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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126825391 | 12682539 | 1 | I | 20160715 | 20160811 | 20160825 | 20160825 | EXP | ES-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-069942 | BRISTOL MYERS SQUIBB | 82.00 | YR | M | Y | 0.00000 | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126825391 | 12682539 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 10 MG, BID | Y | 21436 | 10 | MG | TABLET | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126825391 | 12682539 | 1 | Vascular dementia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126825391 | 12682539 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126825391 | 12682539 | Depressed level of consciousness | |
| 126825391 | 12682539 | Drug prescribing error | |
| 126825391 | 12682539 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 126825391 | 12682539 | 1 | 20160715 | 20160716 | 0 |