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
125246781 12524678 1 I 20110801 20121130 20160704 20160704 EXP GB-PFIZER INC-2012301578 PFIZER 0.00 Y 0.00000 20160704 MD GB GB

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
125246781 12524678 1 PS MITOXANTRONE HCL MITOXANTRONE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 12 MG, ONCE A DAY ON DAY 1 UNK 76871 12 MG
125246781 12524678 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 300 MG, ONCE DAILY ON DAY 1 AND 5 0 300 MG
125246781 12524678 3 SS FLUDARABINE FLUDARABINE PHOSPHATE 1 Oral 50 MG, ONCE DAILY ON DAY 1 AND 5 0 50 MG
125246781 12524678 4 SS RITUXIMAB RITUXIMAB 1 Intravenous (not otherwise specified) 980 MG, ONCE DAILY ON DAY 1 0 980 MG
125246781 12524678 5 C ACYCLOVIR. ACYCLOVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125246781 12524678 1 Chronic lymphocytic leukaemia
125246781 12524678 2 Chronic lymphocytic leukaemia
125246781 12524678 3 Chronic lymphocytic leukaemia
125246781 12524678 4 Chronic lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
125246781 12524678 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125246781 12524678 Febrile neutropenia

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
125246781 12524678 1 20110419 0
125246781 12524678 2 20110419 0
125246781 12524678 3 20110419 0
125246781 12524678 4 20110419 0