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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126259391 | 12625939 | 1 | I | 20160622 | 20160628 | 20160805 | 20160805 | EXP | 365281 | IT-VALIDUS PHARMACEUTICALS LLC-IT-2016VAL002239 | VALIDUS | 90.00 | YR | F | Y | 0.00000 | 20160805 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126259391 | 12625939 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 100 MILLIGRAM (S) ; DAILY | 17400 | MG | Y | UNKNOWN | 16273 | 100 | MG | ||||
| 126259391 | 12625939 | 2 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 1 DOSAGE FORM; TWICE A DAY | 17400 | MG | Y | UNKNOWN | 16273 | 1 | DF | ||||
| 126259391 | 12625939 | 3 | SS | POTASSIUM CANRENOATE | CANRENOATE POTASSIUM | 1 | Oral | 50 MILLIGRAM(S) ;DAILY | 8700 | MG | Y | UNKNOWN | 0 | 50 | MG | ||||
| 126259391 | 12625939 | 4 | C | TRITTICO | TRAZODONE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 126259391 | 12625939 | 5 | C | COUMADIN | WARFARIN SODIUM | 1 | UNK | U | 0 | ||||||||||
| 126259391 | 12625939 | 6 | C | CARVEDILOL. | CARVEDILOL | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126259391 | 12625939 | 1 | Product used for unknown indication |
| 126259391 | 12625939 | 3 | Product used for unknown indication |
| 126259391 | 12625939 | 4 | Product used for unknown indication |
| 126259391 | 12625939 | 5 | Product used for unknown indication |
| 126259391 | 12625939 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126259391 | 12625939 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126259391 | 12625939 | Dehydration | |
| 126259391 | 12625939 | Hypokalaemia | |
| 126259391 | 12625939 | Hyponatraemia | |
| 126259391 | 12625939 | Sopor |
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 |
|---|---|---|---|---|---|---|
| 126259391 | 12625939 | 1 | 20160101 | 20160622 | 0 | |
| 126259391 | 12625939 | 3 | 20160101 | 20160622 | 0 |