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
127541521 12754152 1 I 20160906 20160916 20160916 PER US-ASTRAZENECA-2016SE95661 ASTRAZENECA 0.00 M Y 63.50000 KG 20160916 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
127541521 12754152 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 2 PUFFS TWICE PER DAY Y 21929
127541521 12754152 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 2 PUFFS TWICE PER DAY Y 21929
127541521 12754152 3 SS LISINOPRIL. LISINOPRIL 1 Oral U U 0 20 MG TABLET QD
127541521 12754152 4 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral U 0 20 MG QD
127541521 12754152 5 C MELOXICAM. MELOXICAM 1 Oral 0 7.5 UG/KG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127541521 12754152 1 Chronic obstructive pulmonary disease
127541521 12754152 2 Chronic obstructive pulmonary disease
127541521 12754152 3 Blood pressure abnormal
127541521 12754152 5 Foot deformity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127541521 12754152 Choking
127541521 12754152 Cough
127541521 12754152 Dyspnoea
127541521 12754152 Intentional product misuse

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

no results found

Therapies reported

no results found