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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126635313 | 12663531 | 3 | F | 20160907 | 20160818 | 20160913 | EXP | CA-PFIZER INC-2016388998 | PFIZER | PERRI, G.. DIGOXIN FOR THE CONTROL OF CONGESTIVE HEART FAILURE SYMPTOMS IN PALLIATIVE CARE. ANNALS OF LONG-TERM CARE: CLINICAL CARE AND AGING. 2015;23(8):29-32 | 72.00 | YR | M | Y | 0.00000 | 20160913 | MD | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126635313 | 12663531 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 2.5 MG, DAILY | Y | 19901 | 2.5 | MG | |||||||
| 126635313 | 12663531 | 2 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Unknown | 12.5 MG, DAILY | Y | 12151 | 12.5 | MG | |||||||
| 126635313 | 12663531 | 3 | SS | CARVEDILOL. | CARVEDILOL | 1 | Unknown | 3.25 MG, 2X/DAY | U | 0 | 3.25 | MG | BID | ||||||
| 126635313 | 12663531 | 4 | SS | CARVEDILOL. | CARVEDILOL | 1 | Unknown | 3.25 MG, 1X/DAY | U | 0 | 3.25 | MG | QD | ||||||
| 126635313 | 12663531 | 5 | SS | METOLAZONE. | METOLAZONE | 1 | Unknown | 2.5 MG, 2X/WEEK | Y | 0 | 2.5 | MG | BIW | ||||||
| 126635313 | 12663531 | 6 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 20 MG, 2X/DAY | U | 0 | 20 | MG | BID |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126635313 | 12663531 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126635313 | 12663531 | Blood potassium increased | |
| 126635313 | 12663531 | Blood sodium decreased | |
| 126635313 | 12663531 | Chronic kidney disease | |
| 126635313 | 12663531 | Condition aggravated | |
| 126635313 | 12663531 | Hypotension | |
| 126635313 | 12663531 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |