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
121626118 12162611 8 F 20160706 20160309 20160714 PER US-PFIZER INC-2016128114 PFIZER 82.00 YR M Y 83.00000 KG 20160714 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
121626118 12162611 1 PS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (ONCE DAILY, 28 DAYS ON/14 DAYS OFF) Y 21938 50 MG CAPSULE, HARD
121626118 12162611 2 SS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (ONCE DAILY, 28 DAYS ON/14 DAYS OFF) Y 21938 50 MG CAPSULE, HARD
121626118 12162611 3 C PROSCAR FINASTERIDE 1 UNK 0
121626118 12162611 4 C FLOMAX TAMSULOSIN HYDROCHLORIDE 1 UNK 0
121626118 12162611 5 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
121626118 12162611 6 C COLACE DOCUSATE SODIUM 1 UNK 0
121626118 12162611 7 C LASIX FUROSEMIDE 1 UNK 0
121626118 12162611 8 C POTASSIUM POTASSIUM 1 UNK 0
121626118 12162611 9 C PROTONIX PANTOPRAZOLE SODIUM 1 UNK 0
121626118 12162611 10 C TYLENOL ACETAMINOPHEN 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121626118 12162611 1 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
121626118 12162611 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121626118 12162611 Acne
121626118 12162611 Appetite disorder
121626118 12162611 Dysgeusia
121626118 12162611 Fatigue
121626118 12162611 Glossitis
121626118 12162611 Head discomfort
121626118 12162611 Hypersomnia
121626118 12162611 Insomnia
121626118 12162611 Platelet count decreased
121626118 12162611 Pruritus
121626118 12162611 Renal impairment
121626118 12162611 Scab
121626118 12162611 Skin lesion
121626118 12162611 Tongue disorder
121626118 12162611 Urinary tract infection
121626118 12162611 White blood cell count 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
121626118 12162611 1 20160208 20160306 0
121626118 12162611 2 20160404 20160418 0
121626118 12162611 7 201505 20160629 0