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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126741342 | 12674134 | 2 | F | 20160815 | 20160822 | 20160823 | EXP | PHHY2016CA105263 | SANDOZ | 0.00 | F | Y | 0.00000 | 20160823 | CN | COUNTRY NOT SPECIFIED | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126741342 | 12674134 | 1 | SS | MYFORTIC | MYCOPHENOLATE SODIUM | 1 | Oral | UNK | 0 | ||||||||||
| 126741342 | 12674134 | 2 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | 12.5 MG, QD | U | 0 | 12.5 | MG | QD | ||||||
| 126741342 | 12674134 | 3 | PS | CICLOSPORIN | CYCLOSPORINE | 1 | Unknown | 100 MG, BID | U | 65017 | 100 | MG | BID | ||||||
| 126741342 | 12674134 | 4 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | UNK | 0 | ||||||||||
| 126741342 | 12674134 | 5 | C | DEFEROXAMINE | DEFEROXAMINEDEFEROXAMINE MESYLATE | 1 | Subcutaneous | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126741342 | 12674134 | 1 | Iron overload |
| 126741342 | 12674134 | 2 | Product used for unknown indication |
| 126741342 | 12674134 | 3 | Product used for unknown indication |
| 126741342 | 12674134 | 4 | Product used for unknown indication |
| 126741342 | 12674134 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126741342 | 12674134 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126741342 | 12674134 | Drug intolerance | |
| 126741342 | 12674134 | Haemoglobin decreased | |
| 126741342 | 12674134 | Product use issue | |
| 126741342 | 12674134 | Rheumatoid arthritis |
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 |
|---|---|---|---|---|---|---|
| 126741342 | 12674134 | 1 | 201603 | 0 | ||
| 126741342 | 12674134 | 4 | 201605 | 0 |