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
126673161 12667316 1 I 20160714 0 20160818 20160818 DIR 78.37 YR F N 60.00000 KG 20160817 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
126673161 12667316 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 1250 MG
126673161 12667316 2 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 85 MG
126673161 12667316 3 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 2 MG
126673161 12667316 4 SS RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMERIC) RITUXIMAB 1 0 600 MG
126673161 12667316 5 SS PREDNISONE. PREDNISONE 1 0 850 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126673161 12667316 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126673161 12667316 Febrile neutropenia

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
126673161 12667316 1 20160707 0
126673161 12667316 2 20160707 0
126673161 12667316 3 20160707 0
126673161 12667316 4 20160707 0
126673161 12667316 5 20160710 0