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
127241701 12724170 1 I 20160822 0 20160903 20160903 DIR FDA-CTU 59.48 YR F N 81.60000 KG 20160901 N MD US 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
127241701 12724170 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 1900 MG
127241701 12724170 2 SS CYTARABINE. CYTARABINE 1 0 1120 MG
127241701 12724170 3 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0 1600 MG
127241701 12724170 4 SS METHOTREXATE. METHOTREXATE 1 0 37.5 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127241701 12724170 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127241701 12724170 Diarrhoea
127241701 12724170 Febrile neutropenia
127241701 12724170 Klebsiella bacteraemia
127241701 12724170 Nausea
127241701 12724170 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
127241701 12724170 1 20160801 0
127241701 12724170 2 20160811 0
127241701 12724170 3 20160814 0
127241701 12724170 4 20160815 0