PREDNISOLONE SODIUM PHOSPHATE
Generic: PREDNISOLONE SODIUM PHOSPHATE
PAI HoldingsManufacturer
ORALRoute
PREDNISOLONE SODIUM PHOSPHATEActive Substance
2008-06-09Original Approval
PREDNISOLONE SODIUM PHOSPHATE is FDA application ANDA078988, sponsored by PHARM ASSOC. 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.
Top Reported Reactions
1
DRUG INEFFECTIVE
187 reports
2
OFF LABEL USE
170 reports
3
PYREXIA
157 reports
4
TREATMENT FAILURE
153 reports
5
VOMITING
142 reports
6
CONDITION AGGRAVATED
136 reports
7
PAIN
133 reports
8
RHEUMATOID ARTHRITIS
126 reports
9
HYPERSENSITIVITY
125 reports
10
HEADACHE
124 reports