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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7023068 | 7418288 | F | 7023068-5 | 20100908 | 20100916 | 20100930 | EXP | PHHY2010CA36044 | NOVARTIS PHARMACEUTICAL CORPORATION | 56 | YR | M | Y | 20100930 | OT | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7023068 | 1014812594 | PS | ZOMETA | 1 | INTRAVENOUS | 4 MG, EVERY 4 WEEKS | 021223 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7023068 | 1014812594 | PROSTATE CANCER METASTATIC |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7023068 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7023068 | ABDOMINAL DISTENSION |
| 7023068 | ARTHRITIS |
| 7023068 | BLOOD CHLORIDE DECREASED |
| 7023068 | BLOOD POTASSIUM DECREASED |
| 7023068 | BLOOD PRESSURE INCREASED |
| 7023068 | FIBROMYALGIA |
| 7023068 | GASTROOESOPHAGEAL REFLUX DISEASE |
| 7023068 | MUSCULOSKELETAL STIFFNESS |
| 7023068 | PAIN |
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 |
|---|---|---|---|---|---|
| 7023068 | 1014812594 | 20100526 |