Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6810395 | 7449112 | I | 6810395-7 | 20100611 | 20100617 | 20100630 | EXP | PHHY2010AR39809 | NOVARTIS PHARMACEUTICAL CORPORATION | 81 | YR | M | Y | 20100630 | CN | ARGENTINA |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
6810395 | 1014007721 | PS | DIOVAN | 1 | 160 MG | 020665 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6810395 | HO |
Reactions reported
Event ID | PT |
---|---|
6810395 | BRONCHOPNEUMONIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |