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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127765571 | 12776557 | 1 | I | 2016 | 20160916 | 20160923 | 20160923 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-077468 | BRISTOL MYERS SQUIBB | 20.00 | YR | F | Y | 46.72000 | KG | 20160923 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127765571 | 12776557 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 20 MG, QD | U | 21436 | 20 | MG | QD | ||||||
| 127765571 | 12776557 | 2 | SS | ABILIFY MAINTENA | ARIPIPRAZOLE | 1 | Intramuscular | 400 MG, QMO | U | 0 | 400 | MG | /month |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127765571 | 12776557 | 1 | Psychotic disorder |
| 127765571 | 12776557 | 2 | Psychotic disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127765571 | 12776557 | Off label use | |
| 127765571 | 12776557 | Product use issue | |
| 127765571 | 12776557 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 127765571 | 12776557 | 1 | 201607 | 0 | ||
| 127765571 | 12776557 | 2 | 201607 | 0 |