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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125988301 | 12598830 | 1 | I | 2016 | 20160606 | 20160726 | 20160726 | EXP | DE-CADRBFARM-2016012698 | DE-MYLANLABS-2016M1024118 | MYLAN | 0.00 | Y | 0.00000 | 20160726 | CN | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125988301 | 12598830 | 1 | PS | BISOPROLOL | BISOPROLOL | 1 | Oral | 1.25 DF, UNK | U | U | 75831 | 1.25 | DF |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125988301 | 12598830 | 1 | Arrhythmia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125988301 | 12598830 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125988301 | 12598830 | Bradycardia | |
| 125988301 | 12598830 | Defaecation urgency | |
| 125988301 | 12598830 | Dizziness | |
| 125988301 | 12598830 | Fatigue | |
| 125988301 | 12598830 | Heart rate decreased |
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 |
|---|---|---|---|---|---|---|
| 125988301 | 12598830 | 1 | 20160525 | 0 |