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
127008134 12700813 4 F 2015 20160922 20160830 20160929 EXP US-AMGEN-USASP2016113037 AMGEN 85.00 YR E M Y 77.55000 KG 20160929 OT 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
127008134 12700813 1 PS PROCRIT ERYTHROPOIETIN 1 Subcutaneous 40,000 UNITS, WEEKLY G262423A 103234 SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127008134 12700813 1 Nephrogenic anaemia

Outcome of event

Event ID CASEID OUTC COD
127008134 12700813 HO
127008134 12700813 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127008134 12700813 Aplasia pure red cell
127008134 12700813 Blood iron abnormal
127008134 12700813 Blood product transfusion dependent
127008134 12700813 Drug ineffective
127008134 12700813 Haemoglobin decreased
127008134 12700813 Iron binding capacity total abnormal
127008134 12700813 Serum ferritin abnormal
127008134 12700813 Transferrin abnormal

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
127008134 12700813 1 20160819 0