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
127573671 12757367 1 I 20160318 20160915 20160919 20160919 EXP CN-ROCHE-1830797 ROCHE 69.00 YR M Y 58.00000 KG 20160919 OT CN CN

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
127573671 12757367 1 PS MABTHERA RITUXIMAB 1 Intravenous drip U H0765 103705 600 MG SOLUTION FOR INFUSION QD
127573671 12757367 2 SS EPIRUBICIN HYDROCHLORIDE. EPIRUBICIN HYDROCHLORIDE 1 Intravenous drip U 15042421 0 120 MG QD
127573671 12757367 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous drip U 0 .8 G QD
127573671 12757367 4 SS Vincristine VINCRISTINE 1 Unknown U 0
127573671 12757367 5 SS PREDNISONE. PREDNISONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127573671 12757367 1 B-cell lymphoma
127573671 12757367 2 B-cell lymphoma
127573671 12757367 3 B-cell lymphoma
127573671 12757367 4 B-cell lymphoma
127573671 12757367 5 B-cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
127573671 12757367 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127573671 12757367 Bone marrow failure

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
127573671 12757367 1 20160311 20160311 0
127573671 12757367 2 20160311 20160311 0
127573671 12757367 3 20160312 0