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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121938053 | 12193805 | 3 | F | 20150612 | 20160714 | 20160321 | 20160720 | EXP | JP-ROCHE-1728812 | ROCHE | 77.40 | YR | M | Y | 56.00000 | KG | 20160720 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121938053 | 12193805 | 1 | PS | LUCENTIS | RANIBIZUMAB | 1 | Other | UNK | Y | U | UNKNOWN | 125156 | SOLUTION FOR INJECTION | ||||||
| 121938053 | 12193805 | 2 | SS | LUCENTIS | RANIBIZUMAB | 1 | Other | Y | U | UNKNOWN | 125156 | .05 | ML | ||||||
| 121938053 | 12193805 | 3 | SS | LUCENTIS | RANIBIZUMAB | 1 | Other | Y | U | UNKNOWN | 125156 | .05 | ML |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121938053 | 12193805 | 1 | Age-related macular degeneration |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121938053 | 12193805 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121938053 | 12193805 | Cerebral infarction |
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 |
|---|---|---|---|---|---|---|
| 121938053 | 12193805 | 1 | 20091112 | 0 | ||
| 121938053 | 12193805 | 2 | 20150603 | 20160603 | 0 | |
| 121938053 | 12193805 | 3 | 20151007 | 20151007 | 0 |