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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124176902 | 12417690 | 2 | F | 20160425 | 20160809 | 20160530 | 20160815 | EXP | PHJP2016JP012690 | NOVARTIS | 76.00 | YR | M | Y | 0.00000 | 20160815 | PH | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124176902 | 12417690 | 1 | PS | NEORAL | CYCLOSPORINE | 1 | Oral | 100 MG, UNK | 50715 | 100 | MG | CAPSULE | |||||||
| 124176902 | 12417690 | 2 | SS | NEORAL | CYCLOSPORINE | 1 | Oral | 50 MG, UNK | 50715 | 50 | MG | CAPSULE |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124176902 | 12417690 | 1 | Rheumatic disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124176902 | 12417690 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124176902 | 12417690 | Decreased appetite | |
| 124176902 | 12417690 | Renal impairment |
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 |
|---|---|---|---|---|---|---|
| 124176902 | 12417690 | 1 | 20160502 | 0 | ||
| 124176902 | 12417690 | 2 | 20160502 | 20160525 | 0 |