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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5286005 | 6123474 | F | 5286005-X | 20060101 | 20070326 | 20070404 | EXP | PHBS2006BR13163 | NOVARTIS PHARMACEUTICALS CORP. | 36 | YR | F | Y | 20070404 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5286005 | 1008328617 | PS | ZELNORM | 1 | ORAL | 12 MG/DAY | 21200 | ||||
| 5286005 | 1008328618 | C | LISADOR | 2 | |||||||
| 5286005 | 1008328619 | C | LUFTAL | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5286005 | 1008328617 | CONSTIPATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5286005 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5286005 | FALLOPIAN TUBE OPERATION |
| 5286005 | HAEMORRHAGE |
| 5286005 | LAPAROSCOPY |
| 5286005 | OOPHORECTOMY |
| 5286005 | SURGERY |
| 5286005 | UTERINE OPERATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |