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
126713131 12671313 1 I 20160219 20160222 20160822 20160822 PER US-TEVA-639233USA TEVA 83.07 YR F Y 65.31000 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
126713131 12671313 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; Y 6AR0153 (43F352) 76191 180 MG TABLET QD
126713131 12671313 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 6AR0153 (43F352) 76191
126713131 12671313 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 6AR0153 (43F352) 76191
126713131 12671313 4 C NAPROXEN. NAPROXEN 1 0
126713131 12671313 5 C LOVASTATIN. LOVASTATIN 1 0
126713131 12671313 6 C LEVOTHYROXINE. LEVOTHYROXINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126713131 12671313 1 Rhinorrhoea
126713131 12671313 2 Nasal congestion
126713131 12671313 3 Nasopharyngitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126713131 12671313 Drug administered to patient of inappropriate age
126713131 12671313 Insomnia
126713131 12671313 Off label use

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
126713131 12671313 1 20160219 20160219 0
126713131 12671313 4 201601 0