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
123158213 12315821 3 F 2015 20160823 20160428 20160830 EXP US-DSJP-DSU-2016-114698 DAIICHI 0.00 Y 0.00000 20160830 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
123158213 12315821 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 40 MG, QD U 21286 40 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123158213 12315821 1 Blood pressure measurement

Outcome of event

Event ID CASEID OUTC COD
123158213 12315821 OT
123158213 12315821 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123158213 12315821 Bladder cancer
123158213 12315821 Chronic kidney disease
123158213 12315821 Dizziness
123158213 12315821 Hepatitis B surface antibody
123158213 12315821 Hyperlipidaemia
123158213 12315821 Hypertension
123158213 12315821 Malabsorption
123158213 12315821 Osteoarthritis
123158213 12315821 Pain
123158213 12315821 Seizure
123158213 12315821 Transient ischaemic attack
123158213 12315821 Type 2 diabetes mellitus

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
123158213 12315821 1 2013 2015 0