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
124253362 12425336 2 F 2016 20160629 20160601 20160706 EXP US-AMGEN-USASP2016067591 AMGEN 83.00 YR E F Y 68.93000 KG 20160706 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
124253362 12425336 1 PS PROLIA DENOSUMAB 1 Subcutaneous UNK, Q6MO U 125320 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124253362 12425336 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
124253362 12425336 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124253362 12425336 Asthenia
124253362 12425336 Cough
124253362 12425336 Dizziness
124253362 12425336 Drug intolerance
124253362 12425336 Gait disturbance
124253362 12425336 Hip arthroplasty
124253362 12425336 Hypersensitivity
124253362 12425336 Influenza like illness
124253362 12425336 Musculoskeletal discomfort
124253362 12425336 Pruritus generalised
124253362 12425336 Rhinitis

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
124253362 12425336 1 201503 201605 0