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
126892532 12689253 2 F 201509 20160914 20160826 20160920 EXP CA-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-065600 BRISTOL MYERS SQUIBB 43.00 YR F Y 0.00000 20160920 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
126892532 12689253 1 PS ORENCIA ABATACEPT 1 Subcutaneous U 125118
126892532 12689253 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) U 0
126892532 12689253 3 SS ACTEMRA TOCILIZUMAB 1 Unknown U 0
126892532 12689253 4 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous U 0
126892532 12689253 5 SS HUMIRA ADALIMUMAB 1 Subcutaneous U 0
126892532 12689253 6 SS ENBREL ETANERCEPT 1 Subcutaneous N 0
126892532 12689253 7 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) U 0
126892532 12689253 8 SS ARAVA LEFLUNOMIDE 1 Unknown U 0 TABLET
126892532 12689253 9 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 Unknown U 0
126892532 12689253 10 SS SULFATHALIDINE PHTHALYLSULFATHIAZOLE 1 Unknown U 0
126892532 12689253 11 SS CORTISONE CORTISONEHYDROCORTISONE 1 Oral U 0 ORAL DROPS
126892532 12689253 12 SS FOLIC ACID. FOLIC ACID 1 Unknown U 0
126892532 12689253 13 SS METHOTREXATE. METHOTREXATE 1 Unknown U 0
126892532 12689253 14 SS PREDNISONE. PREDNISONE 1 Unknown U 0
126892532 12689253 15 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown U 0 TABLET
126892532 12689253 16 SS REACTINE /00884302/ CETIRIZINE HYDROCHLORIDE 1 Unknown U 0
126892532 12689253 17 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown U 0 TABLET
126892532 12689253 18 SS SIMPONI GOLIMUMAB 1 Subcutaneous U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126892532 12689253 1 Rheumatoid arthritis
126892532 12689253 2 Rheumatoid arthritis
126892532 12689253 3 Rheumatoid arthritis
126892532 12689253 4 Rheumatoid arthritis
126892532 12689253 5 Rheumatoid arthritis
126892532 12689253 6 Rheumatoid arthritis
126892532 12689253 7 Rheumatoid arthritis
126892532 12689253 8 Rheumatoid arthritis
126892532 12689253 9 Rheumatoid arthritis
126892532 12689253 10 Rheumatoid arthritis
126892532 12689253 11 Rheumatoid arthritis
126892532 12689253 12 Rheumatoid arthritis
126892532 12689253 13 Rheumatoid arthritis
126892532 12689253 14 Rheumatoid arthritis
126892532 12689253 15 Rheumatoid arthritis
126892532 12689253 16 Rheumatoid arthritis
126892532 12689253 17 Rheumatoid arthritis
126892532 12689253 18 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126892532 12689253 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126892532 12689253 Abdominal discomfort
126892532 12689253 Alopecia
126892532 12689253 Drug ineffective
126892532 12689253 Drug intolerance
126892532 12689253 Fatigue
126892532 12689253 Glossodynia
126892532 12689253 Hand deformity
126892532 12689253 Pain
126892532 12689253 Pemphigus
126892532 12689253 Swelling
126892532 12689253 Systemic lupus erythematosus

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

no results found

Therapies reported

no results found