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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126445471 | 12644547 | 1 | I | 20160803 | 20160811 | 20160811 | EXP | GB-MHRA-EYC 00143093 | PHHY2016GB107126 | SANDOZ | 52.00 | YR | F | Y | 0.00000 | 20160811 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126445471 | 12644547 | 1 | PS | BISOPROLOL FUMARATE. | BISOPROLOL FUMARATE | 1 | Oral | 1 DF, QD | Y | U | 8044579 | 75643 | 1 | DF | QD | ||||
| 126445471 | 12644547 | 2 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126445471 | 12644547 | 1 | Hypertension |
| 126445471 | 12644547 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126445471 | 12644547 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126445471 | 12644547 | Diarrhoea | |
| 126445471 | 12644547 | Fatigue | |
| 126445471 | 12644547 | Malaise | |
| 126445471 | 12644547 | Myalgia | |
| 126445471 | 12644547 | Product substitution issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |