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
112821732 11282173 2 F 2014 20160907 20150720 20160924 PER US-ASTRAZENECA-2015SE66524 ASTRAZENECA 0.00 F Y 52.20000 KG 20160924 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
112821732 11282173 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG, 2 PUFFS TWO TIMES A DAY 21929
112821732 11282173 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG, 2 PUFFS TWO TIMES A DAY 21929

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112821732 11282173 1 Chronic obstructive pulmonary disease
112821732 11282173 2 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
112821732 11282173 Asthma
112821732 11282173 Device failure
112821732 11282173 Device issue
112821732 11282173 Off label use

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
112821732 11282173 1 20150702 0
112821732 11282173 2 20150702 0