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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123450062 | 12345006 | 2 | F | 20140512 | 20160805 | 20160507 | 20160912 | PER | US-JNJFOC-20160419554 | JANSSEN | 34.81 | YR | A | M | Y | 0.00000 | 20160912 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123450062 | 12345006 | 1 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | U | UNKNOWN | 0 | 15 | MG | TABLET | |||||
| 123450062 | 12345006 | 2 | PS | XARELTO | RIVAROXABAN | 1 | Oral | Y | U | UNKNOWN | 22406 | 20 | MG | TABLET | |||||
| 123450062 | 12345006 | 3 | SS | NAPROXEN. | NAPROXEN | 1 | Unknown | U | 0 | UNSPECIFIED | |||||||||
| 123450062 | 12345006 | 4 | C | LOVASTATIN. | LOVASTATIN | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 123450062 | 12345006 | 5 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 123450062 | 12345006 | 6 | C | BENAZEPRIL | BENAZEPRIL HYDROCHLORIDE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 123450062 | 12345006 | 7 | C | OXCARBAZEPINE. | OXCARBAZEPINE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123450062 | 12345006 | 1 | Deep vein thrombosis |
| 123450062 | 12345006 | 2 | Deep vein thrombosis |
| 123450062 | 12345006 | 3 | Product used for unknown indication |
| 123450062 | 12345006 | 4 | Product used for unknown indication |
| 123450062 | 12345006 | 5 | Product used for unknown indication |
| 123450062 | 12345006 | 6 | Product used for unknown indication |
| 123450062 | 12345006 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123450062 | 12345006 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123450062 | 12345006 | Epistaxis | |
| 123450062 | 12345006 | Gastrointestinal haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 123450062 | 12345006 | 1 | 20140402 | 201404 | 0 | |
| 123450062 | 12345006 | 2 | 20140424 | 20140626 | 0 |