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
126378522 12637852 2 F 20160809 20160809 20160816 EXP JP-BAUSCH-BL-2016-018864 BAUSCH AND LOMB 60.00 YR M Y 0.00000 20160816 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
126378522 12637852 1 PS VISUDYNE VERTEPORFIN 1 Intravenous (not otherwise specified) Y 21119 15 MG INJECTION
126378522 12637852 2 SS LUCENTIS RANIBIZUMAB 1 Other U 0 .05 ML INJECTION
126378522 12637852 3 C AFLIBERCEPT AFLIBERCEPT 1 Other 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126378522 12637852 1 Age-related macular degeneration
126378522 12637852 2 Age-related macular degeneration
126378522 12637852 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126378522 12637852 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126378522 12637852 Detachment of retinal pigment epithelium
126378522 12637852 Subretinal fluid
126378522 12637852 Vasodilatation
126378522 12637852 Visual acuity reduced

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found