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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98835932 | 9883593 | 2 | F | 20160726 | 20140210 | 20160726 | EXP | JP-BRISTOL-MYERS SQUIBB COMPANY-20161378 | BRISTOL MYERS SQUIBB | 26.00 | YR | F | Y | 0.00000 | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98835932 | 9883593 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | TOOK 60MG | U | 21436 | 6 | MG | TABLET | QD | |||||
| 98835932 | 9883593 | 2 | SS | SEROQUEL | QUETIAPINE FUMARATE | 1 | Oral | TOOK 1500MG | U | 0 | 1550 | MG | QD | ||||||
| 98835932 | 9883593 | 3 | SS | LEVOMEPROMAZINE | LEVOMEPROMAZINE | 1 | Oral | TOOK 20MG | U | 0 | 20 | MG | QD | ||||||
| 98835932 | 9883593 | 4 | SS | SODIUM VALPROATE | VALPROATE SODIUM | 1 | Unknown | 200 MG, UNK | U | 0 | 200 | MG | |||||||
| 98835932 | 9883593 | 5 | SS | LORAZEPAM. | LORAZEPAM | 1 | Unknown | .5 MG, UNK | U | 0 | .5 | MG | |||||||
| 98835932 | 9883593 | 6 | SS | MIDODRINE HCL | MIDODRINE HYDROCHLORIDE | 1 | Unknown | 2 MG, UNK | U | 0 | 2 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 98835932 | 9883593 | 1 | Schizophrenia |
| 98835932 | 9883593 | 2 | Product used for unknown indication |
| 98835932 | 9883593 | 3 | Product used for unknown indication |
| 98835932 | 9883593 | 4 | Product used for unknown indication |
| 98835932 | 9883593 | 5 | Product used for unknown indication |
| 98835932 | 9883593 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 98835932 | 9883593 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 98835932 | 9883593 | Overdose | |
| 98835932 | 9883593 | Pulmonary embolism | |
| 98835932 | 9883593 | Rhabdomyolysis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |