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
125440541 12544054 1 I 20160530 20160627 20160711 20160711 EXP JP-GLAXOSMITHKLINE-JP2016JPN091925 GLAXOSMITHKLINE 0.00 E M Y 0.00000 20160711 CN JP JP

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
125440541 12544054 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 250 ?G, BID 353000 UG Y 21077 250 UG INHALATION POWDER BID
125440541 12544054 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 250 ?G, BID 353000 UG Y 21077 250 UG INHALATION POWDER BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125440541 12544054 1 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
125440541 12544054 OT
125440541 12544054 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125440541 12544054 Chronic obstructive pulmonary disease
125440541 12544054 Hypercapnia
125440541 12544054 Pneumonia bacterial
125440541 12544054 Tongue coated

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
125440541 12544054 1 20140624 20160602 0
125440541 12544054 2 20160607 0