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
127601681 12760168 1 I 20160823 20160907 20160919 20160919 EXP GB-MHRA-EYC 00144677 GB-TEVA-693022ACC TEVA 51.00 YR F Y 82.55000 KG 20160919 CN 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
127601681 12760168 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral U UM11515 76191 120 MG
127601681 12760168 2 C AMITRIPTYLIN AMITRIPTYLINE 1 0
127601681 12760168 3 C REFRESH CELLUVISC CARBOXYMETHYLCELLULOSE SODIUM 1 0
127601681 12760168 4 C CLENIL MODULITE BECLOMETHASONE DIPROPIONATE 1 0
127601681 12760168 5 C CODEINE CODEINE 1 OCCASIONAL USE. 0
127601681 12760168 6 C DIAZEPAM. DIAZEPAM 1 OCCASIONAL USE. 0
127601681 12760168 7 C SALMETEROL SALMETEROL 1 0
127601681 12760168 8 C VENTOLIN ALBUTEROL SULFATE 1 ONLY USED VERY OCCASIONALLY. 0
127601681 12760168 9 C ZOLPIDEM TARTRATE. ZOLPIDEM TARTRATE 1 OCCASIONAL USE ONLY. 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127601681 12760168 1 Urticaria
127601681 12760168 5 Migraine
127601681 12760168 6 Migraine
127601681 12760168 9 Migraine

Outcome of event

Event ID CASEID OUTC COD
127601681 12760168 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127601681 12760168 Fatigue
127601681 12760168 Myalgia
127601681 12760168 Nausea
127601681 12760168 Sinus headache

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
127601681 12760168 1 20160822 0