Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5080776 | 6081615 | I | 5080776-3 | 20060628 | 20060809 | EXP | PHBS2006JP09844 | SANDOZ INC | 49 | YR | F | N | 20060712 | MD | JAPAN |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5080776 | 1007581243 | PS | CYCLOSPORINE | 1 | 100 MG/D, | U | U | 80339 | |||
| 5080776 | 1007598297 | SS | PREDNISOLONE TAB | 1 | 25 MG/D, | U | U |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5080776 | 1007581243 | DERMATOMYOSITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5080776 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5080776 | PNEUMOMEDIASTINUM |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5080776 | FGN |
| 5080776 | HP |
| 5080776 | LIT |
| 5080776 | OTH |
Therapies reported
| no results found |