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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7584793 | 8010691 | F | 7584793-0 | 20110621 | 20110630 | EXP | PHHY2011US54195 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | Y | 20110630 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7584793 | 1016909641 | PS | TASIGNA | 1 | ORAL | 022068 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
7584793 | OT |
Reactions reported
Event ID | PT |
---|---|
7584793 | HEADACHE |
7584793 | RETINAL HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |