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
126713621 12671362 1 I 20160622 20160623 20160822 20160822 PER US-TEVA-672860USA TEVA 66.91 YR F Y 52.15000 KG 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
126713621 12671362 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral Y 6CR0233 (43F457) 76191 TABLET QD
126713621 12671362 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 6CR0233 (43F457) 76191
126713621 12671362 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 6CR0233 (43F457) 76191
126713621 12671362 4 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 6CR0233 (43F457) 76191

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126713621 12671362 1 Seasonal allergy
126713621 12671362 2 Eye pruritus
126713621 12671362 3 Rhinorrhoea
126713621 12671362 4 Sneezing

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126713621 12671362 Drug administered to patient of inappropriate age
126713621 12671362 Nausea
126713621 12671362 Paranasal sinus discomfort

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
126713621 12671362 1 20160622 20160623 0