The Safety Rates Drug Report

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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
126712491 12671249 1 I 2015 20150924 20160822 20160822 PER US-TEVA-597721USA TEVA 0.00 M Y 90.70000 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
126712491 12671249 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; Y 4MR0247 (43F130) 76191 180 MG TABLET QD
126712491 12671249 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 4MR0247 (43F130) 76191
126712491 12671249 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 4MR0247 (43F130) 76191
126712491 12671249 4 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 4MR0247 (43F130) 76191
126712491 12671249 5 C SINGULAIR MONTELUKAST SODIUM 1 0
126712491 12671249 6 C AMLODIPINE AMLODIPINE BESYLATE 1 0
126712491 12671249 7 C CRESTOR ROSUVASTATIN CALCIUM 1 0
126712491 12671249 8 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
126712491 12671249 9 C ALLERGEN EXTRACTS 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712491 12671249 1 Hypersensitivity
126712491 12671249 2 Rhinorrhoea
126712491 12671249 3 Eye pruritus
126712491 12671249 4 Lacrimation increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712491 12671249 Drug administered to patient of inappropriate age
126712491 12671249 Dry mouth
126712491 12671249 Dry throat
126712491 12671249 Mucosal dryness

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
126712491 12671249 1 2015 201509 0