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
127629211 12762921 1 I 20160524 20160915 20160920 20160920 EXP AU-SA-2016SA171214 AVENTIS 70.00 YR E F Y 53.00000 KG 20160920 CN AU AU

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
127629211 12762921 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral F008 20872 180 MG FILM-COATED TABLET QD
127629211 12762921 2 I ADALAT NIFEDIPINE 1 Unknown ADALAT (NIFEDIPINE) 10MG U UNKNOWN 0
127629211 12762921 3 SS FELODUR ER FELODIPINE 1 Unknown U UNKNOWN 0
127629211 12762921 4 C AMOXICILLIN. AMOXICILLIN 1 Unknown 0
127629211 12762921 5 C AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Unknown 0
127629211 12762921 6 C DOXYCYCLINE. DOXYCYCLINE 1 Unknown 0
127629211 12762921 7 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown 0
127629211 12762921 8 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127629211 12762921 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127629211 12762921 Blood pressure decreased
127629211 12762921 Chest pain
127629211 12762921 Drug interaction
127629211 12762921 Dry mouth
127629211 12762921 Feeling hot
127629211 12762921 Heart rate increased
127629211 12762921 Malaise
127629211 12762921 Pruritus

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
127629211 12762921 1 20150927 20160628 0
127629211 12762921 2 20160524 0