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
85070423 8507042 3 F 20110829 20120412 20160927 PER US-ASTRAZENECA-2011SE38855 ASTRAZENECA 0.00 M Y 0.00000 20160927 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
85070423 8507042 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U U 21153 40 MG QD
85070423 8507042 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U U 0 40 MG CAPSULE QD
85070423 8507042 3 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U U 0 20 MG CAPSULE BID
85070423 8507042 4 C DEXILANT DEXLANSOPRAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
85070423 8507042 1 Gastrooesophageal reflux disease
85070423 8507042 2 Gastrooesophageal reflux disease
85070423 8507042 3 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
85070423 8507042 Abdominal distension
85070423 8507042 Dizziness
85070423 8507042 Drug dose omission
85070423 8507042 Drug ineffective
85070423 8507042 Dyspnoea
85070423 8507042 Dyspnoea paroxysmal nocturnal
85070423 8507042 Hypoaesthesia
85070423 8507042 Limb injury
85070423 8507042 Neck injury
85070423 8507042 Somnolence

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

no results found

Therapies reported

no results found