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
126481121 12648112 1 I 20160726 0 20160811 20160811 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
126481121 12648112 1 PS DEXAMETHASONE. DEXAMETHASONE 1 0 84 MG
126481121 12648112 2 SS DAUNORUBICIN DAUNORUBICIN 1 0 45.5 MG
126481121 12648112 3 SS ONCASPAR PEGASPARGASE 1 0 1400 IU
126481121 12648112 4 SS CYTARABINE. CYTARABINE 1 0 50 MG
126481121 12648112 5 SS METHOTREXATE. METHOTREXATE 1 0 20 MG
126481121 12648112 6 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 3.01 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126481121 12648112 HO
126481121 12648112 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126481121 12648112 Histiocytosis haematophagic
126481121 12648112 Human papilloma virus test positive
126481121 12648112 Mucormycosis
126481121 12648112 Neutropenia
126481121 12648112 Pyrexia
126481121 12648112 Respiratory failure
126481121 12648112 Septic shock

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

Event ID CASEID RPSR COD
126481121 12648112 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126481121 12648112 1 20160713 0
126481121 12648112 2 20160721 0
126481121 12648112 3 20160702 0
126481121 12648112 4 20160629 0
126481121 12648112 5 20160728 0
126481121 12648112 6 20160721 0