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
126481721 12648172 1 I 20160731 0 20160811 20160811 DIR 51.42 YR M N 112.70000 KG 20160808 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
126481721 12648172 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 D D 0 2430 MG
126481721 12648172 2 SS CYTARABINE. CYTARABINE 1 0 2912 MG
126481721 12648172 3 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0 2100 MG
126481721 12648172 4 SS METHOTREXATE. METHOTREXATE 1 0 48 MG
126481721 12648172 5 SS ONCASPAR PEGASPARGASE 1 3750 UNIT? 0 3750 DF

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126481721 12648172 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126481721 12648172 Body temperature increased
126481721 12648172 Chills
126481721 12648172 Diarrhoea
126481721 12648172 Nausea
126481721 12648172 Neutrophil count abnormal
126481721 12648172 Vomiting

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
126481721 12648172 1 20160707 0
126481721 12648172 2 20160717 0
126481721 12648172 3 20160720 0
126481721 12648172 4 20160707 0
126481721 12648172 5 20160623 0