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
122276862 12227686 2 F 2015 20160923 20160401 20160930 EXP US-ASTRAZENECA-2016SE31006 ASTRAZENECA 62.00 YR M Y 86.20000 KG 20160930 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
122276862 12227686 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG TOW PUFFS, TWO TIMES A DAY U U 3001241C00 21929 BID
122276862 12227686 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG TOW PUFFS, TWO TIMES A DAY U U 21929 BID
122276862 12227686 3 C VENTOLIN INH 2 Respiratory (inhalation) 0
122276862 12227686 4 C OXYGEN. OXYGEN 1 Nasal 2.0L CONTINUOUSLY 0 2 L

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122276862 12227686 1 Chronic obstructive pulmonary disease
122276862 12227686 2 Chronic obstructive pulmonary disease
122276862 12227686 3 Chronic obstructive pulmonary disease
122276862 12227686 4 Dyspnoea

Outcome of event

Event ID CASEID OUTC COD
122276862 12227686 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122276862 12227686 Adenosquamous cell lung cancer
122276862 12227686 Device malfunction
122276862 12227686 Drug dose omission
122276862 12227686 Dyspnoea
122276862 12227686 Incorrect dose administered by device

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
122276862 12227686 1 2013 0
122276862 12227686 2 201603 0