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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125896461 | 12589646 | 1 | I | 201604 | 20160607 | 20160725 | 20160725 | EXP | ES-BAYER-2016-112832 | BAYER | 78.00 | YR | E | M | Y | 0.00000 | 20160725 | CN | ES | ES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125896461 | 12589646 | 1 | PS | NEXAVAR | SORAFENIB | 1 | UNK | 21923 | FILM-COATED TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125896461 | 12589646 | OT |
| 125896461 | 12589646 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125896461 | 12589646 | Abdominal injury | |
| 125896461 | 12589646 | Abdominal pain | |
| 125896461 | 12589646 | Blood glucose increased | |
| 125896461 | 12589646 | Blood pressure increased | |
| 125896461 | 12589646 | Fluid retention | |
| 125896461 | 12589646 | Nipple pain | |
| 125896461 | 12589646 | Occult blood positive | |
| 125896461 | 12589646 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 125896461 | 12589646 | 1 | 20160421 | 2016 | 0 |