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
126156161 12615616 1 I 201512 20160726 20160802 20160802 EXP US-AMGEN-USASP2016097133 AMGEN 75.00 YR E F Y 0.00000 20160802 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
126156161 12615616 1 PS PROLIA DENOSUMAB 1 Unknown 60 MG/ML, Q6MO U 125320 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126156161 12615616 1 Osteoporosis postmenopausal

Outcome of event

Event ID CASEID OUTC COD
126156161 12615616 HO
126156161 12615616 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126156161 12615616 Blister
126156161 12615616 Brain operation
126156161 12615616 Eosinophil count increased
126156161 12615616 Eosinophilic granulomatosis with polyangiitis
126156161 12615616 Fall
126156161 12615616 Head injury
126156161 12615616 Hospitalisation
126156161 12615616 Ileostomy
126156161 12615616 Pain in extremity
126156161 12615616 Peroneal nerve palsy
126156161 12615616 Skin ulcer
126156161 12615616 Spinal fracture
126156161 12615616 Tendon disorder

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
126156161 12615616 1 2010 0