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
127781491 12778149 1 I 20050104 20160925 20160925 PER US-ASTRAZENECA-2005UW00148 ASTRAZENECA 0.00 F Y 0.00000 20160926 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
127781491 12778149 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40.0MG UNKNOWN 21153 40 MG CAPSULE
127781491 12778149 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 0 40 MG CAPSULE BID
127781491 12778149 3 C RANITIDINE. RANITIDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127781491 12778149 1 Gastrooesophageal reflux disease
127781491 12778149 2 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127781491 12778149 Drug hypersensitivity
127781491 12778149 Drug ineffective
127781491 12778149 Dyspepsia
127781491 12778149 Epistaxis
127781491 12778149 Hypertension
127781491 12778149 Hypotension
127781491 12778149 Intentional product misuse
127781491 12778149 Laryngeal polyp
127781491 12778149 Off label use

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
127781491 12778149 1 1989 0