The Safety Rates Drug Report

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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
1023578512 10235785 12 F 20160801 20140613 20160812 EXP NO-PFIZER INC-2014156420 PFIZER LAURITZSEN G. HIGH 7 YEAR-SURVIVAL RATES IN ADULT LYMPHOBLASTIC LYMPHOMA AFTER TREATMENT WITH A NORWEGIAN INTENSIFIED ALL INDUCTION, HIGH-DOSE BEAM, AUTOLOGOUS STEM CELL SUPPORT AND MEDIASTINAL RATIATION THERAPY. HAEMATOLOGICA. 2012;97 (S1):183 46.00 YR M Y 0.00000 20160812 OT NO NO

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
1023578512 10235785 1 PS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 Intravenous (not otherwise specified) 1.5 MG/M2, MAX 2.0 MG (DAYS 1, 8, 15, 22, AND 29) 71484 1.5 MG/M**2
1023578512 10235785 2 SS CYTARABINE. CYTARABINE 1 Intravenous (not otherwise specified) 200 MG/M2,(DAYS 43-47) 71868 200 MG/M**2
1023578512 10235785 3 SS CYTARABINE. CYTARABINE 1 Intrathecal 40 MG, (DAYS 78, 92, 106) 71868 40 MG
1023578512 10235785 4 SS DOXORUBICIN HCL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) 30 MG/M2, (DAYS 8, 15, AND 22) 50467 30 MG/M**2
1023578512 10235785 5 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intrathecal 15 MG, (DAYS 15, 29, 43, 64) 11719 15 MG
1023578512 10235785 6 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intravenous (not otherwise specified) 1500 MG/M2,(DAYS 64 AND 78) 11719 1500 MG/M**2
1023578512 10235785 7 SS DAUNORUBICIN DAUNORUBICIN 1 Intravenous (not otherwise specified) 50 MG/M2,(DAYS 43, 45, AND 47) 0 50 MG/M**2
1023578512 10235785 8 SS MERCAPTOPURINE. MERCAPTOPURINE 1 Intravenous (not otherwise specified) 35 MG/M2, (DAYS 64-111) 0 35 MG/M**2
1023578512 10235785 9 SS L-ASPARAGINASE ASPARAGINASE 1 Intravenous (not otherwise specified) 10000 IU, (DAYS 8-21) 0 10000 IU
1023578512 10235785 10 SS THIOGUANINE THIOGUANINE 1 Intravenous (not otherwise specified) 150 MG/M2, (DAYS 43-47) 0 150 MG/M**2
1023578512 10235785 11 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) 750 MG/M2,(DAYS 15, 22, AND 29) 0 750 MG/M**2
1023578512 10235785 12 SS G-CSF GRANULOCYTE COLONY-STIMULATING FACTOR NOS 1 10 MCG/KG/DAY 0
1023578512 10235785 13 SS PREDNISOLONE. PREDNISOLONE 1 Oral 40 MG/M2, (DAY 1-29, TAPER TO DAY 35) 0 40 MG/M**2
1023578512 10235785 14 SS PREDNISOLONE. PREDNISOLONE 1 Intrathecal 10 MG, UNK 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1023578512 10235785 1 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 2 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 4 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 5 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 7 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 8 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 9 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 10 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 11 Precursor T-lymphoblastic lymphoma/leukaemia
1023578512 10235785 12 Peripheral blood stem cell apheresis
1023578512 10235785 13 Precursor T-lymphoblastic lymphoma/leukaemia

Outcome of event

Event ID CASEID OUTC COD
1023578512 10235785 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
1023578512 10235785 Multiple organ dysfunction syndrome
1023578512 10235785 Venoocclusive disease

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

no results found

Therapies reported

no results found