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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5742247 | 6610683 | F | 5742247-8 | 20080331 | 20080508 | 20080519 | EXP | PHHY2008JP04572 | NOVARTIS PHARMACEUTICALS CORP. | 53 | YR | Y | 53 | KG | 20080517 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5742247 | 1009923973 | PS | SANDOSTATIN | 1 | SUBCUTANEOUS | 300 UG/DAY | 019667 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5742247 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5742247 | DIALYSIS |
| 5742247 | HYPONATRAEMIA |
| 5742247 | NAUSEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5742247 | 1009923973 | 20080330 | 20080401 | 4320 | MIN |