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
127265621 12726562 1 I 201607 20160906 20160908 20160908 PER US-GLAXOSMITHKLINE-US2016130117 GLAXOSMITHKLINE 51.78 YR F Y 0.00000 20160908 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
127265621 12726562 1 PS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 1 PUFF(S), QD 203975 1 DF INHALATION POWDER QD
127265621 12726562 2 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 203975 INHALATION POWDER
127265621 12726562 3 SS FLOVENT DISKUS FLUTICASONE PROPIONATE 1 1 PUFF(S), BID 0 1 DF BID
127265621 12726562 4 C MORPHINE PUMP MORPHINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127265621 12726562 1 Chronic obstructive pulmonary disease
127265621 12726562 2 Asthma
127265621 12726562 3 Dyspnoea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127265621 12726562 Dyspnoea

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
127265621 12726562 1 201607 0
127265621 12726562 3 201607 0