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
102982263 10298226 3 F 201401 20160711 20140711 20160721 EXP US-GLAXOSMITHKLINE-A1060546A GLAXOSMITHKLINE 60.52 YR F Y 0.00000 20160721 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
102982263 10298226 1 PS FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 220 MCG, 2 PUFFS U F0358 21433 2 DF BID
102982263 10298226 2 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 U 0 INHALATION POWDER
102982263 10298226 3 C MAXAIR PIRBUTEROL ACETATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102982263 10298226 1 Asthma
102982263 10298226 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
102982263 10298226 Asthma
102982263 10298226 Extra dose administered
102982263 10298226 Product packaging confusion
102982263 10298226 Product quality issue

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
102982263 10298226 1 2013 0