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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126366071 | 12636607 | 1 | I | 20160613 | 20160729 | 20160809 | 20160809 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-062574 | BRISTOL MYERS SQUIBB | 82.08 | YR | M | Y | 85.00000 | KG | 20160809 | CN | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126366071 | 12636607 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 5 MG, QD | 35 | MG | Y | 9218 | 5 | MG | TABLET | QD | |||
126366071 | 12636607 | 2 | I | ENOXAPARIN SODIUM. | ENOXAPARIN SODIUM | 1 | Subcutaneous | 16000 IU, QD | 112000 | IU | Y | 0 | 16000 | IU | SOLUTION FOR INJECTION | QD | |||
126366071 | 12636607 | 3 | I | IBUPROFEN SODIUM. | IBUPROFEN SODIUM | 1 | Oral | 1200 MG, QD | 16800 | MG | Y | 0 | 1200 | MG | TABLET | QD | |||
126366071 | 12636607 | 4 | C | PANTOPRAZOLE SODIUM. | PANTOPRAZOLE SODIUM | 1 | Oral | 20 MG, UNK | U | 0 | 20 | MG | TABLET | ||||||
126366071 | 12636607 | 5 | C | PROPAFENONE. | PROPAFENONE | 1 | Oral | 450 MG, UNK | U | 0 | 450 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126366071 | 12636607 | 1 | Atrial fibrillation |
126366071 | 12636607 | 2 | Anticoagulant therapy |
126366071 | 12636607 | 3 | Pericarditis |
126366071 | 12636607 | 4 | Prophylaxis |
126366071 | 12636607 | 5 | Arrhythmia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126366071 | 12636607 | LT |
126366071 | 12636607 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126366071 | 12636607 | Drug interaction | |
126366071 | 12636607 | Subdural haematoma | |
126366071 | 12636607 | Subdural haematoma evacuation | |
126366071 | 12636607 | Transfusion |
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 |
---|---|---|---|---|---|---|
126366071 | 12636607 | 1 | 20160606 | 20160612 | 0 | |
126366071 | 12636607 | 2 | 20160606 | 20160612 | 0 | |
126366071 | 12636607 | 3 | 20160531 | 20160613 | 0 | |
126366071 | 12636607 | 4 | 20160531 | 20160721 | 0 | |
126366071 | 12636607 | 5 | 20160607 | 20160613 | 0 |