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
126355611 12635561 1 I 20160727 20160803 20160809 20160809 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201608-003964 CONCORDIA 47.00 YR F Y 0.00000 20160809 OT 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
126355611 12635561 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown 1 MG, U U 21959 1 MG TABLET
126355611 12635561 2 SS ADOPORT TACROLIMUS 1 Unknown 0.5 MG, U U 0 .5 MG CAPSULE
126355611 12635561 3 SS ADOPORT TACROLIMUS 1 Unknown 1 MG, U U 0 1 MG CAPSULE
126355611 12635561 4 SS ARANESP DARBEPOETIN ALFA 1 Unknown 200 UG/ML, ` U U 0 INJECTION
126355611 12635561 5 SS SANDOZ LTD AZATHIOPRINE AZATHIOPRINE 1 Unknown 25 MG, U U 0 25 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126355611 12635561 1 Immunosuppression
126355611 12635561 2 Immunosuppression
126355611 12635561 4 Erythropoiesis abnormal
126355611 12635561 5 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126355611 12635561 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126355611 12635561 Infection

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

no results found

Therapies reported

no results found