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
125695561 12569556 1 I 20160708 0 20160718 20160718 DIR 14.68 YR F N 84.50000 KG 20160715 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
125695561 12569556 1 PS DAUNORUBICIN DAUNORUBICIN 1 0 145 MG
125695561 12569556 2 SS ONCASPAR PEGASPARGASE 1 0 4750 IU
125695561 12569556 3 SS PREDNISONE. PREDNISONE 1 0 2880 MG
125695561 12569556 4 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 6 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125695561 12569556 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125695561 12569556 Activated partial thromboplastin time prolonged
125695561 12569556 Bilirubin conjugated increased
125695561 12569556 Blood bilirubin increased
125695561 12569556 Blood fibrinogen decreased
125695561 12569556 Catheter site discharge
125695561 12569556 Condition aggravated
125695561 12569556 Gamma-glutamyltransferase increased
125695561 12569556 Hepatic congestion
125695561 12569556 Prothrombin time prolonged

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

Event ID CASEID RPSR COD
125695561 12569556 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125695561 12569556 1 20160706 0
125695561 12569556 2 20160625 0
125695561 12569556 3 20160715 0
125695561 12569556 4 20160706 0