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
122913432 12291343 2 F 20160202 20160901 20160421 20160909 EXP GB-MHRA-EYC 00137739 GB-MYLANLABS-2016M1015277 MYLAN 0.00 Y 0.00000 20160909 OT 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
122913432 12291343 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Oral 75 MG, QD 77665 75 MG QD
122913432 12291343 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 40 MG, UNK Y U 0 40 MG
122913432 12291343 3 C ALENDRONIC ACID ALENDRONIC ACID 1 UNK U 0
122913432 12291343 4 C CELLUVISC /00007002/ 2 UNK U 0
122913432 12291343 5 C EZETIMIBE. EZETIMIBE 1 UNK U 0
122913432 12291343 6 C LATANOPROST. LATANOPROST 1 UNK U 0
122913432 12291343 7 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK U 0
122913432 12291343 8 C RAMIPRIL. RAMIPRIL 1 10 MG, QD U 0 10 MG QD
122913432 12291343 9 C SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK U 0
122913432 12291343 10 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 UNK U 0
122913432 12291343 11 C ASPIRIN /00002701/ ASPIRIN 1 300 MG, UNK U 0 300 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122913432 12291343 1 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
122913432 12291343 OT
122913432 12291343 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122913432 12291343 Facial paralysis
122913432 12291343 Labelled drug-drug interaction medication error
122913432 12291343 Transient ischaemic attack

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
122913432 12291343 1 201503 0
122913432 12291343 2 20150301 20160202 0