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
125780731 12578073 1 I 20160406 20160719 20160721 20160721 EXP CH-ROCHE-1798521 ROCHE 76.00 YR F Y 71.00000 KG 20160721 MD CH CH

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
125780731 12578073 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) Y 103705 SOLUTION FOR INFUSION
125780731 12578073 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) Y 103705 SOLUTION FOR INFUSION
125780731 12578073 3 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) Y 103705 SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125780731 12578073 1 Non-Hodgkin's lymphoma
125780731 12578073 2 B-cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
125780731 12578073 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125780731 12578073 Arthralgia
125780731 12578073 Back pain
125780731 12578073 Chills
125780731 12578073 Dyspnoea
125780731 12578073 Feeling hot
125780731 12578073 Flank pain
125780731 12578073 Hypotension

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
125780731 12578073 1 20160406 20160406 0
125780731 12578073 2 20160502 20160502 0
125780731 12578073 3 20160601 20160622 0