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
127173731 12717373 1 I 20160821 20160829 20160906 20160906 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201608-004358 CONCORDIA 71.00 YR M Y 0.00000 20160906 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
127173731 12717373 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 21959 TABLET
127173731 12717373 2 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown U 0 TABLET
127173731 12717373 3 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown U 0 TABLET
127173731 12717373 4 SS NEORAL CYCLOSPORINE 1 Unknown U 0 CAPSULE
127173731 12717373 5 SS NEORAL CYCLOSPORINE 1 Unknown U 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127173731 12717373 1 Immunosuppression
127173731 12717373 2 Immunosuppression
127173731 12717373 4 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
127173731 12717373 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127173731 12717373 Death

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

no results found

Therapies reported

no results found