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
127381361 12738136 1 I 20160102 20160905 20160913 20160913 EXP CN-ASTRAZENECA-2016SE96120 ASTRAZENECA 70.00 YR M Y 70.00000 KG 20160913 MD CN CN

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
127381361 12738136 1 PS ESOMEPRAZOLE MAGNESIUM. ESOMEPRAZOLE MAGNESIUM 1 Oral N 21153 40 MG MODIFIED-RELEASE TABLET QD
127381361 12738136 2 SS ESOMEPRAZOLE MAGNESIUM. ESOMEPRAZOLE MAGNESIUM 1 Oral 6.0DF ONCE/SINGLE ADMINISTRATION N 21153 6 DF MODIFIED-RELEASE TABLET
127381361 12738136 3 C LANSOPRAZOLE. LANSOPRAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127381361 12738136 1 Abdominal pain upper
127381361 12738136 2 Abdominal pain upper
127381361 12738136 3 Abdominal pain upper

Outcome of event

Event ID CASEID OUTC COD
127381361 12738136 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127381361 12738136 Blood creatinine increased
127381361 12738136 Blood potassium increased
127381361 12738136 Blood urea increased
127381361 12738136 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
127381361 12738136 1 20160101 20160102 0
127381361 12738136 2 20160102 20160102 0