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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126259581 | 12625958 | 1 | I | 20160702 | 20160722 | 20160805 | 20160805 | EXP | GR20160773 | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002378 | VALIDUS | 81.00 | YR | M | Y | 0.00000 | 20160805 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126259581 | 12625958 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Intravenous (not otherwise specified) | 80 MG, DAILY | N | UNKNOWN | 16363 | 80 | MG | INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126259581 | 12625958 | 1 | Cardiac failure |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126259581 | 12625958 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126259581 | 12625958 | Fall |
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 |
---|---|---|---|---|---|---|
126259581 | 12625958 | 1 | 20160702 | 20160702 | 0 |