Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122802253 | 12280225 | 3 | F | 20160713 | 20160419 | 20160725 | EXP | JP-ROCHE-1741239 | ROCHE | 73.00 | YR | M | Y | 0.00000 | 20160725 | MD | JP | JP |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122802253 | 12280225 | 1 | PS | LUCENTIS | RANIBIZUMAB | 1 | Other | U | 125156 | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122802253 | 12280225 | 1 | Age-related macular degeneration |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122802253 | 12280225 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122802253 | 12280225 | Detachment of retinal pigment epithelium | |
122802253 | 12280225 | Drug resistance | |
122802253 | 12280225 | Retinal disorder | |
122802253 | 12280225 | Visual acuity reduced |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |