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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125433081 | 12543308 | 1 | I | 20160624 | 20160711 | 20160711 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-056392 | BRISTOL MYERS SQUIBB | 0.00 | F | Y | 0.00000 | 20160711 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125433081 | 12543308 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | N | 21436 | TABLET | |||||||||
125433081 | 12543308 | 2 | SS | ARIPIPRAZOLE TEVA | ARIPIPRAZOLE | 1 | Oral | 5 MG, QD | U | TV7569 | 0 | 5 | MG | QD | |||||
125433081 | 12543308 | 3 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Unknown | U | 0 | ||||||||||
125433081 | 12543308 | 4 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | Unknown | U | 0 | ||||||||||
125433081 | 12543308 | 5 | C | CHLORTHALIDONE. | CHLORTHALIDONE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125433081 | 12543308 | 1 | Anxiety |
125433081 | 12543308 | 2 | Anxiety |
125433081 | 12543308 | 3 | Product used for unknown indication |
125433081 | 12543308 | 4 | Product used for unknown indication |
125433081 | 12543308 | 5 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125433081 | 12543308 | Blood glucose increased | |
125433081 | 12543308 | Glucose tolerance impaired | |
125433081 | 12543308 | Hypertension | |
125433081 | 12543308 | Product use issue | |
125433081 | 12543308 | Weight increased |
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 |
---|---|---|---|---|---|---|
125433081 | 12543308 | 2 | 20160527 | 0 |