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
126276232 12627623 2 F 20160804 20160805 20160812 EXP JP-BAUSCH-BL-2016-018557 BAUSCH AND LOMB 77.00 YR M Y 0.00000 20160812 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
126276232 12627623 1 PS VISUDYNE VERTEPORFIN 1 Intravenous (not otherwise specified) 21119 6 MG/M**2 INJECTION
126276232 12627623 2 SS VISUDYNE VERTEPORFIN 1 21119
126276232 12627623 3 SS LUCENTIS RANIBIZUMAB 1 Other N 0 .05 ML INJECTION
126276232 12627623 4 SS LUCENTIS RANIBIZUMAB 1 N 0
126276232 12627623 5 C EYLEA AFLIBERCEPT 1 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126276232 12627623 1 Polypoidal choroidal vasculopathy
126276232 12627623 2 Age-related macular degeneration
126276232 12627623 3 Polypoidal choroidal vasculopathy
126276232 12627623 4 Age-related macular degeneration
126276232 12627623 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126276232 12627623 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126276232 12627623 Polypoidal choroidal vasculopathy
126276232 12627623 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