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
125416311 12541631 1 I 2015 20151012 20160708 20160708 PER US-DSJP-DSU-2015-131718 DAIICHI 0.00 M Y 72.56000 KG 20160708 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
125416311 12541631 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 20/12.5 MG, ONCE DAILY N 21532 FILM-COATED TABLET
125416311 12541631 2 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/12.5 MG, UNK N 21532 FILM-COATED TABLET
125416311 12541631 3 SS AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 AZOR 10/40 MG N 0 TABLET
125416311 12541631 4 SS AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 5/40 MG, UNK N 0 TABLET
125416311 12541631 5 SS AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 Oral 10-40 MG, ONCE DAILY N 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125416311 12541631 1 Hypertension
125416311 12541631 3 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125416311 12541631 Anxiety
125416311 12541631 Depression
125416311 12541631 Dizziness
125416311 12541631 Insomnia
125416311 12541631 Malabsorption
125416311 12541631 Visual impairment

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
125416311 12541631 1 2009 201407 0
125416311 12541631 2 20140811 0
125416311 12541631 3 2009 201407 0
125416311 12541631 4 20140811 0
125416311 12541631 5 20140814 0