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
126712221 12671222 1 I 2014 20150819 20160822 20160822 PER US-TEVA-588663USA TEVA 0.00 M Y 74.83000 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
126712221 12671222 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 90 MILLIGRAM DAILY; 1/2 TABLET 4HR0189 (43F032) 76191 90 MG TABLET QD
126712221 12671222 2 C COPPER COPPER 1 0
126712221 12671222 3 C ZINC ZINCINC CHLORIDE 1 0
126712221 12671222 4 C VITAMIN E .ALPHA.-TOCOPHEROL 1 0
126712221 12671222 5 C VITAMIN C ASCORBIC ACID 1 0
126712221 12671222 6 C NITROGLYCERIN. NITROGLYCERIN 1 0
126712221 12671222 7 C METOPROLOL. METOPROLOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712221 12671222 1 Urticaria

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712221 12671222 Drug administered to patient of inappropriate age
126712221 12671222 Drug effect decreased
126712221 12671222 Off label use
126712221 12671222 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
126712221 12671222 1 2014 0
126712221 12671222 2 201508 0
126712221 12671222 3 201508 0
126712221 12671222 4 201508 0
126712221 12671222 5 201508 0