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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5688587 | 6555498 | F | 5688587-2 | 20080319 | 20080331 | EXP | PHHY2008AT01504 | NOVARTIS PHARMACEUTICALS CORP. | F | Y | 74 | KG | 20080328 | MD | AUSTRIA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5688587 | 1009725589 | PS | ZOMETA | 1 | 4 MG/YEAR | 021223 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5688587 | 1009725589 | OSTEOGENESIS IMPERFECTA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5688587 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5688587 | NEPHROLITHIASIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |