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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125222811 | 12522281 | 1 | I | 20160616 | 20160701 | 20160701 | EXP | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002196 | VALIDUS | 67.00 | YR | F | Y | 0.00000 | 20160701 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125222811 | 12522281 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 0.5 UNITS, DAILY | 16273 | TABLET | |||||||||
| 125222811 | 12522281 | 2 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 500 MG, UNK | U | 0 | 500 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125222811 | 12522281 | 1 | Cardiac failure |
| 125222811 | 12522281 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125222811 | 12522281 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125222811 | 12522281 | Drug ineffective | |
| 125222811 | 12522281 | Incorrect dose administered | |
| 125222811 | 12522281 | Product physical issue |
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 |
|---|---|---|---|---|---|---|
| 125222811 | 12522281 | 1 | 2015 | 0 |