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
121966313 12196631 3 F 201002 20160902 20160321 20160910 EXP US-DSJP-DSU-2015-131212 DAIICHI 0.00 Y 0.00000 20160909 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
121966313 12196631 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 20 MG, QD U 21286 20 MG TABLET QD
121966313 12196631 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 U 21286 TABLET
121966313 12196631 3 SS BENICAR OLMESARTAN MEDOXOMIL 1 U 21286 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121966313 12196631 1 Myocardial infarction
121966313 12196631 2 Stent placement
121966313 12196631 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
121966313 12196631 OT
121966313 12196631 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121966313 12196631 Aortic aneurysm
121966313 12196631 Cholecystitis
121966313 12196631 Cholelithiasis
121966313 12196631 Constipation
121966313 12196631 Diverticulitis
121966313 12196631 Haemorrhoids
121966313 12196631 Malabsorption
121966313 12196631 Off label use
121966313 12196631 Rectal haemorrhage

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
121966313 12196631 1 20100222 2015 0