The Safety Rates Drug Report

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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
125273091 12527309 1 I 200810 20160621 20160705 20160705 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-40923BP BOEHRINGER INGELHEIM 60.56 YR F Y 0.00000 20160705 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
125273091 12527309 1 PS MELOXICAM. MELOXICAM 1 Unknown 20938
125273091 12527309 2 C LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown 0
125273091 12527309 3 C PREDNISONE. PREDNISONE 1 Unknown 0
125273091 12527309 4 C CLOBETASOL CLOBETASOL 1 Unknown 0
125273091 12527309 5 C XELJANZ TOFACITINIB CITRATE 1 Oral EXTENDED RELEASE (XR); STRENGTH: 5MG 0 TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125273091 12527309 1 Product used for unknown indication
125273091 12527309 2 Product used for unknown indication
125273091 12527309 3 Product used for unknown indication
125273091 12527309 4 Product used for unknown indication
125273091 12527309 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125273091 12527309 Drug ineffective

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
125273091 12527309 1 200810 201202 0
125273091 12527309 2 201504 201507 0
125273091 12527309 3 201507 201604 0
125273091 12527309 4 201403 201405 0