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
116036733 11603673 3 F 20160831 20151007 20160920 PER US-ASTRAZENECA-2015SE93420 ASTRAZENECA 0.00 F Y 54.40000 KG 20160920 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
116036733 11603673 1 PS EKLIRA ACLIDINIUM BROMIDE 1 Respiratory (inhalation) U U 08142015,1145539 202450 400 UG INHALATION POWDER QD
116036733 11603673 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral 0
116036733 11603673 3 C VITAMIN D CHOLECALCIFEROL 1 Oral 0
116036733 11603673 4 C MULTIVITAMIN VITAMINS 1 Oral 0
116036733 11603673 5 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
116036733 11603673 6 C UNSPECIFIED MEDICATION UNSPECIFIED INGREDIENT 1 0
116036733 11603673 7 C UNSPECIFIED MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116036733 11603673 1 Chronic obstructive pulmonary disease
116036733 11603673 6 Anxiety
116036733 11603673 7 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
116036733 11603673 Activities of daily living impaired
116036733 11603673 Cough
116036733 11603673 Device issue
116036733 11603673 Drug dose omission
116036733 11603673 Drug ineffective
116036733 11603673 Intentional product misuse
116036733 11603673 Product quality issue
116036733 11603673 Productive cough

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
116036733 11603673 1 2015 0