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
126731921 12673192 1 I 201509 20160712 20160822 20160822 EXP CA-ORION CORPORATION ORION PHARMA-TREX2016-1052 ORION 43.00 YR F Y 0.00000 20160822 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
126731921 12673192 1 PS METHOTREXATE. METHOTREXATE 1 Oral N 0 25 MG
126731921 12673192 2 SS ENBREL ETANERCEPT 1 Subcutaneous N 0
126731921 12673192 3 SS SULFASALAZINE. SULFASALAZINE 1 Oral N 0 1 G BID
126731921 12673192 4 SS REMICADE INFLIXIMAB 1 Unknown N 0 POWDER FOR SOLUTION FOR INJECTION
126731921 12673192 5 SS ACTEMRA TOCILIZUMAB 1 Unknown N 0
126731921 12673192 6 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) N 0
126731921 12673192 7 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous N 0
126731921 12673192 8 SS HUMIRA ADALIMUMAB 1 Subcutaneous N 0
126731921 12673192 9 SS RITUXAN RITUXIMAB 1 Unknown N 0
126731921 12673192 10 SS SIMPONI GOLIMUMAB 1 Subcutaneous N 0
126731921 12673192 11 SS ARAVA LEFLUNOMIDE 1 Oral N 0 TABLET
126731921 12673192 12 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown N 0 400 MG TABLET QD
126731921 12673192 13 SS CORTISONE CORTISONEHYDROCORTISONE 1 Oral N 0 ORAL DROPS
126731921 12673192 14 SS FOLIC ACID. FOLIC ACID 1 Unknown 0
126731921 12673192 15 SS PREDNISONE. PREDNISONE 1 Unknown 0
126731921 12673192 16 SS HYDROXYCHLOROQUINE SULFATE. HYDROXYCHLOROQUINE SULFATE 1 Unknown U 0
126731921 12673192 17 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown U 0
126731921 12673192 18 C XELJANZ TOFACITINIB CITRATE 1 Unknown 0
126731921 12673192 19 C FOSAMAX ALENDRONATE SODIUM 1 Unknown 0 TABLET
126731921 12673192 20 C REACTINE CETIRIZINE HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126731921 12673192 1 Rheumatoid arthritis
126731921 12673192 2 Rheumatoid arthritis
126731921 12673192 3 Rheumatoid arthritis
126731921 12673192 4 Rheumatoid arthritis
126731921 12673192 5 Rheumatoid arthritis
126731921 12673192 6 Rheumatoid arthritis
126731921 12673192 7 Rheumatoid arthritis
126731921 12673192 8 Rheumatoid arthritis
126731921 12673192 9 Rheumatoid arthritis
126731921 12673192 10 Rheumatoid arthritis
126731921 12673192 11 Rheumatoid arthritis
126731921 12673192 12 Rheumatoid arthritis
126731921 12673192 13 Rheumatoid arthritis
126731921 12673192 14 Rheumatoid arthritis
126731921 12673192 15 Rheumatoid arthritis
126731921 12673192 16 Rheumatoid arthritis
126731921 12673192 17 Rheumatoid arthritis
126731921 12673192 19 Rheumatoid arthritis
126731921 12673192 20 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126731921 12673192 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126731921 12673192 Abdominal discomfort
126731921 12673192 Alopecia
126731921 12673192 Drug ineffective
126731921 12673192 Fatigue
126731921 12673192 Glossodynia
126731921 12673192 Hand deformity
126731921 12673192 Pain
126731921 12673192 Pemphigus
126731921 12673192 Swelling
126731921 12673192 Systemic lupus erythematosus

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
126731921 12673192 1 2006 2016 0
126731921 12673192 3 2006 2007 0
126731921 12673192 6 201005 201103 0
126731921 12673192 9 2009 2010 0
126731921 12673192 12 2006 0