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
125745201 12574520 1 I 201509 20160718 20160720 20160720 EXP US-GLAXOSMITHKLINE-US2016GSK102655 GLAXOSMITHKLINE 52.86 YR F Y 0.00000 20160720 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
125745201 12574520 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 100/50 MCG UNK, U U 21077 INHALATION POWDER
125745201 12574520 2 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 21077 INHALATION POWDER
125745201 12574520 3 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 21077 INHALATION POWDER
125745201 12574520 4 SS ALBUTEROL. ALBUTEROL 1 UNK, U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125745201 12574520 1 Chronic obstructive pulmonary disease
125745201 12574520 2 Asthma
125745201 12574520 3 Emphysema
125745201 12574520 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125745201 12574520 LT
125745201 12574520 HO
125745201 12574520 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125745201 12574520 Cardio-respiratory arrest
125745201 12574520 Dyspnoea
125745201 12574520 Hospitalisation
125745201 12574520 Malaise
125745201 12574520 Nasopharyngitis
125745201 12574520 Resuscitation

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

no results found

Therapies reported

no results found