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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122315153 | 12231515 | 3 | F | 201503 | 20160804 | 20160401 | 20160810 | EXP | US-JNJFOC-20160318784 | JANSSEN | 41.02 | YR | A | F | Y | 0.00000 | 20160810 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122315153 | 12231515 | 1 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN | 0 | 20 | MG | TABLET | |||||
122315153 | 12231515 | 2 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN | 0 | 15 | MG | TABLET | |||||
122315153 | 12231515 | 3 | SS | XARELTO | RIVAROXABAN | 1 | Oral | DOSE VARYING FROM 15MG TO 20 MG. | Y | N | UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN | 0 | 20 | MG | TABLET | ||||
122315153 | 12231515 | 4 | SS | XARELTO | RIVAROXABAN | 1 | Oral | DOSE VARYING FROM 15MG TO 20 MG. | Y | N | UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN | 0 | 20 | MG | TABLET | ||||
122315153 | 12231515 | 5 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN | 0 | 15 | MG | TABLET | |||||
122315153 | 12231515 | 6 | PS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN | 22406 | 20 | MG | TABLET | |||||
122315153 | 12231515 | 7 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | Y | N | 19012 | UNSPECIFIED | ||||||||
122315153 | 12231515 | 8 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | Y | N | 19012 | UNSPECIFIED | ||||||||
122315153 | 12231515 | 9 | C | TAMOXIFEN | TAMOXIFEN | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
122315153 | 12231515 | 10 | C | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
122315153 | 12231515 | 11 | C | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122315153 | 12231515 | 1 | Thrombosis prophylaxis |
122315153 | 12231515 | 2 | Thrombosis prophylaxis |
122315153 | 12231515 | 3 | Thrombosis prophylaxis |
122315153 | 12231515 | 4 | Thrombosis prophylaxis |
122315153 | 12231515 | 5 | Thrombosis prophylaxis |
122315153 | 12231515 | 6 | Thrombosis prophylaxis |
122315153 | 12231515 | 7 | Abdominal pain |
122315153 | 12231515 | 8 | Back pain |
122315153 | 12231515 | 9 | Product used for unknown indication |
122315153 | 12231515 | 10 | Product used for unknown indication |
122315153 | 12231515 | 11 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122315153 | 12231515 | HO |
122315153 | 12231515 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122315153 | 12231515 | Gastrointestinal haemorrhage | |
122315153 | 12231515 | Pulmonary embolism | |
122315153 | 12231515 | Rectal 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 |
---|---|---|---|---|---|---|
122315153 | 12231515 | 1 | 20150530 | 20150830 | 0 | |
122315153 | 12231515 | 2 | 20150324 | 20150413 | 0 | |
122315153 | 12231515 | 3 | 20150324 | 20150504 | 0 | |
122315153 | 12231515 | 4 | 20150324 | 20150504 | 0 | |
122315153 | 12231515 | 5 | 20150324 | 20150413 | 0 | |
122315153 | 12231515 | 6 | 20150530 | 20150830 | 0 | |
122315153 | 12231515 | 7 | 20120426 | 0 | ||
122315153 | 12231515 | 8 | 20120426 | 0 | ||
122315153 | 12231515 | 9 | 20130110 | 20150323 | 0 |