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
7298370 7816706 I 7298370-2 20100101 20110208 20110217 EXP NL-US-EMD SERONO, INC.-7031485 US-EMD SERONO, INC. 24 YR F Y 20110217 OT NETHERLANDS

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
7298370 1015804073 C CALCIUMCARBONAAT/COLECALCIFEROL (CALCIUM CARBONATE/COLECALCIFEROL) 2 ORAL
7298370 1015804074 C CALCIUMCARBONAAT/COLECALCIFEROL (CALCIUM CARBONATE/COLECALCIFEROL) 2 ORAL
7298370 1015804077 C HYDROXOCOBALAMINE 2
7298370 1015804078 C VIT B12 (VITAMIN B12) 2
7298370 1015804070 PS REBIF 1 SUBCUTANEOUS
7298370 1015804071 C ACETYLSALILZURR 2 ORAL
7298370 1015804072 C AMITRIPTYLINE 2 ORAL
7298370 1015804081 C RANITIDINE 1 ORAL
7298370 1015804076 C LYNESTRENOL 2
7298370 1015804075 C ETHINYL ESTRADIOL 1
7298370 1015804080 C NAPROXEN 1
7298370 1015804082 C TRAMADOL 2 ORAL
7298370 1015804079 C METOCLOPRAMIDE HCL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7298370 1015804073 OSTEOPOROSIS PROPHYLAXIS
7298370 1015804074 VITAMIN D DECREASED
7298370 1015804070 MULTIPLE SCLEROSIS
7298370 1015804071 ANTICOAGULANT THERAPY
7298370 1015804072 PAIN
7298370 1015804081 DYSPEPSIA
7298370 1015804076 CONTRACEPTION
7298370 1015804075 CONTRACEPTION
7298370 1015804079 NAUSEA

Outcome of event

Event ID OUTC COD
7298370 HO

Reactions reported

Event ID PT
7298370 DYSPNOEA
7298370 INSOMNIA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7298370 1015804073 20100701
7298370 1015804070 20100816
7298370 1015804071 20080101