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
125977891 12597789 1 I 20160714 20160726 20160726 EXP GB-BAUSCH-BL-2016-016970 BAUSCH AND LOMB 70.00 YR M Y 0.00000 20160726 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
125977891 12597789 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070 ENTERIC-COATED TABLET
125977891 12597789 2 SS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070 TABLET
125977891 12597789 3 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown U 0 TABLET
125977891 12597789 4 SS NEORAL CYCLOSPORINE 1 Unknown U 0 CAPSULE
125977891 12597789 5 SS NEORAL CYCLOSPORINE 1 Unknown U 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125977891 12597789 1 Immunosuppression
125977891 12597789 3 Immunosuppression
125977891 12597789 4 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
125977891 12597789 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125977891 12597789 Intestinal perforation

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

no results found

Therapies reported

no results found