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
125303831 12530383 1 I 20160501 0 20160705 20160705 DIR 2.08 YR F N 10.74000 KG 20160630 N 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
125303831 12530383 1 PS DEXAMETHASONE. DEXAMETHASONE 1 0 68.6 MG
125303831 12530383 2 SS ONCASPAR PEGASPARGASE 1 0 1200 IU
125303831 12530383 4 C CYTARABINE. CYTARABINE 1 0 30 MG
125303831 12530383 5 SS LEUCOVORIN CALCIUM. LEUCOVORIN CALCIUM 1 0 4.8 MG
125303831 12530383 6 SS METHOTREXATE. METHOTREXATE 1 0 8 MG
125303831 12530383 7 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 2.14 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125303831 12530383 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125303831 12530383 Abdominal pain
125303831 12530383 Hepatic ischaemia
125303831 12530383 Intestinal ischaemia
125303831 12530383 Ischaemic pancreatitis
125303831 12530383 Necrosis
125303831 12530383 Neutrophil count increased
125303831 12530383 Pyrexia
125303831 12530383 Spleen disorder
125303831 12530383 Superior mesenteric artery syndrome
125303831 12530383 Systemic mycosis
125303831 12530383 Thrombosis

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
125303831 12530383 1 20160430 0
125303831 12530383 2 20160408 0
125303831 12530383 4 20160404 0
125303831 12530383 5 20160415 0
125303831 12530383 6 20160412 0
125303831 12530383 7 20160419 0