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
6856743 7536559 I 6856743-3 20100408 20100630 PER 1000013110 FOREST LABORATORIES, INC. 62 YR F N 20100610 MD UNITED STATES

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
6856743 1014174901 PS BYSTOLIC 1 ORAL 5 MG (5 MG, 1 IN 1 D), ORAL Y D 21742
6856743 1014390463 C ZOCOR 1
6856743 1014390470 C DIOVAN HCT (TABLETS) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6856743 1014174901 HYPERTENSION

Outcome of event

no results found

Reactions reported

Event ID PT
6856743 DIZZINESS
6856743 FATIGUE

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

Event ID RPSR COD
6856743 CR
6856743 HP

Therapies reported

no results found