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
102707225 10270722 5 F 20140414 20160728 20140701 20160802 EXP CA-MERCK-1406CAN013886 MERCK 76.17 YR F Y 0.00000 20160802 MD CA CA

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
102707225 10270722 1 PS SINGULAIR MONTELUKAST SODIUM 1 Oral 10 MG, QD 20829 10 MG TABLET QD
102707225 10270722 2 SS EZETROL EZETIMIBE 1 Oral 10 MG, QD 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102707225 10270722 1 Asthma
102707225 10270722 2 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
102707225 10270722 HO
102707225 10270722 LT
102707225 10270722 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102707225 10270722 Aortic valve replacement
102707225 10270722 Aortic valvotomy
102707225 10270722 Cardiac valve disease
102707225 10270722 Coronary artery bypass
102707225 10270722 Cough
102707225 10270722 Endocarditis
102707225 10270722 Influenza
102707225 10270722 Malaise
102707225 10270722 Myalgia
102707225 10270722 Nasopharyngitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found