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
107972822 10797282 2 F 20160708 20150216 20160713 EXP US-ASTRAZENECA-2015SE11543 ASTRAZENECA 71.00 YR F Y 0.00000 20160713 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
107972822 10797282 1 PS ESOMEPRAZOLE MAGNESIUM. ESOMEPRAZOLE MAGNESIUM 1 Oral U 0
107972822 10797282 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral U 0
107972822 10797282 3 SS OMEPRAZOLE. OMEPRAZOLE 1 Unknown GASEC U 0
107972822 10797282 4 SS GAS-X DIMETHICONE 1 Unknown U 0
107972822 10797282 5 C PROTONIX PANTOPRAZOLE SODIUM 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
107972822 10797282 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107972822 10797282 Aplasia
107972822 10797282 Drug ineffective
107972822 10797282 Dyspepsia
107972822 10797282 Gastrooesophageal reflux disease
107972822 10797282 Hernia
107972822 10797282 Malaise
107972822 10797282 Nausea
107972822 10797282 Vomiting

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

no results found

Therapies reported

no results found