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
125896221 12589622 1 I 20150724 20160712 20160725 20160725 EXP CA-HQ SPECIALTY-CA-2016INT000596 INTERCHEM 65.00 YR F Y 0.00000 20160725 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
125896221 12589622 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK Y 201749
125896221 12589622 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK Y 201749
125896221 12589622 3 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 MG (5 MG,2 IN 1 D) 0 5 MG
125896221 12589622 4 SS XELJANZ TOFACITINIB CITRATE 1 UNK 0
125896221 12589622 5 SS SULFASALAZINE. SULFASALAZINE 1 UNK U 0
125896221 12589622 6 SS SULFASALAZINE. SULFASALAZINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125896221 12589622 1 Rheumatoid arthritis
125896221 12589622 3 Rheumatoid arthritis
125896221 12589622 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125896221 12589622 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125896221 12589622 Diabetes mellitus
125896221 12589622 Diarrhoea
125896221 12589622 Gastric polyps
125896221 12589622 Influenza
125896221 12589622 Oesophageal polyp

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
125896221 12589622 1 201501 0
125896221 12589622 2 201502 0
125896221 12589622 3 20140721 201501 0
125896221 12589622 4 201502 0
125896221 12589622 5 201501 0
125896221 12589622 6 201502 0