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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124437142 | 12443714 | 2 | F | 20160713 | 20160607 | 20160721 | EXP | JP-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-039540 | BRISTOL MYERS SQUIBB | 13.00 | YR | M | Y | 0.00000 | 20160721 | CN | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124437142 | 12443714 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 6 MG, QD | 21436 | 6 | MG | TABLET | QD | ||||||
| 124437142 | 12443714 | 2 | SS | SERTRALINE HYDROCHLORIDE. | SERTRALINE HYDROCHLORIDE | 1 | Oral | 50 MG, QD | 0 | 50 | MG | QD | |||||||
| 124437142 | 12443714 | 3 | SS | SERTRALINE HYDROCHLORIDE. | SERTRALINE HYDROCHLORIDE | 1 | Oral | 50 MG, QD | 0 | 50 | MG | QD | |||||||
| 124437142 | 12443714 | 4 | SS | SERTRALINE HYDROCHLORIDE. | SERTRALINE HYDROCHLORIDE | 1 | Oral | 50 MG, QD | 0 | 50 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124437142 | 12443714 | 1 | Autism |
| 124437142 | 12443714 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124437142 | 12443714 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124437142 | 12443714 | Hyperglycaemia | |
| 124437142 | 12443714 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |