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
126893341 12689334 1 I 20160722 0 20160825 20160825 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
126893341 12689334 1 PS ONCASPAR PEGASPARGASE 1 0 4475 IU
126893341 12689334 2 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 8 MG
126893341 12689334 3 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0 800 MG
126893341 12689334 4 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0 865 MG
126893341 12689334 5 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 5596 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126893341 12689334 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126893341 12689334 Apnoea
126893341 12689334 Blood pressure decreased
126893341 12689334 Feeling abnormal
126893341 12689334 Generalised tonic-clonic seizure
126893341 12689334 Hyperhidrosis
126893341 12689334 Loss of consciousness
126893341 12689334 Pallor
126893341 12689334 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
126893341 12689334 1 20160617 0
126893341 12689334 1 20160722 0
126893341 12689334 2 20160722 0
126893341 12689334 3 20160616 0
126893341 12689334 4 20160712 0
126893341 12689334 5 20160712 0