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
125696991 12569699 1 I 20160712 20160719 20160719 EXP CA-AMGEN-CANSP2016091118 AMGEN 57.00 YR A M Y 0.00000 20160719 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
125696991 12569699 1 PS PROLIA DENOSUMAB 1 Subcutaneous 60 MG, Q6MO U 125320 60 MG SOLUTION FOR INJECTION
125696991 12569699 2 SS COUMADIN WARFARIN SODIUM 1 Unknown 0
125696991 12569699 3 SS PREDNISONE. PREDNISONE 1 Unknown 0
125696991 12569699 4 C BENTYL DICYCLOMINE HYDROCHLORIDE 1 Unknown 0
125696991 12569699 5 C PAROXETINE. PAROXETINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125696991 12569699 1 Osteoporosis
125696991 12569699 2 Product used for unknown indication
125696991 12569699 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125696991 12569699 OT
125696991 12569699 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125696991 12569699 Epigastric discomfort
125696991 12569699 Malaise
125696991 12569699 Thrombosis

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

no results found

Therapies reported

no results found