Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127506091 | 12750609 | 1 | I | 201512 | 20160105 | 20160915 | 20160915 | PER | US-ASTELLAS-2016US000539 | ASTELLAS | 75.69 | YR | M | Y | 0.00000 | 20160915 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127506091 | 12750609 | 1 | PS | XTANDI | ENZALUTAMIDE | 1 | Oral | U | 1516825PC/1521458PC/1539683PC | 203415 | 160 | MG | CAPSULE | QD | |||||
| 127506091 | 12750609 | 2 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127506091 | 12750609 | 1 | Prostate cancer |
| 127506091 | 12750609 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127506091 | 12750609 | Abdominal distension | |
| 127506091 | 12750609 | Decreased appetite | |
| 127506091 | 12750609 | Dysgeusia | |
| 127506091 | 12750609 | Nausea | |
| 127506091 | 12750609 | Prostatic specific antigen increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |