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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125252502 | 12525250 | 2 | F | 20151102 | 20160706 | 20160704 | 20160711 | EXP | IE-JNJFOC-20160627093 | JANSSEN | 84.50 | YR | E | F | Y | 0.00000 | 20160711 | CN | IE | IE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125252502 | 12525250 | 1 | PS | STELARA | USTEKINUMAB | 1 | Subcutaneous | N | UNKNOWN | 125261 | 90 | MG | SOLUTION FOR INJECTION | ||||||
| 125252502 | 12525250 | 2 | C | CITALOPRAM HYDROBROMIDE. | CITALOPRAM HYDROBROMIDE | 1 | Unknown | 0 | 20 | MG | UNSPECIFIED | ||||||||
| 125252502 | 12525250 | 3 | C | NEBILET | NEBIVOLOL | 1 | Unknown | 0 | .5 | MG | UNSPECIFIED | ||||||||
| 125252502 | 12525250 | 4 | C | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | 0 | 5 | MG | UNSPECIFIED | ||||||||
| 125252502 | 12525250 | 5 | C | DELTACORTRIL | PREDNISOLONE | 1 | Unknown | 0 | 5 | MG | UNSPECIFIED | ||||||||
| 125252502 | 12525250 | 6 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 0 | 40 | MG | UNSPECIFIED | ||||||||
| 125252502 | 12525250 | 7 | C | ASPIRIN. | ASPIRIN | 1 | Unknown | 0 | 75 | MG | UNSPECIFIED | ||||||||
| 125252502 | 12525250 | 8 | C | PANTOLAX | 2 | Unknown | 0 | 20 | MG | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125252502 | 12525250 | 1 | Vasculitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125252502 | 12525250 | HO |
| 125252502 | 12525250 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125252502 | 12525250 | Death | |
| 125252502 | 12525250 | Hospitalisation | |
| 125252502 | 12525250 | Off label use | |
| 125252502 | 12525250 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 125252502 | 12525250 | 1 | 20151102 | 0 |