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
126134491 12613449 1 I 20160627 20160729 20160802 20160802 EXP FR-ROCHE-1806339 ROCHE 56.00 YR M Y 0.00000 20160802 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
126134491 12613449 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
126134491 12613449 2 SS BENDAMUSTINE BENDAMUSTINE 1 Intravenous (not otherwise specified) U 0
126134491 12613449 3 C PREDNISOLONE. PREDNISOLONE 1 Unknown 0 80 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126134491 12613449 1 Non-Hodgkin's lymphoma
126134491 12613449 2 Non-Hodgkin's lymphoma
126134491 12613449 3 Premedication

Outcome of event

Event ID CASEID OUTC COD
126134491 12613449 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126134491 12613449 Progressive multifocal leukoencephalopathy

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
126134491 12613449 1 20160530 20160628 0
126134491 12613449 2 20160530 20160628 0