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
126968801 12696880 1 I 20151109 20160822 20160830 20160830 EXP IT-AMGEN-ITASP2016111251 AMGEN 60.00 YR A F Y 0.00000 20160830 OT IT IT

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
126968801 12696880 1 PS XGEVA DENOSUMAB 1 Unknown 120 MG, QMO Y 125320 120 MG UNKNOWN FORMULATION /month
126968801 12696880 2 SS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 4 MG, QMO 20 MG 0 4 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126968801 12696880 1 Metastases to bone
126968801 12696880 2 Metastasis

Outcome of event

Event ID CASEID OUTC COD
126968801 12696880 DS
126968801 12696880 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126968801 12696880 Bone fistula
126968801 12696880 Dysaesthesia
126968801 12696880 Mouth swelling
126968801 12696880 Oral mucosal erythema

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
126968801 12696880 1 20150102 0
126968801 12696880 2 20140901 20150101 0