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
126398101 12639810 1 I 20160727 20160803 20160810 20160810 EXP GB-AMGEN-GBRSP2016101138 AMGEN 47.00 YR A F Y 0.00000 20160810 CN 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
126398101 12639810 1 PS ARANESP DARBEPOETIN ALFA 1 Unknown 200 MUG/ML, UNK U 103951 SOLUTION FOR INJECTION
126398101 12639810 2 SS ADOPORT TACROLIMUS 1 Unknown 1 MG, UNK 0 1 MG
126398101 12639810 3 SS ADOPORT TACROLIMUS 1 Unknown 0.5 MG, UNK 0 .5 MG
126398101 12639810 4 SS PREDNISOLON PREDNISOLONE 1 Unknown 1 MG, UNK 0 1 MG
126398101 12639810 5 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown 25 MG, UNK 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126398101 12639810 1 Erythropoiesis abnormal
126398101 12639810 2 Immunosuppression
126398101 12639810 4 Immunosuppression
126398101 12639810 5 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126398101 12639810 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126398101 12639810 Infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found