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
126026541 12602654 1 I 2016 20160722 20160728 20160728 EXP US-GLAXOSMITHKLINE-US2016GSK107428 GLAXOSMITHKLINE 46.39 YR F Y 0.00000 20160728 CN US US

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
126026541 12602654 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 21077 INHALATION POWDER
126026541 12602654 2 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 21077 INHALATION POWDER
126026541 12602654 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 U KA5M 0
126026541 12602654 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126026541 12602654 1 Chronic obstructive pulmonary disease
126026541 12602654 2 Emphysema
126026541 12602654 3 Emphysema
126026541 12602654 4 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
126026541 12602654 OT
126026541 12602654 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126026541 12602654 Chest pain
126026541 12602654 Condition aggravated
126026541 12602654 Dialysis
126026541 12602654 Hospitalisation
126026541 12602654 Medical device removal
126026541 12602654 Renal failure
126026541 12602654 Staphylococcal infection

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

no results found

Therapies reported

no results found