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
104112092 10411209 2 F 201401 20160913 20140826 20160928 PER US-ASTRAZENECA-2014SE19350 ASTRAZENECA 654.00 MON M Y 81.60000 KG 20160928 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
104112092 10411209 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG; 2 INHALATIONS BID U U 21929
104112092 10411209 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG; 2 INHALATIONS BID U U 21929
104112092 10411209 3 C COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 20-100 MCG DAILY 0
104112092 10411209 4 C ALBUTEROL SULFATE. ALBUTEROL SULFATE 1 Respiratory (inhalation) NOT REPORTED PRN 0
104112092 10411209 5 C MONTELUKAST MONTELUKAST SODIUM 1 Oral 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104112092 10411209 1 Asthma
104112092 10411209 2 Chronic obstructive pulmonary disease
104112092 10411209 3 Asthma
104112092 10411209 5 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104112092 10411209 Drug dose omission
104112092 10411209 Feeding disorder
104112092 10411209 Oral candidiasis
104112092 10411209 Oral discomfort
104112092 10411209 Oral pain
104112092 10411209 Tongue discomfort

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
104112092 10411209 1 201401 20141219 0
104112092 10411209 2 201401 20141219 0