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
121323472 12132347 2 F 20160223 20160817 20160301 20160822 EXP US-ASTRAZENECA-2016SE20347 ASTRAZENECA 21344.00 DY M Y 0.00000 20160822 CN 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
121323472 12132347 1 PS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) U 1147663 202450 400 UG INHALATION POWDER BID
121323472 12132347 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
121323472 12132347 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121323472 12132347 Asthma
121323472 12132347 Chronic obstructive pulmonary disease
121323472 12132347 Drug dose omission
121323472 12132347 Exposure to chemical pollution
121323472 12132347 Hypersensitivity
121323472 12132347 Product quality issue
121323472 12132347 Pulmonary function test decreased
121323472 12132347 Throat irritation

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
121323472 12132347 1 2015 0