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
86084563 8608456 3 F 20160809 20120611 20160814 EXP US-ROCHE-1076550 ROCHE 0.00 M Y 0.00000 20160815 MD US US

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
86084563 8608456 1 PS LUCENTIS RANIBIZUMAB 1 Other U 475546 125156 .5 MG SOLUTION FOR INJECTION
86084563 8608456 2 C LEVOMET 2 0
86084563 8608456 3 C ATORVASTATIN ATORVASTATIN 1 0
86084563 8608456 4 C SIMVASTATIN. SIMVASTATIN 1 0
86084563 8608456 5 C ENALAPRIL ENALAPRIL 1 0
86084563 8608456 6 C FAMOTIDINE. FAMOTIDINE 1 0
86084563 8608456 7 C ASA ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86084563 8608456 1 Diabetic retinal oedema

Outcome of event

Event ID CASEID OUTC COD
86084563 8608456 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86084563 8608456 Cardiac failure congestive
86084563 8608456 Localised infection
86084563 8608456 Myocardial infarction

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
86084563 8608456 1 20120825 20121127 0