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
126713301 12671330 1 I 20160511 20160511 20160822 20160822 PER US-TEVA-660775USA TEVA 68.17 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
126713301 12671330 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral N 6AE1509 (43F377) 76191 180 MG TABLET
126713301 12671330 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 N 6AE1509 (43F377) 76191
126713301 12671330 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 N 6AE1509 (43F377) 76191

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126713301 12671330 1 Eye pruritus
126713301 12671330 2 Sinus congestion
126713301 12671330 3 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126713301 12671330 Drug administered to patient of inappropriate age
126713301 12671330 Product use issue
126713301 12671330 Tinnitus

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
126713301 12671330 1 20160511 20160511 0