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
125269013 12526901 3 F 20160802 20160705 20160809 EXP GB-AMGEN-GBRSP2016086184 AMGEN 44.00 YR A M Y 0.00000 20160809 OT GB GB

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
125269013 12526901 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 UNKNOWN FORMULATION
125269013 12526901 2 SS AVASTIN BEVACIZUMAB 1 Unknown UNK 0
125269013 12526901 3 SS METOCHLOPRAMIDE METOCLOPRAMIDE HYDROCHLORIDE 1 Unknown UNK 0
125269013 12526901 4 SS PEMETREXED PEMETREXED 1 Unknown UNK 0
125269013 12526901 5 SS CARBOPLATIN. CARBOPLATIN 1 Unknown UNK 0
125269013 12526901 6 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK 0
125269013 12526901 7 SS ONDANSETRON ONDANSETRON 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125269013 12526901 1 Product used for unknown indication
125269013 12526901 2 Product used for unknown indication
125269013 12526901 3 Product used for unknown indication
125269013 12526901 4 Product used for unknown indication
125269013 12526901 5 Product used for unknown indication
125269013 12526901 6 Product used for unknown indication
125269013 12526901 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125269013 12526901 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125269013 12526901 Diarrhoea
125269013 12526901 Vomiting

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

no results found

Therapies reported

no results found