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
124535092 12453509 2 F 2007 20151007 20160609 20160720 EXP US-DSJP-DSU-2015-119462 DAIICHI 67.54 YR F Y 72.56000 KG 20160718 MD 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
124535092 12453509 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40-25 MG, QD Y 21532 FILM-COATED TABLET QD
124535092 12453509 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 UNK U 0 TABLET
124535092 12453509 3 C LOSARTAN AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM 1 100-25 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124535092 12453509 1 Hypertension
124535092 12453509 2 Hypertension
124535092 12453509 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
124535092 12453509 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124535092 12453509 Abdominal pain
124535092 12453509 Adenomatous polyposis coli
124535092 12453509 Constipation
124535092 12453509 Dizziness
124535092 12453509 Fatigue
124535092 12453509 Gallbladder disorder
124535092 12453509 Gastrointestinal haemorrhage
124535092 12453509 Gastrooesophageal reflux disease
124535092 12453509 Haemangioma of liver
124535092 12453509 Irritable bowel syndrome
124535092 12453509 Malabsorption

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
124535092 12453509 1 2012 2014 0
124535092 12453509 2 2007 2007 0
124535092 12453509 3 2014 0