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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121823672 | 12182367 | 2 | F | 20160212 | 20160822 | 20160316 | 20160826 | EXP | SE-ROCHE-1724693 | ROCHE | 80.00 | YR | F | Y | 0.00000 | 20160826 | MD | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121823672 | 12182367 | 1 | PS | LUCENTIS | RANIBIZUMAB | 1 | Other | U | 212800LOT06201752027D | 125156 | |||||||||
| 121823672 | 12182367 | 2 | SS | LUCENTIS | RANIBIZUMAB | 1 | Other | U | 212800LOT06201752027D | 125156 | |||||||||
| 121823672 | 12182367 | 3 | C | OMEPRAZOL | OMEPRAZOLE | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 4 | C | SODIUM BICARBONATE. | SODIUM BICARBONATE | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 5 | C | NOVONORM | REPAGLINIDE | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 6 | C | ETALPHA | ALFACALCIDOL | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 7 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 8 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 9 | C | BISOPROLOL SANDOZ | BISOPROLOL | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 10 | C | LATANOPROST. | LATANOPROST | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 11 | C | RENVELA | SEVELAMER CARBONATE | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 12 | C | ALVEDON | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 121823672 | 12182367 | 13 | C | ZOPIKLON | ZOPICLONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121823672 | 12182367 | 1 | Age-related macular degeneration |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121823672 | 12182367 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121823672 | 12182367 | Myocardial 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 |
|---|---|---|---|---|---|---|
| 121823672 | 12182367 | 1 | 20140703 | 0 | ||
| 121823672 | 12182367 | 2 | 20151013 | 0 |