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
126019511 12601951 1 I 20160720 20160728 20160728 EXP US-ASTELLAS-2016US028137 ASTELLAS 0.00 M Y 0.00000 20160728 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
126019511 12601951 1 PS TACROLIMUS. TACROLIMUS 1 Topical 0.03 %, UNKNOWN FREQ. U 50777 .03 PCT OINTMENT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126019511 12601951 1 Dermatitis atopic

Outcome of event

Event ID CASEID OUTC COD
126019511 12601951 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126019511 12601951 Off label use
126019511 12601951 Peliosis hepatis

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
126019511 12601951 1 20040216 0