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
124320172 12432017 2 F 20160516 20160718 20160603 20160725 EXP US-AMGEN-USASP2016069406 AMGEN 75.00 YR E F Y 67.12000 KG 20160724 CN 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
124320172 12432017 1 PS PROLIA DENOSUMAB 1 Subcutaneous 60 UNK, UNK U 125320 SOLUTION FOR INJECTION
124320172 12432017 2 SS PROLIA DENOSUMAB 1 U 125320 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124320172 12432017 1 Osteoporosis
124320172 12432017 2 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
124320172 12432017 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124320172 12432017 Arthralgia
124320172 12432017 Bone pain
124320172 12432017 Gait disturbance
124320172 12432017 Hypoaesthesia
124320172 12432017 Limb operation
124320172 12432017 Off label use
124320172 12432017 Pain
124320172 12432017 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
124320172 12432017 1 20160516 0