The Safety Rates Drug Report

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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
113880844 11388084 4 F 201507 20160727 20150817 20160812 EXP US-GLAXOSMITHKLINE-US2015116209 GLAXOSMITHKLINE 72.09 YR M Y 0.00000 20160812 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
113880844 11388084 1 PS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), QD R668888 203975 1 DF INHALATION POWDER QD
113880844 11388084 2 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), QD R691609 203975 1 DF INHALATION POWDER QD
113880844 11388084 3 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 62.5/25 MCG, 1 PUFF(S), QD 6ZP3472 203975 1 DF INHALATION POWDER QD
113880844 11388084 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 PUFF(S), PRN 5ZP0167 0 2 DF
113880844 11388084 5 C COREG CARVEDILOL 1 U 0
113880844 11388084 6 C COUMADIN WARFARIN SODIUM 1 U 0
113880844 11388084 7 C NIASPAN NIACIN 1 U 0
113880844 11388084 8 C ZOCOR SIMVASTATIN 1 U 0
113880844 11388084 9 C AZELASTINE AZELASTINE 1 U 0
113880844 11388084 10 C ASPIRIN (BABY) ASPIRIN 1 U 0
113880844 11388084 11 C DIGOXIN. DIGOXIN 1 U 0
113880844 11388084 12 C LISINOPRIL. LISINOPRIL 1 U 0
113880844 11388084 13 C METFORMIN METFORMIN HYDROCHLORIDE 1 U 0
113880844 11388084 14 C OXYGEN. OXYGEN 1 U 0
113880844 11388084 15 C LUTEIN LUTEIN 1 0
113880844 11388084 16 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
113880844 11388084 17 C WARFARIN WARFARIN 1 0
113880844 11388084 18 C FUROSEMIDE. FUROSEMIDE 1 0
113880844 11388084 19 C ALPRAZOLAM. ALPRAZOLAM 1 0
113880844 11388084 20 C PROAIR HFA ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113880844 11388084 1 Chronic obstructive pulmonary disease
113880844 11388084 4 Dyspnoea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113880844 11388084 Blood glucose increased
113880844 11388084 Dyspnoea
113880844 11388084 Nasopharyngitis
113880844 11388084 Product quality issue
113880844 11388084 Rhinorrhoea

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
113880844 11388084 1 201507 0
113880844 11388084 4 2013 0