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
115807094 11580709 4 F 20160721 20160812 20150930 20160822 EXP CA-ABBVIE-15K-028-1471671-00 ABBVIE 43.00 YR F Y 0.00000 20160822 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
115807094 11580709 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous N UNKNOWN 125057
115807094 11580709 2 SS REMICADE INFLIXIMAB 1 Unknown N UNKNOWN 0
115807094 11580709 3 SS ACTEMRA TOCILIZUMAB 1 Unknown N UNKNOWN 0
115807094 11580709 4 SS ORENCIA ABATACEPT 1 Unknown N UNKNOWN 0
115807094 11580709 5 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown N UNKNOWN 0
115807094 11580709 6 SS ENBREL ETANERCEPT 1 Unknown N UNKNOWN 0
115807094 11580709 7 SS RITUXAN RITUXIMAB 1 Unknown N UNKNOWN 0
115807094 11580709 8 SS SIMPONI GOLIMUMAB 1 Unknown N UNKNOWN 0
115807094 11580709 9 SS ARAVA LEFLUNOMIDE 1 Unknown N UNKNOWN 0
115807094 11580709 10 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown N UNKNOWN 0
115807094 11580709 11 SS SULFASALAZINE. SULFASALAZINE 1 Unknown N UNKNOWN 0
115807094 11580709 12 SS METHOTREXATE. METHOTREXATE 1 Unknown UNKNOWN 0
115807094 11580709 13 SS FOLIC ACID. FOLIC ACID 1 Unknown UNKNOWN 0
115807094 11580709 14 SS PREDNISONE. PREDNISONE 1 Unknown UNKNOWN 0
115807094 11580709 15 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNKNOWN 0
115807094 11580709 16 SS REACTINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNKNOWN 0
115807094 11580709 17 SS CORTISONE CORTISONEHYDROCORTISONE 1 Oral N UNKNOWN 0 ORAL DROPS
115807094 11580709 18 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 0
115807094 11580709 19 C XELJANZ TOFACITINIB CITRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115807094 11580709 1 Rheumatoid arthritis
115807094 11580709 2 Rheumatoid arthritis
115807094 11580709 3 Rheumatoid arthritis
115807094 11580709 4 Rheumatoid arthritis
115807094 11580709 5 Rheumatoid arthritis
115807094 11580709 6 Rheumatoid arthritis
115807094 11580709 7 Rheumatoid arthritis
115807094 11580709 8 Rheumatoid arthritis
115807094 11580709 9 Rheumatoid arthritis
115807094 11580709 10 Rheumatoid arthritis
115807094 11580709 11 Rheumatoid arthritis
115807094 11580709 12 Rheumatoid arthritis
115807094 11580709 13 Rheumatoid arthritis
115807094 11580709 14 Rheumatoid arthritis
115807094 11580709 15 Rheumatoid arthritis
115807094 11580709 16 Rheumatoid arthritis
115807094 11580709 17 Rheumatoid arthritis
115807094 11580709 18 Product used for unknown indication
115807094 11580709 19 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
115807094 11580709 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115807094 11580709 Abdominal discomfort
115807094 11580709 Alopecia
115807094 11580709 Anti-cyclic citrullinated peptide antibody positive
115807094 11580709 Drug ineffective
115807094 11580709 Drug intolerance
115807094 11580709 Fatigue
115807094 11580709 Glossodynia
115807094 11580709 Hand deformity
115807094 11580709 Hip arthroplasty
115807094 11580709 Infusion related reaction
115807094 11580709 Joint swelling
115807094 11580709 Knee arthroplasty
115807094 11580709 Pain
115807094 11580709 Pemphigus
115807094 11580709 Rash
115807094 11580709 Rheumatoid factor positive
115807094 11580709 Swelling
115807094 11580709 Systemic lupus erythematosus
115807094 11580709 Wound

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

no results found

Therapies reported

no results found