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
125347091 12534709 1 I 20160527 20160706 20160706 PER US-ASTRAZENECA-2016SE58347 ASTRAZENECA 0.00 F Y 0.00000 20160707 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
125347091 12534709 1 PS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 19810
125347091 12534709 2 SS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral U 0 MODIFIED-RELEASE TABLET
125347091 12534709 3 C REGLAN METOCLOPRAMIDE HYDROCHLORIDE 1 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125347091 12534709 Depression
125347091 12534709 Drug dose omission

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found