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
126511711 12651171 1 I 20160724 0 20160812 20160812 DIR 1.81 YR F N 12.40000 KG 20160811 N OT 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
126511711 12651171 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 D D 0 520 MG
126511711 12651171 2 SS CYTARABINE. CYTARABINE 1 0 312 MG
126511711 12651171 3 SS MERCAPTOPURINE. MERCAPTOPURINE 1 0
126511711 12651171 4 SS ONCASPAR PEGASPARGASE 1 0 1275 IU
126511711 12651171 5 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 .64 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126511711 12651171 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126511711 12651171 Atelectasis
126511711 12651171 Bacillus infection
126511711 12651171 Bacterial infection
126511711 12651171 Enterovirus infection
126511711 12651171 Febrile neutropenia
126511711 12651171 Pneumonia
126511711 12651171 Pseudomonas test positive
126511711 12651171 Rhinovirus infection
126511711 12651171 Skin disorder

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

Event ID CASEID RPSR COD
126511711 12651171 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126511711 12651171 1 20160708 0
126511711 12651171 2 20160718 0
126511711 12651171 4 20160722 0
126511711 12651171 5 20160729 0