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
126837011 12683701 1 I 20160722 0 20160824 20160824 DIR 16.06 YR M N 62.90000 KG 20160823 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
126837011 12683701 1 PS ONCASPAR PEGASPARGASE 1 D D 0 4475 IU
126837011 12683701 2 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 8 MG
126837011 12683701 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 5596 MG
126837011 12683701 4 SS CYTARABINE. CYTARABINE 1 0 1040 MG
126837011 12683701 5 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0 865 MG
126837011 12683701 6 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0 800 MG
126837011 12683701 7 SS METHOTREXATE. METHOTREXATE 1 0 60 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126837011 12683701 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126837011 12683701 Apnoea
126837011 12683701 Blood pressure decreased
126837011 12683701 Feeling abnormal
126837011 12683701 Generalised tonic-clonic seizure
126837011 12683701 Hyperhidrosis
126837011 12683701 Loss of consciousness
126837011 12683701 Pallor
126837011 12683701 Vomiting

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

Event ID CASEID RPSR COD
126837011 12683701 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126837011 12683701 1 20160617 0
126837011 12683701 1 20160722 0
126837011 12683701 2 20160722 0
126837011 12683701 3 20160712 0
126837011 12683701 4 20160613 0
126837011 12683701 5 20160712 0
126837011 12683701 6 20160616 0
126837011 12683701 7 20160624 0