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
125586571 12558657 1 I 201607 20160708 20160715 20160715 EXP US-AMGEN-USASP2016089313 AMGEN 59.00 YR A F Y 0.00000 20160714 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
125586571 12558657 1 PS PROLIA DENOSUMAB 1 Unknown UNK U 125320 SOLUTION FOR INJECTION
125586571 12558657 2 C FENTANYL. FENTANYL 1 0
125586571 12558657 3 C ELIQUIS APIXABAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125586571 12558657 1 Osteoporosis postmenopausal
125586571 12558657 2 Pain

Outcome of event

Event ID CASEID OUTC COD
125586571 12558657 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125586571 12558657 Abdominal discomfort
125586571 12558657 Dental caries
125586571 12558657 Gait disturbance
125586571 12558657 General physical health deterioration
125586571 12558657 Mouth haemorrhage
125586571 12558657 Osteoarthritis
125586571 12558657 Pain in extremity
125586571 12558657 Pain in jaw
125586571 12558657 Toothache
125586571 12558657 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
125586571 12558657 1 20160324 0