Table 2.
Disease-modifying antirheumatic drugs.
Drug | Use | Dosage | Adverse effects | Mechanism |
---|---|---|---|---|
Abatacept | Monotherapy in moderate severe RA or with DMARDs | 500/1000 mg iv for 2 weeks then for 4 weeks | Headache, blood hypertension, nausea, infections respiratory system, vertigo, and severe infection | Modulator of T-lymphocyte activation |
| ||||
Adalimumab | Moderate or severe AR | 40 mg sc. for 2 weeks | Myositis, headache, rash, nausea, blood hypertension, hyperlipidemia, and higher plasma transaminases levels | Anti-TNF-α |
| ||||
Anakinra | Monotherapy in moderate/severe RA in patient with ≥1 DMARD not efficacy | 100 mg/die sc. | Abdominal pain, diarrhea, headache, fever, and infections of respiratory system | Anti-IL-1 |
| ||||
Certolizumab | Moderate or severe AR | 400 mg sc. for 2 weeks then 200 mg for 2 weeks | Rash, headache, blood hypertension, fever, and asthenia | Anti-TNF-α |
| ||||
Etanercept | Moderate or severe AR with DMARD | 50 mg/weeks sc. | Pain into injection site, infections, headache, rash, vertigo, and asthenia | Anti-TNF-α |
| ||||
Golimumab | RA M/S with MTX | 50 mg/month sc. | Blood hypertension, higher plasma transaminases levels, and vertigo, rhinitis |
Anti-TNF-α |
| ||||
Infliximab | Moderate or severe AR with MTX | 3 mg/kg iv one time then on 2 and 6 weeks | Fever, headache, rash, myalgia, asthenia, dyspnea, and higher plasma transaminases levels | Anti-TNF-α |
| ||||
Rituximab | Moderate or severe AR, with MTX in patient and without response to ≥1 anti-TNF-α agent | 1000 mg iv in days 1 and 15 then at 24 weeks | Fever, nausea, hypotension, itching, and myelosuppression | Modulator of B-cell activation |