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
116821234 11682123 4 F 201505 20160823 20151029 20160830 EXP US-ASTELLAS-2015US039650 ASTELLAS 5.59 YR M Y 0.00000 20160830 MD 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
116821234 11682123 1 PS TACROLIMUS. TACROLIMUS 1 Topical 0.03 %, ONCE DAILY 50777 .03 PCT OINTMENT QD
116821234 11682123 2 SS TACROLIMUS. TACROLIMUS 1 50777 OINTMENT
116821234 11682123 3 C TRIAMCINOLONE TRIAMCINOLONE 1 Topical UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
116821234 11682123 4 C FLUCONAZOLE. FLUCONAZOLE 1 Topical UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
116821234 11682123 5 C EPICERAM 2 Topical UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
116821234 11682123 6 C TOPICORT /00370301/ 2 Topical 0.25 %, UNKNOWN FREQ. U 0 .25 PCT FORMULATION UNKNOWN
116821234 11682123 7 C BANA 2 Topical UNK, UNKNOWN FREQ. U 0 CREAM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116821234 11682123 1 Dermatitis atopic
116821234 11682123 2 Eczema
116821234 11682123 3 Dermatitis atopic
116821234 11682123 4 Dermatitis atopic
116821234 11682123 5 Dermatitis atopic
116821234 11682123 6 Dermatitis atopic
116821234 11682123 7 Dermatitis atopic

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
116821234 11682123 Off label use
116821234 11682123 Staphylococcal infection

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
116821234 11682123 1 2011 0