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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127495382 | 12749538 | 2 | F | 20160919 | 20160916 | 20160921 | EXP | PHHY2016CR127426 | NOVARTIS | 0.00 | E | F | Y | 0.00000 | 20160921 | MD | CR | CR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127495382 | 12749538 | 1 | PS | DIOVAN | VALSARTAN | 1 | Unknown | 80 MG | D | 21283 | 80 | MG | TABLET | ||||||
| 127495382 | 12749538 | 2 | SS | DIOVAN | VALSARTAN | 1 | Unknown | 160 MG | D | 21283 | 160 | MG | TABLET | ||||||
| 127495382 | 12749538 | 3 | SS | DIOVAN | VALSARTAN | 1 | Unknown | 320 MG | D | 21283 | 320 | MG | TABLET | ||||||
| 127495382 | 12749538 | 4 | SS | DIOVAN | VALSARTAN | 1 | Unknown | 80 MG | D | 21283 | 80 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127495382 | 12749538 | 1 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127495382 | 12749538 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127495382 | 12749538 | Blood pressure decreased | |
| 127495382 | 12749538 | Blood pressure inadequately controlled | |
| 127495382 | 12749538 | Lung disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |