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
126712401 12671240 1 I 20150912 20150923 20160822 20160822 PER US-TEVA-597291USA TEVA 67.12 YR M Y 76.19000 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
126712401 12671240 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral SINGLE Y Y 5ER0280 (43F243) 76191 180 MG TABLET
126712401 12671240 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral SINGLE Y Y 5ER0280 (43F243) 76191 180 MG TABLET
126712401 12671240 3 C ULORIC FEBUXOSTAT 1 0
126712401 12671240 4 C ATORVASTATIN ATORVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712401 12671240 1 Nasal congestion

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712401 12671240 Drug administered to patient of inappropriate age
126712401 12671240 Off label use
126712401 12671240 Pruritus Pruritus
126712401 12671240 Urticaria Urticaria

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
126712401 12671240 1 20150912 20150912 0
126712401 12671240 2 20150914 20150914 0
126712401 12671240 3 2008 0
126712401 12671240 4 2008 0