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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127725962 | 12772596 | 2 | F | 201609 | 20160927 | 20160922 | 20160930 | EXP | PHJP2016JP026937 | NOVARTIS | 70.00 | YR | M | Y | 0.00000 | 20160930 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127725962 | 12772596 | 1 | PS | NEORAL | CYCLOSPORINE | 1 | Oral | 75 MG, BID | D | 50716 | 75 | MG | SOLUTION | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127725962 | 12772596 | 1 | Interstitial lung disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127725962 | 12772596 | DE |
| 127725962 | 12772596 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127725962 | 12772596 | Bone marrow failure | |
| 127725962 | 12772596 | Death | |
| 127725962 | 12772596 | 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 |
|---|---|---|---|---|---|---|
| 127725962 | 12772596 | 1 | 20160909 | 0 |