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
125497231 12549723 1 I 20160704 20160712 20160712 EXP SE-PURDUE PHARMA-GBR-2016-0038110 PURDUE 57.00 YR M Y 0.00000 20160708 OT SE SE

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
125497231 12549723 1 SS TRAMADOL HCL TRAMADOL HYDROCHLORIDE 1 Unknown U 0
125497231 12549723 2 PS TARGINIQ ER NALOXONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE 1 Unknown U 205777 PROLONGED-RELEASE TABLET
125497231 12549723 3 SS IBUPROFEN. IBUPROFEN 1 Unknown U 0
125497231 12549723 4 SS ZOPICLONE ZOPICLONE 1 Unknown U 0
125497231 12549723 5 SS PARACETAMOL ACETAMINOPHEN 1 Unknown U 0
125497231 12549723 6 SS AMITRIPTYLINE AMITRIPTYLINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125497231 12549723 1 Product used for unknown indication
125497231 12549723 2 Product used for unknown indication
125497231 12549723 3 Product used for unknown indication
125497231 12549723 4 Product used for unknown indication
125497231 12549723 5 Product used for unknown indication
125497231 12549723 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125497231 12549723 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125497231 12549723 Agitation
125497231 12549723 Fatigue
125497231 12549723 Toxicity to various agents

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

no results found

Therapies reported

no results found