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
126900431 12690043 1 I 20160811 20160826 20160826 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-122687 RANBAXY 0.00 M Y 0.00000 20160826 CN 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
126900431 12690043 1 PS OXALIPLATIN. OXALIPLATIN 1 Unknown 85 MG/M2 EVERY 14 DAY CYCLE 202922
126900431 12690043 2 SS JAKAFI RUXOLITINIB 1 Oral 20 MG, BID AD2761Q 0 20 MG TABLET Q12H
126900431 12690043 3 SS ARANESP DARBEPOETIN ALFA 1 Unknown UNK U 0
126900431 12690043 4 C CAPECITABINE. CAPECITABINE 1 Unknown UNK U 0
126900431 12690043 5 C XELODA CAPECITABINE 1 Unknown 1500 MG, BID (ONE WEEK ON AND ONE WEEK OFF) U 0 1500 MG Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126900431 12690043 1 Product used for unknown indication
126900431 12690043 2 Myelofibrosis
126900431 12690043 3 Product used for unknown indication
126900431 12690043 4 Product used for unknown indication
126900431 12690043 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126900431 12690043 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126900431 12690043 Abdominal discomfort
126900431 12690043 Anaemia
126900431 12690043 Arthralgia
126900431 12690043 Balance disorder
126900431 12690043 Decreased appetite
126900431 12690043 Dyspnoea
126900431 12690043 Early satiety
126900431 12690043 Malaise
126900431 12690043 Neuropathy peripheral
126900431 12690043 Oedema peripheral
126900431 12690043 Weight decreased
126900431 12690043 Wound

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
126900431 12690043 1 20160415 0
126900431 12690043 2 20160205 0
126900431 12690043 5 201603 0