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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5286968 | 6456844 | I | 5286968-2 | 20070101 | 20070116 | 20070404 | EXP | PHBS2007CN05658 | NOVARTIS PHARMACEUTICALS CORP. | 39 | YR | F | Y | 20070404 | MD | CHINA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5286968 | 1008332273 | PS | ZELNORM | 1 | ORAL | 6 MG, BID | 21200 | ||||
| 5286968 | 1008332274 | C | POLYETHYLENE GLYCOL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5286968 | 1008332273 | IRRITABLE BOWEL SYNDROME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5286968 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5286968 | MUSCLE SPASTICITY |
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 |
|---|---|---|---|---|---|
| 5286968 | 1008332273 | 20070101 | |||
| 5286968 | 1008332274 | 20070101 |