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
126712431 12671243 1 I 20150901 20160822 20160822 PER US-TEVA-591471USA TEVA 0.00 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
126712431 12671243 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral AS NEEDED 5DV0660 (43F198) 76191 180 MG TABLET
126712431 12671243 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral AS NEEDED 5DV0660 (43F198) 76191 180 MG TABLET
126712431 12671243 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 5DV0660 (43F198) 76191
126712431 12671243 4 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 5DV0660 (43F198) 76191
126712431 12671243 5 C AFRIN OXYMETAZOLINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712431 12671243 1 Seasonal allergy
126712431 12671243 2 Rhinorrhoea
126712431 12671243 3 Eye pruritus
126712431 12671243 4 Sneezing

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712431 12671243 Drug effect decreased

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
126712431 12671243 1 201507 201507 0
126712431 12671243 2 201104 0