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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123299952 | 12329995 | 2 | F | 20160426 | 20160711 | 20160504 | 20160718 | EXP | PHHY2016BR060271 | NOVARTIS | 87.93 | YR | F | Y | 72.00000 | KG | 20160718 | MD | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123299952 | 12329995 | 1 | PS | DIOVAN | VALSARTAN | 1 | Oral | 1 DF, QD | Y | 21283 | 1 | DF | TABLET | QD | |||||
| 123299952 | 12329995 | 2 | SS | DIOVAN HCT | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Oral | 1 DF (120 MG/SOME MILLIGRAM), QD (IN THE MORNING) | 0 | 1 | DF | TABLET | QD | ||||||
| 123299952 | 12329995 | 3 | SS | DIOVAN HCT | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Oral | 1 DF (HYDROCHLOROTHIAZIDE 12.5 MG, VALSARTAN 160 MG), QD | 0 | 1 | DF | TABLET | QD | ||||||
| 123299952 | 12329995 | 4 | SS | DIOVAN HCT | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Oral | 1 DF (HYDROCHLOROTHIAZIDE 25 MG, VALSARTAN 320 MG) ,UNK | 0 | 1 | DF | TABLET | |||||||
| 123299952 | 12329995 | 5 | SS | DIOVAN HCT | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Oral | 1 DF (HYDROCHLOROTHIAZIDE 12.5 MG, VALSARTAN 160 MG), UNK | 1526526,1536528 | 0 | 1 | DF | TABLET | ||||||
| 123299952 | 12329995 | 6 | C | RIVOTRIL | CLONAZEPAM | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123299952 | 12329995 | 1 | Hypertension |
| 123299952 | 12329995 | 2 | Hypertension |
| 123299952 | 12329995 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123299952 | 12329995 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123299952 | 12329995 | Blood pressure increased | |
| 123299952 | 12329995 | Body height decreased | |
| 123299952 | 12329995 | Deafness | |
| 123299952 | 12329995 | Feeling abnormal | |
| 123299952 | 12329995 | Irritability | |
| 123299952 | 12329995 | Malaise | |
| 123299952 | 12329995 | Nervousness |
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 |
|---|---|---|---|---|---|---|
| 123299952 | 12329995 | 1 | 1999 | 0 | ||
| 123299952 | 12329995 | 3 | 2007 | 0 |