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
126140381 12614038 1 I 20160709 0 20160801 20160801 DIR 56.94 YR M N 103.45000 KG 20160721 N US

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
126140381 12614038 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 2410 MG
126140381 12614038 3 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 128 MG
126140381 12614038 5 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0 644 MG
126140381 12614038 6 SS PREDNISONE. PREDNISONE 1 0 1300 MG
126140381 12614038 8 SS RITUXIMAB (MOAB C2B8 ANTI C20, CHIMERIC) RITUXIMAB 1 0 840 MG
126140381 12614038 9 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 3.6 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126140381 12614038 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126140381 12614038 Febrile neutropenia
126140381 12614038 Haemoglobin decreased
126140381 12614038 Platelet count decreased

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
126140381 12614038 1 20160703 0
126140381 12614038 3 20160702 0
126140381 12614038 5 20160702 0
126140381 12614038 6 20160704 0
126140381 12614038 8 20160629 0
126140381 12614038 9 20160702 0