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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126491871 | 12649187 | 1 | I | 20160805 | 20160812 | 20160812 | EXP | KR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-065666 | BRISTOL MYERS SQUIBB | 0.00 | F | Y | 0.00000 | 20160812 | OT | KR | KR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126491871 | 12649187 | 1 | PS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | 5 MG, UNK | 21436 | 5 | MG | ||||||||
| 126491871 | 12649187 | 2 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | 15 MG, UNK | 21436 | 15 | MG | ||||||||
| 126491871 | 12649187 | 3 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | 20 MG, UNK | 21436 | 20 | MG | ||||||||
| 126491871 | 12649187 | 4 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | 30 MG, UNK | 21436 | 30 | MG | ||||||||
| 126491871 | 12649187 | 5 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | 15 MG, UNK | 21436 | 15 | MG | ||||||||
| 126491871 | 12649187 | 6 | C | VALPORATE CHRONO | 2 | Unknown | 600 MG, UNK | Y | 0 | 600 | MG | ||||||||
| 126491871 | 12649187 | 7 | C | VALPORATE CHRONO | 2 | Unknown | 800 MG, UNK | Y | 0 | 800 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126491871 | 12649187 | 1 | Tuberous sclerosis |
| 126491871 | 12649187 | 6 | Major depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126491871 | 12649187 | OT |
| 126491871 | 12649187 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126491871 | 12649187 | Akathisia | |
| 126491871 | 12649187 | Product use issue | |
| 126491871 | 12649187 | Psychomotor retardation | |
| 126491871 | 12649187 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |