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
125661132 12566113 2 F 201606 20160713 20160718 20160718 EXP US-GLAXOSMITHKLINE-US2016100715 GLAXOSMITHKLINE 66.97 YR M Y 0.00000 20160718 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
125661132 12566113 1 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 1 PUFF(S), BID Y 0 1 DF INHALATION POWDER BID
125661132 12566113 2 SS COREG CARVEDILOL 1 UNK, BID 0 BID
125661132 12566113 3 PS VENTOLIN HFA ALBUTEROL SULFATE 1 UNK, PRN UB9S 20983
125661132 12566113 4 C ASPIRIN. ASPIRIN 1 U 0
125661132 12566113 5 C DIGOXIN. DIGOXIN 1 U 0
125661132 12566113 6 C INCRUSE ELLIPTA UMECLIDINIUM BROMIDE 1 U 0
125661132 12566113 7 C LASIX FUROSEMIDE 1 U 0
125661132 12566113 8 C PLAVIX CLOPIDOGREL BISULFATE 1 U 0
125661132 12566113 9 C THEOPHYLLINE THEOPHYLLINE ANHYDROUS 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125661132 12566113 1 Chronic obstructive pulmonary disease
125661132 12566113 2 Product used for unknown indication
125661132 12566113 3 Dyspnoea

Outcome of event

Event ID CASEID OUTC COD
125661132 12566113 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125661132 12566113 Dyspnoea
125661132 12566113 Oxygen saturation decreased
125661132 12566113 Respiratory disorder

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
125661132 12566113 1 2014 201606 0
125661132 12566113 2 2013 0
125661132 12566113 3 2007 0