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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112686372 | 11268637 | 2 | F | 20150121 | 20160803 | 20150714 | 20160912 | PER | US-JNJFOC-20150704862 | JANSSEN | 89.82 | YR | E | F | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112686372 | 11268637 | 1 | SS | RIVAROXABAN | RIVAROXABAN | 1 | Oral | N | 0 | 10 | MG | TABLET | |||||||
112686372 | 11268637 | 2 | SS | RIVAROXABAN | RIVAROXABAN | 1 | Oral | N | 0 | 10 | MG | TABLET | |||||||
112686372 | 11268637 | 3 | PS | RIVAROXABAN | RIVAROXABAN | 1 | Oral | N | 22406 | 10 | MG | TABLET | |||||||
112686372 | 11268637 | 4 | SS | ALLOPURINOL. | ALLOPURINOL | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
112686372 | 11268637 | 5 | SS | ASPIRIN. | ASPIRIN | 1 | Unknown | 0 | 81 | MG | UNSPECIFIED | ||||||||
112686372 | 11268637 | 6 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | U | 0 | UNSPECIFIED | |||||||||
112686372 | 11268637 | 7 | SS | NEURONTIN | GABAPENTIN | 1 | Unknown | 0 | 300 | MG | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
112686372 | 11268637 | 1 | Thrombosis |
112686372 | 11268637 | 2 | Deep vein thrombosis |
112686372 | 11268637 | 3 | Pulmonary embolism |
112686372 | 11268637 | 4 | Product used for unknown indication |
112686372 | 11268637 | 5 | Cardiac disorder |
112686372 | 11268637 | 6 | Product used for unknown indication |
112686372 | 11268637 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
112686372 | 11268637 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
112686372 | 11268637 | Gastrointestinal haemorrhage | |
112686372 | 11268637 | International normalised ratio increased |
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 |
---|---|---|---|---|---|---|
112686372 | 11268637 | 1 | 20150114 | 20150325 | 0 | |
112686372 | 11268637 | 2 | 20150114 | 20150325 | 0 | |
112686372 | 11268637 | 3 | 20150114 | 20150325 | 0 |