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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6683578 7330275 F 6683578-7 20090409 20100406 20100413 EXP TCI2010A00626 TAKEDA PHARMACEUTICALS NORTH AMERICA 69 YR F N 20100412 JAPAN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6683578 1013512199 PS ACTOS 1 ORAL 7.5 MG (7.5 MG, 1 IN 1 D), ORAL D D 21073
6683578 1013566280 C VENTANEURIN (PO) (FURSULTIAMINE, PYRIDOXAL 5- PHOSPHATE, HYDROXCOBA) 2
6683578 1013566281 C DEPAS (ETIZOLAM) 2
6683578 1013566282 C STAYBLA (IMIDAFENACIN) (UROLOGICALS) 2
6683578 1013566286 C AMARYL 1
6683578 1013566288 C DIOVAN 1
6683578 1013566290 C AMLODIPINE BESYLATE 1
6683578 1013566295 C TATSUPLAMIN (PRAVASTATIN SODIUM) 2
6683578 1013566297 C LIVALO (ITAVASTATIN CALCIUM) 2
6683578 1013566302 C FLUITRAN (TRICHLORMETHIZIDE) 2
6683578 1013566305 C NORVASC 1
6683578 1013566309 C PREMINENT (HYDROCHLOROTHIAZIDE, LOSARTAN POTASSIUM) 2
6683578 1013566429 C CRESTOR 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6683578 1013512199 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6683578 HO

Reactions reported

Event ID PT
6683578 EYELID OEDEMA
6683578 LACUNAR INFARCTION
6683578 WHITE BLOOD CELL COUNT DECREASED

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
6683578 FGN
6683578 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6683578 1013512199 20090323 20090723 121 DAY