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
123104724 12310472 4 F 20150922 20160628 20160427 20160706 PER US-AMGEN-USASP2016046831 AMGEN 85.00 YR E F Y 61.22000 KG 20160706 MD 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
123104724 12310472 1 PS PROLIA DENOSUMAB 1 Subcutaneous 60 MG, UNK U 1057143 125320 60 MG SOLUTION FOR INJECTION
123104724 12310472 2 C VITAMIN B12 CYANOCOBALAMIN 1 Oral 1000 MUG, QD 0 1000 UG QD
123104724 12310472 3 C TRAMADOL HCL TRAMADOL HYDROCHLORIDE 1 Oral 50 MG, Q8H 0 50 MG TID
123104724 12310472 4 C MELOXICAM. MELOXICAM 1 Oral 7.5 MG, UNK 0 7.5 MG
123104724 12310472 5 C FLUOROMETHOLONE. FLUOROMETHOLONE 1 Unknown 0.1 %, UNK 0 .1 PCT
123104724 12310472 6 C VITAMIN D CHOLECALCIFEROL 1 Oral UNK UNK, QD 0 QD
123104724 12310472 7 C LUTEIN LUTEIN 1 Oral UNK UNK, BID 0 BID
123104724 12310472 8 C CEPHALEXIN. CEPHALEXIN 1 Oral 500 MG, 1 CAP THREE TIMES A DAY 0 500 MG
123104724 12310472 9 C CALCIUM CALCIUM 1 UNK 0
123104724 12310472 10 C ALEVE NAPROXEN SODIUM 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123104724 12310472 1 Osteoporosis postmenopausal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123104724 12310472 Anaemia
123104724 12310472 Arthralgia
123104724 12310472 Back pain
123104724 12310472 Bone contusion
123104724 12310472 C-reactive protein increased
123104724 12310472 Chills
123104724 12310472 Contusion
123104724 12310472 Fall
123104724 12310472 Fatigue
123104724 12310472 Headache
123104724 12310472 Joint injury
123104724 12310472 Ligament sprain
123104724 12310472 Myalgia
123104724 12310472 Oropharyngeal pain
123104724 12310472 Osteoporosis
123104724 12310472 Red blood cell sedimentation rate increased
123104724 12310472 Rhinalgia
123104724 12310472 Skin ulcer
123104724 12310472 Temporal arteritis
123104724 12310472 Upper respiratory tract infection
123104724 12310472 Urinary tract infection
123104724 12310472 Viral pharyngitis
123104724 12310472 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
123104724 12310472 1 20150922 0
123104724 12310472 2 20151021 0
123104724 12310472 3 20151030 0
123104724 12310472 4 20151113 0
123104724 12310472 5 20151016 0
123104724 12310472 6 20130816 0
123104724 12310472 7 20150518 0
123104724 12310472 8 20151021 0
123104724 12310472 9 20130529 0
123104724 12310472 10 20150125 0