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
126712671 12671267 1 I 20160124 20160129 20160822 20160822 PER US-TEVA-632579USA TEVA 59.67 YR F Y 81.63000 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
126712671 12671267 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; 5KR0247 (43F326) 76191 180 MG TABLET QD
126712671 12671267 2 C LIPITOR ATORVASTATIN CALCIUM 1 0
126712671 12671267 3 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
126712671 12671267 4 C BABY ASPIRIN ASPIRIN 1 0
126712671 12671267 5 C One a Day Womens 50 Plus Multivitamin 2 0
126712671 12671267 6 C TAMSULOSIN TAMSULOSIN 1 0
126712671 12671267 7 C FENOFIBRATE. FENOFIBRATE 1 0
126712671 12671267 8 C ATENOLOL. ATENOLOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712671 12671267 1 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712671 12671267 Drug ineffective

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
126712671 12671267 1 20160124 20160129 0