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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125044324 | 12504432 | 4 | F | 2016 | 20160901 | 20160628 | 20160907 | EXP | IE-JNJFOC-20160617716 | JANSSEN | 0.00 | F | Y | 0.00000 | 20160907 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125044324 | 12504432 | 1 | PS | STELARA | USTEKINUMAB | 1 | Subcutaneous | N | N | FKS06NB | 125261 | 90 | MG | SOLUTION FOR INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125044324 | 12504432 | 1 | Temporal arteritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125044324 | 12504432 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125044324 | 12504432 | Kidney infection | |
| 125044324 | 12504432 | Nephrolithiasis | |
| 125044324 | 12504432 | Off label use | |
| 125044324 | 12504432 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |