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
113839152 11383915 2 F 20160510 20150815 20160812 PER US-ASTRAZENECA-2015SE76564 ASTRAZENECA 0.00 M Y 127.00000 KG 20160812 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
113839152 11383915 1 PS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) 400UG, ONE PUFF, TWO TIMES A DAY 1136201 202450 INHALATION POWDER
113839152 11383915 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) N U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113839152 11383915 1 Chronic obstructive pulmonary disease
113839152 11383915 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113839152 11383915 Adverse drug reaction
113839152 11383915 Drug ineffective
113839152 11383915 Dry mouth
113839152 11383915 Dyspnoea
113839152 11383915 Gait disturbance
113839152 11383915 Product quality issue

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
113839152 11383915 1 20150715 0