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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127619501 | 12761950 | 1 | I | 20140704 | 20160908 | 20160920 | 20160920 | EXP | BR20160603 | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002657 | VALIDUS | 72.00 | YR | F | Y | 0.00000 | 20160920 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127619501 | 12761950 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 750 MG, DAILY | Y | 16273 | 750 | MG | |||||||
| 127619501 | 12761950 | 2 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 500 MG, QD | Y | 16273 | 500 | MG | |||||||
| 127619501 | 12761950 | 3 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 40 MG, QD | Y | 16273 | 40 | MG | |||||||
| 127619501 | 12761950 | 4 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Oral | 50 MG, DAILY | Y | 0 | 50 | MG | |||||||
| 127619501 | 12761950 | 5 | SS | ESIDREX | HYDROCHLOROTHIAZIDE | 1 | Oral | 25 MG, DAILY | Y | 0 | 25 | MG | TABLET | ||||||
| 127619501 | 12761950 | 6 | C | PREVISCAN | FLUINDIONE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127619501 | 12761950 | 7 | C | FUMAFER | FERROUS FUMARATE | 1 | Unknown | UNK | 0 | ||||||||||
| 127619501 | 12761950 | 8 | C | MOVICOL | POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 127619501 | 12761950 | 9 | C | LANTUS | INSULIN GLARGINE | 1 | Unknown | UNK | 0 | ||||||||||
| 127619501 | 12761950 | 10 | C | NOVORAPID | INSULIN ASPART | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127619501 | 12761950 | 1 | Product used for unknown indication |
| 127619501 | 12761950 | 4 | Product used for unknown indication |
| 127619501 | 12761950 | 5 | Product used for unknown indication |
| 127619501 | 12761950 | 6 | Product used for unknown indication |
| 127619501 | 12761950 | 7 | Product used for unknown indication |
| 127619501 | 12761950 | 8 | Product used for unknown indication |
| 127619501 | 12761950 | 9 | Product used for unknown indication |
| 127619501 | 12761950 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127619501 | 12761950 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127619501 | 12761950 | Acute kidney injury | |
| 127619501 | 12761950 | Dehydration | |
| 127619501 | 12761950 | Hypokalaemia |
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 |
|---|---|---|---|---|---|---|
| 127619501 | 12761950 | 1 | 20140708 | 0 | ||
| 127619501 | 12761950 | 4 | 20140708 | 0 | ||
| 127619501 | 12761950 | 5 | 20140708 | 0 |