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
117165503 11716550 3 F 2007 20151104 20151109 20160720 PER US-DSJP-DSU-2015-125968 DAIICHI 39.82 YR F Y 76.19000 KG 20160718 OT 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
117165503 11716550 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/12.5 MG, QD 21532 FILM-COATED TABLET QD
117165503 11716550 2 SS AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117165503 11716550 1 Hypertension
117165503 11716550 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117165503 11716550 Alopecia
117165503 11716550 Constipation
117165503 11716550 Dizziness
117165503 11716550 Gastrooesophageal reflux disease
117165503 11716550 Malabsorption
117165503 11716550 Peptic ulcer

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
117165503 11716550 1 20060412 20100601 0
117165503 11716550 2 2006 0