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
117885523 11788552 3 F 20160704 20151201 20160714 EXP GB-AMGEN-GBRSP2015125497 AMGEN 35.00 YR A F Y 0.00000 20160714 MD GB GB

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
117885523 11788552 1 PS ARANESP DARBEPOETIN ALFA 1 Unknown 130 MUG, EVERY FIVE DAYS 103951 130 UG SOLUTION FOR INJECTION
117885523 11788552 2 SS EPOGEN ERYTHROPOIETIN 1 Unknown U 0 UNKNOWN FORMULATION
117885523 11788552 3 C PREDNISOLONE. PREDNISOLONE 1 10 MG, QD 0 10 MG QD
117885523 11788552 4 C MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 1 G, BID 0 1 G BID
117885523 11788552 5 C RAMIPRIL. RAMIPRIL 1 0
117885523 11788552 6 C SODIUM BICARBONATE. SODIUM BICARBONATE 1 0
117885523 11788552 7 C ALFACALCIDOL ALFACALCIDOL 1 0
117885523 11788552 8 C CALCICHEW CALCIUM CARBONATE 1 0
117885523 11788552 9 C RANITIDINE. RANITIDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117885523 11788552 1 Anaemia
117885523 11788552 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117885523 11788552 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117885523 11788552 Anaemia
117885523 11788552 Feeling abnormal
117885523 11788552 Reticulocyte count decreased
117885523 11788552 Therapeutic response decreased

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
117885523 11788552 1 2009 0