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
126288462 12628846 2 F 201607 20160825 20160808 20160831 EXP JP-ROCHE-1809766 ROCHE 67.00 YR F Y 0.00000 20160831 MD JP JP

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
126288462 12628846 1 PS LUCENTIS RANIBIZUMAB 1 Other UNK 125156 SOLUTION FOR INJECTION
126288462 12628846 2 SS LUCENTIS RANIBIZUMAB 1 Other UNK 125156 SOLUTION FOR INJECTION
126288462 12628846 3 SS LUCENTIS RANIBIZUMAB 1 Other UNK 125156 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126288462 12628846 1 Retinal vein occlusion
126288462 12628846 2 Macular oedema

Outcome of event

Event ID CASEID OUTC COD
126288462 12628846 OT
126288462 12628846 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126288462 12628846 Haemorrhage
126288462 12628846 Macular fibrosis
126288462 12628846 Vitreous haemorrhage

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
126288462 12628846 1 201508 0
126288462 12628846 2 201603 0