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
125063232 12506323 2 F 2012 20160719 20160628 20160801 EXP CA-HQ SPECIALTY-CA-2016INT000422 INTERCHEM 58.00 YR F Y 0.00000 20160801 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
125063232 12506323 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 201749
125063232 12506323 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 25 MG, UNK U 201749 25 MG
125063232 12506323 3 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown UNK 0
125063232 12506323 4 C ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) 17.8571 MG (500 MG,1 IN 4 W) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125063232 12506323 1 Rheumatoid arthritis
125063232 12506323 3 Rheumatoid arthritis
125063232 12506323 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125063232 12506323 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125063232 12506323 Breast cancer
125063232 12506323 Gait disturbance
125063232 12506323 Peripheral swelling
125063232 12506323 Synovitis

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
125063232 12506323 2 201407 0
125063232 12506323 4 201509 20160605 0