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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 80190443 | 8019044 | 3 | F | 201105 | 20160823 | 20110701 | 20160823 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-15859713 | BRISTOL MYERS SQUIBB | 27.68 | YR | F | Y | 0.00000 | 20160823 | CN | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 80190443 | 8019044 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | FOR SOME TIME | 21436 | 15 | MG | TABLET | |||||||
| 80190443 | 8019044 | 2 | SS | XANAX | ALPRAZOLAM | 1 | Unknown | UNK UNK, PRN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 80190443 | 8019044 | 1 | Schizophrenia |
| 80190443 | 8019044 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 80190443 | 8019044 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 80190443 | 8019044 | Maternal exposure during pregnancy | |
| 80190443 | 8019044 | Selective abortion | |
| 80190443 | 8019044 | Twin pregnancy |
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 |
|---|---|---|---|---|---|---|
| 80190443 | 8019044 | 1 | 2011 | 201104 | 0 | |
| 80190443 | 8019044 | 2 | 201104 | 0 |