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
85067664 8506766 4 F 20160902 20120412 20160924 PER US-ASTRAZENECA-2011SE29121 ASTRAZENECA 63.00 YR M Y 0.00000 20160924 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
85067664 8506766 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40.0MG UNKNOWN U 21153 40 MG CAPSULE
85067664 8506766 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40.0MG UNKNOWN U 21153 40 MG TABLET
85067664 8506766 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) U 0
85067664 8506766 4 C ZANTAC RANITIDINE 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
85067664 8506766 Abdominal pain upper
85067664 8506766 Drug dose omission
85067664 8506766 Dyspepsia
85067664 8506766 Intentional product misuse
85067664 8506766 Muscle spasms
85067664 8506766 Peripheral swelling
85067664 8506766 Regurgitation

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
85067664 8506766 3 201502 0