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
125518931 12551893 1 I 20160619 20160705 20160713 20160713 EXP FR-ASTRAZENECA-2016SE74005 ASTRAZENECA 31879.00 DY F Y 0.00000 20160713 MD FR FR

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
125518931 12551893 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral 16 MG Y U 20838 8 MG TABLET BID
125518931 12551893 2 SS LOXEN NICARDIPINE HYDROCHLORIDE 1 Oral 50 MG Y U 0 50 MG QD
125518931 12551893 3 SS TEMERIT NEBIVOLOL 1 Oral 5 MG Y U 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125518931 12551893 1 Hypertension
125518931 12551893 2 Hypertension
125518931 12551893 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125518931 12551893 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125518931 12551893 Bradycardia
125518931 12551893 Hypotension
125518931 12551893 Product use issue

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
125518931 12551893 1 20160619 20160619 0
125518931 12551893 2 20160619 20160619 0
125518931 12551893 3 20160619 20160619 0