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
122342944 12234294 4 F 201512 20160808 20160404 20160812 EXP DE-ROCHE-1736449 ROCHE 67.31 YR M Y 71.00000 KG 20160812 MD DE DE

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
122342944 12234294 1 PS MABTHERA RITUXIMAB 1 Unknown FOR 5 MONTHS 103705
122342944 12234294 2 SS MABTHERA RITUXIMAB 1 Unknown 103705
122342944 12234294 3 SS IDELALISIB IDELALISIB 1 Unknown 0
122342944 12234294 4 SS IDELALISIB IDELALISIB 1 Unknown 0
122342944 12234294 5 C BENDAMUSTINE BENDAMUSTINE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122342944 12234294 1 Chronic lymphocytic leukaemia
122342944 12234294 3 Chronic lymphocytic leukaemia
122342944 12234294 5 Chronic lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
122342944 12234294 DS
122342944 12234294 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122342944 12234294 Dementia
122342944 12234294 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
122342944 12234294 1 201412 201505 0
122342944 12234294 2 201103 201106 0
122342944 12234294 3 201412 201509 0
122342944 12234294 4 201103 201106 0
122342944 12234294 5 201103 201106 0