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
127611591 12761159 1 I 20160808 20160914 20160920 20160920 EXP DE-ROCHE-1831372 ROCHE 0.00 E F Y 0.00000 20160920 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
127611591 12761159 1 PS Ranibizumab RANIBIZUMAB 1 Intraocular LEFT EYE, VIAL, 1X 125156 .5 MG SOLUTION FOR INJECTION
127611591 12761159 2 SS Ranibizumab RANIBIZUMAB 1 Intraocular LEFT EYE, VIAL, 1X 125156 .5 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127611591 12761159 1 Neovascular age-related macular degeneration

Outcome of event

Event ID CASEID OUTC COD
127611591 12761159 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127611591 12761159 Detachment of retinal pigment epithelium

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
127611591 12761159 1 20160707 0
127611591 12761159 2 20160804 20160804 0