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
126712881 12671288 1 I 201601 20160211 20160822 20160822 PER US-TEVA-636195USA TEVA 0.00 M 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
126712881 12671288 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; Y 5BR0162 (43F159) 76191 180 MG TABLET QD
126712881 12671288 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 5BR0162 (43F159) 76191
126712881 12671288 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 5BR0162 (43F159) 76191
126712881 12671288 4 C ANTIHYPERTENSIVES UNSPECIFIED INGREDIENT 1 0
126712881 12671288 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712881 12671288 1 Rhinorrhoea
126712881 12671288 2 Eye pruritus
126712881 12671288 3 Lacrimation increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712881 12671288 Drug ineffective
126712881 12671288 Pruritus
126712881 12671288 Rash

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
126712881 12671288 1 201512 201601 0
126712881 12671288 4 2015 0
126712881 12671288 5 2015 0