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
126026551 12602655 1 I 20160119 20160718 20160728 20160728 EXP CN-GLAXOSMITHKLINE-CN2016GSK108067 GLAXOSMITHKLINE 83.14 YR F Y 53.00000 KG 20160728 OT CN CN

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
126026551 12602655 1 PS VOLTAREN DICLOFENAC SODIUM 1 Oral 1 DF, BID 36 DF 22122 1 DF FILM-COATED TABLET BID
126026551 12602655 2 SS COLCHICINE. COLCHICINE 1 Oral 1 DF, QD 18 DF 0 1 DF TABLET QD
126026551 12602655 3 SS PREDNISONE. PREDNISONE 1 Oral 10 MG, QD 180 MG 0 10 MG QD
126026551 12602655 4 C CELECOXIB. CELECOXIB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126026551 12602655 1 Rheumatoid arthritis
126026551 12602655 2 Gout
126026551 12602655 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126026551 12602655 DS
126026551 12602655 OT
126026551 12602655 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126026551 12602655 Bone marrow failure
126026551 12602655 Hepatic function abnormal
126026551 12602655 Renal impairment

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
126026551 12602655 1 20160101 20160619 0
126026551 12602655 2 20160101 20160119 0
126026551 12602655 3 20160101 20160119 0