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
125809011 12580901 1 I 20160714 20160721 20160721 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201607-003638 CONCORDIA 70.00 YR M Y 0.00000 20160721 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
125809011 12580901 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown 5 MG, UNK U U 21959 5 MG
125809011 12580901 2 SS PREDNISOLONE. PREDNISOLONE 1 Unknown 2.5 MG, UNK U U 21959 2.5 MG
125809011 12580901 3 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown 25 MG, UNK U U 0 25 MG TABLET
125809011 12580901 4 SS NEORAL CYCLOSPORINE 1 Unknown 25 MG, UNK U U 0 25 MG CAPSULE
125809011 12580901 5 SS NEORAL CYCLOSPORINE 1 Unknown 50 MG, UNK U U 0 50 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125809011 12580901 1 Immunosuppression
125809011 12580901 3 Immunosuppression
125809011 12580901 4 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
125809011 12580901 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125809011 12580901 Intestinal perforation

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

no results found

Therapies reported

no results found