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
124672703 12467270 3 F 201604 20160902 20160615 20160909 EXP US-AMGEN-USASL2016073829 AMGEN 37.00 YR A F Y 0.00000 20160909 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
124672703 12467270 1 PS NPLATE ROMIPLOSTIM 1 Unknown 75 MUG, QWK U 125268 75 UG POWDER FOR INJECTION /wk
124672703 12467270 2 SS NPLATE ROMIPLOSTIM 1 Unknown 100 MUG, UNK U 125268 100 UG POWDER FOR INJECTION
124672703 12467270 3 SS NPLATE ROMIPLOSTIM 1 Unknown 144 MUG, UNK U 125268 144 UG POWDER FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124672703 12467270 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
124672703 12467270 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124672703 12467270 Abdominal pain upper
124672703 12467270 Arthralgia
124672703 12467270 Asthenia
124672703 12467270 Blood disorder
124672703 12467270 Epistaxis
124672703 12467270 Grip strength decreased
124672703 12467270 Headache
124672703 12467270 Heat stroke
124672703 12467270 Hypoaesthesia
124672703 12467270 Injection site pain
124672703 12467270 Mobility decreased
124672703 12467270 Musculoskeletal stiffness
124672703 12467270 Myalgia
124672703 12467270 Neuralgia
124672703 12467270 Pain in extremity
124672703 12467270 Paraesthesia
124672703 12467270 Peripheral swelling
124672703 12467270 Petechiae
124672703 12467270 Platelet count abnormal

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
124672703 12467270 1 2015 0
124672703 12467270 3 20160201 0