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
125378181 12537818 1 I 2015 20150609 20160707 20160707 PER US-DSJP-DSU-2015-118213 DAIICHI 0.00 M Y 97.51000 KG 20160707 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
125378181 12537818 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40/12.5MG, QAM N 21532 1 DF FILM-COATED TABLET QD
125378181 12537818 2 SS CLONIDINE. CLONIDINE 1 Topical 1 PATCH, ONCE EVERY 1 WK 0 TRANSDERMAL PATCH /wk
125378181 12537818 3 SS EDARBYCLOR AZILSARTAN KAMEDOXOMILCHLORTHALIDONE 1 Oral 40/25 MG, QD 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125378181 12537818 1 Hypertension
125378181 12537818 2 Hypertension
125378181 12537818 3 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125378181 12537818 Dizziness
125378181 12537818 Dyspepsia
125378181 12537818 Hypotension
125378181 12537818 Malaise
125378181 12537818 Treatment noncompliance

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
125378181 12537818 1 201505 0
125378181 12537818 2 201505 0
125378181 12537818 3 201505 20150608 0