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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125547112 | 12554711 | 2 | F | 20160726 | 20160713 | 20160801 | EXP | PHHY2016FR093262 | NOVARTIS | 62.00 | YR | M | Y | 0.00000 | 20160801 | CN | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125547112 | 12554711 | 1 | PS | RASILEZ | ALISKIREN | 1 | Unknown | 150 MG, TID | Y | 21985 | 150 | MG | TABLET | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125547112 | 12554711 | 1 | Cardiac disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125547112 | 12554711 | Alopecia | |
| 125547112 | 12554711 | Bladder disorder | |
| 125547112 | 12554711 | Decreased appetite | |
| 125547112 | 12554711 | Hot flush | |
| 125547112 | 12554711 | Palpitations | |
| 125547112 | 12554711 | Product use issue | |
| 125547112 | 12554711 | Visual acuity reduced |
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 |
|---|---|---|---|---|---|---|
| 125547112 | 12554711 | 1 | 201605 | 0 |