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
122875533 12287553 3 F 20160314 20160429 20160420 20160805 PER US-ASTRAZENECA-2016SE32785 ASTRAZENECA 54.00 YR F Y 0.00000 20160806 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
122875533 12287553 1 PS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral Y U 21229 1 DF MODIFIED-RELEASE TABLET QD
122875533 12287553 2 SS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral 20.0MG UNKNOWN Y U 21229 20 MG MODIFIED-RELEASE TABLET
122875533 12287553 3 SS DIPHENHYDRAMINE. DIPHENHYDRAMINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122875533 12287553 1 Dyspepsia
122875533 12287553 2 Dyspepsia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122875533 12287553 Condition aggravated
122875533 12287553 Drug ineffective
122875533 12287553 Fatigue
122875533 12287553 Product colour issue
122875533 12287553 Product quality issue
122875533 12287553 Product shape issue
122875533 12287553 Somnolence
122875533 12287553 Wrong drug administered

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

no results found

Therapies reported

no results found