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
125244832 12524483 2 F 20160816 20160704 20160820 EXP FR-AUROBINDO-AUR-APL-2016-08349 AUROBINDO 59.00 YR M Y 0.00000 20160820 OT FR FR

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
125244832 12524483 1 SS Mycophenolate MYCOPHENOLIC ACID 1 Unknown 2 G, DAILY U U 0 2 G
125244832 12524483 2 PS PREDNISONE. PREDNISONE 1 Unknown 10 MG, DAILY U U 84774 10 MG
125244832 12524483 3 SS TACROLIMUS. TACROLIMUS 1 Unknown 3.5 MG, DAILY U U 0 3.5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125244832 12524483 1 Product used for unknown indication
125244832 12524483 2 Product used for unknown indication
125244832 12524483 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125244832 12524483 HO
125244832 12524483 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125244832 12524483 Abscess
125244832 12524483 Condition aggravated
125244832 12524483 Pain
125244832 12524483 Phaehyphomycosis
125244832 12524483 Purulent discharge

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

no results found

Therapies reported

no results found