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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040494 | 6075483 | F | 5040494-4 | 20060321 | 20060405 | 20060630 | EXP | US-ROCHE-443529 | ROCHE | 79 | YR | F | Y | 56.2 | KG | 20060630 | CN | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040494 | 1007431407 | PS | BONIVA | 1 | ORAL | 021455 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5040494 | 1007431407 | OSTEOPOROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5040494 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5040494 | AORTIC ANEURYSM |
| 5040494 | ARTERIOSCLEROSIS |
| 5040494 | DIARRHOEA |
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 |
|---|---|---|---|---|---|
| 5040494 | 1007431407 | 20060321 | 20060321 | 1 | DAY |