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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122809722 | 12280972 | 2 | F | 201601 | 20160720 | 20160419 | 20160722 | EXP | AR-ROCHE-1743464 | ROCHE | 70.48 | YR | F | Y | 0.00000 | 20160722 | OT | AR | AR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122809722 | 12280972 | 1 | PS | LUCENTIS | RANIBIZUMAB | 1 | Other | UNK (RIGHT EYE) | U | 125156 | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122809722 | 12280972 | 1 | Age-related macular degeneration |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122809722 | 12280972 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122809722 | 12280972 | Cholelithiasis | |
122809722 | 12280972 | Visual acuity reduced |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
122809722 | 12280972 | 1 | 2013 | 0 |