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
126663341 12666334 1 I 20160810 20160818 20160818 EXP NL-ASTRAZENECA-2016SE88022 ASTRAZENECA 0.00 F Y 0.00000 20160818 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
126663341 12666334 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) U 21929 INHALATION POWDER
126663341 12666334 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) U 21929 INHALATION POWDER
126663341 12666334 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) U 21929 INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126663341 12666334 1 Chronic obstructive pulmonary disease
126663341 12666334 2 Asthma
126663341 12666334 3 Lower respiratory tract infection fungal

Outcome of event

Event ID CASEID OUTC COD
126663341 12666334 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126663341 12666334 Balance disorder
126663341 12666334 Fall
126663341 12666334 Wrist fracture

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found