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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124948132 | 12494813 | 2 | F | 20160601 | 20160725 | 20160624 | 20160802 | EXP | DE-ROCHE-1782442 | ROCHE | 70.00 | YR | M | Y | 0.00000 | 20160802 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124948132 | 12494813 | 1 | PS | LUCENTIS | RANIBIZUMAB | 1 | Other | Y | U | HG S2053D | 125156 | SOLUTION FOR INJECTION | |||||||
| 124948132 | 12494813 | 2 | SS | LUCENTIS | RANIBIZUMAB | 1 | Y | U | HG S2053D | 125156 | |||||||||
| 124948132 | 12494813 | 3 | C | GODAMED | ASPIRIN | 1 | Unknown | U | 0 | ||||||||||
| 124948132 | 12494813 | 4 | C | CARVEDILOL. | CARVEDILOL | 1 | Unknown | U | 0 | TABLET | |||||||||
| 124948132 | 12494813 | 5 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | 0 | ||||||||||
| 124948132 | 12494813 | 6 | C | CANDESARTAN | CANDESARTAN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124948132 | 12494813 | 1 | Macular oedema |
| 124948132 | 12494813 | 2 | Retinal vein occlusion |
| 124948132 | 12494813 | 3 | Product used for unknown indication |
| 124948132 | 12494813 | 4 | Product used for unknown indication |
| 124948132 | 12494813 | 5 | Product used for unknown indication |
| 124948132 | 12494813 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124948132 | 12494813 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124948132 | 12494813 | Cerebrovascular accident |
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 |
|---|---|---|---|---|---|---|
| 124948132 | 12494813 | 1 | 20160530 | 20160530 | 0 |