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
126552881 12655288 1 I 20160802 20160816 20160816 EXP SE-PFIZER INC-2016373083 PFIZER PAUL, C.. A RANDOMIZED COMPARISON OF DOXORUBICIN AND DOXORUBICIN-DNA IN THE TREATMENT OF ACUTE NONLYMPHOBLASTIC LEUKEMIA. LEUKEMIA AND LYMPHOMA. 1991;3(5-6):355-364 10.00 YR F Y 0.00000 20160816 OT SE SE

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
126552881 12655288 1 PS DOXORUBICIN HCL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) 45 MG/M2, COURSES 1-4 U 50467 45 MG/M**2
126552881 12655288 2 SS DOXORUBICIN HCL DOXORUBICIN HYDROCHLORIDE 1 30 MG/M2, 1X/DAY (ON DAY 1 ) U 50467 30 MG/M**2 QD
126552881 12655288 3 C ARA-C CYTARABINE 1 Intravenous (not otherwise specified) 200 MG/M2, (DURING 6 H ON DAYS 1-5) 0 200 MG/M**2
126552881 12655288 4 C VINCRISTINE VINCRISTINE 1 Intravenous (not otherwise specified) 2 MG, (ON DAY 1) 0 2 MG
126552881 12655288 5 C PREDNISOLONE. PREDNISOLONE 1 Intravenous bolus 7.5 MG/M2, (ON DAYS 1-5) 0 7.5 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126552881 12655288 1 Lymphocytic leukaemia
126552881 12655288 3 Acute myeloid leukaemia
126552881 12655288 4 Acute myeloid leukaemia
126552881 12655288 5 Acute myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
126552881 12655288 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126552881 12655288 Atrial fibrillation

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found