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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126209671 | 12620967 | 1 | I | 20160718 | 20160728 | 20160804 | 20160804 | EXP | PHEH2016US018853 | NOVARTIS | 66.62 | YR | F | Y | 75.28000 | KG | 20160804 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126209671 | 12620967 | 1 | PS | MYFORTIC | MYCOPHENOLATE SODIUM | 1 | Oral | 360 MG, BID | U | 50791 | 360 | MG | BID | ||||||
| 126209671 | 12620967 | 2 | SS | MYFORTIC | MYCOPHENOLATE SODIUM | 1 | U | 50791 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126209671 | 12620967 | 1 | Renal transplant |
| 126209671 | 12620967 | 2 | Prophylaxis against transplant rejection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126209671 | 12620967 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126209671 | 12620967 | Diarrhoea | |
| 126209671 | 12620967 | Pancreatic disorder |
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 |
|---|---|---|---|---|---|---|
| 126209671 | 12620967 | 1 | 20150215 | 0 |