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
126261771 12626177 1 I 20160720 20160805 20160805 EXP E2B_00498826 CA-HQ SPECIALTY-CA-2016INT000709 INTERCHEM 0.00 F Y 0.00000 20160805 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
126261771 12626177 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 201749
126261771 12626177 2 SS ENBREL ETANERCEPT 1 Subcutaneous UNK U 0
126261771 12626177 3 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK U 0
126261771 12626177 4 SS FOLIC ACID. FOLIC ACID 1 Unknown UNK U 0
126261771 12626177 5 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK U 0
126261771 12626177 6 SS ARAVA LEFLUNOMIDE 1 Unknown UNK U 0
126261771 12626177 7 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK U 0
126261771 12626177 8 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK U 0
126261771 12626177 9 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
126261771 12626177 10 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) UNK U 0
126261771 12626177 11 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK U 0
126261771 12626177 12 SS PREDNISONE. PREDNISONE 1 Unknown UNK U 0
126261771 12626177 13 SS REACTINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNK U 0
126261771 12626177 14 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK U 0
126261771 12626177 15 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK U 0
126261771 12626177 16 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126261771 12626177 1 Rheumatoid arthritis
126261771 12626177 2 Rheumatoid arthritis
126261771 12626177 3 Rheumatoid arthritis
126261771 12626177 4 Rheumatoid arthritis
126261771 12626177 5 Rheumatoid arthritis
126261771 12626177 6 Rheumatoid arthritis
126261771 12626177 7 Rheumatoid arthritis
126261771 12626177 8 Rheumatoid arthritis
126261771 12626177 9 Rheumatoid arthritis
126261771 12626177 10 Rheumatoid arthritis
126261771 12626177 11 Rheumatoid arthritis
126261771 12626177 12 Rheumatoid arthritis
126261771 12626177 13 Rheumatoid arthritis
126261771 12626177 14 Rheumatoid arthritis
126261771 12626177 15 Rheumatoid arthritis
126261771 12626177 16 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126261771 12626177 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126261771 12626177 Abdominal discomfort
126261771 12626177 Alopecia
126261771 12626177 Fatigue
126261771 12626177 Glossodynia
126261771 12626177 Hand deformity
126261771 12626177 Hip arthroplasty
126261771 12626177 Knee arthroplasty
126261771 12626177 Pain
126261771 12626177 Pemphigus
126261771 12626177 Swelling
126261771 12626177 Systemic lupus erythematosus
126261771 12626177 Wound

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

no results found

Therapies reported

no results found