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
114275942 11427594 2 F 201506 20150821 20150827 20160831 PER US-SA-2015SA088421 AVENTIS 0.00 E F Y 0.00000 20160831 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
114275942 11427594 1 PS AVAPRO IRBESARTAN 1 Unknown Y UNKNOWN 20757 300 MG FILM-COATED TABLET QD
114275942 11427594 2 SS AVAPRO IRBESARTAN 1 Unknown Y UNKNOWN 20757 150 MG FILM-COATED TABLET QD
114275942 11427594 3 C AVAPRO IRBESARTAN 1 AVAPRO 300 MG BY BRISTOL MEYER SQUIBB 0 300 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114275942 11427594 1 Hypertension
114275942 11427594 2 Hypertension
114275942 11427594 3 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
114275942 11427594 Adverse event
114275942 11427594 Asthenia
114275942 11427594 Chest discomfort
114275942 11427594 Nervousness

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
114275942 11427594 1 201506 201506 0
114275942 11427594 2 201506 201506 0
114275942 11427594 3 1980 2015 0