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
125794401 12579440 1 I 20160708 20160721 20160721 EXP BR-GLAXOSMITHKLINE-BR2016GSK100626 GLAXOSMITHKLINE 0.00 F Y 55.00000 KG 20160721 CN BR BR

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
125794401 12579440 1 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 1 PUFF(S), BID 5ZP0931 0 1 DF INHALATION POWDER BID
125794401 12579440 2 PS Aerolin ALBUTEROL 1 20983 OROMUCOSAL SPRAY

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125794401 12579440 1 Bronchitis
125794401 12579440 2 Bronchitis

Outcome of event

Event ID CASEID OUTC COD
125794401 12579440 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125794401 12579440 Bronchitis
125794401 12579440 Drug ineffective
125794401 12579440 Dyspnoea
125794401 12579440 Extra dose administered
125794401 12579440 Fatigue
125794401 12579440 Hypersensitivity
125794401 12579440 Inappropriate schedule of drug administration
125794401 12579440 Influenza
125794401 12579440 Laryngeal oedema
125794401 12579440 Medication error
125794401 12579440 Mobility decreased
125794401 12579440 Off label use
125794401 12579440 Tachycardia

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
125794401 12579440 1 2009 0