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
126963051 12696305 1 I 20160813 20160824 20160830 20160830 EXP AU-ROCHE-1821505 ROCHE 52.46 YR M Y 108.00000 KG 20160830 MD AU AU

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
126963051 12696305 1 PS Ranibizumab RANIBIZUMAB 1 Other Y 125156 50 ML SOLUTION FOR INJECTION
126963051 12696305 2 SS Ranibizumab RANIBIZUMAB 1 Other Y 125156 50 ML SOLUTION FOR INJECTION
126963051 12696305 3 C CANDESARTAN CANDESARTAN 1 Unknown 32 MG, UNK U 0 32 MG
126963051 12696305 4 C ARGININE ARGININE 1 Unknown PRN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126963051 12696305 1 Diabetic retinal oedema
126963051 12696305 3 Hypertension
126963051 12696305 4 Angina pectoris

Outcome of event

Event ID CASEID OUTC COD
126963051 12696305 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126963051 12696305 Cerebrovascular accident

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
126963051 12696305 1 20160602 20160602 0
126963051 12696305 2 20160811 20160811 0
126963051 12696305 3 20151130 20160812 0
126963051 12696305 4 20151229 0