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
126339661 12633966 1 I 20160731 0 20160808 20160808 DIR 50.58 YR M N 111.40000 KG 20160805 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
126339661 12633966 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 2250 MG
126339661 12633966 2 SS CYTARABINE. CYTARABINE 1 0 1352 MG
126339661 12633966 3 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0 1950 MG
126339661 12633966 4 SS METHOTREXATE. METHOTREXATE 1 0 25 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126339661 12633966 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126339661 12633966 Arthralgia
126339661 12633966 Blood culture positive
126339661 12633966 Chills
126339661 12633966 Malaise
126339661 12633966 Mucosal inflammation
126339661 12633966 Myalgia
126339661 12633966 Night sweats
126339661 12633966 Pancytopenia
126339661 12633966 Pseudomonas test positive

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
126339661 12633966 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126339661 12633966 1 20160718 0
126339661 12633966 2 20160728 0
126339661 12633966 3 20160730 0
126339661 12633966 4 20160725 0