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
126462161 12646216 1 I 2009 20100628 20160811 20160811 EXP US-ASTRAZENECA-2010SE30307 ASTRAZENECA 48.00 YR M Y 0.00000 20160812 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
126462161 12646216 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 21153 40 MG QD
126462161 12646216 2 SS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral U 0 MODIFIED-RELEASE TABLET
126462161 12646216 3 C PROTONIX PANTOPRAZOLE SODIUM 1 0
126462161 12646216 4 C RABEPRAZOLE RABEPRAZOLE 1 0
126462161 12646216 5 C ZEGRID 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126462161 12646216 1 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
126462161 12646216 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126462161 12646216 Chest discomfort
126462161 12646216 Diarrhoea
126462161 12646216 Drug ineffective
126462161 12646216 Drug intolerance
126462161 12646216 Dysphagia
126462161 12646216 Irritable bowel syndrome
126462161 12646216 Nerve injury
126462161 12646216 Oesophageal disorder
126462161 12646216 Panic disorder
126462161 12646216 Pharyngeal disorder

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
126462161 12646216 1 2009 0