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
96853139 9685313 9 F 2003 20160803 20131113 20160810 EXP US-009507513-1311USA004017 MERCK 0.00 F Y 72.56000 KG 20160810 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
96853139 9685313 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 40180 MG 20560 70 MG TABLET /wk
96853139 9685313 2 SS FOSAMAX ALENDRONATE SODIUM 1 40180 MG 20560 TABLET
96853139 9685313 3 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 Oral U 0 TABLET
96853139 9685313 4 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 U 0 TABLET
96853139 9685313 5 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW U U 0 70 MG /wk
96853139 9685313 6 C VITAMINS (UNSPECIFIED) VITAMINS 1 Unknown UNK U U 0
96853139 9685313 7 C calcium (unspecified) (+) vitamin D (unspecified) CALCIUM CARBONATEVITAMIN D 1 Unknown 1200 MG, UNK U U 0 1200 MG
96853139 9685313 8 C CHOLECALCIFEROL CHOLECALCIFEROL 1 Unknown 2000 IU, QD U U 0 2000 IU QD
96853139 9685313 9 C FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 Oral 10 MG, PRN U U 0 10 MG
96853139 9685313 10 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 50MG 1/2 Q, QD U U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96853139 9685313 1 Osteopenia
96853139 9685313 2 Osteoporosis
96853139 9685313 3 Osteopenia
96853139 9685313 4 Osteoporosis
96853139 9685313 9 Back pain
96853139 9685313 10 Depression

Outcome of event

Event ID CASEID OUTC COD
96853139 9685313 OT
96853139 9685313 HO
96853139 9685313 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
96853139 9685313 Acute sinusitis
96853139 9685313 Anaemia postoperative
96853139 9685313 Anxiety
96853139 9685313 Chest pain
96853139 9685313 Cutaneous lupus erythematosus
96853139 9685313 Ear congestion
96853139 9685313 Femur fracture
96853139 9685313 Foot fracture
96853139 9685313 Intramedullary rod insertion
96853139 9685313 Large intestine polyp
96853139 9685313 Migraine
96853139 9685313 Myalgia
96853139 9685313 Nasal turbinate hypertrophy
96853139 9685313 Pain in extremity
96853139 9685313 Palpitations
96853139 9685313 Papule
96853139 9685313 Pyrexia
96853139 9685313 Reflux laryngitis
96853139 9685313 Stress
96853139 9685313 Upper respiratory tract infection
96853139 9685313 Vitamin D deficiency

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
96853139 9685313 1 20010821 20120813 0
96853139 9685313 6 2001 2012 0
96853139 9685313 7 2001 2012 0
96853139 9685313 8 2001 2007 0