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
106475888 10647588 8 F 20031219 20160901 20141211 20160907 EXP US-009507513-1412USA005258 MERCK 0.00 F Y 89.80000 KG 20160907 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
106475888 10647588 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
106475888 10647588 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral UNK U 20560 TABLET
106475888 10647588 3 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 Oral 70 MG, QW 3196.549 MG 0 70 MG TABLET /wk
106475888 10647588 4 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW U 0 70 MG /wk
106475888 10647588 5 C PREDNISONE. PREDNISONE 1 Unknown UNK U U 0
106475888 10647588 6 C THEOPHYLLINE THEOPHYLLINE ANHYDROUS 1 Unknown UNK U U 0
106475888 10647588 7 C PREVACID LANSOPRAZOLE 1 UNK U U 0
106475888 10647588 8 C CALCIUM (UNSPECIFIED) CALCIUM 1 Unknown 500 MG, QD U U 0 500 MG QD
106475888 10647588 9 C CHOLECALCIFEROL CHOLECALCIFEROL 1 Unknown 5000 IU, QD U U 0 5000 IU QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106475888 10647588 1 Osteoporosis
106475888 10647588 3 Osteoporosis
106475888 10647588 4 Osteoporosis
106475888 10647588 5 Asthma
106475888 10647588 6 Asthma
106475888 10647588 7 Product used for unknown indication
106475888 10647588 8 Product used for unknown indication
106475888 10647588 9 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106475888 10647588 OT
106475888 10647588 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106475888 10647588 Anxiety
106475888 10647588 Arthralgia
106475888 10647588 Asthenia
106475888 10647588 Back pain
106475888 10647588 Calcium deficiency
106475888 10647588 Depression
106475888 10647588 Escherichia urinary tract infection
106475888 10647588 Fall
106475888 10647588 Femoral neck fracture
106475888 10647588 Femur fracture
106475888 10647588 Fracture malunion
106475888 10647588 Fungal infection
106475888 10647588 Gait disturbance
106475888 10647588 Haematoma
106475888 10647588 Leukocytosis
106475888 10647588 Lumbar vertebral fracture
106475888 10647588 Multiple fractures
106475888 10647588 Neuropathy peripheral
106475888 10647588 Pain
106475888 10647588 Rib fracture
106475888 10647588 Upper respiratory tract infection
106475888 10647588 Vitamin D deficiency
106475888 10647588 Vulval cancer

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
106475888 10647588 1 200801 0
106475888 10647588 2 1999 0
106475888 10647588 3 20080222 20091010 0
106475888 10647588 4 200911 201012 0
106475888 10647588 5 1987 2015 0
106475888 10647588 6 1994 0
106475888 10647588 7 200001 200512 0
106475888 10647588 8 2005 2015 0
106475888 10647588 9 2005 2015 0