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
127353931 12735393 1 I 2007 20160826 20160912 20160912 PER US-ASTRAZENECA-2016SE92411 ASTRAZENECA 0.00 M Y 59.00000 KG 20160912 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
127353931 12735393 1 PS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral 21229 20 MG MODIFIED-RELEASE TABLET QD
127353931 12735393 2 C SUCRALFATE. SUCRALFATE 1 0
127353931 12735393 3 C PEPCID FAMOTIDINE 1 80 MG,UNKNOWN 0
127353931 12735393 4 C VALIUM DIAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127353931 12735393 1 Gastrooesophageal reflux disease
127353931 12735393 4 Oesophageal disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127353931 12735393 Abdominal pain upper
127353931 12735393 Chest discomfort
127353931 12735393 Chills
127353931 12735393 Dysphagia
127353931 12735393 Malaise
127353931 12735393 Weight decreased

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
127353931 12735393 1 2007 2007 0