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
101764987 10176498 7 F 20140111 20160808 20140516 20160818 EXP US-PFIZER INC-2014125475 PFIZER 16.00 YR F Y 72.30000 KG 20160818 MD 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
101764987 10176498 1 PS CRIZOTINIB CRIZOTINIB 1 Oral COURSE A: 165 MG/M2, (250MG) 2X/DAY ON DAYS 1-21 Y 202570 250 MG BID
101764987 10176498 2 SS CRIZOTINIB CRIZOTINIB 1 Oral UNK Y 202570
101764987 10176498 3 SS CRIZOTINIB CRIZOTINIB 1 Oral LOWER DOSE PER PROTOCOL (DOSE GROUP C) Y 202570
101764987 10176498 4 SS HYDROCORTISONE ACETATE. HYDROCORTISONE ACETATE 1 Intrathecal PROPHASE (CYCLE= 5 DAYS): 7.5-12 MG ON DAY 1 (AGE BASED DOSING) 8917
101764987 10176498 5 SS CYTARABINE. CYTARABINE 1 Intrathecal PROPHASE (CYCLE= 5 DAYS): 15-24 MG ON DAY 1 (AGE BASED DOSING), (24 MG) 71868 24 MG
101764987 10176498 6 SS CYTARABINE. CYTARABINE 1 Intravenous (not otherwise specified) COURSE A: 150MG/M2 IV OVER 1-30 MINUTES Q12 HOURS ON DAYS 4 AND 5 71868 150 MG/M**2
101764987 10176498 7 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intrathecal PROPHASE (CYCLE= 5 DAYS): 7.5-12 MG ON DAY 1 (AGE BASED DOSING) 11719
101764987 10176498 8 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intravenous (not otherwise specified) COURSE A: 3000 MG/M2, IV OVER 3 HOURS ON DAY 1 11719 3000 MG/M**2
101764987 10176498 9 SS ETOPOSIDE. ETOPOSIDE 1 Intravenous (not otherwise specified) COURSE A: 100 MG/M2, OVER 2 HOURS ON DAYS 4 AND 5 0 100 MG/M**2
101764987 10176498 10 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral PROPHASE (CYCLE= 5 DAYS): 5MG/M2 1X/DAY ON DAYS 1-2 AND 5MG/M2 PO BID ON DAYS 3-5, (72 MG) 0 72 MG
101764987 10176498 11 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral COURSE A: 5 MG/M2, 2X/DAY ON DAYS 1-5 0 90 MG
101764987 10176498 12 SS IFOSFAMIDE. IFOSFAMIDE 1 Intravenous (not otherwise specified) COURSE A: 800 MG/M2, IV OVER 60 MINUTES ON DAYS 1-5 0 800 MG/M**2
101764987 10176498 13 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) PROPHASE (CYCLE= 5 DAYS): 200 MG/M2, IV OVER 30-60 MIN ON DAYS 1 AND 2 0 200 MG/M**2
101764987 10176498 14 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 UNK 0
101764987 10176498 15 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101764987 10176498 1 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 4 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 5 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 7 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 9 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 10 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 12 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 13 Anaplastic large cell lymphoma T- and null-cell types
101764987 10176498 14 Nausea

Outcome of event

Event ID CASEID OUTC COD
101764987 10176498 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
101764987 10176498 Colitis
101764987 10176498 Ileus
101764987 10176498 Posterior reversible encephalopathy syndrome
101764987 10176498 Seizure
101764987 10176498 Vomiting

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
101764987 10176498 1 20140111 20140111 0
101764987 10176498 2 20140112 201401 0
101764987 10176498 3 20140122 20140124 0
101764987 10176498 4 20140106 20140106 0
101764987 10176498 5 20140106 20140106 0
101764987 10176498 6 20140114 0
101764987 10176498 7 20140106 20140106 0
101764987 10176498 8 20140111 0
101764987 10176498 9 20140114 0
101764987 10176498 10 20140106 20140110 0
101764987 10176498 11 20140111 0
101764987 10176498 12 20140111 0
101764987 10176498 13 20140106 20140107 0
101764987 10176498 15 20140111 0