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
105684758 10568475 8 F 20141028 20151217 20141106 20151231 EXP DE-CELGENE-DEU-2014105352 CELGENE 45.00 YR F Y 76.50000 KG 20151231 OT DE DE

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
105684758 10568475 1 PS CC-10004 APREMILAST 1 Oral U 70270 TABLETS
105684758 10568475 2 SS CC-10004 APREMILAST 1 Oral 300 MILLIGRAM U 70270 TABLETS
105684758 10568475 3 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 20 MG UNKNOWN
105684758 10568475 4 C IBUPROFEN. IBUPROFEN 1 Oral 0 800 MG TABLETS
105684758 10568475 5 C CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Oral 40 MILLIGRAM 0 300 MG UNKNOWN QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105684758 10568475 1 Psoriasis
105684758 10568475 3 Product used for unknown indication
105684758 10568475 4 Arthralgia
105684758 10568475 5 Otitis media

Outcome of event

Event ID CASEID OUTC COD
105684758 10568475 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
105684758 10568475 Deafness unilateral

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
105684758 10568475 1 201403 20141023 0
105684758 10568475 2 20141105 0
105684758 10568475 3 20140408 0
105684758 10568475 4 20140728 0
105684758 10568475 5 20141204 20141214 0