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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124991462 | 12499146 | 2 | F | 201601 | 20160628 | 20160627 | 20160706 | EXP | PHHY2016AR084567 | NOVARTIS | 62.80 | YR | M | Y | 0.00000 | 20160707 | CN | COUNTRY NOT SPECIFIED | AR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124991462 | 12499146 | 1 | PS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Unknown | 50 MG, BID | U | 207620 | 50 | MG | TABLET | BID | |||||
| 124991462 | 12499146 | 2 | SS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Unknown | 100 MG TABLET (HALF TABLET IN THE MORNING, AND HALF TABLET IN THE AFTERNOON) | U | 207620 | .5 | DF | TABLET | BID | |||||
| 124991462 | 12499146 | 3 | SS | SINTROM | ACENOCOUMAROL | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124991462 | 12499146 | 1 | Cardiac failure |
| 124991462 | 12499146 | 3 | Anticoagulant therapy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124991462 | 12499146 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124991462 | 12499146 | Arrhythmia | |
| 124991462 | 12499146 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |