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
123838022 12383802 2 F 20160524 20160519 20160819 PER US-ASTRAZENECA-2016SE38535 ASTRAZENECA 0.00 F Y 52.20000 KG 20160819 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
123838022 12383802 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG, 2 PUFFS, TWO TIMES A DAY 21929
123838022 12383802 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG, 2 PUFFS, TWO TIMES A DAY 21929
123838022 12383802 3 C FLONASE FLUTICASONE PROPIONATE 1 0
123838022 12383802 4 C ATROVENT IPRATROPIUM BROMIDE 1 AS REQUIRED 0
123838022 12383802 5 C OTHER MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123838022 12383802 1 Asthma
123838022 12383802 2 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123838022 12383802 Asthma
123838022 12383802 Cough
123838022 12383802 Device defective
123838022 12383802 Drug dose omission
123838022 12383802 Intentional product misuse

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
123838022 12383802 1 201512 0
123838022 12383802 2 201603 0