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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100850392 | 10085039 | 2 | F | 20160711 | 20140417 | 20160714 | EXP | IN-BRISTOL-MYERS SQUIBB COMPANY-20622676 | BRISTOL MYERS SQUIBB | 28.00 | YR | M | Y | 0.00000 | 20160714 | CN | US | IN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100850392 | 10085039 | 1 | PS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | 5MG:2 WEEKS,DOSE INCRSD:10MG(6WEEKS),15MG. | 21436 | 5 | MG | TABLET | |||||||
| 100850392 | 10085039 | 2 | SS | RISPERIDONE. | RISPERIDONE | 1 | Unknown | DOSE INCRSD:8MG,12MG,16MG,20MG | 0 | 3 | MG | ||||||||
| 100850392 | 10085039 | 3 | SS | OLANZAPINE. | OLANZAPINE | 1 | Unknown | DOSE INCRSD TO:20MG 15MG FOR 1 MONTH | 0 | 15 | MG | ||||||||
| 100850392 | 10085039 | 4 | C | SODIUM VALPROATE | VALPROATE SODIUM | 1 | Unknown | 1000 MG, UNK | 0 | 1000 | MG | ||||||||
| 100850392 | 10085039 | 5 | C | TRIHEXYPHENIDYL | TRIHEXYPHENIDYL | 1 | Unknown | 4MG,6MG,8MG(4WEEKS),10MG | U | 0 | 2 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 100850392 | 10085039 | 1 | Schizophrenia |
| 100850392 | 10085039 | 2 | Schizophrenia |
| 100850392 | 10085039 | 3 | Schizophrenia |
| 100850392 | 10085039 | 4 | Schizophrenia |
| 100850392 | 10085039 | 5 | Schizophrenia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 100850392 | 10085039 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 100850392 | 10085039 | Condition aggravated | |
| 100850392 | 10085039 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |