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
124189603 12418960 3 F 20160101 20160707 20160531 20160713 EXP GB-ROCHE-1712362 ROCHE 81.69 YR F Y 0.00000 20160713 MD GB GB

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
124189603 12418960 1 PS Ranibizumab RANIBIZUMAB 1 Unknown N S2014B 125156 SOLUTION FOR INJECTION
124189603 12418960 2 SS Ranibizumab RANIBIZUMAB 1 Unknown LAST DOSE PRIOR TO SAE N S2014B 125156 SOLUTION FOR INJECTION
124189603 12418960 3 C WARFARIN WARFARIN 1 Unknown U 0
124189603 12418960 4 C BISOPROLOL BISOPROLOL 1 Unknown U 0
124189603 12418960 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124189603 12418960 1 Diabetic retinal oedema
124189603 12418960 3 Atrial fibrillation
124189603 12418960 4 Atrial fibrillation
124189603 12418960 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
124189603 12418960 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124189603 12418960 Cerebral 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
124189603 12418960 1 20140920 0
124189603 12418960 2 20150310 20150310 0
124189603 12418960 3 20131216 0
124189603 12418960 4 20111116 0
124189603 12418960 5 20080402 0