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
126712741 12671274 1 I 20151130 20151208 20160822 20160822 PER US-TEVA-617654USA TEVA 50.07 YR F Y 55.78000 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
126712741 12671274 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral EVERY DAY AS NEEDED Y 5FE1406 (43F251) 76191 180 MG TABLET
126712741 12671274 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 5FE1406 (43F251) 76191
126712741 12671274 3 C METOPROLOL. METOPROLOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712741 12671274 1 Sinus disorder
126712741 12671274 2 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712741 12671274 Dysgeusia
126712741 12671274 Feeling abnormal
126712741 12671274 Gingival bleeding
126712741 12671274 Off label use
126712741 12671274 Product use issue

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
126712741 12671274 1 20151130 20151205 0