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
126399231 12639923 1 I 20160726 0 20160809 20160809 DIR 2.15 YR F N 13.00000 KG 20160808 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
126399231 12639923 1 PS DEXAMETHASONE. DEXAMETHASONE 1 0 84 MG
126399231 12639923 2 SS DAUNORUBICIN DAUNORUBICIN 1 0 45.5 MG
126399231 12639923 3 SS ONCASPAR PEGASPARGASE 1 0 1400 IU
126399231 12639923 4 SS CYTARABINE. CYTARABINE 1 0 50 MG
126399231 12639923 5 SS METHOTREXATE. METHOTREXATE 1 0 20 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126399231 12639923 DE
126399231 12639923 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126399231 12639923 Abdominal distension
126399231 12639923 Histiocytosis haematophagic
126399231 12639923 Human metapneumovirus test positive
126399231 12639923 Mucormycosis
126399231 12639923 Neutropenia
126399231 12639923 Pyrexia
126399231 12639923 Respiratory failure
126399231 12639923 Septic shock

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
126399231 12639923 1 20160713 0
126399231 12639923 2 20160721 0
126399231 12639923 3 20160702 0
126399231 12639923 4 20160629 0
126399231 12639923 5 20160728 0