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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 67093334 | 6709333 | 4 | F | 20080612 | 20160824 | 20080724 | 20160831 | EXP | PE-ASTRAZENECA-2008UW14172 | ASTRAZENECA | 73.00 | YR | F | Y | 74.00000 | KG | 20160901 | MD | PE | PE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 67093334 | 6709333 | 1 | PS | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | Y | U | 0 | 20 | MG | CAPSULE | ||||||
| 67093334 | 6709333 | 2 | SS | NAPROXEN. | NAPROXEN | 1 | Oral | 3 IN 1D | Y | U | 06-046542 | 0 | TABLET | ||||||
| 67093334 | 6709333 | 3 | C | RISEDRONATE | RISEDRONATE SODIUM | 1 | Oral | 0 | |||||||||||
| 67093334 | 6709333 | 4 | C | CALCIUM CARBONATE. | CALCIUM CARBONATE | 1 | Oral | 0 | |||||||||||
| 67093334 | 6709333 | 5 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | 0 | |||||||||||
| 67093334 | 6709333 | 6 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 | |||||||||||
| 67093334 | 6709333 | 7 | C | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Oral | 0 | |||||||||||
| 67093334 | 6709333 | 8 | C | ENALAPRIL | ENALAPRIL | 1 | Unknown | 0 | |||||||||||
| 67093334 | 6709333 | 9 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 0 | |||||||||||
| 67093334 | 6709333 | 10 | C | CELECOXIB. | CELECOXIB | 1 | Unknown | 0 | |||||||||||
| 67093334 | 6709333 | 11 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | 0 | |||||||||||
| 67093334 | 6709333 | 12 | C | SIORBIDE | 2 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 67093334 | 6709333 | 1 | Rheumatoid arthritis |
| 67093334 | 6709333 | 2 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 67093334 | 6709333 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 67093334 | 6709333 | Atrial fibrillation | |
| 67093334 | 6709333 | Myocardial infarction |
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 |
|---|---|---|---|---|---|---|
| 67093334 | 6709333 | 1 | 20080606 | 20080611 | 0 | |
| 67093334 | 6709333 | 2 | 20080606 | 20080611 | 0 | |
| 67093334 | 6709333 | 3 | 200703 | 20080611 | 0 | |
| 67093334 | 6709333 | 4 | 200703 | 20080611 | 0 | |
| 67093334 | 6709333 | 5 | 200703 | 20080611 | 0 | |
| 67093334 | 6709333 | 6 | 2000 | 20080611 | 0 | |
| 67093334 | 6709333 | 7 | 2002 | 20080611 | 0 | |
| 67093334 | 6709333 | 8 | 200506 | 20080611 | 0 | |
| 67093334 | 6709333 | 9 | 200603 | 20080611 | 0 | |
| 67093334 | 6709333 | 10 | 200501 | 20080526 | 0 |