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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118869012 | 11886901 | 2 | F | 20160627 | 20160104 | 20160704 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-091852 | BRISTOL MYERS SQUIBB | 0.00 | F | Y | 0.00000 | 20160704 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118869012 | 11886901 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | 30 MG, UNK | 21436 | 30 | MG | TABLET | |||||||
| 118869012 | 11886901 | 2 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | UNK | 21436 | TABLET | |||||||||
| 118869012 | 11886901 | 3 | SS | SEROQUEL | QUETIAPINE FUMARATE | 1 | Unknown | UNK | 0 | ||||||||||
| 118869012 | 11886901 | 4 | SS | TEGRETOL | CARBAMAZEPINE | 1 | Unknown | U | 0 | ||||||||||
| 118869012 | 11886901 | 5 | SS | LITHIUM. | LITHIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 118869012 | 11886901 | 6 | SS | LATUDA | LURASIDONE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118869012 | 11886901 | 1 | Bipolar disorder |
| 118869012 | 11886901 | 3 | Product used for unknown indication |
| 118869012 | 11886901 | 4 | Product used for unknown indication |
| 118869012 | 11886901 | 5 | Product used for unknown indication |
| 118869012 | 11886901 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118869012 | 11886901 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118869012 | 11886901 | Insomnia |
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 |
|---|---|---|---|---|---|---|
| 118869012 | 11886901 | 1 | 2002 | 0 | ||
| 118869012 | 11886901 | 2 | 201404 | 201504 | 0 | |
| 118869012 | 11886901 | 3 | 201301 | 201402 | 0 | |
| 118869012 | 11886901 | 6 | 201505 | 0 |