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
125615471 12561547 1 I 20160708 20160715 20160715 EXP CN-GLAXOSMITHKLINE-CN2016GSK098339 GLAXOSMITHKLINE 12.00 YR M Y 0.00000 20160715 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
125615471 12561547 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID Y 21077 1 DF INHALATION POWDER BID
125615471 12561547 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), QD Y 21077 1 DF INHALATION POWDER QD
125615471 12561547 3 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), PRN (WHEN ASTHMA RECURRENT) Y 21077 1 DF INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125615471 12561547 1 Asthma
125615471 12561547 2 Wheezing

Outcome of event

Event ID CASEID OUTC COD
125615471 12561547 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125615471 12561547 Asthma
125615471 12561547 Drug ineffective
125615471 12561547 Inappropriate schedule of drug administration

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found