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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127096191 | 12709619 | 1 | I | 20160503 | 20160830 | 20160902 | 20160902 | EXP | US-009507513-1608USA015322 | MERCK | 80.00 | YR | M | Y | 54.10000 | KG | 20160902 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127096191 | 12709619 | 1 | PS | PRINIVIL | LISINOPRIL | 1 | Oral | UNK | Y | 19558 | TABLET | ||||||||
127096191 | 12709619 | 2 | SS | PRINIVIL | LISINOPRIL | 1 | UNK | Y | 19558 | TABLET | |||||||||
127096191 | 12709619 | 3 | SS | CARDIZEM | DILTIAZEM HYDROCHLORIDE | 1 | Intravenous drip | 10 MG/HR | Y | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127096191 | 12709619 | OT |
127096191 | 12709619 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127096191 | 12709619 | Angioedema | |
127096191 | 12709619 | Atrial flutter |
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 |
---|---|---|---|---|---|---|
127096191 | 12709619 | 1 | 20160506 | 0 | ||
127096191 | 12709619 | 2 | 20160607 | 0 | ||
127096191 | 12709619 | 3 | 201605 | 201605 | 0 |