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
124523093 12452309 3 F 20160715 20160609 20160729 EXP CA-HQ SPECIALTY-CA-2016INT000346 INTERCHEM 91.00 YR F Y 0.00000 20160729 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
124523093 12452309 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 2.8571 MG (20 MG,1 IN 1 W) Y 201749
124523093 12452309 2 SS ARAVA LEFLUNOMIDE 1 Oral 20 MG (20 MG,1 IN 1 D) Y 0
124523093 12452309 3 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 Oral 400 MG (400 MG,1 IN 1 D) 0
124523093 12452309 4 SS SULFASALAZINE. SULFASALAZINE 1 UNK Y 0
124523093 12452309 5 SS PREDNISONE. PREDNISONE 1 UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124523093 12452309 1 Rheumatoid arthritis
124523093 12452309 2 Rheumatoid arthritis
124523093 12452309 3 Rheumatoid arthritis
124523093 12452309 4 Rheumatoid arthritis
124523093 12452309 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
124523093 12452309 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124523093 12452309 Abasia
124523093 12452309 Drug ineffective
124523093 12452309 Rheumatoid arthritis

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
124523093 12452309 1 20151123 20160620 0
124523093 12452309 2 20150723 20151123 0
124523093 12452309 3 20150723 0