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
126025611 12602561 1 I 20160119 20160718 20160728 20160728 EXP PHHY2016CN100860 NOVARTIS 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
126025611 12602561 1 PS VOLTAREN DICLOFENAC SODIUM 1 Oral 1 DF, BID 38 DF Y 19201 1 DF ENTERIC-FILM-COATED TABLET BID
126025611 12602561 2 SS PREDNISONE. PREDNISONE 1 Oral 10 MG, QD 190 MG Y 0 10 MG TABLET QD
126025611 12602561 3 SS COLCHICINE. COLCHICINE 1 Oral 1 DF, QD 19 DF Y 0 1 DF TABLET QD
126025611 12602561 4 C CELECOXIB. CELECOXIB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126025611 12602561 1 Rheumatoid arthritis
126025611 12602561 2 Rheumatoid arthritis
126025611 12602561 3 Gout

Outcome of event

Event ID CASEID OUTC COD
126025611 12602561 HO
126025611 12602561 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126025611 12602561 Bone marrow failure
126025611 12602561 Liver function test abnormal
126025611 12602561 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
126025611 12602561 1 20160101 20160619 0
126025611 12602561 2 20160101 20160119 0
126025611 12602561 3 20160101 20160119 0