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
125976131 12597613 1 I 20160623 0 20160726 20160726 DIR 42.23 YR M N 72.40000 KG 20160715 N MD 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
125976131 12597613 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 1500 MG
125976131 12597613 2 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 80 MG
125976131 12597613 4 C ETOPOSIDE (VP-16) ETOPOSIDE 1 0 400 MG
125976131 12597613 6 C PREDNISONE. PREDNISONE 1 0 600 MG
125976131 12597613 8 C RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMERIC) RITUXIMAB 1 0 759 MG
125976131 12597613 10 C VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 3.2 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125976131 12597613 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125976131 12597613 Anaemia
125976131 12597613 Febrile neutropenia
125976131 12597613 Parainfluenzae virus infection

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
125976131 12597613 1 20160617 0
125976131 12597613 2 20160616 0
125976131 12597613 4 20160616 0
125976131 12597613 6 20160617 0
125976131 12597613 8 20160613 0
125976131 12597613 10 20160616 0