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
127555691 12755569 1 I 2012 20160914 20160916 20160916 EXP MX-SA-2016SA170542 AVENTIS 40.00 YR A M Y 67.50000 KG 20160916 CN MX MX

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
127555691 12755569 1 PS AVAPRO IRBESARTAN 1 Oral U 20757 1 DF TABLET QD
127555691 12755569 2 C CAPTOPRIL. CAPTOPRIL 1 Oral 0 TABLET
127555691 12755569 3 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 CAPSULE
127555691 12755569 4 C TELMISARTAN. TELMISARTAN 1 Oral 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127555691 12755569 1 Hypertension
127555691 12755569 2 Hypertension
127555691 12755569 3 Gastritis

Outcome of event

Event ID CASEID OUTC COD
127555691 12755569 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127555691 12755569 Hypertension
127555691 12755569 Thyroid disorder

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
127555691 12755569 1 2012 2015 0
127555691 12755569 2 2012 2015 0
127555691 12755569 4 2012 0