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
126672681 12667268 1 I 20160625 0 20160818 20160818 DIR 19.56 YR M N 75.00000 KG 20160817 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
126672681 12667268 1 PS DAUNORUBICIN DAUNORUBICIN 1 0 141 MG
126672681 12667268 2 SS PREDNISONE. PREDNISONE 1 0 3300 MG
126672681 12667268 3 SS ONCASPAR PEGASPARGASE 1 0 4700 IU
126672681 12667268 4 SS CYTARABINE. CYTARABINE 1 0 70 MG
126672681 12667268 5 SS METHOTREXATE. METHOTREXATE 1 0 15 MG
126672681 12667268 6 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 6 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126672681 12667268 HO
126672681 12667268 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126672681 12667268 Abdominal pain
126672681 12667268 Colitis
126672681 12667268 Gastrointestinal necrosis
126672681 12667268 Haemodynamic instability
126672681 12667268 Multiple organ dysfunction syndrome
126672681 12667268 Nausea
126672681 12667268 Neutropenic colitis
126672681 12667268 Pancytopenia
126672681 12667268 Peritonitis
126672681 12667268 Pyrexia
126672681 12667268 Vomiting

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
126672681 12667268 1 20160614 0
126672681 12667268 2 20160624 0
126672681 12667268 3 20160604 0
126672681 12667268 4 20160531 0
126672681 12667268 5 20160608 0
126672681 12667268 6 20160614 0