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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126474421 | 12647442 | 1 | I | 2008 | 20160809 | 20160812 | 20160812 | EXP | PHHY2016AR110125 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160812 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126474421 | 12647442 | 1 | PS | DIOVAN | VALSARTAN | 1 | Unknown | 20665 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126474421 | 12647442 | 1 | Cardiac disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126474421 | 12647442 | HO |
126474421 | 12647442 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126474421 | 12647442 | Diabetes mellitus | |
126474421 | 12647442 | Drug interaction | |
126474421 | 12647442 | Malaise | |
126474421 | 12647442 | Memory impairment | |
126474421 | 12647442 | Product use issue | |
126474421 | 12647442 | Vein disorder | |
126474421 | 12647442 | Vein rupture |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |