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
124666852 12466685 2 F 20160802 20160615 20160812 EXP GB-BAUSCH-BL-2016-013818 BAUSCH AND LOMB 52.00 YR M Y 0.00000 20160812 MD 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
124666852 12466685 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070 5 MG TABLET
124666852 12466685 2 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown U 0 50 MG
124666852 12466685 3 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown U 0 25 MG
124666852 12466685 4 SS ADOPORT TACROLIMUS 1 Unknown U 0 1 MG CAPSULE
124666852 12466685 5 SS ADOPORT TACROLIMUS 1 Unknown U 0 .5 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124666852 12466685 1 Immunosuppression
124666852 12466685 2 Immunosuppression
124666852 12466685 4 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
124666852 12466685 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124666852 12466685 Abdominal pain
124666852 12466685 Malaise

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

no results found

Therapies reported

no results found