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
126592932 12659293 2 F 20160809 20160914 20160817 20160923 EXP TH-ROCHE-1812726 ROCHE 55.21 YR M Y 0.00000 20160923 MD TH TH

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
126592932 12659293 1 PS LUCENTIS RANIBIZUMAB 1 Other 0.5 MG, UNK 125156 .5 MG SOLUTION FOR INJECTION
126592932 12659293 2 SS LUCENTIS RANIBIZUMAB 1 Other 0.5 MG, UNK 125156 .5 MG SOLUTION FOR INJECTION
126592932 12659293 3 C POLY-OPH 2 Unknown UNK UNK, QID U 0 QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126592932 12659293 1 Diabetic retinal oedema
126592932 12659293 3 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126592932 12659293 OT
126592932 12659293 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126592932 12659293 Endophthalmitis
126592932 12659293 Eye irritation
126592932 12659293 Eye pain
126592932 12659293 Inappropriate schedule of drug administration
126592932 12659293 Injection site irritation
126592932 12659293 Injection site pain
126592932 12659293 Ocular hyperaemia
126592932 12659293 Vision blurred
126592932 12659293 Visual acuity reduced

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
126592932 12659293 1 20160729 0
126592932 12659293 2 20160809 20160809 0
126592932 12659293 3 20160729 0