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
123157962 12315796 2 F 20160414 20160718 20160428 20160721 EXP DE-SEATTLE GENETICS-2016SGN00672 SEATTLE GENETICS 0.00 Y 0.00000 20160721 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
123157962 12315796 1 PS brentuximab vedotin BRENTUXIMAB VEDOTIN 1 Unknown 1.8 MG/KG, UNK U 125388 1.8 MG/KG INJECTION
123157962 12315796 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown 750 MG/M2, UNK U 0 750 MG/M**2 INJECTION
123157962 12315796 3 SS DOXORUBICIN DOXORUBICIN 1 Unknown 50 MG/M2, UNK U 0 50 MG/M**2 INJECTION
123157962 12315796 4 SS PREDNISONE. PREDNISONE 1 Unknown 100 MG, UNK U 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123157962 12315796 1 Hodgkin's disease
123157962 12315796 2 Hodgkin's disease
123157962 12315796 3 Hodgkin's disease
123157962 12315796 4 Hodgkin's disease

Outcome of event

Event ID CASEID OUTC COD
123157962 12315796 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123157962 12315796 Pyrexia
123157962 12315796 Respiratory tract infection
123157962 12315796 Syncope

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
123157962 12315796 1 20160204 20160407 0
123157962 12315796 2 20160204 20160407 0
123157962 12315796 3 20160204 20160207 0
123157962 12315796 4 20160205 20160412 0