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
125282191 12528219 1 I 20110801 20121106 20160705 20160705 EXP GB-PFIZER INC-1485198 PFIZER 0.00 Y 0.00000 20160705 MD GB GB

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
125282191 12528219 1 PS MITOXANTRONE HCL MITOXANTRONE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 12 MG, ONCE A DAY ON DAY 1 76871 12 MG SOLUTION FOR INJECTION
125282191 12528219 2 SS FLUDARABINE PHOSPHATE. FLUDARABINE PHOSPHATE 1 Oral 50 MG, ONCE DAILY ON DAY 1 AND 5 77790 50 MG POWDER FOR INJECTION
125282191 12528219 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 300 MG, ONCE DAILY ON DAY 1 AND 5 0 300 MG
125282191 12528219 4 SS RITUXIMAB RITUXIMAB 1 Intravenous (not otherwise specified) 980 MG, ONCE DAILY ON DAY 1 0 980 MG
125282191 12528219 5 C ACYCLOVIR /00587301/ ACYCLOVIR 1 UNK 0
125282191 12528219 6 C GABAPENTIN. GABAPENTIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125282191 12528219 1 Chronic lymphocytic leukaemia
125282191 12528219 2 Chronic lymphocytic leukaemia
125282191 12528219 3 Chronic lymphocytic leukaemia
125282191 12528219 4 Chronic lymphocytic leukaemia
125282191 12528219 5 Product used for unknown indication
125282191 12528219 6 Neuralgia

Outcome of event

Event ID CASEID OUTC COD
125282191 12528219 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125282191 12528219 Febrile neutropenia

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
125282191 12528219 1 20110419 0
125282191 12528219 2 20110419 0
125282191 12528219 3 20110419 0
125282191 12528219 4 20110419 0