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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126899741 | 12689974 | 1 | I | 20160817 | 20160826 | 20160826 | EXP | US-009507513-1608USA009463 | MERCK | 0.00 | Y | 0.00000 | 20160826 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126899741 | 12689974 | 1 | PS | PRINIVIL | LISINOPRIL | 1 | Oral | U | 19558 | TABLET | |||||||||
126899741 | 12689974 | 2 | C | ARHALOFENATE | 2 | 600 MG, QD | 0 | 600 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126899741 | 12689974 | 2 | Gout |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126899741 | 12689974 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126899741 | 12689974 | Angioedema |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |