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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126495571 | 12649557 | 1 | I | 20160803 | 20160812 | 20160812 | EXP | GB-MHRA-EYC 00143093 | GB-MYLANLABS-2016M1032767 | MYLAN | 0.00 | Y | 0.00000 | 20160812 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126495571 | 12649557 | 1 | PS | BISOPROLOL | BISOPROLOL | 1 | Oral | 1 DF, QD | Y | U | 8044579 | 75831 | 1 | DF | QD | ||||
126495571 | 12649557 | 2 | C | OMEPRAZOLE /00661202/ | 2 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126495571 | 12649557 | 1 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126495571 | 12649557 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126495571 | 12649557 | Diarrhoea | |
126495571 | 12649557 | Fatigue | |
126495571 | 12649557 | Malaise | |
126495571 | 12649557 | Myalgia | |
126495571 | 12649557 | 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 |