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
126360411 12636041 1 I 201605 20160408 20160809 20160809 PER US-ASTRAZENECA-2016SE82633 ASTRAZENECA 0.00 F Y 0.00000 20160809 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
126360411 12636041 1 PS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) 400 MCG, UNKNOWN 202450 INHALATION POWDER
126360411 12636041 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, 1 PUFF TWICE DAILY 0
126360411 12636041 3 C XOPENEX HFA LEVALBUTEROL TARTRATE 1 AS REQUIRED 0
126360411 12636041 4 C MEDICATION UNSPECIFIED INGREDIENT 1 0
126360411 12636041 5 C MEDICATION UNSPECIFIED INGREDIENT 1 0
126360411 12636041 6 C MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126360411 12636041 1 Asthma
126360411 12636041 2 Asthma
126360411 12636041 4 Blood cholesterol abnormal
126360411 12636041 5 Hypotension
126360411 12636041 6 Inhalation therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126360411 12636041 Asthma
126360411 12636041 Discomfort
126360411 12636041 Dysphonia
126360411 12636041 Fatigue
126360411 12636041 Fluid retention
126360411 12636041 Off label use
126360411 12636041 Pain
126360411 12636041 Pneumonia

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
126360411 12636041 2 201601 0