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
123264713 12326471 3 F 20160713 20160503 20160722 EXP PHEH2016US010586 SANDOZ 0.00 F Y 51.50000 KG 20160722 CN COUNTRY NOT SPECIFIED US

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
123264713 12326471 1 SS ILARIS CANAKINUMAB 1 Subcutaneous UNK Y 0 POWDER FOR SOL FOR INJ
123264713 12326471 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 20 MG, UNK Y 90029 20 MG
123264713 12326471 3 SS HYDROCORTISONE. HYDROCORTISONE 1 Oral 15MG IN AM, 5MG IN PM U 0 20 MG OINTMENT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123264713 12326471 1 Juvenile idiopathic arthritis
123264713 12326471 2 Arthritis
123264713 12326471 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123264713 12326471 OT
123264713 12326471 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
123264713 12326471 Drug ineffective
123264713 12326471 Inappropriate schedule of drug administration
123264713 12326471 Juvenile idiopathic arthritis
123264713 12326471 Red blood cell sedimentation rate increased

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
123264713 12326471 1 20160119 20160420 0
123264713 12326471 2 20160329 201606 0