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
125818813 12581881 3 F 20160710 20160830 20160722 20160906 EXP CA-AMGEN-CANSL2016092109 AMGEN 81.00 YR E M Y 104.31000 KG 20160906 CN CA CA

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
125818813 12581881 1 PS ARANESP DARBEPOETIN ALFA 1 Subcutaneous 60 MUG, QWK 240 UG N 1068045 103951 60 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
125818813 12581881 2 C INSULIN INSULIN NOS 1 0
125818813 12581881 3 C ASPIRIN. ASPIRIN 1 UNK UNK, AS NECESSARY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125818813 12581881 1 Nephrogenic anaemia

Outcome of event

Event ID CASEID OUTC COD
125818813 12581881 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125818813 12581881 Arthralgia
125818813 12581881 Balance disorder
125818813 12581881 Blood potassium increased
125818813 12581881 Drug ineffective
125818813 12581881 Fatigue
125818813 12581881 Feeling abnormal
125818813 12581881 Haemoglobin decreased
125818813 12581881 Headache
125818813 12581881 Mobility decreased
125818813 12581881 Muscular weakness
125818813 12581881 Myalgia
125818813 12581881 Pain in extremity
125818813 12581881 Red blood cell count decreased
125818813 12581881 Renal 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
125818813 12581881 1 20160622 20160713 0