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
125348491 12534849 1 I 20160622 0 20160706 20160706 DIR 4.89 YR M N 20.90000 KG 20160705 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
125348491 12534849 1 PS DEXAMETHASONE. DEXAMETHASONE 1 D D 0 19 MG
125348491 12534849 2 SS ERWINIA ASPARAGINASE ASPARAGINASE ERWINIA CHRYSANTHEMI 1 0 2050 IU
125348491 12534849 3 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 2.46 MG
125348491 12534849 4 SS CYTARABINE. CYTARABINE 1 0 70 MG
125348491 12534849 5 SS METHOTREXATE. METHOTREXATE 1 0 12 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125348491 12534849 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125348491 12534849 Escherichia sepsis
125348491 12534849 Hypoxia
125348491 12534849 Ischaemia
125348491 12534849 Pupil fixed
125348491 12534849 Septic shock
125348491 12534849 Tonsillar disorder

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

Event ID CASEID RPSR COD
125348491 12534849 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125348491 12534849 1 20160629 0
125348491 12534849 2 20160614 0
125348491 12534849 3 20160618 0
125348491 12534849 4 20160610 0
125348491 12534849 5 20160617 0