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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123070172 | 12307017 | 2 | F | 20160721 | 20160426 | 20160721 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-032507 | BRISTOL MYERS SQUIBB | 61.00 | YR | M | Y | 0.00000 | 20160721 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123070172 | 12307017 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | 30 MG, BID | 21436 | 30 | MG | BID | |||||||
| 123070172 | 12307017 | 2 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | 15 UNK, UNK | 21436 | 15 | MG | ||||||||
| 123070172 | 12307017 | 3 | SS | CLONIDINE. | CLONIDINE | 1 | Unknown | 50 MG, UNK | U | 0 | 50 | MG | |||||||
| 123070172 | 12307017 | 4 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 123070172 | 12307017 | 5 | C | ATENOLOL. | ATENOLOL | 1 | Unknown | 50 MG, UNK | U | 0 | 50 | MG | QD | ||||||
| 123070172 | 12307017 | 6 | C | VITAMIN E /00110501/ | TOCOPHEROL | 1 | Unknown | U | 0 | ||||||||||
| 123070172 | 12307017 | 7 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123070172 | 12307017 | 1 | Product used for unknown indication |
| 123070172 | 12307017 | 3 | Product used for unknown indication |
| 123070172 | 12307017 | 4 | Product used for unknown indication |
| 123070172 | 12307017 | 5 | Product used for unknown indication |
| 123070172 | 12307017 | 6 | Product used for unknown indication |
| 123070172 | 12307017 | 7 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123070172 | 12307017 | Off label use | |
| 123070172 | 12307017 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |