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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127193732 | 12719373 | 2 | F | 20160229 | 20160920 | 20160907 | 20160928 | EXP | FR-ROCHE-1826642 | ROCHE | 69.70 | YR | M | Y | 0.00000 | 20160928 | MD | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127193732 | 12719373 | 1 | PS | LUCENTIS | RANIBIZUMAB | 1 | Intraocular | UNK | S2052B | 125156 | SOLUTION FOR INJECTION | ||||||||
| 127193732 | 12719373 | 2 | SS | LUCENTIS | RANIBIZUMAB | 1 | Intraocular | UNK | S2052B | 125156 | SOLUTION FOR INJECTION | ||||||||
| 127193732 | 12719373 | 3 | SS | LUCENTIS | RANIBIZUMAB | 1 | Intraocular | UNK | S2052B | 125156 | SOLUTION FOR INJECTION | ||||||||
| 127193732 | 12719373 | 4 | C | PARIET | RABEPRAZOLE SODIUM | 1 | Unknown | 1 OT, QD | U | 0 | QD | ||||||||
| 127193732 | 12719373 | 5 | C | TENORETIC | ATENOLOLCHLORTHALIDONE | 1 | Unknown | 1 OT, QD | U | 0 | QD | ||||||||
| 127193732 | 12719373 | 6 | C | CANDESARTAN | CANDESARTAN | 1 | Unknown | 0.5 OT, QD | U | 0 | QD | ||||||||
| 127193732 | 12719373 | 7 | C | MECIR | TAMSULOSIN HYDROCHLORIDE | 1 | Unknown | 1 OT, QD | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127193732 | 12719373 | 1 | Age-related macular degeneration |
| 127193732 | 12719373 | 4 | Product used for unknown indication |
| 127193732 | 12719373 | 5 | Product used for unknown indication |
| 127193732 | 12719373 | 6 | Product used for unknown indication |
| 127193732 | 12719373 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127193732 | 12719373 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127193732 | 12719373 | Aphasia | |
| 127193732 | 12719373 | Hemianopia | |
| 127193732 | 12719373 | Transient ischaemic attack | |
| 127193732 | 12719373 | Vision blurred | |
| 127193732 | 12719373 | 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 |
|---|---|---|---|---|---|---|
| 127193732 | 12719373 | 1 | 20140915 | 20160203 | 0 | |
| 127193732 | 12719373 | 2 | 20160203 | 20160203 | 0 | |
| 127193732 | 12719373 | 3 | 20160309 | 0 |