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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4817149 | 6040619 | I | 4817149-1 | 20050318 | 20050523 | 20051018 | PER | PHEH2005US05832 | NOVARTIS PHARMACEUTICALS CORP. | 58 | YR | M | N | 20050829 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4817149 | 1006582234 | PS | ZOMETA | 1 | INTRAVENOUS | 4 MG, ONCE/SINGLE, INTRAVENOUS | Y | D | 21223 | ||
| 4817149 | 1006612769 | C | ATENOLOL | 1 | |||||||
| 4817149 | 1006612771 | C | CASODEX | 1 | |||||||
| 4817149 | 1006612773 | C | LISINOPRIL | 1 | |||||||
| 4817149 | 1006612777 | C | PERCOCET | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4817149 | 1006582234 | METASTASES TO BONE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4817149 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4817149 | BLOOD CREATININE INCREASED |
| 4817149 | FEELING ABNORMAL |
| 4817149 | RENAL FAILURE ACUTE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4817149 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4817149 | 1006582234 | 20050318 | 20050318 |