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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126417651 | 12641765 | 1 | I | 20160801 | 20160810 | 20160810 | EXP | NZ-BAYER-2016-152154 | BAYER | 0.00 | Y | 0.00000 | 20160810 | MD | NZ | NZ |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126417651 | 12641765 | 1 | PS | NEXAVAR | SORAFENIB | 1 | Oral | UNK | 21923 | FILM-COATED TABLET | |||||||||
| 126417651 | 12641765 | 2 | SS | NEXAVAR | SORAFENIB | 1 | Oral | UNK | 21923 | FILM-COATED TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126417651 | 12641765 | 1 | Fibromatosis |
| 126417651 | 12641765 | 2 | Fibromatosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126417651 | 12641765 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126417651 | 12641765 | Fibromatosis | |
| 126417651 | 12641765 | General physical health deterioration | |
| 126417651 | 12641765 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |