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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577637 | 6517023 | I | 5577637-X | 20071101 | 20071221 | 20071231 | EXP | PHBS2007CH21344 | NOVARTIS PHARMACEUTICALS CORP. | M | Y | 20071229 | OT | SWITZERLAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577637 | 1009349357 | PS | LEPONEX | 2 | 19758 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577637 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5577637 | DIABETES MELLITUS |
| 5577637 | GENERAL PHYSICAL HEALTH DETERIORATION |
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 |
|---|---|---|---|---|---|
| 5577637 | 1009349357 | 20070901 |