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
126712731 12671273 1 I 20151214 20151215 20160822 20160822 PER US-TEVA-620024USA TEVA 67.97 YR F Y 61.22000 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
126712731 12671273 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral Y 5HE1191 (43F271) 76191 TABLET
126712731 12671273 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 5HE1191 (43F271) 76191
126712731 12671273 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Y 5HE1191 (43F271) 76191
126712731 12671273 4 C SIMVASTATIN. SIMVASTATIN 1 0
126712731 12671273 5 C AMLODIPINE AMLODIPINE BESYLATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712731 12671273 1 Rhinorrhoea
126712731 12671273 2 Eye pruritus
126712731 12671273 3 Lacrimation increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712731 12671273 Chest discomfort
126712731 12671273 Drug administered to patient of inappropriate age
126712731 12671273 Insomnia

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
126712731 12671273 1 20151214 20151214 0