The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

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
114972253 11497225 3 F 20150117 20160831 20150911 20160909 EXP US-PFIZER INC-2015297305 PFIZER 14.00 YR F Y 56.00000 KG 20160909 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
114972253 11497225 1 PS CRIZOTINIB CRIZOTINIB 1 Oral COURSE A, B: 165 MG/M2, CYCLIC TWICE DAILY ON DAYS 1-21 33990 MG/M2 Y 202570 165 MG/M**2
114972253 11497225 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intrathecal PROPHASE: 7.5-12MG INTRATHECAL (IT) ON DAY 1 (AGE BASED DOSING) Y 11719
114972253 11497225 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intravenous (not otherwise specified) COURSE A, B: 3000 MG/M2, CYCLIC (OVER 3 HOURS ON DAY 1) Y 11719 3000 MG/M**2
114972253 11497225 4 SS CYTARABINE. CYTARABINE 1 Intrathecal PROPHASE: 15-24 MG ON DAY 1 (AGE BASED DOSING) Y 71868
114972253 11497225 5 SS CYTARABINE. CYTARABINE 1 Intravenous (not otherwise specified) COURSE A: 150 MG/M2, CYCLIC OVER 1-30 MINUTES EVERY 12 HOURS ON DAYS 4 AND 5 (TOTAL 4 DOSES) Y 71868 150 MG/M**2
114972253 11497225 6 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral PROPHASE: 5MG/M2 ORAL (PO) ONCE DAILY (QD) ON DAYS 1-2, AND 5MG/M2 PO TWICE DAILY (BID) ON DAYS 3-5 82 MG Y 0 5 MG/M**2
114972253 11497225 7 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral COURSE A, B: 5 MG, CYCLIC (TWICE DAILY ON DAYS 1-5) 82 MG Y 0 5 MG
114972253 11497225 8 SS ETOPOSIDE. ETOPOSIDE 1 Intravenous (not otherwise specified) COURSE A: 100 MG/M2, CYCLIC (OVER 2 HOURS ON DAYS 4 AND 5) Y 0 100 MG/M**2
114972253 11497225 9 SS IFOSFAMIDE. IFOSFAMIDE 1 Intravenous (not otherwise specified) COURSE A: 800 MG/M2, CYCLIC (OVER 60 MIN ON DAYS 1-5) Y 0 800 MG/M**2
114972253 11497225 10 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) PROPHASE: 200MG/M2 INTRAVENOUS (IV) OVER 15-30 MINUTES ON DAYS 1 AND 2 0 200 MG/M**2
114972253 11497225 11 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) COURSE B: 200 MG/M2, CYCLIC ( OVER 15-30 MINUTES ON DAYS 1 AND 2) 0 200 MG/M**2
114972253 11497225 12 C HYDROCORTISONE. HYDROCORTISONE 1 Intrathecal PROPHASE: 7.5-12MG, ON DAY 1 0
114972253 11497225 13 C DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) COURSE B: 25 MG/M2, CYCLIC (OVER 1-15 MIN ON DAYS 4 AND 5) 0 25 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114972253 11497225 1 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 2 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 4 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 6 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 8 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 9 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 10 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 12 Anaplastic large cell lymphoma T- and null-cell types
114972253 11497225 13 Anaplastic large cell lymphoma T- and null-cell types

Outcome of event

Event ID CASEID OUTC COD
114972253 11497225 HO
114972253 11497225 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114972253 11497225 Pyrexia
114972253 11497225 White blood cell count decreased

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
114972253 11497225 1 20141007 20150121 0
114972253 11497225 3 20141007 20150108 0
114972253 11497225 5 20141010 20150112 0
114972253 11497225 7 20141007 20150112 0
114972253 11497225 8 20141010 20150112 0
114972253 11497225 9 20141007 20150111 0
114972253 11497225 11 20141220 0
114972253 11497225 13 20141220 0