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
125844071 12584407 1 I 20160709 20160715 20160722 20160722 EXP PE-AMGEN-PERSP2016094986 AMGEN 77.00 YR E F Y 0.00000 20160722 CN PE PE

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
125844071 12584407 1 PS PROLIA DENOSUMAB 1 Subcutaneous 60 MG/ML, CYCLICAL 125320 SOLUTION FOR INJECTION
125844071 12584407 2 SS PROLIA DENOSUMAB 1 Subcutaneous UNK 125320 SOLUTION FOR INJECTION
125844071 12584407 3 SS PROLIA DENOSUMAB 1 Subcutaneous UNK 125320 SOLUTION FOR INJECTION
125844071 12584407 4 SS PROLIA DENOSUMAB 1 Subcutaneous UNK 125320 SOLUTION FOR INJECTION
125844071 12584407 5 SS PROLIA DENOSUMAB 1 Subcutaneous UNK 125320 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125844071 12584407 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
125844071 12584407 HO
125844071 12584407 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125844071 12584407 Aphasia
125844071 12584407 Arthritis
125844071 12584407 Cerebrovascular accident
125844071 12584407 Pain in extremity

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
125844071 12584407 1 20140128 0
125844071 12584407 2 20140723 0
125844071 12584407 3 20150122 0
125844071 12584407 4 20150818 0
125844071 12584407 5 20160212 0