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
126431611 12643161 1 I 20160801 20160811 20160811 EXP AU-BAUSCH-BL-2016-018571 BAUSCH AND LOMB 0.00 M Y 0.00000 20160811 OT AU AU

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
126431611 12643161 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070
126431611 12643161 2 SS CYCLOSPORIN CYCLOSPORINE 1 Unknown U 0
126431611 12643161 3 SS METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Unknown U 0
126431611 12643161 4 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown U 0
126431611 12643161 5 SS TACROLIMUS. TACROLIMUS 1 Unknown U 0
126431611 12643161 6 SS STELARA USTEKINUMAB 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126431611 12643161 1 Product used for unknown indication
126431611 12643161 2 Product used for unknown indication
126431611 12643161 3 Product used for unknown indication
126431611 12643161 4 Product used for unknown indication
126431611 12643161 5 Product used for unknown indication
126431611 12643161 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126431611 12643161 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126431611 12643161 Cushingoid
126431611 12643161 Disease progression
126431611 12643161 Drug ineffective

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

no results found

Therapies reported

no results found