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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127657691 | 12765769 | 1 | I | 2016 | 20160902 | 20160921 | 20160921 | PER | US-JNJFOC-20160903921 | JANSSEN | 0.00 | E | F | Y | 0.00000 | 20160921 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127657691 | 12765769 | 1 | SS | XARELTO | RIVAROXABAN | 1 | Oral | U | 0 | 20 | MG | TABLET | |||||||
| 127657691 | 12765769 | 2 | PS | XARELTO | RIVAROXABAN | 1 | Oral | U | 202439 | 20 | MG | TABLET | |||||||
| 127657691 | 12765769 | 3 | SS | MULTAQ | DRONEDARONE | 1 | Unknown | 0 | 40 | MG | UNSPECIFIED | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127657691 | 12765769 | 1 | Cerebrovascular accident prophylaxis |
| 127657691 | 12765769 | 2 | Atrial fibrillation |
| 127657691 | 12765769 | 3 | Atrial fibrillation |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127657691 | 12765769 | Malaise | |
| 127657691 | 12765769 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 127657691 | 12765769 | 1 | 20160107 | 20160520 | 0 | |
| 127657691 | 12765769 | 2 | 20160107 | 20160520 | 0 |