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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123520334 | 12352033 | 4 | F | 2016 | 20160727 | 20160510 | 20160803 | EXP | ID-BAYER-2016-085147 | BAYER | 48.00 | YR | A | F | Y | 0.00000 | 20160803 | CN | ID | ID |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123520334 | 12352033 | 1 | PS | NEXAVAR | SORAFENIB | 1 | Oral | 200 MG, BID | 26000 | MG | 21923 | 200 | MG | FILM-COATED TABLET | BID | ||||
| 123520334 | 12352033 | 2 | SS | NEXAVAR | SORAFENIB | 1 | 2 X 200 MG | 26000 | MG | 21923 | FILM-COATED TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123520334 | 12352033 | 1 | Hepatocellular carcinoma |
| 123520334 | 12352033 | 2 | Hepatocellular carcinoma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123520334 | 12352033 | HO |
| 123520334 | 12352033 | OT |
| 123520334 | 12352033 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123520334 | 12352033 | Abdominal pain upper | |
| 123520334 | 12352033 | Abdominal rigidity | |
| 123520334 | 12352033 | Asthenia | |
| 123520334 | 12352033 | Death | |
| 123520334 | 12352033 | Decreased appetite | |
| 123520334 | 12352033 | Diarrhoea | |
| 123520334 | 12352033 | Erythema | |
| 123520334 | 12352033 | Faeces discoloured | |
| 123520334 | 12352033 | Fatigue | |
| 123520334 | 12352033 | Feeling hot | |
| 123520334 | 12352033 | Haematemesis | |
| 123520334 | 12352033 | Hospitalisation | |
| 123520334 | 12352033 | Hypophagia | |
| 123520334 | 12352033 | Intentional product misuse | |
| 123520334 | 12352033 | Mobility decreased | |
| 123520334 | 12352033 | Myalgia | |
| 123520334 | 12352033 | Nausea | |
| 123520334 | 12352033 | Ocular icterus | |
| 123520334 | 12352033 | Pharyngeal haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 123520334 | 12352033 | 1 | 20160408 | 20160611 | 0 | |
| 123520334 | 12352033 | 2 | 20160620 | 20160622 | 0 |