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
125427331 12542733 1 I 2014 20160701 20160709 20160709 EXP US-AMGEN-USASP2016086743 AMGEN 90.00 YR E M Y 0.00000 20160709 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
125427331 12542733 1 PS PROLIA DENOSUMAB 1 Unknown UNK U 125320 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125427331 12542733 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125427331 12542733 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125427331 12542733 Back pain
125427331 12542733 Blood potassium abnormal
125427331 12542733 Bone density abnormal
125427331 12542733 Bronchitis
125427331 12542733 Fatigue
125427331 12542733 Hip fracture
125427331 12542733 Muscle rupture
125427331 12542733 Muscular weakness
125427331 12542733 Pain
125427331 12542733 Urinary incontinence
125427331 12542733 Walking aid user

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
125427331 12542733 1 2013 0