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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125516962 | 12551696 | 2 | F | 20160707 | 20160713 | 20160714 | EXP | PHHY2016AR093937 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160714 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125516962 | 12551696 | 1 | PS | DIOVAN | VALSARTAN | 1 | Unknown | 80 OT, QD | B8051 | 20665 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125516962 | 12551696 | 1 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125516962 | 12551696 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125516962 | 12551696 | Apparent death | |
| 125516962 | 12551696 | Back injury | |
| 125516962 | 12551696 | Back pain | |
| 125516962 | 12551696 | Bone pain | |
| 125516962 | 12551696 | Fall | |
| 125516962 | 12551696 | Fatigue | |
| 125516962 | 12551696 | Head injury | |
| 125516962 | 12551696 | Hypokinesia | |
| 125516962 | 12551696 | Memory impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |