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
96980715 9698071 5 F 20130404 20160817 20131120 20160830 EXP IT-CELGENEUS-083-50794-13111902 CELGENE 65.00 YR M Y 0.00000 20160830 MD IT IT

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
96980715 9698071 1 PS VIDAZA AZACITIDINE 1 Subcutaneous Y U 50794 INJECTION
96980715 9698071 2 SS VIDAZA AZACITIDINE 1 Subcutaneous Y U 50794 INJECTION
96980715 9698071 3 SS VIDAZA AZACITIDINE 1 Subcutaneous Y U 50794 INJECTION
96980715 9698071 4 SS VIDAZA AZACITIDINE 1 Subcutaneous Y U 50794 142 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96980715 9698071 1 Myelodysplastic syndrome

Outcome of event

Event ID CASEID OUTC COD
96980715 9698071 HO
96980715 9698071 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
96980715 9698071 Pneumonia

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
96980715 9698071 1 20121102 0
96980715 9698071 2 20121130 0
96980715 9698071 3 20121227 0
96980715 9698071 4 20130124 20130131 0