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
126967561 12696756 1 I 20160224 20160818 20160830 20160830 EXP DE-ROCHE-1821501 ROCHE 74.00 YR M Y 0.00000 20160830 MD DE DE

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
126967561 12696756 1 PS Ranibizumab RANIBIZUMAB 1 Other 0.5 MG, UNK, RIGHT EYE S2045F,S2046A,S2046A,S2047D 125156 .5 MG SOLUTION FOR INJECTION
126967561 12696756 2 SS Ranibizumab RANIBIZUMAB 1 Other 0.5 UNK,RIGHT EYE S2045F,S2046A,S2046A,S2047D 125156 .5 MG SOLUTION FOR INJECTION
126967561 12696756 3 SS Ranibizumab RANIBIZUMAB 1 Other 0.5 MG, UNK, RIGHT EYE S2045F,S2046A,S2046A,S2047D 125156 .5 MG SOLUTION FOR INJECTION
126967561 12696756 4 SS Ranibizumab RANIBIZUMAB 1 Other 0.5 MG, UNK, RIGHT EYE S2045F,S2046A,S2046A,S2047D 125156 .5 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126967561 12696756 1 Visual impairment
126967561 12696756 2 Macular oedema
126967561 12696756 3 Retinal vein occlusion

Outcome of event

Event ID CASEID OUTC COD
126967561 12696756 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126967561 12696756 Eye pain
126967561 12696756 Sensation of foreign body
126967561 12696756 Vision blurred
126967561 12696756 Visual acuity reduced
126967561 12696756 Visual impairment

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
126967561 12696756 1 20160224 20160224 0
126967561 12696756 2 20160406 20160406 0
126967561 12696756 3 20160518 20160518 0
126967561 12696756 4 20160803 0