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
123164093 12316409 3 F 20160303 20160901 20160429 20160906 EXP DE-ROCHE-1748869 ROCHE 68.37 YR M Y 0.00000 20160906 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
123164093 12316409 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) AS PALLIATIVE TREATMENT U N7033B20,N7020B12,N7022B16 103705 100 MG SOLUTION FOR INFUSION
123164093 12316409 2 SS MABTHERA RITUXIMAB 1 U N7033B20,N7020B12,N7022B16 103705
123164093 12316409 3 C ZYDELIG IDELALISIB 1 Unknown AS PALLIATIVE THERAPY N7020B12,N7033B20,N7022B16 0
123164093 12316409 4 C ZYDELIG IDELALISIB 1 N7020B12,N7033B20,N7022B16 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123164093 12316409 1 Non-Hodgkin's lymphoma
123164093 12316409 2 Chronic lymphocytic leukaemia
123164093 12316409 3 Non-Hodgkin's lymphoma
123164093 12316409 4 Chronic lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
123164093 12316409 LT
123164093 12316409 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123164093 12316409 Blood pressure abnormal
123164093 12316409 Chills
123164093 12316409 Oxygen saturation decreased
123164093 12316409 Pyrexia
123164093 12316409 Tachycardia

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
123164093 12316409 1 201310 0
123164093 12316409 3 201310 0