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
126713651 12671365 1 I 20160624 20160624 20160822 20160822 PER US-TEVA-673412USA TEVA 75.56 YR F Y 72.56000 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
126713651 12671365 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral Y 6BE1128 (43F397 76191 180 MG TABLET
126713651 12671365 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 6BE1128 (43F397 76191
126713651 12671365 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 6BE1128 (43F397 76191

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126713651 12671365 1 Eye pruritus
126713651 12671365 2 Sneezing
126713651 12671365 3 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126713651 12671365 Drug administered to patient of inappropriate age
126713651 12671365 Dry mouth
126713651 12671365 Extra dose administered

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
126713651 12671365 1 20160624 20160624 0