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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127138441 | 12713844 | 1 | I | 20160901 | 20160905 | 20160905 | EXP | DE-009507513-1609DEU000588 | MERCK | 67.00 | YR | F | Y | 0.00000 | 20160905 | MD | DE | DE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127138441 | 12713844 | 1 | PS | TEMODAL | TEMOZOLOMIDE | 1 | Oral | U | 21029 | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127138441 | 12713844 | 1 | Astrocytoma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127138441 | 12713844 | DS |
127138441 | 12713844 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127138441 | 12713844 | Fall | |
127138441 | 12713844 | Gait disturbance | |
127138441 | 12713844 | Helplessness | |
127138441 | 12713844 | Neuropathy peripheral | |
127138441 | 12713844 | Prescribed overdose | |
127138441 | 12713844 | Product use issue | |
127138441 | 12713844 | Walking aid user |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |