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
89287262 8928726 2 F 2012 20121115 20121128 20130702 EXP US-PFIZER INC-2012294086 PFIZER 29.00 YR M Y 0.00000 20130702 OT 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
89287262 8928726 1 PS IBUPROFEN 1 UNKNOWN UNK D 18989
89287262 8928726 2 SS IBUPROFEN 1 D 18989
89287262 8928726 3 SS TYLENOL 1 UNKNOWN UNK D 0
89287262 8928726 4 SS TYLENOL 1 D 0
89287262 8928726 5 SS REBIF 1 SUBCUTANEOUS 3 TIMES PER WEEK D AU003961 0 INJECTION
89287262 8928726 6 SS REBIF 1 SUBCUTANEOUS 22 UG, UNK D AU003961 0 22 UG INJECTION
89287262 8928726 7 SS ALEVE 1 UNKNOWN D 0
89287262 8928726 8 SS ALEVE 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89287262 8928726 1 Headache
89287262 8928726 2 Premedication
89287262 8928726 3 Headache
89287262 8928726 4 Premedication
89287262 8928726 5 Multiple sclerosis
89287262 8928726 7 Headache
89287262 8928726 8 Premedication

Outcome of event

Event ID CASEID OUTC COD
89287262 8928726 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89287262 8928726 Asthenia
89287262 8928726 Balance disorder
89287262 8928726 Feeling abnormal
89287262 8928726 Gait disturbance
89287262 8928726 Headache
89287262 8928726 Injection site erythema
89287262 8928726 Liver function test abnormal
89287262 8928726 Malaise
89287262 8928726 Memory impairment
89287262 8928726 Multiple sclerosis
89287262 8928726 Pain in extremity

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
89287262 8928726 1 201204 0
89287262 8928726 3 201204 0
89287262 8928726 5 20110311 0
89287262 8928726 6 201204 0
89287262 8928726 7 201204 0