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
124935692 12493569 2 F 20160704 20160623 20160708 PER US-PFIZER INC-2016306653 PFIZER 33.00 YR F Y 0.00000 20160708 OT 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
124935692 12493569 1 PS CYTARABINE. CYTARABINE 1 UNK U 71868
124935692 12493569 2 SS BLINATUMOMAB BLINATUMOMAB 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124935692 12493569 1 B-cell type acute leukaemia
124935692 12493569 2 B-cell type acute leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124935692 12493569 Acute lymphocytic leukaemia recurrent
124935692 12493569 Disease progression

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
124935692 12493569 1 20151020 0
124935692 12493569 2 20151103 0