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
126712261 12671226 1 I 20150804 20150806 20160822 20160822 PER US-TEVA-585620USA TEVA 61.95 YR 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
126712261 12671226 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; 5DE1303 (43F181) 76191 180 MG TABLET QD
126712261 12671226 2 SS CETIRIZINE CETIRIZINE HYDROCHLORIDE 1 Oral 10 MILLIGRAM DAILY; 5EE1316 77279 10 MG QD
126712261 12671226 3 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
126712261 12671226 4 C ESTRACE ESTRADIOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712261 12671226 1 Urticaria
126712261 12671226 2 Urticaria

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712261 12671226 Eye swelling
126712261 12671226 Inappropriate schedule of drug administration
126712261 12671226 Off label use
126712261 12671226 Therapeutic response unexpected

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
126712261 12671226 1 20150804 0
126712261 12671226 2 20150804 0
126712261 12671226 4 2011 0