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
127428121 12742812 1 I 20160910 0 20160914 20160914 DIR FDA-CTU 9.86 YR M N 61.10000 KG 20160913 N MD COUNTRY NOT SPECIFIED 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
127428121 12742812 1 PS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 7 MG
127428121 12742812 3 SS ONCASPAR PEGASPARGASE 1 0 7900 IU
127428121 12742812 4 SS METHOTREXATE. METHOTREXATE 1 0 60 MG
127428121 12742812 6 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0 2700 MG
127428121 12742812 8 SS CYTARABINE. CYTARABINE 1 0 1896 MG
127428121 12742812 9 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 3160 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127428121 12742812 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127428121 12742812 Aspartate aminotransferase increased
127428121 12742812 Bacterial test positive
127428121 12742812 Blood bilirubin increased
127428121 12742812 Hypotension
127428121 12742812 Neutropenia
127428121 12742812 Oxygen saturation decreased
127428121 12742812 Pyrexia
127428121 12742812 Sepsis

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

Event ID CASEID RPSR COD
127428121 12742812 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127428121 12742812 1 20160905 0
127428121 12742812 3 20160829 0
127428121 12742812 4 20160808 0
127428121 12742812 8 20160825 0
127428121 12742812 9 20160815 0