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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127829711 | 12782971 | 1 | I | 20160920 | 20160927 | 20160927 | PER | US-PFIZER INC-2016443716 | PFIZER | 77.00 | YR | M | Y | 80.00000 | KG | 20160927 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127829711 | 12782971 | 1 | PS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | UNK UNK, 1X/DAY, (25 QD) | U | 12151 | TABLET | QD | ||||||||
| 127829711 | 12782971 | 2 | SS | LASIX | FUROSEMIDE | 1 | UNK UNK, 1X/DAY, (20 QD) | U | 0 | QD | |||||||||
| 127829711 | 12782971 | 3 | SS | COREG | CARVEDILOL | 1 | UNK UNK, 2X/DAY, (6.25 BID) | U | 0 | BID |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127829711 | 12782971 | Fatigue |
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 |
|---|---|---|---|---|---|---|
| 127829711 | 12782971 | 1 | 20160328 | 0 | ||
| 127829711 | 12782971 | 2 | 20160328 | 0 | ||
| 127829711 | 12782971 | 3 | 20160328 | 0 |