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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125378671 | 12537867 | 1 | I | 201603 | 20160622 | 20160707 | 20160707 | EXP | RS20160656 | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002228 | VALIDUS | 92.00 | YR | F | Y | 0.00000 | 20160707 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125378671 | 12537867 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 250 MG, QD | N | 16273 | 250 | MG | |||||||
| 125378671 | 12537867 | 2 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 375 MG, QD | N | 16273 | 375 | MG | |||||||
| 125378671 | 12537867 | 3 | SS | SOLUDACTONE | CANRENOATE POTASSIUMTROMETHAMINE | 1 | Oral | UNK | N | 0 | |||||||||
| 125378671 | 12537867 | 4 | SS | BURINEX | BUMETANIDE | 1 | Oral | UNK | N | 0 | |||||||||
| 125378671 | 12537867 | 5 | C | CORDARONE | AMIODARONE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 125378671 | 12537867 | 6 | C | PREVISCAN /00789001/ | FLUINDIONE | 1 | UNK | U | 0 | ||||||||||
| 125378671 | 12537867 | 7 | C | SECTRAL | ACEBUTOLOL HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 125378671 | 12537867 | 8 | C | DISCOTRINE | NITROGLYCERIN | 1 | UNK | U | 0 | ||||||||||
| 125378671 | 12537867 | 9 | C | EUPANTOL | PANTOPRAZOLE SODIUM | 1 | UNK | U | 0 | ||||||||||
| 125378671 | 12537867 | 10 | C | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 125378671 | 12537867 | 11 | C | LEXOMIL | BROMAZEPAM | 1 | UNK | U | 0 | ||||||||||
| 125378671 | 12537867 | 12 | C | ZOLPIDEM /00914902/ | ZOLPIDEMOLPIDEM TARTRATE | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125378671 | 12537867 | 1 | Cardiac failure |
| 125378671 | 12537867 | 3 | Cardiac failure |
| 125378671 | 12537867 | 4 | Cardiac failure |
| 125378671 | 12537867 | 5 | Product used for unknown indication |
| 125378671 | 12537867 | 6 | Product used for unknown indication |
| 125378671 | 12537867 | 7 | Product used for unknown indication |
| 125378671 | 12537867 | 8 | Product used for unknown indication |
| 125378671 | 12537867 | 9 | Product used for unknown indication |
| 125378671 | 12537867 | 10 | Product used for unknown indication |
| 125378671 | 12537867 | 11 | Product used for unknown indication |
| 125378671 | 12537867 | 12 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125378671 | 12537867 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125378671 | 12537867 | Acute kidney injury |
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 |
|---|---|---|---|---|---|---|
| 125378671 | 12537867 | 1 | 20150403 | 0 | ||
| 125378671 | 12537867 | 3 | 201503 | 201504 | 0 | |
| 125378671 | 12537867 | 4 | 201503 | 201504 | 0 |