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
125403071 12540307 1 I 2006 20150902 20160708 20160708 PER US-DSJP-DSU-2015-127772 DAIICHI 0.00 M Y 89.80000 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
125403071 12540307 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40/12.5 MG, QD Y 21532 FILM-COATED TABLET
125403071 12540307 2 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 20/12.5 MG, QD Y 21532 FILM-COATED TABLET
125403071 12540307 3 C NAPROXEN. NAPROXEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125403071 12540307 1 Hypertension
125403071 12540307 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125403071 12540307 Constipation
125403071 12540307 Diverticulum
125403071 12540307 Haematochezia
125403071 12540307 Liver function test abnormal
125403071 12540307 Malabsorption
125403071 12540307 Microcytic anaemia
125403071 12540307 Renal failure

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
125403071 12540307 1 2006 2012 0