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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8364540 | 8267284 | F | 8364540-5 | 20111116 | 20120514 | 20120516 | EXP | GB-ROCHE-1016588 | ROCHE | 81 | YR | Y | 20120516 | OT | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8364540 | 1019710226 | PS | RANIBIZUMAB | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8364540 | 1019710226 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
8364540 | DE |
Reactions reported
Event ID | PT |
---|---|
8364540 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |