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
127218691 12721869 1 I 20160823 20160907 20160907 PER US-ASTRAZENECA-2016SE90987 ASTRAZENECA 72.00 YR M Y 0.00000 20160907 OT 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
127218691 12721869 1 PS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral Y U 19810
127218691 12721869 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral Y U 19810 40 MG QD
127218691 12721869 3 C FAMOTADINE 2 Unknown 0 20 MG QD
127218691 12721869 4 C FAMOTADINE 2 Unknown 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127218691 12721869 1 Gastrooesophageal reflux disease
127218691 12721869 2 Gastrooesophageal reflux disease
127218691 12721869 3 Gastrooesophageal reflux disease
127218691 12721869 4 Barrett's oesophagus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127218691 12721869 Barrett's oesophagus
127218691 12721869 Dyspepsia
127218691 12721869 Memory impairment

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
127218691 12721869 2 201607 0
127218691 12721869 3 201607 0
127218691 12721869 4 201607 0