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
113082362 11308236 2 F 20150701 20160530 20150724 20160729 PER US-ASTRAZENECA-2015SE68462 ASTRAZENECA 26535.00 DY F Y 54.40000 KG 20160729 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
113082362 11308236 1 PS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) 400 MCG ONE PUFF TWICE DAILY U U 1136201 202450 INHALATION POWDER
113082362 11308236 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 2 PUFFS TWICE DAILY U U 0 BID
113082362 11308236 3 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) 2.5MG EVERY 4 - 6 HOURS 0 2.5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113082362 11308236 1 Chronic obstructive pulmonary disease
113082362 11308236 2 Chronic obstructive pulmonary disease
113082362 11308236 3 Hypoxia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113082362 11308236 Device malfunction
113082362 11308236 Drug dose omission
113082362 11308236 Dyspnoea
113082362 11308236 Hypoxia

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
113082362 11308236 1 201412 0
113082362 11308236 3 20150701 0