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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126466161 | 12646616 | 1 | I | 20160805 | 20160812 | 20160812 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-065771 | BRISTOL MYERS SQUIBB | 0.00 | F | Y | 63.49000 | KG | 20160812 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126466161 | 12646616 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 0.15 MG, QD | 21436 | .15 | MG | TABLET | QD | ||||||
| 126466161 | 12646616 | 2 | SS | ABILIFY | ARIPIPRAZOLE | 1 | 21436 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126466161 | 12646616 | 1 | Mood swings |
| 126466161 | 12646616 | 2 | Paranoia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126466161 | 12646616 | OT |
| 126466161 | 12646616 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126466161 | 12646616 | Hospitalisation | |
| 126466161 | 12646616 | Off label use | |
| 126466161 | 12646616 | 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 |
|---|---|---|---|---|---|---|
| 126466161 | 12646616 | 1 | 2007 | 0 |