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
103314083 10331408 3 F 2014 20160803 20140722 20160808 EXP US-PFIZER INC-2014200653 PFIZER 27.00 YR M Y 103.86000 KG 20160808 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
103314083 10331408 1 PS LYRICA PREGABALIN 1 Oral 150 MG, 3X/DAY 21446 150 MG CAPSULE, HARD TID
103314083 10331408 2 C SOMA CARISOPRODOL 1 350 MG, AS NEEDED (UP TO FOUR TIMES A DAY) 0 350 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103314083 10331408 1 Spinal cord injury

Outcome of event

Event ID CASEID OUTC COD
103314083 10331408 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103314083 10331408 Blood glucose abnormal
103314083 10331408 Blood pressure abnormal
103314083 10331408 Body temperature fluctuation
103314083 10331408 Decreased appetite
103314083 10331408 Feeling abnormal
103314083 10331408 Hyperhidrosis
103314083 10331408 Insomnia
103314083 10331408 Malaise
103314083 10331408 Memory impairment
103314083 10331408 Paraesthesia
103314083 10331408 Seizure
103314083 10331408 Visual impairment
103314083 10331408 Withdrawal syndrome

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
103314083 10331408 1 201406 2014 0