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
126580681 12658068 1 I 20160816 20160817 20160817 EXP GB-ROCHE-1814568 ROCHE 62.00 YR F Y 0.00000 20160817 CN GB GB

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
126580681 12658068 1 PS Rituximab RITUXIMAB 1 Unknown U U 103705
126580681 12658068 2 SS DOXORUBICIN DOXORUBICIN 1 Unknown SECOND ROUND U U 0
126580681 12658068 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown U U 0
126580681 12658068 4 SS PREDNISOLONE. PREDNISOLONE 1 Unknown SECOND ROUND U U 0
126580681 12658068 5 SS VINCRISTINE VINCRISTINE 1 Unknown SECOND ROUND U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126580681 12658068 1 Product used for unknown indication
126580681 12658068 2 Non-Hodgkin's lymphoma
126580681 12658068 3 Product used for unknown indication
126580681 12658068 4 Non-Hodgkin's lymphoma
126580681 12658068 5 Non-Hodgkin's lymphoma

Outcome of event

Event ID CASEID OUTC COD
126580681 12658068 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126580681 12658068 Adverse drug reaction
126580681 12658068 Oral pain
126580681 12658068 Pyrexia
126580681 12658068 Sepsis
126580681 12658068 Transfusion
126580681 12658068 Vomiting
126580681 12658068 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found