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
124189122 12418912 2 F 201603 20160708 20160531 20160713 EXP DK-DKMA-WBS-0003561 DK-ROCHE-1765645 ROCHE 65.86 YR F Y 0.00000 20160713 MD DK DK

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
124189122 12418912 1 PS MABTHERA RITUXIMAB 1 Subcutaneous 1 DOSE/CYCLE 103705 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124189122 12418912 1 Diffuse large B-cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
124189122 12418912 OT
124189122 12418912 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124189122 12418912 Aphasia
124189122 12418912 JC virus test positive
124189122 12418912 Nervous system disorder
124189122 12418912 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
124189122 12418912 1 201508 0