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
125073662 12507366 2 F 2012 20160629 20160629 20160705 EXP JP-ROCHE-1782458 ROCHE 71.00 YR F Y 0.00000 20160705 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
125073662 12507366 1 PS LUCENTIS RANIBIZUMAB 1 Other UNK U 125156 SOLUTION FOR INJECTION
125073662 12507366 2 SS LUCENTIS RANIBIZUMAB 1 Other IN LEFT EYE U 125156

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125073662 12507366 1 Optic disc disorder
125073662 12507366 2 Age-related macular degeneration

Outcome of event

Event ID CASEID OUTC COD
125073662 12507366 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125073662 12507366 Cataract cortical
125073662 12507366 Detachment of retinal pigment epithelium
125073662 12507366 Injection site pain
125073662 12507366 Intraocular pressure increased
125073662 12507366 Macular degeneration
125073662 12507366 Off label use
125073662 12507366 Optic discs blurred
125073662 12507366 Retinal degeneration
125073662 12507366 Retinal detachment
125073662 12507366 Staphyloma
125073662 12507366 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
125073662 12507366 2 2005 2005 0