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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127612461 | 12761246 | 1 | I | 20160114 | 20160920 | 20160920 | PER | US-TEVA-626169USA | TEVA | 0.00 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127612461 | 12761246 | 1 | PS | CARVEDILOL. | CARVEDILOL | 1 | 76373 | 6.25 | MG | TABLET | |||||||||
127612461 | 12761246 | 2 | C | COUMADIN | WARFARIN SODIUM | 1 | 0 | ||||||||||||
127612461 | 12761246 | 3 | C | ELIQUIS | APIXABAN | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127612461 | 12761246 | 1 | Stent placement |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127612461 | 12761246 | Blood pressure increased | |
127612461 | 12761246 | Chest discomfort | |
127612461 | 12761246 | Crying | |
127612461 | 12761246 | Dizziness | |
127612461 | 12761246 | Feeling abnormal | |
127612461 | 12761246 | Strabismus | |
127612461 | 12761246 | Thinking abnormal |
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 |
---|---|---|---|---|---|---|
127612461 | 12761246 | 1 | 201509 | 0 | ||
127612461 | 12761246 | 2 | 201509 | 0 | ||
127612461 | 12761246 | 3 | 20160113 | 0 |