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
126141121 12614112 1 I 20140831 20150119 20160802 20160802 EXP US-ASTELLAS-2015US002083 ASTELLAS 17.10 YR F Y 0.00000 20160802 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
126141121 12614112 1 PS TACROLIMUS. TACROLIMUS 1 Topical 0.1 %, UNKNOWN FREQ. 50777 .1 PCT OINTMENT
126141121 12614112 2 C MUPIROCIN. MUPIROCIN 1 Topical UNK UNK, UNKNOWN FREQ. U 0 OINTMENT
126141121 12614112 3 C ALTABAX RETAPAMULIN 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126141121 12614112 1 Dermatitis atopic
126141121 12614112 2 Impetigo
126141121 12614112 3 Dermatitis atopic

Outcome of event

Event ID CASEID OUTC COD
126141121 12614112 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126141121 12614112 Endometriosis
126141121 12614112 Off label use
126141121 12614112 Ovarian cyst

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
126141121 12614112 1 200001 0