The Safety Rates Drug Report

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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
126712951 12671295 1 I 201604 20160502 20160822 20160822 PER US-TEVA-657965USA TEVA 59.57 YR F Y 0.00000 20160822 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
126712951 12671295 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; Y 5KR0129, (43F335) 76191 180 MG TABLET QD
126712951 12671295 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 5KR0129, (43F335) 76191
126712951 12671295 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 5KR0129, (43F335) 76191
126712951 12671295 4 C MULTIVITAMIN VITAMINS 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712951 12671295 1 Rhinorrhoea
126712951 12671295 2 Eye pruritus
126712951 12671295 3 Perennial allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712951 12671295 Back pain
126712951 12671295 Feeling jittery
126712951 12671295 Irritability
126712951 12671295 Pollakiuria

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
126712951 12671295 1 201604 201604 0
126712951 12671295 4 2012 0