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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127101191 | 12710119 | 1 | I | 20160824 | 20160902 | 20160902 | EXP | JP-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-070922 | BRISTOL MYERS SQUIBB | 0.00 | M | Y | 0.00000 | 20160902 | CN | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127101191 | 12710119 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 3 MG, UNK | U | 21436 | 3 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127101191 | 12710119 | 1 | Confusional state |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127101191 | 12710119 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127101191 | 12710119 | Insomnia | |
| 127101191 | 12710119 | Logorrhoea | |
| 127101191 | 12710119 | Product use issue | |
| 127101191 | 12710119 | Suicidal ideation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |