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
127808431 12780843 1 I 20160912 20160915 20160926 20160926 EXP US-SA-2016SA172850 AVENTIS 70.00 YR E M Y 0.00000 20160926 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
127808431 12780843 1 PS ALLEGRA-D 24 HOUR FEXOFENADINE HYDROCHLORIDEPSEUDOEPHEDRINE HYDROCHLORIDE 1 Oral DOSE 180/240MG N HG104T 21704 PROLONGED-RELEASE TABLET 1X
127808431 12780843 2 SS ALLEGRA-D 24 HOUR FEXOFENADINE HYDROCHLORIDEPSEUDOEPHEDRINE HYDROCHLORIDE 1 Oral DOSE 180/240MG N HG104T 21704 PROLONGED-RELEASE TABLET 1X
127808431 12780843 3 SS ALLEGRA-D 24 HOUR FEXOFENADINE HYDROCHLORIDEPSEUDOEPHEDRINE HYDROCHLORIDE 1 Oral DOSE 180/240MG N HG104T 21704 PROLONGED-RELEASE TABLET 1X

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127808431 12780843 1 Nasal congestion
127808431 12780843 2 Multiple allergies
127808431 12780843 3 Nasal congestion

Outcome of event

Event ID CASEID OUTC COD
127808431 12780843 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127808431 12780843 Dysuria
127808431 12780843 Insomnia
127808431 12780843 Thrombosis

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
127808431 12780843 1 20160912 20160912 0
127808431 12780843 2 20160912 20160912 0
127808431 12780843 3 20160912 20160912 0