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
127506173 12750617 3 F 20160823 20160916 20160915 20160919 EXP DE-PFIZER INC-2016416168 PFIZER 53.00 YR M Y 118.00000 KG 20160919 MD DE DE

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
127506173 12750617 1 SS GEMTUZUMAB OZOGAMICIN GEMTUZUMAB OZOGAMICIN 1 6.90 MG, DAILY Y 0 6.9 MG
127506173 12750617 2 PS Idarubicin IDARUBICIN 1 27.60 MG, DAILY Y 50734 27.6 MG SOLUTION FOR INJECTION
127506173 12750617 3 SS CYTARABINE. CYTARABINE 1 230 MG, DAILY Y 0 230 MG
127506173 12750617 4 SS ATRA TRETINOIN 1 90 MG, DAILY Y 0 90 MG
127506173 12750617 5 SS ATRA TRETINOIN 1 30 MG, DAILY Y 0 30 MG
127506173 12750617 6 SS ETOPOSIDE. ETOPOSIDE 1 230 MG, DAILY Y 0 230 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127506173 12750617 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127506173 12750617 Pancytopenia

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
127506173 12750617 1 20160719 20160719 0
127506173 12750617 2 20160719 20160723 0
127506173 12750617 3 20160719 20160725 0
127506173 12750617 4 20160724 20160726 0
127506173 12750617 5 20160727 20160808 0
127506173 12750617 6 20160719 20160721 0