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
126172791 12617279 1 I 20160511 20160726 20160803 20160803 EXP NL-ASTRAZENECA-2016SE81037 ASTRAZENECA 8032.00 DY F Y 0.00000 20160803 CN NL NL

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
126172791 12617279 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 200/6MCG/DOSIS SPUITBUS 120DO, 1 DF EVERYDAY N U 21929 INHALATION POWDER
126172791 12617279 2 C NON SPECIFIED O.A.C. 2 Intramuscular 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126172791 12617279 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
126172791 12617279 HO
126172791 12617279 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126172791 12617279 Chest discomfort
126172791 12617279 Dyspnoea
126172791 12617279 Fatigue
126172791 12617279 Palpitations
126172791 12617279 Tachycardia

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
126172791 12617279 1 20160427 20160514 0
126172791 12617279 2 2012 0