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
125029443 12502944 3 F 20150618 20160712 20160628 20160718 EXP JP-ROCHE-1784295 ROCHE 74.00 YR F Y 48.00000 KG 20160718 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
125029443 12502944 1 PS LUCENTIS RANIBIZUMAB 1 Other UNK U 125156 SOLUTION FOR INJECTION
125029443 12502944 2 C TELMISARTAN. TELMISARTAN 1 Oral 20 MG, QD Y 0 20 MG QD
125029443 12502944 3 C TELMISARTAN. TELMISARTAN 1 Oral 40 MG, QD Y 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125029443 12502944 1 Retinal vein occlusion
125029443 12502944 2 Blood pressure systolic increased

Outcome of event

Event ID CASEID OUTC COD
125029443 12502944 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125029443 12502944 Blood pressure increased
125029443 12502944 Blood pressure systolic increased
125029443 12502944 Brain natriuretic peptide increased
125029443 12502944 Macular oedema
125029443 12502944 Vision blurred

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
125029443 12502944 1 20150401 0