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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126625671 | 12662567 | 1 | I | 20160727 | 20160803 | 20160818 | 20160818 | PER | US-ASTRAZENECA-2016SE85417 | ASTRAZENECA | 23328.00 | DY | M | Y | 96.60000 | KG | 20160818 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126625671 | 12662567 | 1 | PS | BYDUREON | EXENATIDE | 1 | Subcutaneous | 22200 | 2 | MG | /wk | ||||||||
| 126625671 | 12662567 | 2 | SS | METOPROLOL SUCCINATE. | METOPROLOL SUCCINATE | 1 | Oral | 0 | 50 | MG | MODIFIED-RELEASE TABLET | QD | |||||||
| 126625671 | 12662567 | 3 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 0 | 5000 | MG | QD | ||||||||
| 126625671 | 12662567 | 4 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 0 | 81 | MG | QD | ||||||||
| 126625671 | 12662567 | 5 | C | HYDROCHLOROT | HYDROCHLOROTHIAZIDE | 1 | Oral | 0 | 25 | MG | QD | ||||||||
| 126625671 | 12662567 | 6 | C | ATORVASTATIN | ATORVASTATIN | 1 | Oral | 0 | 20 | MG | QD | ||||||||
| 126625671 | 12662567 | 7 | C | GEMFIBROZIL. | GEMFIBROZIL | 1 | Oral | 0 | 1200 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126625671 | 12662567 | 1 | Type 2 diabetes mellitus |
| 126625671 | 12662567 | 4 | Cardiac disorder |
| 126625671 | 12662567 | 5 | Cardiac disorder |
| 126625671 | 12662567 | 7 | Cardiac disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126625671 | 12662567 | Injection site haemorrhage | |
| 126625671 | 12662567 | Product quality issue |
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 |
|---|---|---|---|---|---|---|
| 126625671 | 12662567 | 1 | 2016 | 0 | ||
| 126625671 | 12662567 | 3 | 2015 | 0 |