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
125637991 12563799 1 I 201604 20160707 20160716 20160716 EXP US-AMGEN-USASP2016089225 AMGEN 71.00 YR E F Y 63.50000 KG 20160716 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
125637991 12563799 1 PS PROCRIT ERYTHROPOIETIN 1 Unknown 40000 UNIT, QWK G198941A 103234 SOLUTION FOR INJECTION /wk
125637991 12563799 2 SS RAPAMUNE SIROLIMUS 1 Oral 1 MG, QD 0 1 MG QD
125637991 12563799 3 C WARFARIN WARFARIN 1 Oral 2 MG, TWO DAYS OUT OF WEEK 0 2 MG
125637991 12563799 4 C WARFARIN WARFARIN 1 Oral 4 MG, THREE DAYS 0 4 MG
125637991 12563799 5 C CLONIDINE. CLONIDINE 1 Oral 2 MG, THREE TIMES A DAY 0 2 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125637991 12563799 1 Haemoglobin decreased
125637991 12563799 2 Prophylaxis
125637991 12563799 3 Hypercoagulation
125637991 12563799 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125637991 12563799 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125637991 12563799 Blood viscosity increased
125637991 12563799 Dyspnoea
125637991 12563799 Haemoglobin decreased
125637991 12563799 Swelling

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
125637991 12563799 2 2005 0
125637991 12563799 3 20160406 0
125637991 12563799 4 20160406 0