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
89185983 8918598 3 F 2012 20160526 20121120 20160725 PER US-ASTRAZENECA-2012SE19377 ASTRAZENECA 71.00 YR F Y 64.40000 KG 20160725 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
89185983 8918598 1 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral GENERIC 0
89185983 8918598 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 0 40 MG CAPSULE BID
89185983 8918598 3 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 0 22 MG BID
89185983 8918598 4 PS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral 21229 MODIFIED-RELEASE TABLET
89185983 8918598 5 C RECLAST ZOLEDRONIC ACID 1 0
89185983 8918598 6 C RECLAST ZOLEDRONIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89185983 8918598 1 Gastrooesophageal reflux disease
89185983 8918598 2 Gastrooesophageal reflux disease
89185983 8918598 3 Gastrooesophageal reflux disease
89185983 8918598 5 Bone disorder
89185983 8918598 6 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
89185983 8918598 Appetite disorder
89185983 8918598 Decreased appetite
89185983 8918598 Drug dose omission
89185983 8918598 Drug ineffective
89185983 8918598 Gastrooesophageal reflux disease
89185983 8918598 Off label use
89185983 8918598 Osteoporosis

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
89185983 8918598 2 2006 2016 0
89185983 8918598 3 2016 0