Drug Guide
Adalimumab-aqvh
Classification
Therapeutic: Immunosuppressant, TNF inhibitor
Pharmacological: Monoclonal antibody
FDA Approved Indications
- Crohn's Disease
- Ulcerative Colitis
- Rheumatoid Arthritis
- Psoriatic Arthritis
- Ankylosing Spondylitis
- Plaque Psoriasis
- Hidradenitis Suppurativa
- Juvenile Idiopathic Arthritis
Mechanism of Action
Adalimumab is a recombinant IgG1 monoclonal antibody that binds specifically to tumor necrosis factor-alpha (TNF-α), a cytokine involved in systemic inflammation. By inhibiting TNF-α, it reduces inflammation and immune system activity.
Dosage and Administration
Adult: Variable depending on the condition; typically 40 mg subcutaneously every other week.
Pediatric: Dosing varies by age and condition; consult specific prescribing information.
Geriatric: Adjust based on comorbidities and tolerability; no specific dose reduction recommended solely due to age.
Renal Impairment: No specific dosage adjustment required.
Hepatic Impairment: No specific dosage adjustment required.
Pharmacokinetics
Absorption: Subcutaneous absorption with bioavailability approximately 64%.
Distribution: Distributed primarily in the vascular and extravascular compartments.
Metabolism: Metabolized via proteolytic degradation to small peptides and amino acids.
Excretion: Eliminated through proteolytic degradation pathways; not primarily renal.
Half Life: Approximately 2 weeks.
Contraindications
- Hypersensitivity to adalimumab or its components.
- Active infections, including tuberculosis.
Precautions
- Screen for latent TB before initiation.
- Monitor for infections during therapy.
- Assess for heart failure symptoms; use with caution in patients with NYHA Class III/IV.
Adverse Reactions - Common
- Injection site reactions (Common)
- Upper respiratory infections (Common)
Adverse Reactions - Serious
- Serious infections (e.g., sepsis, pneumonia) (Less common)
- Malignancies (e.g., lymphoma) (Rare)
- Demyelinating diseases (Rare)
- Heart failure exacerbation (Rare)
Drug-Drug Interactions
- Other immunosuppressants
- Live vaccines
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for signs of infection, TB screening results, injection site reactions.
Diagnoses:
- Risk for infection
Implementation: Administer as prescribed, monitor patient response, educate patient on infection risk.
Evaluation: Assess for reduction in disease symptoms, monitor for adverse effects.
Patient/Family Teaching
- Report signs of infection or unusual symptoms immediately.
- Do not receive live vaccines during therapy.
- Understand the importance of adherence to dosing schedule.
Special Considerations
Black Box Warnings:
- Serious infections including tuberculosis and fungal infections.
- Malignancies, including lymphoma and other cancers.
Genetic Factors: Limited data on genetic influences on response.
Lab Test Interference: May affect immune markers; interpret results cautiously.
Overdose Management
Signs/Symptoms: Possible severe infections, hypersensitivity reactions.
Treatment: Supportive care, monitor vital signs, ensure airway patency, consult poison control.
Storage and Handling
Storage: Store in a refrigerator (2°C to 8°C). Do not freeze.
Stability: Stable until the expiration date when refrigerated; can be kept at room temperature for up to 14 days.