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
126926831 12692683 1 I 20160209 20160826 20160829 20160829 EXP FR-ROCHE-1821281 ROCHE 13.00 YR M Y 0.00000 20160829 MD 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
126926831 12692683 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 375 MG/M**2 SOLUTION FOR INFUSION /cycle
126926831 12692683 2 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown 0
126926831 12692683 3 C NEORAL CYCLOSPORINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126926831 12692683 1 Nephrotic syndrome

Outcome of event

Event ID CASEID OUTC COD
126926831 12692683 HO
126926831 12692683 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126926831 12692683 C-reactive protein increased
126926831 12692683 Fatigue
126926831 12692683 Off label use
126926831 12692683 Pain in extremity
126926831 12692683 Product use issue
126926831 12692683 Pyrexia

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126926831 12692683 1 20150605 20160613 0