The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
120371222 12037122 2 F 20160824 20160208 20160826 EXP CA-ROCHE-1707749 ROCHE 0.00 M Y 0.00000 20160826 OT CA CA

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
120371222 12037122 1 PS LUCENTIS RANIBIZUMAB 1 Ophthalmic 125156 .5 MG SOLUTION FOR INJECTION
120371222 12037122 2 SS AVASTIN BEVACIZUMAB 1 Intravenous (not otherwise specified) 125085

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120371222 12037122 1 Product used for unknown indication
120371222 12037122 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120371222 12037122 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
120371222 12037122 Death

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
120371222 12037122 1 20100202 20100602 0