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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119808232 | 11980823 | 2 | F | 20160729 | 20160129 | 20160802 | PER | PHEH2015US008133 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160802 | OT | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119808232 | 11980823 | 1 | PS | GLEEVEC | IMATINIB MESYLATE | 1 | Unknown | 400 MG, UNK | U | 21588 | 400 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
119808232 | 11980823 | 1 | Neoplasm |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
119808232 | 11980823 | Amnesia | |
119808232 | 11980823 | Confusional state | |
119808232 | 11980823 | Diarrhoea | |
119808232 | 11980823 | Malaise | |
119808232 | 11980823 | Memory impairment | |
119808232 | 11980823 | Thinking abnormal |
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 |
---|---|---|---|---|---|---|
119808232 | 11980823 | 1 | 2013 | 0 |