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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281461 | 12528146 | 1 | I | 20160625 | 20160627 | 20160705 | 20160705 | EXP | BE-JNJFOC-20160624938 | JANSSEN | 0.00 | M | Y | 0.00000 | 20160705 | MD | BE | BE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281461 | 12528146 | 1 | PS | ZYTIGA | ABIRATERONE ACETATE | 1 | Oral | SINCE 3 TO 4 MONTHS | U | U | 202379 | TABLET | |||||||
| 125281461 | 12528146 | 2 | SS | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125281461 | 12528146 | 1 | Product used for unknown indication |
| 125281461 | 12528146 | 2 | Pharyngeal abscess |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125281461 | 12528146 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125281461 | 12528146 | Pharyngeal abscess | |
| 125281461 | 12528146 | Rash |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125281461 | 12528146 | 2 | 20160624 | 0 |