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
125972611 12597261 1 I 20160715 0 20160726 20160726 DIR 41.37 YR F N 148.40000 KG 20160725 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
125972611 12597261 1 PS MERCAPTOPURINE. MERCAPTOPURINE 1 D D 0 1400 MG
125972611 12597261 2 SS METHOTREXATE. METHOTREXATE 1 0 200 MG
125972611 12597261 3 SS PREDNISONE. PREDNISONE 1 0 800 MG
125972611 12597261 4 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 2 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125972611 12597261 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125972611 12597261 Abdominal pain
125972611 12597261 Acute lymphocytic leukaemia
125972611 12597261 Atelectasis
125972611 12597261 Chest pain
125972611 12597261 Dyspnoea
125972611 12597261 Fatigue
125972611 12597261 Hyperbilirubinaemia
125972611 12597261 Neutropenia
125972611 12597261 Pyrexia
125972611 12597261 Splenomegaly
125972611 12597261 Thrombocytopenia

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

Event ID CASEID RPSR COD
125972611 12597261 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125972611 12597261 1 20160502 0
125972611 12597261 2 20160502 0
125972611 12597261 3 20160506 0
125972611 12597261 4 20160502 0