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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118657912 | 11865791 | 2 | F | 20151029 | 20160826 | 20151223 | 20160902 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-088746 | BRISTOL MYERS SQUIBB | 11.92 | YR | M | Y | 40.00000 | KG | 20160902 | CN | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118657912 | 11865791 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 10 MG, QD | 370 | MG | U | 21436 | 10 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118657912 | 11865791 | 1 | Tourette's disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118657912 | 11865791 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118657912 | 11865791 | Chest pain | |
| 118657912 | 11865791 | Drug administered to patient of inappropriate age | |
| 118657912 | 11865791 | Dyspnoea | |
| 118657912 | 11865791 | Electrocardiogram QT prolonged | |
| 118657912 | 11865791 | Fumbling | |
| 118657912 | 11865791 | Product use issue | |
| 118657912 | 11865791 | Sinus bradycardia |
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 |
|---|---|---|---|---|---|---|
| 118657912 | 11865791 | 1 | 20150923 | 20151211 | 0 |