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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112002583 | 11200258 | 3 | F | 20160809 | 20150618 | 20160818 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-040986 | BRISTOL MYERS SQUIBB | 7.00 | YR | M | Y | 0.00000 | 20160818 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112002583 | 11200258 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | U | 21436 | TABLET | |||||||||
| 112002583 | 11200258 | 2 | SS | DEXTROAMPHETAMINE /00016601/ | DEXTROAMPHETAMINE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 112002583 | 11200258 | 1 | Attention deficit/hyperactivity disorder |
| 112002583 | 11200258 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 112002583 | 11200258 | Dystonia | |
| 112002583 | 11200258 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |