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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126693671 | 12669367 | 1 | I | 20160603 | 20160810 | 20160819 | 20160819 | EXP | FR-JNJFOC-20160813219 | JANSSEN | 81.98 | YR | E | M | Y | 0.00000 | 20160819 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126693671 | 12669367 | 1 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | 0 | TABLET | ||||||||
| 126693671 | 12669367 | 2 | PS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | 202439 | TABLET | ||||||||
| 126693671 | 12669367 | 3 | SS | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Oral | Y | 0 | UNSPECIFIED | |||||||||
| 126693671 | 12669367 | 4 | SS | CANDESARTAN CILEXETIL. | CANDESARTAN CILEXETIL | 1 | Oral | Y | 0 | UNSPECIFIED | |||||||||
| 126693671 | 12669367 | 5 | C | MACROGOL | POLYETHYLENE GLYCOLS | 1 | Oral | 0 | UNSPECIFIED | ||||||||||
| 126693671 | 12669367 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 0 | UNSPECIFIED | ||||||||||
| 126693671 | 12669367 | 7 | C | HYDROXYZINE | HYDROXYZINEHYDROXYZINE HYDROCHLORIDE | 1 | Oral | 0 | UNSPECIFIED | ||||||||||
| 126693671 | 12669367 | 8 | C | SPASFON | PHLOROGLUCINOL | 1 | Oral | 0 | UNSPECIFIED | ||||||||||
| 126693671 | 12669367 | 9 | C | ZOPICLONE | ZOPICLONE | 1 | Oral | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126693671 | 12669367 | 1 | Cerebrovascular accident prophylaxis |
| 126693671 | 12669367 | 2 | Atrial fibrillation |
| 126693671 | 12669367 | 3 | Hypertension |
| 126693671 | 12669367 | 4 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126693671 | 12669367 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126693671 | 12669367 | Anaemia | |
| 126693671 | 12669367 | Renal failure | |
| 126693671 | 12669367 | Traumatic haematoma |
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 |
|---|---|---|---|---|---|---|
| 126693671 | 12669367 | 1 | 20160603 | 0 | ||
| 126693671 | 12669367 | 2 | 20160603 | 0 | ||
| 126693671 | 12669367 | 3 | 20160603 | 0 | ||
| 126693671 | 12669367 | 4 | 20160603 | 0 |