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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 86455143 | 8645514 | 3 | F | 2008 | 20160919 | 20120702 | 20160927 | EXP | BR-ASTRAZENECA-2012SE42528 | ASTRAZENECA | 66.00 | YR | F | Y | 74.00000 | KG | 20160927 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 86455143 | 8645514 | 1 | PS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | DAILY | 19810 | ||||||||||
| 86455143 | 8645514 | 2 | SS | SEROQUEL | QUETIAPINE FUMARATE | 1 | Oral | 365.5 | DF | 0 | .5 | DF | FILM-COATED TABLET | QD | |||||
| 86455143 | 8645514 | 3 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 4870 | MG | 0 | 10 | MG | TABLET | QD | |||||
| 86455143 | 8645514 | 4 | SS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Oral | Y | 0 | ||||||||||
| 86455143 | 8645514 | 5 | C | NORVASC | AMLODIPINE BESYLATE | 1 | Oral | 5.0MG UNKNOWN | 0 | 5 | MG | ||||||||
| 86455143 | 8645514 | 6 | C | ENDOFOLIN | FOLIC ACID | 1 | Oral | 0 | 5 | MG | BID | ||||||||
| 86455143 | 8645514 | 7 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 0 | |||||||||||
| 86455143 | 8645514 | 8 | C | ETNA | UNSPECIFIED INGREDIENT | 1 | 0 | ||||||||||||
| 86455143 | 8645514 | 9 | C | XARELTO | RIVAROXABAN | 1 | 20.0MG UNKNOWN | 0 | 20 | MG | |||||||||
| 86455143 | 8645514 | 10 | C | ASPIRINA PREVENT | ASPIRIN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 86455143 | 8645514 | 2 | Depression |
| 86455143 | 8645514 | 3 | Blood cholesterol increased |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 86455143 | 8645514 | HO |
| 86455143 | 8645514 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 86455143 | 8645514 | Abdominal pain | |
| 86455143 | 8645514 | Aortic aneurysm | |
| 86455143 | 8645514 | Fall | |
| 86455143 | 8645514 | Off label use | |
| 86455143 | 8645514 | Platelet count decreased | |
| 86455143 | 8645514 | Somnolence |
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 |
|---|---|---|---|---|---|---|
| 86455143 | 8645514 | 1 | 2008 | 0 | ||
| 86455143 | 8645514 | 2 | 2008 | 0 | ||
| 86455143 | 8645514 | 3 | 200811 | 0 | ||
| 86455143 | 8645514 | 4 | 2008 | 201012 | 0 | |
| 86455143 | 8645514 | 5 | 2008 | 0 | ||
| 86455143 | 8645514 | 6 | 2008 | 0 | ||
| 86455143 | 8645514 | 7 | 2008 | 0 |