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
124787482 12478748 2 F 201604 20160817 20160619 20160829 PER US-ASTRAZENECA-2016SE50283 ASTRAZENECA 1128.00 MON M Y 72.60000 KG 20160827 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
124787482 12478748 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, 2 PUFFS TWO TIMES A DAY Y U 3001131C00 21929
124787482 12478748 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, ONE PUFF TWO TIMES A DAY Y U 3001131C00 21929

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124787482 12478748 1 Chronic obstructive pulmonary disease
124787482 12478748 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124787482 12478748 Dry mouth
124787482 12478748 Dysphonia
124787482 12478748 Off label use
124787482 12478748 Product quality issue
124787482 12478748 Wrong technique in product usage process

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
124787482 12478748 1 20160413 0