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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5153815 | 6127894 | I | 5153815-9 | 20061107 | 20061120 | EXP | US-JNJFOC-20060900270 | ALZA CORPORATION | M | Y | 72.58 | KG | 20061120 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5153815 | 1007865262 | PS | VIADUR | 1 | SUBCUTANEOUS | 021088 | |||||
| 5153815 | 1007865263 | C | MANY UNKNOWN MEDICATIONS | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5153815 | 1007865262 | PROSTATE CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5153815 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5153815 | CHOLECYSTECTOMY |
| 5153815 | DEHYDRATION |
| 5153815 | HOT FLUSH |
| 5153815 | NAUSEA |
| 5153815 | NEPHROLITHIASIS |
| 5153815 | RENAL FAILURE |
| 5153815 | VOMITING |
| 5153815 | WEIGHT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |