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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125976442 | 12597644 | 2 | F | 20160722 | 20160727 | 20160802 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-061337 | BRISTOL MYERS SQUIBB | 0.00 | M | Y | 0.00000 | 20160802 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125976442 | 12597644 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | UNK | Y | 21436 | |||||||||
125976442 | 12597644 | 2 | SS | ABILIFY MAINTENA | ARIPIPRAZOLE | 1 | Intramuscular | 400 MG, QMO | Y | 0 | 400 | MG | /month | ||||||
125976442 | 12597644 | 3 | C | COGENTIN | BENZTROPINE MESYLATE | 1 | Unknown | U | 0 | ||||||||||
125976442 | 12597644 | 4 | C | DEPAKOTE | DIVALPROEX SODIUM | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125976442 | 12597644 | 1 | Bipolar II disorder |
125976442 | 12597644 | 2 | Product used for unknown indication |
125976442 | 12597644 | 3 | Product used for unknown indication |
125976442 | 12597644 | 4 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125976442 | 12597644 | Angular cheilitis | |
125976442 | 12597644 | Blood prolactin increased | |
125976442 | 12597644 | Glossitis | |
125976442 | 12597644 | Gynaecomastia | |
125976442 | 12597644 | Mood altered | |
125976442 | 12597644 | Mouth swelling | |
125976442 | 12597644 | Product use issue |
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 |
---|---|---|---|---|---|---|
125976442 | 12597644 | 1 | 201606 | 0 | ||
125976442 | 12597644 | 2 | 20160501 | 20160620 | 0 |