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
122975592 12297559 2 F 20160223 20160527 20160422 20160727 PER US-ASTRAZENECA-2016SE29517 ASTRAZENECA 25368.00 DY F Y 83.90000 KG 20160727 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
122975592 12297559 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, TWO PUFFS TWICE A DAY 21929 BID
122975592 12297559 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, TWO PUFFS TWICE A DAY 3001131C00 21929 BID
122975592 12297559 3 C PREDNISONE. PREDNISONE 1 0
122975592 12297559 4 C ALBUTEROL. ALBUTEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122975592 12297559 1 Allergic bronchitis
122975592 12297559 2 Allergic bronchitis
122975592 12297559 3 Allergic bronchitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122975592 12297559 Circumstance or information capable of leading to medication error
122975592 12297559 Device malfunction
122975592 12297559 Wheezing

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
122975592 12297559 1 2014 0
122975592 12297559 2 201602 0