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
116860082 11686008 2 F 20160531 20151030 20160728 PER US-ASTRAZENECA-2015SF02043 ASTRAZENECA 0.00 F Y 81.60000 KG 20160729 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
116860082 11686008 1 PS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) 400 UG, ONE PUFF TWO TIMES A DAY 1136132 202450 INHALATION POWDER
116860082 11686008 2 SS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) 400 UG, ONE PUFF TWO TIMES A DAY 1136132 202450 INHALATION POWDER
116860082 11686008 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 2 PUFFS,TWO TIMES A DAY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116860082 11686008 1 Emphysema
116860082 11686008 2 Emphysema
116860082 11686008 3 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
116860082 11686008 Body height decreased
116860082 11686008 Choking
116860082 11686008 Dysgeusia
116860082 11686008 Intentional product misuse
116860082 11686008 Lung disorder
116860082 11686008 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
116860082 11686008 1 20151008 0
116860082 11686008 2 20151013 0