Ciqorin

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Ciqorin

Property Description
Active Ingredient Cyclosporine (Ciclosporin)
Common Forms Soft gelatin capsules, oral solution, injection, ophthalmic emulsion
Pharmacological Class Immunosuppressant, Calcineurin Inhibitor (CNI)
Origin Semi-synthetic (derived from the fungus Tolypocladium inflatum)
Primary Goal Prevent immune rejection and suppress severe autoimmune activity

Ciqorin: A Definition and Chemical Identity

Ciqorin is a pharmaceutical product containing the active substance Cyclosporine (INN: ciclosporin), a highly specialized and potent medicine. Structurally, Cyclosporine is classified as a cyclic polypeptide, meaning its molecule is a closed ring of eleven amino acids. Its origin is rooted in nature, as it is a semi-synthetic compound originally derived from the fungus Tolypocladium inflatum. This defining chemical characteristic is clinically recognized for its selective inhibition of T-lymphocytes, establishing its critical role in modern medicine. Cyclosporine is recognized for its unique biological properties.


What Type of Medicine is Ciqorin?

Ciqorin is classified as a highly selective Calcineurin Inhibitor (CNI), which is a key subtype of the broader immunosuppressant pharmacological class. The general therapeutic purpose of this medication is to modulate and prevent the body's immune system from mounting an overwhelming or destructive attack. The medication is used to suppress immune responses that lead to chronic inflammation and tissue damage. This underscores its importance in preventing the immune system from rejecting a transplanted organ, which is a typical use scenario.


Available Forms and Pharmaceutical Class

This medicine is available in various forms for different routes of administration, including soft gelatin capsules, an oral solution, a solution for intravenous injection, and an ophthalmic emulsion. The capsule and oral solution forms utilize specialized microemulsion bases, which are necessary to ensure the effective and reliable systemic absorption of the Cyclosporine molecule, a challenging task due to the drug's inherent properties. These delivery systems are crucial for maintaining consistent concentrations for therapeutic drug monitoring.

Regulatory References

  1. MedlinePlus Drug Information on Cyclosporine

What side effects are possible with Ciqorin?

Possible side effects and safety information

The safety profile for Ciqorin (Cyclosporine) is characterized by a spectrum of adverse reactions categorized by frequency and the organ systems affected, as established in official regulatory documents. The most critical safety elements relate to potential major organ system toxicity and the consequences of immunosuppression.

Regulatory Classification of Side Effects

The medicine's safety information classifies effects across several frequency tiers:

  • Very Common (occurring in ge 1 in 10 patients): These frequently reported effects include nephrotoxicity (kidney damage or dysfunction), systemic hypertension (high blood pressure), tremor, headache, and hypertrichosis (excessive hair growth).
  • Common (occurring in ge 1 in 100 patients): Effects typically include hepatotoxicity (liver injury), gingival hypertrophy (enlarged gums), and changes in blood fats (hyperlipidemia).

Serious adverse reactions documented in official labeling include an increased risk of malignancy (such as lymphoma and skin cancer) and a heightened susceptibility to serious opportunistic infections, which stems directly from the drug's immunosuppressive nature. Severe manifestations of neurotoxicity, such as convulsions, are also listed.

Safety Patterns and Constraints

The official safety information notes that the risks of hypertension and nephrotoxicity generally increase with higher doses and longer duration of therapy. Population-specific considerations are noted for older adults, who may require close monitoring of renal function, and for use during pregnancy, where potential benefits must clearly justify the risks. Furthermore, caution is indicated in patients with severe hepatic impairment due to the potential for increased drug exposure.

Overdose and Emergency Response

Overdose with Ciqorin (Cyclosporine) primarily results in the intensification of the drug’s officially documented toxicities. The acute clinical manifestations involve nephrotoxicity and hepatotoxicity, which are officially noted alongside corresponding elevated laboratory markers. Other signs reported in regulatory documents include neurological effects such as tremor, headache, and lethargy, as well as cardiovascular signs like hypertension and tachycardia.

Overdose is classified as potentially severe or life-threatening, with documented outcomes including acute renal failure, seizures, and coma. Massive or prolonged overexposure has been associated with the risk of irreversible renal damage. Increased susceptibility to severe effects is noted for pediatric patients and individuals with existing renal or hepatic impairment.

The official regulatory guidance mandates that you seek immediate medical attention and contact a poison control center for any suspected overdose. Because no specific antidote is known, clinical management is restricted to symptomatic and supportive treatment under continuous hospital monitoring. Procedures such as gastric decontamination (e.g., activated charcoal or gastric lavage) may be administered for recent oral over-ingestion. Continuous monitoring of Cyclosporine blood levels and organ function is required during the period of observation.

Therapeutic Uses of Ciqorin

What Ciqorin Treats: Main Uses and Benefits

Ciqorin is a prescribed medication used to address conditions involving an overactive immune system, providing relief in specific clinical settings. Its primary therapeutic domains include managing the body's response to transplanted organs—specifically kidney, liver, and heart allogeneic transplants—to support their acceptance. It also helps manage specific chronic autoimmune disorders, such as severe, active rheumatoid arthritis that has not responded adequately to methotrexate, and psoriasis in nonimmunocompromised adult patients.

This medication aims to mitigate the disease activity and associated symptoms of these chronic inflammatory and autoimmune conditions. The benefit to the patient is focused on supporting the body's efforts to accept the new organ and managing the underlying inflammatory processes.

Quick Fact: Relief for Inflammatory Symptoms and Transplant Rejection Management

Eligibility and Restrictions for Use

Eligibility Map: Who Can and Cannot Use Ciqorin — Official Regulatory Information

Populations for whom use is allowed (as stated in label):

Ciqorin is approved for use in adults receiving kidney, liver, or heart transplant allografts. It is also indicated for adults with severe rheumatoid arthritis or severe psoriasis when other treatments have failed, and for children (4 years) for specific ophthalmic conditions.

Populations for whom use is contraindicated:

Use is contraindicated in patients with a known hypersensitivity to cyclosporine or any formulation ingredients. For non-transplant indications like rheumatoid arthritis and psoriasis, the medicine is also prohibited for patients with uncontrolled hypertension, abnormal renal function, or active malignancy.

Age-Related and Conditional Use Rules

Systemic use for rheumatoid arthritis or psoriasis has not been established in the pediatric population. Use in older adults requires specific caution and close monitoring of kidney function. The medicine is not recommended during pregnancy and lactation unless the clinical benefit is judged to outweigh the potential risk, as the substance is excreted in breast milk. Conditional use with monitoring is required for patients with hepatic impairment due to the drug's extensive liver metabolism.

Connection to the overall eligibility profile

Official regulatory documents define who can and cannot use Ciqorin by establishing absolute contraindications for high-risk populations and mandating conditional use based on the integrity of major organ systems like the liver and kidneys. Eligibility is strictly structured by age-group and reproductive status to ensure appropriate use.

What should I know about interactions with other medicines?

Ciqorin (Cyclosporine) has a significant interaction profile documented by regulatory authorities, primarily affecting its concentration in the body. Certain combinations are classified as contraindicated. Co-administration with Bosentan is prohibited due to the documented risk of significant reduction in Cyclosporine exposure. The herbal supplement St. John's Wort (Hypericum perforatum) is also contraindicated, as it is documented to decrease Ciqorin blood levels and risks treatment failure.

The majority of documented drug-drug interactions relate to the Cytochrome P-450 3A (CYP3A4) enzyme system and P-glycoprotein activity. Medicines such as Verapamil (Calcium Channel Blockers), Ketoconazole (Antifungals), and Erythromycin (Macrolide Antibiotics) are formally documented to increase Ciqorin plasma concentrations. Conversely, medications like Rifampin (Antibiotics) and Phenytoin (Anticonvulsants) are documented to decrease plasma concentrations.

Regulatory warnings also highlight the risks of additive organ toxicity. Combining Ciqorin with other nephrotoxic agents, such as Non-Steroidal Anti-Inflammatory Drugs (NSAIDs), is formally documented to increase the overall risk of renal toxicity. Co-administration with Digoxin carries a documented risk of severe digitalis toxicity. Dietary restrictions include avoiding Grapefruit and Grapefruit Juice, as they are documented to increase systemic exposure. For the ophthalmic emulsion, co-administered topical eye products must be separated by at least 15 minutes.

Mechanism of Action

How Ciqorin Works

Primary Mechanism: P1R Antagonism and Osteoclast Cascade

Ciqorin functions as a selective non-peptidyl antagonist for the A1 purinergic receptor ( P1 R). Its primary mechanism involves high-affinity competitive binding to the P1 R on the surface of pre-osteoclast cells. This interaction inhibits the cAMP-PKA pathway, which is essential for NFkappa B translocation. The resulting suppression of NFkappa B activity leads to reduced expression of RANKL-induced genes, including TRAP and Cathepsin K. This sequence results in the net inhibition of osteoclast differentiation, thereby affecting skeletal remodeling processes.


Secondary Mechanism and Systemic Effects

Ciqorin also modulates the balance of osteoblast and osteoclast activity. A secondary mechanism involves the downregulation of the transcription of pro-inflammatory cytokines such as IL-6 and TNF-alpha. This occurs by affecting the JAK/STAT pathway via an M3 muscarinic receptor-dependent cascade, which attenuates the signaling cascade that leads to localized tissue degradation.

Dosage and Administration Information

Ciqorin (Cyclosporine) is administered either orally using soft gelatin capsules or a solution, or through intravenous (IV) infusion, a route primarily reserved for patients unable to tolerate the oral form. The medicine is dosed on a body weight basis and must be administered in two equally divided doses (BID), spaced approximately 12 hours apart.

Indication Initial Daily Dose Range (Oral, Divided BID) Maintenance Dose (Oral, Divided BID)
Transplant Prophylaxis 10–18 mg/kg/day, pre-transplant Tapered to 2–10 mg/kg/day
Rheumatoid Arthritis/Psoriasis 2.5–3 mg/kg/day Adjusted to the lowest effective level

To ensure consistent systemic exposure, the medicine must be taken at the same time each day and with the same consistent relationship to meals. The oral solution requires specific preparation: it must be accurately measured, diluted immediately with compatible liquids (e.g., orange or apple juice), and consumed from a glass container. The dosing syringe should be wiped clean and not rinsed with water.

Special Procedural Conditions: The Modified and Non-Modified oral formulations are not bioequivalent and must not be interchanged without strict medical supervision, as this significantly alters drug absorption. For specific populations, pediatric patients may require a higher dose on a milligram-per-kilogram basis than adults.

Recent Clinical Evidence

Research evidence / Overview of Studies for Ciqorin (Cyclosporine)


Evidence for Preventing Solid Organ Transplant Rejection

Research exploring Ciqorin's use in transplantation involved Randomized Controlled Trials (RCTs) and years of long-term observational cohort studies tracking patient populations receiving kidney, liver, and heart allografts. These studies examined the use of the medicine in preventing the body's immune response to a transplanted organ. Outcomes examined included the incidence of acute rejection episodes and tracking the survival rates of the transplanted organ (graft) over multiple years. Studies reported findings related to measurements of patient and graft survival when Ciqorin was included in the immunosuppressive regimen. Research has noted known challenges in managing potential cumulative effects that impact the research on long-term outcomes, which is a focus of continuous therapeutic monitoring in practice.

Evidence for Severe Active Rheumatoid Arthritis and Psoriasis

For severe, active Rheumatoid Arthritis (RA), research primarily involved short- to intermediate-term RCTs focusing on adults who had not responded adequately to initial therapies. The outcomes examined were related to measures of physical discomfort and daily functioning, such as changes in the number of tender and swollen joints. Similarly, studies for severe psoriasis measured changes in the Psoriasis Area and Severity Index (PASI). Trials for both conditions reported measured changes over defined time intervals (typically 12 weeks up to 1 year).

Key Research Limitations and Unanswered Questions

Several limitations are noted in the evidence landscape. For the autoimmune indications (RA and psoriasis), the follow-up durations were often limited when compared to the chronic nature of the conditions. Comparative evidence is lacking for direct, head-to-head trials against all available modern therapies. Across all indications, results apply only to the populations studied, and long-term effects are not fully established without continuous monitoring. Research provides context but not individual predictions, and findings describe group patterns, not personal outcomes.

Key Studies & References A Systematic Review about an Advance in Cyclosporine Monitoring in Kidney Transplant Recipients

Frequently Asked Questions (FAQ)

Common questions about Ciqorin (FAQ)


Q: What are the different conditions that Ciqorin is used to treat, besides transplants?

Official information states that Ciqorin (Cyclosporine) is approved for use in adults for severe active rheumatoid arthritis and severe psoriasis when other treatments have failed. Additionally, the active ingredient is indicated for use in children (age four and older) for specific ophthalmic (eye) conditions.

Q: How quickly should I expect to see an improvement in my symptoms after starting Ciqorin?

The time it takes to see the full therapeutic effect can vary based on the condition being managed. For conditions like Rheumatoid Arthritis, clinical trials suggest that it may take up to 12 weeks of therapy to reach its maximum therapeutic effect. Your individual response will be monitored over time.

Q: Does Ciqorin need to be taken with food, or on an empty stomach?

The medicine can be taken with or without food. However, it is essential that it is taken with the same consistent relationship to meals every single day. Taking the drug in a consistent manner helps ensure the level of medicine in the blood remains stable and predictable.

Q: What happens if I miss a dose of Ciqorin?

If a dose is missed, taking it as soon as it's remembered is advised. However, if it is close to the time for the next scheduled dose, patient information recommends skipping the missed dose completely and returning to the regular schedule. Two doses should never be taken at the same time.

Q: How long does Ciqorin stay in your system after stopping the medication?

Regulatory information indicates that the time it takes for half of the drug to be eliminated from the body (the half-life) typically ranges from 6 to 20 hours. This time is highly variable and may be longer in individuals with certain health conditions, particularly severe liver impairment.

Q: Can taking Ciqorin affect my cholesterol or blood fat levels?

Yes, official safety information documents that changes in blood fats, specifically hyperlipidemia (increased fat levels), are a Common side effect of Ciqorin. Because of this, monitoring of your lipid (fat) profile is routinely performed during treatment.

Q: What is the difference between the modified and non-modified versions of Cyclosporine, and which is Ciqorin?

Cyclosporine comes in Modified and Non-Modified oral formulations, and regulatory labels warn that these are not bioequivalent and should never be interchanged without medical guidance. Ciqorin is generally recognized as the modified microemulsion formulation, which is designed for more consistent drug absorption.

Q: Can elderly patients take Ciqorin safely, or are there special concerns?

Ciqorin can be used in older adults, but regulatory warnings indicate that they may require special caution. This includes close monitoring of renal (kidney) function, as older patients are more likely to have age-related kidney issues that could potentially affect the drug's safety profile.

Q: Is it safe to get vaccinations while I am on Ciqorin?

Due to Ciqorin's immunosuppressive effects, official warnings advise that live-attenuated vaccines should generally be avoided. Other non-live vaccines may also be less effective while the medication is being used. Vaccination status should always be discussed with a healthcare provider.

Q: Why are regular blood tests necessary when taking Ciqorin?

Regular blood tests are necessary to measure the drug's concentration in the blood, known as the trough level, to ensure the dose is therapeutic. Furthermore, testing is essential to monitor for potential side effects on critical organs, such as the kidneys and liver.

Q: Can Ciqorin affect my gums, and what can I do to prevent gum issues?

Yes, gingival hypertrophy (gum enlargement) is a documented Common side effect. Although the regulatory label does not specify prevention, it is generally understood that maintaining excellent oral hygiene, including regular dental check-ups, may help manage this risk.

Q: Is Ciqorin used to treat dry eye disease, and is this the same formulation as the oral capsules?

Yes, the active ingredient, Cyclosporine, is used to treat dry eye disease; however, it is in a different formulation. This treatment utilizes an ophthalmic emulsion (eye drop) for localized application and is not the same as the oral capsules or solution used for systemic conditions.

Q: How long is the typical course of treatment with Ciqorin for conditions like rheumatoid arthritis or psoriasis?

The appropriate treatment duration is an individual medical decision. For Psoriasis, official product information advises that continuous treatment lasting longer than one year is not generally recommended due to the potential for increased kidney toxicity. Treatment is highly individualized based on need and response.

Q: Why is it important to take Ciqorin at exactly the same time every day?

Taking the medicine at the same time daily is critical for achieving consistent systemic exposure. This maintains a stable, steady level of Ciqorin in the blood, which is essential for therapeutic consistency, especially in preventing acute transplant rejection or managing severe autoimmune activity.

Q: What happens if I switch from a brand-name Cyclosporine to a generic like Ciqorin?

Regulatory documents strongly warn that patients should not switch between different brands or formulations of Cyclosporine without strict medical supervision. Because different versions may not be absorbed equally, any change requires close monitoring of blood levels by a healthcare provider.

Q: Does alcohol consumption interfere with Ciqorin's effectiveness or increase side effects?

Some formulations of the Ciqorin oral solution contain a percentage of alcohol (ethanol) as an inactive ingredient. Regulatory documents advise caution for patients with a history of alcohol abuse or liver disease, as the alcohol content in the medicine itself may be a concern for those with these pre-existing conditions.

Q: Are there any common neurological side effects associated with Ciqorin?

Yes, official safety profiles list tremor and headache as Very Common neurological side effects. This means they are reported by a large number of patients (one in ten or more). More serious neurological effects, such as convulsions, are less common.

Q: Can Ciqorin be taken during pregnancy or while breastfeeding?

Official information advises that Ciqorin is generally not recommended for use during pregnancy or while breastfeeding. This is because the drug can cross the placenta and is excreted in breast milk. Use is only considered if the treating physician determines the clinical benefits clearly outweigh the potential risks.

Q: Why do some people experience stomach issues or nausea when starting Ciqorin?

Nausea, vomiting, and general stomach discomfort are documented as known side effects of Ciqorin in the official safety profile. These symptoms may sometimes be minimized by taking the medication with food, provided the consistent relationship to meals is maintained.

Q: Is the long-term safety profile of Ciqorin well-established for autoimmune diseases?

Studies and regulatory summaries note that, for autoimmune indications like RA and psoriasis, the follow-up durations were often limited in clinical trials when compared to the chronic nature of these diseases. Therefore, long-term effects are not fully established without continuous medical monitoring.

Q: Does Ciqorin require a special measuring tool for the liquid form?

Yes, the official patient information confirms that the Ciqorin oral solution must be accurately measured. It is typically dispensed with a specific dosing syringe to ensure that the patient receives the intended amount of medicine.

Q: Are there any specific dental checks or precautions needed while on Ciqorin?

Due to the risk of gingival hypertrophy (gum enlargement) as a common side effect, regular and increased dental care and check-ups are often generally recommended. Maintaining excellent oral hygiene is considered crucial for managing this complication.

Q: If I have a history of gout, is Ciqorin still a treatment option for me?

Regulatory literature and clinical reports indicate that Ciqorin can cause hyperuricemia (high uric acid levels), which is a risk factor for gout. Because gout attacks have been reported, cautious use and monitoring of uric acid levels are relevant considerations if Ciqorin is started.

Q: Can Ciqorin be used for lupus or other systemic autoimmune diseases?

Systemic use of Ciqorin (Cyclosporine) is only officially approved for organ transplant rejection prophylaxis, severe rheumatoid arthritis, and severe psoriasis. Use for other systemic autoimmune conditions like lupus is not listed as an approved indication in regulatory documents.

Q: What is the average time for Ciqorin to reach its full therapeutic effect?

While the drug begins to work right away to suppress the immune system, the full benefit in conditions like Rheumatoid Arthritis is typically measured over a longer period. Official clinical summaries suggest that achieving the maximum effect can take up to 12 weeks of continuous therapy.

Q: Does Ciqorin affect fertility in men or women?

Official regulatory documents focus primarily on the risks of use during pregnancy and while breastfeeding. The regulatory label does not explicitly state the effect of Ciqorin on a person's underlying ability to conceive (fertility) in either men or women.

Q: Can Ciqorin be taken with a cold or flu, or should I stop it if I get sick?

Because Ciqorin is an immunosuppressant, it increases the risk of serious opportunistic infections. If a patient develops symptoms of an infection like a cold or flu, they should contact a healthcare provider immediately. Patients should not discontinue the medication without consulting a healthcare provider.

Q: Does Ciqorin interact with oral contraceptives or other hormone-based medicines?

Yes, regulatory documents list many potential drug interactions involving a specific liver enzyme system (CYP3A4). This system is involved in metabolizing certain oral contraceptives and other hormone-based medicines, meaning these combinations may require careful dose adjustments and monitoring.

Q: Is it common for Ciqorin to cause a burning or tingling sensation in the limbs?

Yes, official safety information documents that paresthesia is a common side effect. Paresthesia is the term used for an abnormal sensation, such as a burning, tingling, or prickling feeling, usually occurring in the hands or feet.

Q: Does Ciqorin affect blood sugar levels?

Regulatory information documents various metabolic effects associated with Ciqorin use. While not always listed as one of the most frequent side effects, reports of high blood sugar, or hyperglycemia, have been noted in clinical contexts.

How should Ciqorin be stored and disposed of?

How to Store and Dispose of Ciqorin

Ciqorin (cyclosporine) must be stored at Controlled Room Temperature, defined as 20 C to 25 C (68 F to 77 F). The official labeling permits temperature excursions between 15 C and 30 C (59 F and 86 F).


Protection and Handling Requirements

The medicine requires protection from light and moisture. It is prohibited to freeze the capsules or oral solution. Capsules must be stored in their original container, and the oral solution bottle must be kept tightly closed. The oral solution is stable for two months after the initial opening of the bottle. All Ciqorin products must be stored out of the sight and reach of children.

Disposal

Disposal of unused or expired product must follow local requirements. The medicine must not be disposed of via wastewater or household trash.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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