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
122948014 12294801 4 F 201602 20160821 20160422 20160829 EXP US-PFIZER INC-2016221538 PFIZER 70.00 YR M Y 75.00000 KG 20160829 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
122948014 12294801 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG (CAPSULE), CYCLIC (ONCE A DAY FOR 4 WEEKS THEN 2 WEEKS OFF) 2800 MG 21938 50 MG CAPSULE, HARD
122948014 12294801 2 SS SUTENT SUNITINIB MALATE 1 50 MG, 1X/DAY 2800 MG 21938 50 MG CAPSULE, HARD QD
122948014 12294801 3 SS SUTENT SUNITINIB MALATE 1 50 MG, 1X/DAY 2800 MG 21938 50 MG CAPSULE, HARD QD
122948014 12294801 4 C CRESTOR ROSUVASTATIN CALCIUM 1 5 MG, 1X/DAY 0 5 MG QD
122948014 12294801 5 C DIGOXIN. DIGOXIN 1 Oral 0.125 MG, 1X/DAY 0 .125 MG QD
122948014 12294801 6 C WARFARIN WARFARIN 1 2.5 MG, 1X/DAY 0 2.5 MG QD
122948014 12294801 7 C IRON IRON 1 1 DF, 2X/DAY (NON-PRESCRIPTION IRON PILL) 0 1 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122948014 12294801 1 Metastatic renal cell carcinoma
122948014 12294801 4 Blood cholesterol abnormal
122948014 12294801 5 Heart rate abnormal
122948014 12294801 6 Thrombosis
122948014 12294801 7 Blood iron abnormal

Outcome of event

Event ID CASEID OUTC COD
122948014 12294801 DE
122948014 12294801 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122948014 12294801 Abscess
122948014 12294801 Asthenia
122948014 12294801 Blood phosphorus increased
122948014 12294801 Blood potassium increased
122948014 12294801 Death
122948014 12294801 Decreased appetite
122948014 12294801 Diarrhoea
122948014 12294801 Fatigue
122948014 12294801 Gastrointestinal disorder
122948014 12294801 Internal haemorrhage
122948014 12294801 Pyrexia
122948014 12294801 Weight 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
122948014 12294801 1 20160210 0
122948014 12294801 2 20160209 20160307 0
122948014 12294801 3 20160404 20160501 0
122948014 12294801 4 2016 0
122948014 12294801 5 201309 0
122948014 12294801 6 201508 0
122948014 12294801 7 201508 0