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
126825831 12682583 1 I 20160819 20160825 20160825 PER US-ASTRAZENECA-2016SE90319 ASTRAZENECA 0.00 F Y 68.00000 KG 20160825 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
126825831 12682583 1 PS NEXIUM 24HR ESOMEPRAZOLE MAGNESIUM 1 Oral BANZ 204655 22.3 MG CAPSULE QD
126825831 12682583 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 0
126825831 12682583 3 C ADVIL IBUPROFEN 1 0
126825831 12682583 4 C ADVIL IBUPROFEN 1 0
126825831 12682583 5 C ADVIL IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126825831 12682583 1 Dyspepsia
126825831 12682583 3 Intervertebral disc protrusion
126825831 12682583 4 Scoliosis
126825831 12682583 5 Arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126825831 12682583 Constipation
126825831 12682583 Diarrhoea
126825831 12682583 Drug dose omission
126825831 12682583 Drug ineffective
126825831 12682583 Flatulence
126825831 12682583 Product use issue

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

no results found

Therapies reported

no results found