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
120593325 12059332 5 F 20160915 20160210 20160921 EXP US-PFIZER INC-2016071559 PFIZER 56.00 YR F Y 97.00000 KG 20160921 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
120593325 12059332 1 PS RELPAX ELETRIPTAN HYDROBROMIDE 1 20 MG, AS NEEDED (ONE TO TWO) D 21016 20 MG FILM-COATED TABLET
120593325 12059332 2 SS RELPAX ELETRIPTAN HYDROBROMIDE 1 20 MG, AS NEEDED (HA Q2HR, DO NOT EXCEED 04/DAY) D 21016 20 MG FILM-COATED TABLET
120593325 12059332 3 SS RELPAX ELETRIPTAN HYDROBROMIDE 1 20 MG, 2X/DAY PRN D 21016 20 MG FILM-COATED TABLET BID
120593325 12059332 4 SS TACROLIMUS. TACROLIMUS 1 1 MG IN THE MORNING AND 0.5MG IN THE EVENING U 0 BID
120593325 12059332 5 SS TACROLIMUS. TACROLIMUS 1 0.1 MG AM, 0.5 MG PM U 0 BID
120593325 12059332 6 C LISINOPRIL. LISINOPRIL 1 20 MG, UNK 0 20 MG
120593325 12059332 7 C LISINOPRIL. LISINOPRIL 1 40 MG, DAILY 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120593325 12059332 1 Migraine
120593325 12059332 4 Liver transplant
120593325 12059332 6 Hypertension

Outcome of event

Event ID CASEID OUTC COD
120593325 12059332 OT
120593325 12059332 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120593325 12059332 Activities of daily living impaired
120593325 12059332 Disease progression
120593325 12059332 Drug intolerance
120593325 12059332 Eating disorder
120593325 12059332 Malaise
120593325 12059332 Migraine
120593325 12059332 Nausea
120593325 12059332 Pain
120593325 12059332 Retching
120593325 12059332 Thinking abnormal
120593325 12059332 Vomiting

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

no results found

Therapies reported

no results found