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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126898072 | 12689807 | 2 | F | 20120926 | 20160912 | 20160826 | 20160915 | EXP | US-BAYER-2016-083433 | BAYER | 64.00 | YR | A | M | Y | 0.00000 | 20160915 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126898072 | 12689807 | 1 | SS | XARELTO | RIVAROXABAN | 1 | Oral | 20 MG, UNK | U | UNKNOWN | 0 | 20 | MG | FILM-COATED TABLET | |||||
| 126898072 | 12689807 | 2 | SS | XARELTO | RIVAROXABAN | 1 | U | 0 | FILM-COATED TABLET | ||||||||||
| 126898072 | 12689807 | 3 | PS | ACETYLSALICYLIC ACID (} 100 MG, FAST RELEASE) | ASPIRIN | 1 | Unknown | UNK | U | 999999 | MODIFIED-RELEASE TABLET | ||||||||
| 126898072 | 12689807 | 4 | SS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Oral | 75 MG, QD | 0 | 75 | MG | QD | |||||||
| 126898072 | 12689807 | 5 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 40 MG, QD | 0 | 40 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126898072 | 12689807 | 1 | Atrial fibrillation |
| 126898072 | 12689807 | 2 | Cerebrovascular accident prophylaxis |
| 126898072 | 12689807 | 3 | Product used for unknown indication |
| 126898072 | 12689807 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126898072 | 12689807 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126898072 | 12689807 | Anaemia | |
| 126898072 | 12689807 | Contraindicated product administered | |
| 126898072 | 12689807 | Haematuria |
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 |
|---|---|---|---|---|---|---|
| 126898072 | 12689807 | 1 | 20120507 | 20150310 | 0 |