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
125378981 12537898 1 I 20160622 20160707 20160707 EXP CA-HQ SPECIALTY-CA-2016INT000470 INTERCHEM 24.00 YR F Y 0.00000 20160707 MD 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
125378981 12537898 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 3.5714 MG (25 MG, 1 IN 1 W) 201749 25 MG
125378981 12537898 2 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 200 MG (200 MG, 1 IN 1 D) 0 200 MG
125378981 12537898 3 SS LEFLUNOMIDE. LEFLUNOMIDE 1 10 MG (10 MG, 1 IN 1 D) 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125378981 12537898 1 Rheumatoid arthritis
125378981 12537898 2 Rheumatoid arthritis
125378981 12537898 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125378981 12537898 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125378981 12537898 Drug ineffective
125378981 12537898 Drug intolerance
125378981 12537898 Fatigue

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
125378981 12537898 1 20160609 0