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
125956821 12595682 1 I 2014 20160715 20160727 20160727 PER US-ASTRAZENECA-2016SE78530 ASTRAZENECA 58.00 YR F Y 86.20000 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
125956821 12595682 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 1 CAPSULE DAILY EVERY OTHER DAY OR AS NEEDED 204655 CAPSULE
125956821 12595682 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral DAILY 0 CAPSULE
125956821 12595682 3 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral DAILY 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125956821 12595682 1 Dyspepsia
125956821 12595682 2 Sleep apnoea syndrome
125956821 12595682 3 Abdominal discomfort

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125956821 12595682 Activities of daily living impaired
125956821 12595682 Back pain
125956821 12595682 Constipation
125956821 12595682 Large intestine polyp
125956821 12595682 Off label use
125956821 12595682 Product use issue
125956821 12595682 Renal pain

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
125956821 12595682 2 2014 0
125956821 12595682 3 2014 0