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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8602291 | 8738405 | I | 8602291-X | 20090427 | 20120423 | PER | PHEH2009US03965 | NOVARTIS PHARMACEUTICALS CORP. | YR | F | N | 20090730 | MD | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8602291 | 1020590545 | PS | FEMARA | 1 | ORAL | 2.5 MG, QD, ORAL | 20726 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
8602291 | OT |
Reactions reported
Event ID | PT |
---|---|
8602291 | DISEASE PROGRESSION |
8602291 | METASTASIS |
8602291 | DRUG INEFFECTIVE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
8602291 | HP |
Therapies reported
no results found |