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
100869205 10086920 5 F 20160831 20140418 20160908 EXP PHHY2014CA046475 NOVARTIS 0.00 F Y 0.00000 20160908 CN COUNTRY NOT SPECIFIED CA

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
100869205 10086920 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, BID 22068 400 MG CAPSULE BID
100869205 10086920 2 SS TASIGNA NILOTINIB 1 Oral 300 MG, BID 22068 300 MG CAPSULE BID
100869205 10086920 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown U 0
100869205 10086920 4 C ELTROXIN LEVOTHYROXINE 1 Unknown U 0
100869205 10086920 5 C METOPROLOL. METOPROLOL 1 Unknown U 0
100869205 10086920 6 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100869205 10086920 1 Chronic myeloid leukaemia
100869205 10086920 3 Gastric ulcer
100869205 10086920 4 Product used for unknown indication
100869205 10086920 5 Product used for unknown indication
100869205 10086920 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
100869205 10086920 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100869205 10086920 Alopecia
100869205 10086920 Back pain
100869205 10086920 Blood pressure increased
100869205 10086920 Dry skin
100869205 10086920 Dyspepsia
100869205 10086920 Eructation
100869205 10086920 Fatigue
100869205 10086920 Incorrect dose administered
100869205 10086920 Intestinal perforation
100869205 10086920 Muscle spasms
100869205 10086920 Pain
100869205 10086920 Polyp
100869205 10086920 Stress

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
100869205 10086920 1 20140404 20140507 0