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
125388381 12538838 1 I 201606 20160629 20160708 20160708 PER US-ASTRAZENECA-2016SE71875 ASTRAZENECA 711.00 MON F Y 77.10000 KG 20160708 CN 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
125388381 12538838 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral 93504 MG U U 20838 16 MG TABLET QD
125388381 12538838 2 SS ATACAND CANDESARTAN CILEXETIL 1 Oral 93504 MG U U 20838 16 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125388381 12538838 1 Renal disorder
125388381 12538838 2 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125388381 12538838 Aortic stenosis
125388381 12538838 Blood pressure increased
125388381 12538838 Cough
125388381 12538838 Drug dose omission
125388381 12538838 Headache
125388381 12538838 Nausea
125388381 12538838 Product use issue
125388381 12538838 Weight increased

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
125388381 12538838 1 2000 201606 0
125388381 12538838 2 2000 201606 0