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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8554089 | 8694878 | I | 8554089-9 | 20120517 | 20120731 | EXP | PHHY2012BR043637 | SANDOZ,INC. | YR | M | Y | 20120731 | CN | BRAZIL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8554089 | 1020404295 | PS | CYCLOSPORINE | 1 | UNK UKN, UNK | 065017 | |||||
| 8554089 | 1020404296 | SS | PREDNISONE | 1 | UNK UKN, UNK | ||||||
| 8554089 | 1020404294 | SS | MYFORTIC | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8554089 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8554089 | NAUSEA |
| 8554089 | ABDOMINAL DISCOMFORT |
| 8554089 | DEPRESSION |
| 8554089 | GASTROINTESTINAL INJURY |
| 8554089 | MEMORY IMPAIRMENT |
| 8554089 | DYSPEPSIA |
| 8554089 | GASTROINTESTINAL MOTILITY DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |