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
125922491 12592249 1 I 20160719 20160726 20160726 EXP US-ENDO PHARMACEUTICALS INC.-2016-004623 ENDO 53.00 YR M Y 0.00000 20160726 MD US 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
125922491 12592249 1 PS RHEUMATREX METHOTREXATE SODIUM 1 Unknown U 8085 UNKNOWN
125922491 12592249 2 SS PREDNISONE TABLETS PREDNISONE 1 Unknown U 40256 UNKNOWN
125922491 12592249 3 SS VINCRISTINE VINCRISTINE 1 Unknown U 0 UNKNOWN
125922491 12592249 4 SS PEG/L-ASPARAGINASE PEGASPARGASE 1 Unknown U 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125922491 12592249 1 Acute lymphocytic leukaemia
125922491 12592249 2 Acute lymphocytic leukaemia
125922491 12592249 3 Acute lymphocytic leukaemia
125922491 12592249 4 Acute lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
125922491 12592249 OT
125922491 12592249 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125922491 12592249 Blood bilirubin increased
125922491 12592249 Blood glucose increased
125922491 12592249 Coagulopathy
125922491 12592249 Jaundice
125922491 12592249 Meningitis bacterial
125922491 12592249 Nausea
125922491 12592249 Vomiting

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

no results found

Therapies reported

no results found