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
127173101 12717310 1 I 201605 20160902 20160906 20160906 EXP CA-GLAXOSMITHKLINE-CA2016GSK129152 GLAXOSMITHKLINE 80.80 YR F Y 0.00000 20160906 CN CA CA

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
127173101 12717310 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK U 21077
127173101 12717310 2 SS VENTOLIN ALBUTEROL SULFATE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127173101 12717310 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127173101 12717310 Dyspnoea
127173101 12717310 Herpes zoster
127173101 12717310 Lower respiratory tract infection
127173101 12717310 Lung infection

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
127173101 12717310 1 2015 0
127173101 12717310 2 2013 0