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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126932832 | 12693283 | 2 | F | 20160912 | 20160829 | 20160914 | EXP | US-009507513-1608USA009135 | MERCK | 65.00 | YR | M | Y | 0.00000 | 20160914 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126932832 | 12693283 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | U | 70017 | TABLET | |||||||||
126932832 | 12693283 | 2 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | Y | 0 | TABLET | |||||||||
126932832 | 12693283 | 3 | C | CARVEDILOL. | CARVEDILOL | 1 | Y | 0 | |||||||||||
126932832 | 12693283 | 4 | C | ASPIRIN. | ASPIRIN | 1 | Oral | U | 0 | TABLET |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126932832 | 12693283 | HO |
126932832 | 12693283 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126932832 | 12693283 | Cardiac failure | |
126932832 | 12693283 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |