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
126024671 12602467 1 I 20160613 20160701 20160728 20160728 EXP US-AMGEN-USASP2016086601 AMGEN 70.00 YR E F Y 45.35000 KG 20160728 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
126024671 12602467 1 PS PROLIA DENOSUMAB 1 Subcutaneous 60 MG, QMO 1970.802 MG Y Y 125320 60 MG SOLUTION FOR INJECTION /month
126024671 12602467 2 C FENOFIBRATE. FENOFIBRATE 1 145 MG, QD 0 145 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126024671 12602467 1 Osteoporosis
126024671 12602467 2 Hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
126024671 12602467 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126024671 12602467 Asthenia
126024671 12602467 Blood calcium abnormal
126024671 12602467 Blood potassium increased
126024671 12602467 Malaise Malaise
126024671 12602467 Mobility decreased
126024671 12602467 Myalgia
126024671 12602467 Pain in extremity
126024671 12602467 Therapeutic response unexpected

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
126024671 12602467 1 20131011 20160704 0
126024671 12602467 2 20160616 0