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
114978224 11497822 4 F 2013 20160909 20150911 20160916 EXP US-DSJP-DSU-2015-120644 DAIICHI 0.00 Y 0.00000 20160916 LW 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
114978224 11497822 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 UNK U 21286 TABLET
114978224 11497822 2 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40MG/12.5 MG, QD N 0 1 DF FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114978224 11497822 1 Product used for unknown indication
114978224 11497822 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
114978224 11497822 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114978224 11497822 Anxiety
114978224 11497822 Change of bowel habit
114978224 11497822 Diverticulum
114978224 11497822 Dyspepsia
114978224 11497822 Irritable bowel syndrome
114978224 11497822 Malabsorption
114978224 11497822 Mesenteritis
114978224 11497822 Rash
114978224 11497822 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
114978224 11497822 2 2012 2013 0