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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126890651 | 12689065 | 1 | I | 20160821 | 20160824 | 20160826 | 20160826 | EXP | PHFR2016GB006893 | NOVARTIS | 71.55 | YR | M | Y | 0.00000 | 20160826 | CN | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126890651 | 12689065 | 1 | PS | NEORAL | CYCLOSPORINE | 1 | Unknown | 50715 | CAPSULE | ||||||||||
126890651 | 12689065 | 2 | SS | AZATHIOPRINE. | AZATHIOPRINE | 1 | Unknown | 0 | TABLET | ||||||||||
126890651 | 12689065 | 3 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | 0 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126890651 | 12689065 | 1 | Immunosuppression |
126890651 | 12689065 | 2 | Immunosuppression |
126890651 | 12689065 | 3 | Immunosuppression |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126890651 | 12689065 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126890651 | 12689065 | Death |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |