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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126146901 | 12614690 | 1 | I | 201605 | 20160513 | 20160802 | 20160802 | EXP | CA-009507513-1605CAN007999 | MERCK | 66.44 | YR | F | Y | 0.00000 | 20160802 | CN | CA | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126146901 | 12614690 | 1 | PS | TEMODAL | TEMOZOLOMIDE | 1 | Oral | 230 MG, DAILY FOR 5 DAYS | 21029 | 230 | MG | CAPSULE | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126146901 | 12614690 | 1 | Glioblastoma multiforme |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126146901 | 12614690 | OT |
126146901 | 12614690 | HO |
126146901 | 12614690 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126146901 | 12614690 | Death | |
126146901 | 12614690 | Seizure |
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 |
---|---|---|---|---|---|---|
126146901 | 12614690 | 1 | 20160502 | 0 |