Drug Guide
Infliximab
Classification
Therapeutic: Immunosuppressant/Anti-inflammatory
Pharmacological: TNF-alpha inhibitor
FDA Approved Indications
- Crohn's disease
- Ulcerative colitis
- Rheumatoid arthritis
- Ankylosing spondylitis
- Psoriatic arthritis
- Plaque psoriasis
Mechanism of Action
Infliximab is a chimeric monoclonal antibody that binds to tumor necrosis factor-alpha (TNF-alpha), a pro-inflammatory cytokine, thereby inhibiting its activity and reducing inflammation.
Dosage and Administration
Adult: Varies by condition; typically 3-10 mg/kg IV at weeks 0, 2, and 6, then every 8 weeks.
Pediatric: Dosing based on weight; administered IV, frequency similar to adults; specific schedules depend on condition.
Geriatric: Adjustments based on renal and hepatic function, with careful monitoring due to increased infection risk.
Renal Impairment: No specific dose adjustment, but caution advised.
Hepatic Impairment: No specific guidelines; caution recommended.
Pharmacokinetics
Absorption: Not absorbed orally; administered IV.
Distribution: Widely distributed; penetrates inflamed tissues.
Metabolism: Metabolized into peptides and amino acids via proteolytic catabolism.
Excretion: Renal and non-renal routes.
Half Life: Approx. 7-10 days.
Contraindications
- Hypersensitivity to infliximab or its components.
- Active infections, including tuberculosis.
Precautions
- Screen for latent TB prior to initiation.
- Monitor for signs of infection during therapy.
- Use with caution in patients with heart failure, demyelinating diseases, or hepatitis B virus infection.
Adverse Reactions - Common
- Infusion reactions (fever, chills, pruritus) (Common)
- Infections (upper respiratory, sinusitis) (Common)
- Headache (Common)
Adverse Reactions - Serious
- Serious infections (pneumonia, sepsis) (Serious, less common)
- Demyelinating disorders (Rare)
- Lupus-like syndrome (Rare)
- Liver injury (Rare)
Drug-Drug Interactions
- Other immunosuppressants, live vaccines, antibiotics
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for signs of infection, infusion reactions, and immunogenicity.
Diagnoses:
- Risk for infection
- Allergic reaction
Implementation: Administer IV per protocol, monitor infusion site and vitals during infusion.
Evaluation: Assess for efficacy and adverse effects, including infection and infusion reactions.
Patient/Family Teaching
- Report signs of infection immediately.
- Understand infusion schedule and importance of adherence.
- Notify healthcare provider of any allergic reactions or side effects.
Special Considerations
Black Box Warnings:
- Serious infections, including tuberculosis and invasive fungal infections.
- Malignant lymphoma and other malignancies.
Genetic Factors: Genetic predisposition may influence response and risk.
Lab Test Interference: Can suppress signs of inflammation, potentially affecting lab tests.
Overdose Management
Signs/Symptoms: Unknown, but may include exaggerated immunosuppressive effects.
Treatment: Supportive care, monitor vital signs, and manage symptoms.
Storage and Handling
Storage: Store vials refrigerated at 2-8°C, do not freeze.
Stability: Stability varies by manufacturer; use within specified shelf life.