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
125483102 12548310 2 F 2011 20160905 20160712 20160912 PER US-ASTRAZENECA-2016SE73862 ASTRAZENECA 64.00 YR M Y 71.70000 KG 20160912 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
125483102 12548310 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 80-4.5 MCG, TWO PUFFS,TWICE A DAY U U 21929 BID
125483102 12548310 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 80-4.5 MCG, TWO PUFFS,TWICE A DAY U U 2000363C00 21929 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125483102 12548310 1 Chronic obstructive pulmonary disease
125483102 12548310 2 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
125483102 12548310 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125483102 12548310 Device failure
125483102 12548310 Musculoskeletal discomfort
125483102 12548310 Off label use
125483102 12548310 Pneumonia
125483102 12548310 Product use 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
125483102 12548310 1 2011 0
125483102 12548310 2 20160704 0