Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102550581 | 10255058 | 1 | I | 20120809 | 0 | 20121217 | 20121217 | DIR | 73.00 | YR | M | N | 0.00000 | 20121213 | N | OT | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102550581 | 10255058 | 1 | PS | MEDROL | 1 | 0 | |||||||||||||
| 102550581 | 10255058 | 2 | SS | TRIAMCINOLONE | 1 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 102550581 | 10255058 | DE |
| 102550581 | 10255058 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 102550581 | 10255058 | Dysphagia | |
| 102550581 | 10255058 | General physical health deterioration | |
| 102550581 | 10255058 | Gout | |
| 102550581 | 10255058 | Hypotension | |
| 102550581 | 10255058 | Infarction | |
| 102550581 | 10255058 | Joint swelling | |
| 102550581 | 10255058 | Photophobia | |
| 102550581 | 10255058 | Pyrexia | |
| 102550581 | 10255058 | Visual impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 102550581 | 10255058 | HP |
Therapies reported
| no results found |