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
126712251 12671225 1 I 20150812 20150814 20160822 20160822 PER US-TEVA-588076USA TEVA 88.85 YR F Y 4101.00000 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
126712251 12671225 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; Y 5B3657 (43F102) 76191 180 MG TABLET QD
126712251 12671225 2 SS ADVANCED COLON CARE DIETARY SUPPLEMENT 1 Oral 0 CAPSULE 1X
126712251 12671225 3 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
126712251 12671225 4 C XANAX ALPRAZOLAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712251 12671225 1 Hypersensitivity
126712251 12671225 2 Irritable bowel syndrome

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712251 12671225 Diarrhoea
126712251 12671225 Drug administered to patient of inappropriate age
126712251 12671225 Dysgeusia
126712251 12671225 Wrong technique in product usage process

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
126712251 12671225 1 20150812 20150813 0
126712251 12671225 2 20150807 20150807 0