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
113879083 11387908 3 F 20150720 20160728 20150817 20160803 EXP US-ASTRAZENECA-2015SE77624 ASTRAZENECA 23053.00 DY M Y 81.60000 KG 20160803 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
113879083 11387908 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 UG, TWO PUFFS TWICE DAILY 21929 BID
113879083 11387908 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 UG, TWO PUFFS TWICE DAILY 3000913C00 21929 BID
113879083 11387908 3 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) 0 8 DF QD
113879083 11387908 4 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 0 2 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113879083 11387908 1 Chronic obstructive pulmonary disease
113879083 11387908 2 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
113879083 11387908 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113879083 11387908 Choking
113879083 11387908 Device breakage
113879083 11387908 Device malfunction
113879083 11387908 Foreign body

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
113879083 11387908 1 2015 0
113879083 11387908 2 201507 0