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
125662442 12566244 2 F 20160720 20160718 20160803 EXP CA-HQ SPECIALTY-CA-2016INT000541 INTERCHEM 72.00 YR M Y 0.00000 20160803 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
125662442 12566244 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 2.8571 MG (20 MG,1 IN 1 W) N 201749 20 MG
125662442 12566244 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 25 MG/ML (1 IN 1 W) N 201749
125662442 12566244 3 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 MG (5 MG, 2 IN 1 D) N 0 5 MG
125662442 12566244 4 SS ARAVA LEFLUNOMIDE 1 Oral 20 MG (20 MG,1 IN 1 D) 0 20 MG
125662442 12566244 5 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 (400 MG,1 D) N 0 400 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125662442 12566244 1 Rheumatoid arthritis
125662442 12566244 3 Rheumatoid arthritis
125662442 12566244 4 Rheumatoid arthritis
125662442 12566244 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125662442 12566244 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125662442 12566244 Drug ineffective
125662442 12566244 Rheumatoid arthritis
125662442 12566244 Sensitivity to weather change

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
125662442 12566244 1 201309 2015 0
125662442 12566244 2 2015 0
125662442 12566244 3 20151120 0
125662442 12566244 4 201402 0
125662442 12566244 5 201309 0