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
127173042 12717304 2 F 2016 20160923 20160906 20160928 EXP CN-GLAXOSMITHKLINE-CN2016GSK125867 GLAXOSMITHKLINE 59.00 YR F Y 0.00000 20160928 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
127173042 12717304 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) UNK 21077 1 DF INHALATION POWDER
127173042 12717304 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 2 PUFF(S), UNK 21077 2 DF INHALATION POWDER
127173042 12717304 3 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK RD9Y 21077 INHALATION POWDER
127173042 12717304 4 SS Salbutamol sulphate ALBUTEROL SULFATE 1 Respiratory (inhalation) UNK Y 0 INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127173042 12717304 1 Asthma
127173042 12717304 4 Asthma

Outcome of event

Event ID CASEID OUTC COD
127173042 12717304 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127173042 12717304 Abdominal discomfort
127173042 12717304 Asthma
127173042 12717304 Bronchospasm
127173042 12717304 Decreased appetite
127173042 12717304 Drug ineffective
127173042 12717304 Intentional product misuse
127173042 12717304 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
127173042 12717304 1 201602 0