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
126061972 12606197 2 F 201606 20160720 20160729 20160801 PER US-ASTRAZENECA-2016SE79097 ASTRAZENECA 1020.00 MON M Y 106.60000 KG 20160801 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
126061972 12606197 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 TWO PUFFS TWICE PER DAY U U 21929 BID
126061972 12606197 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 TWO PUFFS TWICE PER DAY U U 21929 BID
126061972 12606197 3 C ACETYLCYSTEINE. ACETYLCYSTEINE 1 Respiratory (inhalation) AT NIGHT 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126061972 12606197 1 Bronchitis
126061972 12606197 2 Bronchiectasis
126061972 12606197 3 Bronchiectasis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126061972 12606197 Device malfunction
126061972 12606197 Dysphonia
126061972 12606197 Intentional product misuse

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
126061972 12606197 1 20160614 0
126061972 12606197 2 20160614 0