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
125716101 12571610 1 I 20160706 20160719 20160719 EXP CA-HQ SPECIALTY-CA-2016INT000558 INTERCHEM 69.00 YR M Y 0.00000 20160719 CN CA CA

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
125716101 12571610 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 2.8571 MG (20 MG, 1 IN 1 W) 201749 20 MG
125716101 12571610 2 SS SULFASALAZINE. SULFASALAZINE 1 2 G (1 G, 2 IN 1 D) 0 1 G
125716101 12571610 3 SS XELJANZ TOFACITINIB CITRATE 1 UNK U 0
125716101 12571610 4 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 400 MG, UNK 0 400 MG
125716101 12571610 5 SS LEFLUNOMIDE. LEFLUNOMIDE 1 20 MG (20 MG, 1 IN 1 D) 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125716101 12571610 1 Rheumatoid arthritis
125716101 12571610 2 Rheumatoid arthritis
125716101 12571610 3 Rheumatoid arthritis
125716101 12571610 4 Rheumatoid arthritis
125716101 12571610 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125716101 12571610 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125716101 12571610 Arthralgia
125716101 12571610 Interstitial lung disease

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
125716101 12571610 1 200504 201601 0
125716101 12571610 2 1998 201002 0
125716101 12571610 3 20150813 0
125716101 12571610 4 200505 201504 0
125716101 12571610 5 201504 201508 0