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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118480482 | 11848048 | 2 | F | 20160721 | 20151217 | 20160721 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-088262 | BRISTOL MYERS SQUIBB | 41.00 | YR | F | Y | 0.00000 | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118480482 | 11848048 | 1 | PS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | U | 21436 | ||||||||||
| 118480482 | 11848048 | 2 | SS | BUPROPION. | BUPROPION | 1 | Unknown | U | 0 | ||||||||||
| 118480482 | 11848048 | 3 | SS | BUPRENORPHINE AND NALOXONE | BUPRENORPHINENALOXONE | 1 | Unknown | U | 0 | ||||||||||
| 118480482 | 11848048 | 4 | SS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
| 118480482 | 11848048 | 5 | SS | AMPHETAMINE | AMPHETAMINE | 1 | Unknown | U | 0 | ||||||||||
| 118480482 | 11848048 | 6 | SS | DEXTROAMPHETAMINE /00016601/ | DEXTROAMPHETAMINE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118480482 | 11848048 | 1 | Product used for unknown indication |
| 118480482 | 11848048 | 2 | Product used for unknown indication |
| 118480482 | 11848048 | 3 | Product used for unknown indication |
| 118480482 | 11848048 | 4 | Product used for unknown indication |
| 118480482 | 11848048 | 5 | Product used for unknown indication |
| 118480482 | 11848048 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118480482 | 11848048 | OT |
| 118480482 | 11848048 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118480482 | 11848048 | Completed suicide | |
| 118480482 | 11848048 | Intentional overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |