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
126281851 12628185 1 I 2015 20160802 20160808 20160808 PER US-ASTRAZENECA-2016SE84201 ASTRAZENECA 53.00 YR F Y 94.30000 KG 20160808 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
126281851 12628185 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U 21153
126281851 12628185 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 0
126281851 12628185 3 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 40 MG BID
126281851 12628185 4 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 40 MG QD
126281851 12628185 5 SS PURPLE PILL UNSPECIFIED INGREDIENT 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126281851 12628185 1 Gastrooesophageal reflux disease
126281851 12628185 2 Gastrooesophageal reflux disease
126281851 12628185 3 Gastrooesophageal reflux disease
126281851 12628185 4 Gastrooesophageal reflux disease
126281851 12628185 5 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126281851 12628185 Diabetes mellitus
126281851 12628185 Intentional product misuse
126281851 12628185 Off label use
126281851 12628185 Osteoporosis
126281851 12628185 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
126281851 12628185 3 2012 0
126281851 12628185 4 2012 0
126281851 12628185 5 1995 0