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
125863272 12586327 2 F 20150817 20160720 20160725 20160803 PER US-ASTRAZENECA-2016SE77459 ASTRAZENECA 17037.00 DY M Y 140.60000 KG 20160803 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
125863272 12586327 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U U 21153 40 MG CAPSULE QD
125863272 12586327 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U U 21153 40 MG CAPSULE QD
125863272 12586327 3 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U U 21153
125863272 12586327 4 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U U 21153
125863272 12586327 5 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral GENERIC, 40 MG DAILY U U 21153
125863272 12586327 6 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral GENERIC, 40 MG DAILY U U 21153
125863272 12586327 7 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral GENERIC, 40 MG DAILY U U 21153
125863272 12586327 8 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral GENERIC, 40 MG DAILY U U 21153
125863272 12586327 9 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 0 40 MG QD
125863272 12586327 10 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U U 0 20 MG CAPSULE BID
125863272 12586327 11 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U U 0 40 MG CAPSULE QD
125863272 12586327 12 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral OMEPRAZOLE U U 0
125863272 12586327 13 C BENAZEPRIL BENAZEPRIL HYDROCHLORIDE 1 Oral 0 24 MG QD
125863272 12586327 14 C LOTROPRIL 2 Oral 0 20 MG QD
125863272 12586327 15 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
125863272 12586327 16 C PROTONIX PANTOPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125863272 12586327 1 Gastrooesophageal reflux disease
125863272 12586327 2 Gastrooesophageal reflux disease
125863272 12586327 3 Gastrooesophageal reflux disease
125863272 12586327 4 Gastrooesophageal reflux disease
125863272 12586327 5 Gastrooesophageal reflux disease
125863272 12586327 6 Gastrooesophageal reflux disease
125863272 12586327 7 Gastrooesophageal reflux disease
125863272 12586327 8 Gastrooesophageal reflux disease
125863272 12586327 9 Gastrooesophageal reflux disease
125863272 12586327 10 Gastrooesophageal reflux disease
125863272 12586327 11 Gastrooesophageal reflux disease
125863272 12586327 12 Gastrooesophageal reflux disease
125863272 12586327 13 Hypertension
125863272 12586327 14 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125863272 12586327 Condition aggravated
125863272 12586327 Drug effect decreased
125863272 12586327 Drug ineffective
125863272 12586327 Gastric ulcer
125863272 12586327 Gastrooesophageal reflux disease
125863272 12586327 Malaise

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
125863272 12586327 1 2005 20160621 0
125863272 12586327 2 2005 20160621 0
125863272 12586327 3 2012 0
125863272 12586327 4 2012 0
125863272 12586327 5 2015 0
125863272 12586327 6 2015 0
125863272 12586327 7 201606 0
125863272 12586327 8 201606 0
125863272 12586327 9 20160623 0
125863272 12586327 13 201601 0
125863272 12586327 14 1990 201601 0