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
126591211 12659121 1 I 20160809 20160817 20160817 EXP MX-GLAXOSMITHKLINE-MX2016GSK118079 GLAXOSMITHKLINE 0.00 F Y 51.50000 KG 20160817 CN MX MX

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
126591211 12659121 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 2 INHALATIONS, BID HM9L 21254 2 DF BID
126591211 12659121 2 C COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 UNK U 0
126591211 12659121 3 C TEOFILINA 2 UNK U 0 TABLET
126591211 12659121 4 C STIOLTO RESPIMAT OLODATEROL HYDROCHLORIDETIOTROPIUM BROMIDE MONOHYDRATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126591211 12659121 1 Chronic obstructive pulmonary disease
126591211 12659121 2 Chronic obstructive pulmonary disease
126591211 12659121 3 Chronic obstructive pulmonary disease
126591211 12659121 4 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
126591211 12659121 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126591211 12659121 Adverse event
126591211 12659121 Intentional product misuse
126591211 12659121 Therapy cessation

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

no results found

Therapies reported

no results found