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
125959161 12595916 1 I 20160702 20160715 20160727 20160727 PER US-ASTRAZENECA-2016SE78393 ASTRAZENECA 15699.00 DY F Y 70.30000 KG 20160727 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
125959161 12595916 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 4880 MG U 0 40 MG QD
125959161 12595916 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 4880 MG U 0 40 MG QD
125959161 12595916 3 SS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral U U 0 20 MG QD
125959161 12595916 4 SS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral U U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125959161 12595916 1 Gastritis
125959161 12595916 2 Inflammation
125959161 12595916 3 Gastritis
125959161 12595916 4 Inflammation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125959161 12595916 Arthralgia
125959161 12595916 Off label use
125959161 12595916 Product use issue

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
125959161 12595916 1 201603 0
125959161 12595916 2 201603 0
125959161 12595916 3 20160709 0
125959161 12595916 4 20160709 0