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
86444545 8644454 5 F 20160914 20120629 20160922 EXP US-ASTRAZENECA-2012SE27870 ASTRAZENECA 73.00 YR F Y 0.00000 20160922 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
86444545 8644454 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U 21153 40 MG QD
86444545 8644454 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 0 CAPSULE
86444545 8644454 3 SS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) 400 MCG TWICE A DAY U 1147663 0 INHALATION POWDER
86444545 8644454 4 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 0
86444545 8644454 5 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
86444545 8644454 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86444545 8644454 Circumstance or information capable of leading to medication error
86444545 8644454 Device malfunction
86444545 8644454 Drug dose omission
86444545 8644454 Drug ineffective
86444545 8644454 Dysphonia
86444545 8644454 Dyspnoea
86444545 8644454 Gastrooesophageal reflux disease
86444545 8644454 Hiatus hernia
86444545 8644454 Intentional product misuse

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
86444545 8644454 3 20160201 0
86444545 8644454 4 2006 0
86444545 8644454 5 2006 0