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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127951971 | 12795197 | 1 | I | 20160920 | 20160929 | 20160929 | EXP | US-PFIZER INC-2016443713 | PFIZER | 85.00 | YR | M | Y | 0.00000 | 20160929 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127951971 | 12795197 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | 20 MG, 1X/DAY | U | 18667 | 20 | MG | QD | |||||||
127951971 | 12795197 | 2 | SS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | 25 MG, 2X/DAY | U | 74133 | 25 | MG | BID | |||||||
127951971 | 12795197 | 3 | SS | LISINOPRIL. | LISINOPRIL | 1 | 10 MG, 1X/DAY | U | 0 | 10 | MG | QD | |||||||
127951971 | 12795197 | 4 | C | ASPIRIN. | ASPIRIN | 1 | UNK | 0 | |||||||||||
127951971 | 12795197 | 5 | C | PRAVASTATIN. | PRAVASTATIN | 1 | UNK | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127951971 | 12795197 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127951971 | 12795197 | Cardiac failure | |
127951971 | 12795197 | Condition aggravated | |
127951971 | 12795197 | Dyspnoea | |
127951971 | 12795197 | Oedema peripheral |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |