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
127754411 12775441 1 I 20160918 0 20160920 20160920 DIR FDA-CTU 42.71 YR F N 68.00000 KG 20160919 N 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
127754411 12775441 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 3560 MG
127754411 12775441 3 SS CYTARABINE. CYTARABINE 1 0 1608 MG
127754411 12775441 4 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0 1900 MG
127754411 12775441 5 SS METHOTREXATE. METHOTREXATE 1 0 37.5 MG
127754411 12775441 6 SS PEG-L-ASPARAGINASE PEGASPARGASE 1 0 3560 IU

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127754411 12775441 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127754411 12775441 Abdominal pain
127754411 12775441 Constipation
127754411 12775441 Febrile neutropenia
127754411 12775441 Gastrointestinal disorder
127754411 12775441 Haemoglobin decreased
127754411 12775441 Nausea
127754411 12775441 Pneumonia
127754411 12775441 Rhinorrhoea
127754411 12775441 Urinary tract infection
127754411 12775441 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
127754411 12775441 1 20160913 0
127754411 12775441 3 20160916 0
127754411 12775441 4 20160917 0
127754411 12775441 5 20160830 0
127754411 12775441 6 20160823 0