
Cyclosporine: A strong oral immune-suppressing drug used in short bursts for severe eczema and psoriasis. It works faster than anything else, and blood pressure and kidney function set a hard limit on how long anyone stays on it. Prednisone: A steroid tablet that calms severe skin inflammation within a day or two. Dermatologists use it in short, planned courses, because most skin disease flares again when it stops.


Choose for a fast, short burst of control in severe eczema or psoriasis while a longer-term treatment is set up.
Choose for a short rescue course in severe inflammation like poison ivy — not for ongoing eczema or psoriasis.
Can you take them together?
Both suppress the immune system, so they are only combined briefly in hospital-level situations. Neither is a long-term plan for skin disease.
Compare uses by strength of evidence. Evidence level describes confidence in a benefit, not its size.











Inhibits calcineurin: Binds cyclophilin to block a T-cell activation switch. Reduces IL-2 signals: Limits a messenger that helps T cells become active. Calms skin inflammation: Overactive immune responses in skin decrease.
Cyclosporine binds cyclophilin; that complex inhibits calcineurin and T-cell cytokine production. This is a simplified skin-focused explanation of systemic immunosuppression.

Becomes active prednisolone: The body converts prednisone into its active form. Activates steroid receptors: Binds receptors inside immune and other cells. Turns down inflammatory signals: Changes gene activity to reduce inflammation.
Prednisone is converted to active prednisolone and acts through glucocorticoid receptors with multiple genomic and non-genomic effects. Diagram explains selected mechanisms, not tapering, suitability, or dosing.
The dose is set by body weight, then adjusted by blood pressure and kidney tests, not by how the skin looks.
Starting dose: About 2.5 mg per kilogram of body weight a day, split into two doses. A severe flare may start around 4 to 5 mg per kilogram a day to get control quickly.
Going up: Raised in small steps every two to four weeks if response is poor, and only if the tests are stable.
Coming down: Once the skin is calm, the dose comes down in stages, to give the next treatment time to work.
Total course: Short by design. Many courses run 8 to 16 weeks. Guidelines advise no more than about a year of continuous treatment, less where possible.
The dose is set by the severity of the flare and by body weight, not a standard tablet count, with an end date written in from the start.
Starting dose: For a severe rash, commonly 0.5 to 1 mg per kilogram per day as a single morning dose. Milder problems need much less.
Going up: Rarely in dermatology. If a rash has not responded in a few days, the next step is a different treatment, not a higher dose.
Usual dose: The starting dose held a few days to a week, then stepped down.
Total course: For severe allergic contact dermatitis such as poison ivy, around two to three weeks with a taper — shorter courses are a common cause of rebound. Blistering disease can need months, but that is specialist care with a plan to come off, alongside a second drug that lets the steroid dose fall.
Twice a day, about 12 hours apart, at the same times daily. Be consistent about food: always with meals or always without, because switching changes absorption. Swallow capsules whole and leave them in the foil until you take them.
On the liquid, mix it with orange or apple juice in a glass cup, stir and drink it straight away, then rinse the cup with more juice and drink that too. Never use grapefruit juice.
Once a day in the morning, with food or milk. Morning matters — it matches your own cortisol rhythm and is the best thing you can do about steroid insomnia. Food reduces stomach upset; take it with a full glass of water. Split doses are used in some conditions, only when a doctor asks.
Take it when you remember unless the next dose is close, then skip it. Never take two at once. Tell the prescriber if you miss more than a dose or two, or vomit soon after taking it, because the dose is built around your blood level.
Take it as soon as you remember on the same day. If you do not remember until the next day, take only that day's dose — never two together. On a longer course, if you have missed more than a day, call the prescriber rather than restarting yourself; stopping suddenly is what causes trouble.
Cyclosporine is monitored more closely than any other skin drug, and that monitoring is why it can be used at all. Blood pressure is measured at every visit, often at home. Kidney function is checked by blood test, twice before starting for a reliable baseline, then every couple of weeks for a month or two, then monthly once the dose is steady. The same draws cover potassium, magnesium, uric acid, liver enzymes, blood counts and cholesterol. Drug blood levels are routine in transplant care, not usually needed at dermatology doses.
Two numbers drive the decisions. A rise in creatinine of about a quarter above your baseline, confirmed on a repeat test, means dropping the dose; about half means stopping. New high blood pressure means lowering the dose or adding a blood pressure medicine, and the choice matters: diltiazem and verapamil push levels up, amlodipine does not.
The interaction list is long. Drugs that raise levels include the azole antifungals, clarithromycin and erythromycin, and some HIV and hepatitis C medicines. Drugs that lower it include rifampin, phenytoin, carbamazepine and St John's wort. It also raises statin levels, so that dose is often reduced, and it interacts with colchicine, digoxin, methotrexate and potassium-sparing water tablets. Bring every prescription, supplement and herbal product to the first visit.
The time limit is the point of all this. Kidney damage builds with continuous use and part of it can be permanent, so guidelines cap continuous treatment at about a year and most dermatology courses are far shorter. Long or repeated use also raises the risk of skin cancer, lymphoma and serious infection, so skin checks continue afterward.
For a short course in a healthy person, no routine blood tests are needed. What gets watched is blood sugar in anyone with diabetes or borderline sugars, blood pressure, weight, sleep and signs of infection.
On a longer course — more than about three months, or repeated courses — monitoring becomes real: blood pressure and blood sugar, weight, a bone density scan with calcium and vitamin D, an eye check for cataracts and raised eye pressure, and a plan for protecting the stomach and bones. Usually shared care, not a dermatologist alone.
Prednisone is not a drug to stay on for skin disease. Almost every serious side effect is dose multiplied by time, so the monitoring plan and the exit plan are one conversation.
Approximate windows, not promises.
First 2 weeksStarting: Itch settles first, often within days, and sleep improves. Tingling or burning in the hands and feet, headache and mild nausea are common early. Blood pressure and kidney tests get checked.
Weeks 2 to 6Working: Redness, weeping and thickness improve clearly. Chronic hives that antihistamines do not control usually settle within a month. Extra hair growth on the face, arms and body and swollen or tender gums start now; both are dose-related and reverse after stopping.
Weeks 8 to 16Plaque psoriasis: Large improvement, often near-clear at the higher end of the dose range. Usually where the course ends and another treatment takes over.
VariableSevere inflammatory ulcers: In pyoderma gangrenosum it stops the ulcer spreading while healing catches up. Response times differ a lot.
ThroughoutThe tests: Blood pressure creeping up and kidney numbers drifting decide whether the dose drops or the drug stops. Neither causes symptoms, which is why the tests are not optional.
First 24 to 48 hoursStarting: Itch and swelling ease first; severe hives respond faster to this than to anything else, with antihistamines alongside. Early side effects arrive in the same window — poor sleep, big appetite, restlessness, flushed face, indigestion.
Days 2 to 7Working: The rash flattens and fades. Poison ivy and contact dermatitis settle here, and a severe eczema flare clears fast. Fluid retention and facial puffiness may appear, blood sugar rises in those prone to it, blood pressure can go up.
Days to 2 weeksBlistering disease: New blisters usually stop forming. Healing takes longer, and a steroid-sparing drug is started early so the dose can come down.
Weeks 2 to 3Stepping down: Run the course out rather than stopping early — stopping early brings the rash back. Side effects step down with the dose, and sleep and appetite settle within days of finishing.
After stoppingWatch for rebound: Usually within a few days to two weeks, which is why a longer-term treatment starts at the same time. After a longer course, weeks of tiredness while the adrenal glands restart is normal.
Only with long coursesThe long-term risks: Bone thinning, cataracts, thigh muscle weakness, easy bruising, thin skin, hip pain from reduced blood supply to the bone. Reasons to keep courses short, not to refuse a short one.
Sorted by what to do about them.
Generic capsules are cheap next to biologics, part of why the drug is still used. Branded versions cost more without working better.
The visible cost is not the whole cost. Repeated blood tests, blood pressure checks and appointments add up, and none are optional. It is cheaper per month than a biologic but taken for only a few months, so the comparison depends on what comes after.
Insurance generally covers it for severe psoriasis. Eczema coverage varies more in the United States, where that use is off-label.
Generic prednisone is among the cheapest prescription drugs, stocked everywhere. Cost is almost never the reason it is or is not used.
The delayed-release brand costs far more with no clear advantage in skin disease. The liquid costs more and is kept for children and anyone who cannot swallow.
Faster than anything else for these conditions. Itch improves within days, clearing by four to six weeks.
Most courses run months. Guidelines cap continuous use at about one year, because kidney effects build and some can be permanent.
It raises blood pressure in a meaningful share of people, and that causes no symptoms. Catching it early usually means lowering the dose rather than stopping.
No. Grapefruit, pomelo and Seville oranges block the enzyme that clears it, so levels rise unpredictably. Other citrus is fine.
Both are dose-related. Not dangerous, usually better if the dose comes down, and gone after stopping.
Usually, within weeks to a few months, unless another treatment is running. Planning that before the taper is the point of the short course.
Usually within 24 to 48 hours for itch and swelling. If a rash has not moved after several days, revisit the diagnosis or treatment.
Your adrenal glands slow down and need time to restart, and many skin conditions flare hard if it is dropped suddenly.
Often — particularly eczema, hives and psoriasis. Expected, and why a longer-term treatment is usually started at the same time.
Side effects are dose multiplied by time — bone loss, cataracts, blood sugar, blood pressure, infection risk all build with the months. Safer long-term treatments exist for every condition it is used for.
Both are common and dose-related and settle within days of stopping. Morning dosing helps a lot with sleep.
An occasional drink is not dangerous, but alcohol adds to the stomach irritation, poor sleep and the effect on blood sugar.