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
123363903 12336390 3 F 20160209 20160719 20160505 20160726 EXP US-AMGEN-USASL2016056134 AMGEN 76.00 YR E F Y 81.60000 KG 20160725 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
123363903 12336390 1 PS PROLIA DENOSUMAB 1 Subcutaneous 60 MG/ML, Q6MO 125320 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123363903 12336390 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
123363903 12336390 DE
123363903 12336390 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123363903 12336390 Acute sinusitis
123363903 12336390 Arthralgia
123363903 12336390 Cardiac disorder
123363903 12336390 Dacryostenosis acquired
123363903 12336390 Death
123363903 12336390 Depression
123363903 12336390 Essential hypertension
123363903 12336390 Gastroenteritis viral
123363903 12336390 Ingrowing nail
123363903 12336390 Joint dislocation
123363903 12336390 Onychomycosis
123363903 12336390 Post-traumatic stress disorder
123363903 12336390 Rhinitis allergic
123363903 12336390 Sleep disorder due to general medical condition, insomnia type

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
123363903 12336390 1 20151117 0