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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6451955 | 7185580 | I | 6451955-5 | 20091110 | 20091123 | EXP | FR-GENENTECH-294296 | GNEFDAAERSPRD | Y | 20091123 | MD | SWITZERLAND |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6451955 | 1012629168 | PS | LUCENTIS | 1 | INTRAOCULAR | NOT REPORTED |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6451955 | 1012629168 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6451955 | OT |
Reactions reported
Event ID | PT |
---|---|
6451955 | CEREBROVASCULAR ACCIDENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |