reported Reactions
1
DRUG INEFFECTIVE
9,808 reports
2
PAIN
8,824 reports
3
FATIGUE
8,718 reports
4
RHEUMATOID ARTHRITIS
8,173 reports
5
ALOPECIA
8,078 reports
6
SYSTEMIC LUPUS ERYTHEMATOSUS
8,003 reports
7
PEMPHIGUS
7,745 reports
8
ABDOMINAL DISCOMFORT
7,734 reports
9
GLOSSODYNIA
7,513 reports
10
SWELLING
7,062 reports