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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127867431 | 12786743 | 1 | I | 20150127 | 20160920 | 20160927 | 20160927 | EXP | US-PFIZER INC-2016443817 | PFIZER | 45.00 | YR | M | Y | 83.90000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127867431 | 12786743 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | 40 MG, DAILY | U | 18667 | 40 | MG | ||||||||
| 127867431 | 12786743 | 2 | SS | CARVEDILOL. | CARVEDILOL | 1 | 3.125, 2X/DAY | U | 0 | BID | |||||||||
| 127867431 | 12786743 | 3 | SS | CARVEDILOL. | CARVEDILOL | 1 | 6.25, 2X/DAY | U | 0 | BID | |||||||||
| 127867431 | 12786743 | 4 | SS | LISINOPRIL. | LISINOPRIL | 1 | 5 MG, DAILY | U | 0 | 5 | MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127867431 | 12786743 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127867431 | 12786743 | Dyspnoea | |
| 127867431 | 12786743 | Oedema |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |