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
101450322 10145032 2 F 20100820 20111116 20140501 20150930 EXP US-ROCHE-1392889 ROCHE 46.42 YR F Y 0.00000 20150930 N MD US US

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
101450322 10145032 1 PS AVASTIN BEVACIZUMAB 1 Other 0.5ML D 125085 125 MG
101450322 10145032 2 SS AVASTIN BEVACIZUMAB 1 D 125085
101450322 10145032 3 SS LUCENTIS RANIBIZUMAB 1 Intravesical 19-NOV-2013 MOST RECENT INJECTION D 125156 .5 MG /month
101450322 10145032 4 SS LUCENTIS RANIBIZUMAB 1 D 125156

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101450322 10145032 1 Cystoid macular oedema
101450322 10145032 2 Retinal oedema
101450322 10145032 3 Macular degeneration
101450322 10145032 4 Retinal oedema

Outcome of event

Event ID CASEID OUTC COD
101450322 10145032 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101450322 10145032 Drug hypersensitivity
101450322 10145032 Eye swelling
101450322 10145032 Iritis
101450322 10145032 Ocular hyperaemia
101450322 10145032 Product use issue
101450322 10145032 Punctate keratitis
101450322 10145032 Uveitis

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
101450322 10145032 1 20091217 20100820 0