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
126828571 12682857 1 I 20160801 20160825 20160825 PER US-ASTRAZENECA-2016SE83783 ASTRAZENECA 44.00 YR F Y 0.00000 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
126828571 12682857 1 PS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral U U 21229 MODIFIED-RELEASE TABLET
126828571 12682857 2 SS CHANTIX VARENICLINE TARTRATE 1 Unknown U 0
126828571 12682857 3 C LISINOPRIL. LISINOPRIL 1 0
126828571 12682857 4 C METOPROLOL. METOPROLOL 1 0
126828571 12682857 5 C ANTACID ALUMINUM HYDROXIDECALCIUM CARBONATEDIMETHICONEMAGNESIUM HYDROXIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126828571 12682857 1 Antacid therapy
126828571 12682857 2 Tobacco withdrawal symptoms
126828571 12682857 3 Blood pressure abnormal
126828571 12682857 4 Blood pressure abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126828571 12682857 Drug ineffective
126828571 12682857 Enuresis

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

no results found

Therapies reported

no results found