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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4784846 | 5889108 | I | 4784846-6 | 20050923 | 20050930 | EXP | PHEH2005US10627 | NOVARTIS PHARMACEUTICALS CORP. | F | Y | 20050930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4784846 | 1006472009 | PS | TRILEPTAL | 1 | 021014 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4784846 | OT |
Reactions reported
Event ID | PT |
---|---|
4784846 | MACULAR DEGENERATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |