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
125699481 12569948 1 I 2014 20160716 20160719 20160719 EXP CN-GLAXOSMITHKLINE-CN2016GSK102366 GLAXOSMITHKLINE 55.00 YR F Y 57.50000 KG 20160719 CN CN CN

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
125699481 12569948 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 50/250 MCG U 21077 1 DF INHALATION POWDER QD
125699481 12569948 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 50/250 MCG U PW3F 21077 INHALATION POWDER
125699481 12569948 3 SS CEPHALOSPORIN UNSPECIFIED INGREDIENT 1 Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125699481 12569948 1 Asthma
125699481 12569948 3 Asthma

Outcome of event

Event ID CASEID OUTC COD
125699481 12569948 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125699481 12569948 Ageusia
125699481 12569948 Asthma
125699481 12569948 Off label use
125699481 12569948 Underdose
125699481 12569948 Vomiting
125699481 12569948 Weight decreased

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
125699481 12569948 1 2014 0
125699481 12569948 2 20160708 0