Classes
DEA Class; Rx
Common Brand Names; Neoral, Sandimmune, Gengraf
- DMARDs, Immunomodulators;
- Immunosuppressants;
- Calcineurin Inhibitors
Description
Immunosuppressive; cyclic polypeptide consisting of 11 amino acids
Used to prevent organ rejection and in various autoimmune conditions; ophthalmic 0.05% emulsion and 0.09% solution used to increase tear production in patients with ocular inflammation associated with keratoconjunctivitis; 0.1% ophthalmic emulsion used to treat vernal keratoconjunctivitis
Microemulsion formulation (cyclosporine, USP (Modified)) has been introduced to improve the bioavailability
Indications
Prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants; has been used in combination with azathioprine and corticosteroids
Indicated for severe active, rheumatoid arthritis where the disease has not adequately responded to methotrexate; may be used in combination with methotrexate
Indicated for treatment of adult, nonimmunocompromised patients with severe, recalcitrant, plaque psoriasis who have failed to respond to at least 1 systemic therapy (eg, PUVA, retinoids, or methotrexate) or in patients for whom other systemic therapies are contraindicated, or cannot be tolerated
Orphan Designations
ALS
- Treatment of amyotropohic lateral sclerosis and its variants
Traumatic Brain Injury
- Treatment of moderate-to-severe traumatic brain injury
Lung Transplant
- Prophylaxis of organ rejection in patients receiving allogeneic lung transplant
- Treatment of acute rejection in recipients of allogeneic lung transplants
GVHD
- Prophylaxis and treatment of graft versus host disease
Lung Allograft Rejection
- Liposomal: For aerosolized administration in the prevention and treatment of lung allograft rejection
Pulmonary Rejection With BMT
- Liposomal: For aerosolized administration in the prevention and treatment of pulmonary rejection events associated with bone marrow transplant (BMT)
Bronchioitis Obliterans (Orphan)
- Liposomal cyclosporine for inhalation
Contraindications
Hypersensitivity
Breastfeeding
(RA/Psoriasis use): Abnormal renal function, uncontrolled HTN, malignancies
(Psoriasis use) Concomitant PUVA, UVB radiation, coal tar, methotrexate, other immunosuppressants
Adverse Effects
- Tremor (12-55%)
- Nephrotoxicity (32%)
- Hypertension (26%)
- Infection (3-25%)
- Headache (2-25%)
- Nausea (23%)
- Hirsutism (21%)
- Hypertrichosis (5-19%)
- Female reproductive disorder (5-19%)
- Gum hyperplasia (2-16%)
- Triglycerides increased (15%)
- Abdominal discomfort (1-15%)
- URI (1-14%)
- Diarrhea (3-13%)
- Dyspepsia (2-12%)
- Leg cramps (2-12%)
- Parathesia (1-11%)
- Acne
- Convulsions
- Pruitus
- Hyperkalemia, hypomagnesemia
- Pancreatitis
- Hepatotoxicity
- Flu-like syndrome
Warnings
Injection: monitor closely for at least 30 min
Risk of hepatotoxicity and nephrotoxicity
Myelosuppression may be severe and prolonged; monitor complete blood and platelet counts
Potential increase risk for optic disk edema and infusion-related anaphylactic reactions
Some malignancies caused by cyclosporine immunosuppression may be fatal (eg, lymphoma)
Serious and fatal cerebral, gastrointestinal and pulmonary hemorrhage; monitor platelets and coagulation parameters and treat accordingly
Anticipate and monitor for signs and symptoms of tumor lysis syndrome occur; treat promptly
Monitor for and discontinue promptly if systemic inflammatory response or capillary leak syndrome suspected
Monitor for signs and symptoms of infection; severe and fatal sepsis as a result of bone marrow suppression; discontinue therapy promptly if infection occur
Monitor for and discontinue if venous occlusive disease of the liver suspected
Monitor liver enzymes and discontinue therapy at first signs of severe hepatotoxicity; fatal hepatotoxicity may occur
Monitor renal function and interrupt or discontinue if creatinine levels increase or acute renal failure occur
Increased risk for serious infection with fatal outcome because of immunosuppression, including activation of latent viruses, eg, BK virus-induced nephropathy
Patients with psoriasis who received coal tar, PUVA, methotrexate, or other immunosuppressants have higher risk of skin cancer with Neoral
Discontinue therapy if exfoliative or bullous rash suspected or if Stevens-Johnson syndrome or toxic epidermal necrolysis suspected
Pregnancy and Lactation
Pregnancy Category: C; take into consideration alcohol content of various cyclosporine formulations
Lactation: excreted in breast milk, do not nurse
Maximum Dosage
4 drops/day per affected eye for 0.1% ophthalmic emulsion; 2 drops/day per affected eye for 0.05% ophthalmic emulsion and 0.09% ophthalmic solution. For systemic formulations, the maximum dosage is dependent on indication, route of therapy, and cyclosporine serum concentrations.
4 drops/day per affected eye for 0.1% ophthalmic emulsion; 2 drops/day per affected eye for 0.05% ophthalmic emulsion and 0.09% ophthalmic solution. For systemic formulations, the maximum dosage is dependent on indication, route of therapy, and cyclosporine serum concentrations.
16 to 17 years: 4 drops/day per affected eye for 0.1% ophthalmic emulsion; 2 drops/day per affected eye for 0.05% ophthalmic emulsion. For systemic formulations, the maximum dosage is dependent on indication, route of therapy, and cyclosporine serum concentrations. Safety and efficacy have not been established for the 0.09% ophthalmic solution.
13 to 16 years: 4 drops/day per affected eye for 0.1% ophthalmic emulsion. For systemic formulations, the maximum dosage is dependent on indication, route of therapy, and cyclosporine serum concentrations. Safety and efficacy have not been established for the 0.05% ophthalmic emulsion or 0.09% ophthalmic solution.
4 to 12 years: 4 drops/day per affected eye for 0.1% ophthalmic emulsion. For systemic formulations, the maximum dosage is dependent on indication, route of therapy, and cyclosporine serum concentrations. Safety and efficacy have not been established for the 0.05% ophthalmic emulsion or 0.09% ophthalmic solution.
1 to 3 years: For systemic formulations, the maximum dosage is dependent on indication, route of therapy, and cyclosporine serum concentrations. Safety and efficacy have not been established for the ophthalmic emulsions or solution.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
Cyclosporine
capsule
- 25mg (Gengraf, Neoral, Sandimmune)
- 50mg (Gengraf, Sandimmune)
- 100mg (Gengraf, Neoral, Sandimmune)
oral solution
- 100mg/mL (Gengraf, Neoral, Sandimmune)
injectable solution
- 50mg/mL (Sandimmune)