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
127097631 12709763 1 I 20160822 20160902 20160902 EXP CA-ORION CORPORATION ORION PHARMA-TREX2016-1561 ORION 61.00 YR M Y 0.00000 20160902 OT 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
127097631 12709763 1 PS METHOTREXATE (TRADE NAME UNKNOWN) METHOTREXATE 1 Oral U 0 10 MG TABLET /wk
127097631 12709763 2 SS METHOTREXATE. METHOTREXATE 1 Subcutaneous U 0 25 MG /wk
127097631 12709763 3 SS ENBREL ETANERCEPT 1 Subcutaneous U 0 50 MG /wk
127097631 12709763 4 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) U 0 200 MG
127097631 12709763 5 SS VIOXX ROFECOXIB 1 Unknown U 0 12.5 MG TABLET
127097631 12709763 6 C MOBICOX MELOXICAM 1 Unknown 0
127097631 12709763 7 C MOTRIN IBUPROFEN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127097631 12709763 3 Ankylosing spondylitis

Outcome of event

Event ID CASEID OUTC COD
127097631 12709763 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127097631 12709763 Drug ineffective
127097631 12709763 Hypertension
127097631 12709763 Iritis
127097631 12709763 Nervous system disorder
127097631 12709763 Rheumatoid arthritis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found