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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472334 | 6418782 | F | 5472334-3 | 20070301 | 20070920 | 20070929 | EXP | PHBS2007JP15089 | NOVARTIS PHARMACEUTICALS CORP. | F | Y | 20070927 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472334 | 1008989605 | PS | ZOMETA | 1 | INTRAVENOUS DRIP | 4 MG, QD | 021223 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5472334 | 1008989605 | METASTASES TO BONE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5472334 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5472334 | OSTEOMYELITIS |
| 5472334 | OSTEONECROSIS |
| 5472334 | SEQUESTRECTOMY |
| 5472334 | TOOTH EXTRACTION |
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 |
|---|---|---|---|---|---|
| 5472334 | 1008989605 | 20060901 |