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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127616601 | 12761660 | 1 | I | 201609 | 20160913 | 20160920 | 20160920 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-076068 | BRISTOL MYERS SQUIBB | 81.00 | YR | M | Y | 0.00000 | 20160920 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127616601 | 12761660 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 2.5 MG, QD | 21436 | 2.5 | MG | TABLET | QD | ||||||
| 127616601 | 12761660 | 2 | C | DONEPEZIL. | DONEPEZIL | 1 | Unknown | U | 0 | ||||||||||
| 127616601 | 12761660 | 3 | C | NAMENDA | MEMANTINE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
| 127616601 | 12761660 | 4 | C | DEPAKOTE | DIVALPROEX SODIUM | 1 | Unknown | UNK, BID | U | 0 | BID | ||||||||
| 127616601 | 12761660 | 5 | C | POTASSIUM | POTASSIUM | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127616601 | 12761660 | 1 | Agitation |
| 127616601 | 12761660 | 2 | Product used for unknown indication |
| 127616601 | 12761660 | 3 | Product used for unknown indication |
| 127616601 | 12761660 | 4 | Product used for unknown indication |
| 127616601 | 12761660 | 5 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127616601 | 12761660 | Agitation | |
| 127616601 | 12761660 | Hypersomnia | |
| 127616601 | 12761660 | Insomnia | |
| 127616601 | 12761660 | Myoclonus | |
| 127616601 | 12761660 | Product use issue | |
| 127616601 | 12761660 | Restlessness |
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 |
|---|---|---|---|---|---|---|
| 127616601 | 12761660 | 1 | 201609 | 20160912 | 0 |