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
127276381 12727638 1 I 20160825 20160909 20160909 PER US-ASTRAZENECA-2016SE91887 ASTRAZENECA 0.00 M Y 0.00000 20160909 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
127276381 12727638 1 PS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U U 19810 20 MG BID
127276381 12727638 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U U 19810 20 MG BID
127276381 12727638 3 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U U 19810 20 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127276381 12727638 1 Ulcer
127276381 12727638 2 Abdominal pain upper
127276381 12727638 3 Gastritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127276381 12727638 Off label use
127276381 12727638 Pain
127276381 12727638 Product use issue
127276381 12727638 Throat tightness

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
127276381 12727638 1 20160804 0
127276381 12727638 2 20160804 0
127276381 12727638 3 20160804 0