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
126712901 12671290 1 I 20151106 20151216 20160822 20160822 PER US-TEVA-619992USA TEVA 83.39 YR F Y 60.77000 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
126712901 12671290 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; Y 4MR0199 (43F129) 76191 180 MG TABLET QD
126712901 12671290 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 4MR0199 (43F129) 76191
126712901 12671290 3 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
126712901 12671290 4 C EVISTA RALOXIFENE HYDROCHLORIDE 1 0
126712901 12671290 5 C BISOPROLOL W/HYDROCHLOROTHIAZIDE BISOPROLOL FUMARATEHYDROCHLOROTHIAZIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712901 12671290 1 Rhinorrhoea
126712901 12671290 2 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712901 12671290 Dizziness
126712901 12671290 Drug administered to patient of inappropriate age
126712901 12671290 Feeling abnormal

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
126712901 12671290 1 20151106 20151209 0