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
126456873 12645687 3 F 201503 20160822 20160811 20160826 EXP CN-GLAXOSMITHKLINE-CN2016GSK113774 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160826 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
126456873 12645687 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) UNK Y RD9X-A 21077 INHALATION POWDER
126456873 12645687 2 SS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126456873 12645687 1 Asthma
126456873 12645687 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
126456873 12645687 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126456873 12645687 Condition aggravated
126456873 12645687 Drug ineffective
126456873 12645687 Inappropriate schedule of drug administration
126456873 12645687 Nausea
126456873 12645687 Overdose
126456873 12645687 Product odour abnormal
126456873 12645687 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
126456873 12645687 1 2011 2016 0