Tianke

Tianke Uses, Dosage, Side Effects, Food Interaction and all others data.

Sporium Sterile Ophthalmic Emulsion is a preparation of Tianke 0.05% whichacts as immunomodulator in patients whose tear production is suppressed due toocular inflammation associated with keratoconjunctivitis sicca.

Tianke exerts potent immunosuppressive actions on T cells, thereby prolonging survival following organ and bone marrow transplants. This drug prevents and controls serious immune-mediated reactions including allograft rejection, graft versus host disease, and inflammatory autoimmune disease.

Some notable effects of cyclosporine are hypertrichosis, gingival hyperplasia, and hyperlipidemia. There is also some debate about this drug causing nephrotoxicity.

Trade Name Tianke
Availability Prescription only
Generic Cyclosporine
Cyclosporine Other Names Ciclosporin, Ciclosporina, Ciclosporine, Ciclosporinum, Cyclosporin, Cyclosporin A, Cyclosporine
Related Drugs Humira, Cosentyx, methotrexate, hydroxychloroquine, tacrolimus, azathioprine, Enbrel, Remicade, Stelara, mycophenolate mofetil
Type
Formula C62H111N11O12
Weight Average: 1202.635
Monoisotopic: 1201.841368058
Protein binding

About 50% of the administered dose is taken up by erythrocytes while about 34% is bound to lipoproteins. Prescribing information for Sandimmune states that 90% is mainly bound to lipoproteins.

Groups Approved, Investigational, Vet approved
Therapeutic Class Drugs for Dry eyes
Manufacturer
Available Country China
Last Updated: September 19, 2023 at 7:00 am
Tianke
Tianke

How Tianke works

Tianke is a calcineurin inhibitor that inhibits T cell activation. Its binding to the receptor cyclophilin-1 inside cells produces a complex known as cyclosporine-cyclophilin. This complex subsequently inhibits calcineurin, which in turn stops the dephosphorylation as well as the activation of the nuclear factor of activated T cells (NF-AT) that normally cause inflammatory reactions. NF-AT is a transcription factor that promotes the production of cytokines such as IL-2, IL-4, interferon-gamma and TNF-alpha, all of which are involved in the inflammatory process. Specifically, the inhibition of IL-2, which is necessary for T cell activation or proliferation, is believed to be responsible for cyclosporine's immunosuppressive actions. In addition to the above, the inhibition of NF-AT leads to lower levels of other factors associated with T helper cell function and thymocyte development.

Dosage

Tianke dosage

Instill one drop of this drug twice a day in each eye approximately 12 hours apart. Itcan be used concomitantly with artificial tears, allowing a 15 minute interval betweenproducts

Side Effects

The most common adverse event is ocular burning. Other events reported includeconjunctival hyperemia, discharge, epiphora, eye pain, foreign body sensation,pruritus, stinging and visual disturbance (most often blurring).

Toxicity

The oral LD50 in rats is 1480 mg/kg and the TDLO in humans is 12 mg/kg.

Overdose information

In cases of overdose with oral cyclosporine, forced emesis and gastric lavage are recommended 2 hours after ingestion. There are little data available in the literature regarding overdoses with cyclosporine, but hepatotoxicity and nephrotoxicity may occur. One case report of an cyclosporine overdose due to medical error was made involving a 26 year old female and noted the occurrence of nausea, flushing, tremor, vertigo and vomiting, which resolved within about 1 day. Anorexia and a feeling of increased body girth were also experienced by this patient and resolved within about 2 weeks. When overdose with cyclosporine is observed, it is important to consider that dialysis and charcoal, hemoperfusion are not effective techniques to remove cyclosporine from the body.

Precaution

This drug should not be administered while wearing contact lenses. Patients withdecreased tear production typically should not wear contact lenses. If contact lensesare worn, they should be removed prior to the administration of the emulsion. Lensesmay be reinserted 15 minutes following administration of this medication.This drug may cause blurred vision. Do not drive, use machinery, or do any activitythat requires clear vision until you are sure you can perform such activities safely.

Food Interaction

  • Avoid grapefruit products.
  • Avoid potassium-containing products. Taking products that increase serum potassium may increase the risk of hyperkalemia.
  • Avoid St. John's Wort.
  • Take at the same time every day. Take consistently with regard to food.

[Moderate] GENERALLY AVOID: Administration with grapefruit juice (compared to water or orange juice) has been shown to increase blood concentrations of cyclosporine with a relatively high degree of interpatient variability.

The mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits.

GENERALLY AVOID: Administration with red wine or purple grape juice may decrease blood concentrations of cyclosporine.

In 12 healthy volunteers, 12 ounces total of a merlot consumed 15 minutes prior to and during cyclosporine administration (single 8 mg

The time to reach peak concentration (Tmax) doubled, and oral clearance increased 50%.

Similarly, one study were 12 healthy patients were administered purple grape juice and a single dose of cyclosporine showed a 30% and a 36% decrease in cyclosporine systemic exposure (AUC) and peak blood concentration (Cmax), respectively.

The exact mechanism of interaction is unknown but may involve decreased cyclosporine absorption.

MONITOR: Food has been found to have variable effects on the absorption of cyclosporine.

There have been reports of impaired, unchanged, and enhanced absorption during administration with meals relative to the fasting state.

The mechanisms are unclear.

Some investigators found an association with the fat content of food.

In one study, increased fat intake resulted in significantly increased cyclosporine bioavailability and clearance.

However, the AUC and pharmacodynamics of cyclosporine were not significantly affected, thus clinical relevance of these findings may be minimal.

MANAGEMENT: Patients receiving cyclosporine therapy should be advised to either refrain from or avoid fluctuations in the consumption of grapefruits and grapefruit juice.

Until more data are available, the consumption of red wine or purple grape juice should preferably be avoided or limited.

All oral formulations of cyclosporine should be administered on a consistent schedule with regard to time of day and relation to meals so as to avoid large fluctuations in plasma drug levels.

Tianke Hypertension interaction

[Major] The use of cyclosporine is contraindicated in patients with rheumatoid arthritis or psoriasis with uncontrolled hypertension.

Hypertension, possibly due to renal vasoconstriction, has occurred in 50% of patients receiving cyclosporine.

Antihypertensive therapy may be necessary for kidney, liver, and heart transplant recipients treated with cyclosporine.

Hypertension may decline with continued used, but has persisted in some patients.

Volume of Distribution

The distribution of cyclosporine in the blood consists of 33%-47% in plasma, 4%-9% in the lymphocytes, 5%-12% in the granulocytes, and 41%-58% in the erythrocytes. The reported volume of distribution of cyclosporine ranges from 4-8 L/kg. It concentrates mainly in leucocyte-rich tissues as well as tissues that contain high amounts of fat because it is highly lipophilic. Tianke, in the eye drop formulation, crosses the blood-retinal barrier.

Elimination Route

The absorption of cyclosporine occurs mainly in the intestine. Absorption of cyclosporine is highly variable with a peak bioavailability of 30% sometimes occurring 1-8 hours after administration with a second peak observed in certain patients. The absorption of cyclosporine from the GI tract has been found to be incomplete, likely due to first pass effects. Cmax in both the blood and plasma occurs at approximately 3.5 hours post-dose.

The Cmax of a 0.1% cyclosporine ophthalmic emulsion is 0.67 ng/mL after instilling one drop four times daily.

A note on erratic absorption

During chronic administration, the absorption of Sandimmune Soft Gelatin Capsules and Oral Solution have been observed to be erratic, according to Novartis prescribing information. Those being administered the soft gelatin capsules or oral solution over the long term should be regularly monitored by testing cyclosporine blood concentrations and adjusting the dose accordingly. When compared with the other oral forms of Sandimmune, Neoral capsules and solution have a higher rate of absorption that results in a higher Tmax and a 59% higher Cmax with a 29 % higher bioavailability.

Half Life

The half-life of cyclosporine is biphasic and very variable on different conditions but it is reported in general to last 19 hours. Prescribing information also states a terminal half-life of approximately 19 hours, but with a range between 10 to 27 hours.

Clearance

Cyclosporin shows a linear clearance profile that ranges from 0.38 to 3 Lxh/kg, however, there is substantial inter- patient variability. A 250 mg dose of cyclosporine in the oral soft gelatin capsule of a lipid micro-emulsion formulation shows an approximate clearance of 22.5 L/h.

Elimination Route

After sulfate conjugation, cyclosporine remains in the bile where it is broken down to the original compound and then re-absorbed into the circulation. Tianke excretion is primarily biliary with only 3-6% of the dose (including the parent drug and metabolites) excreted in the urine while 90% of the administered dose is eliminated in the bile. From the excreted proportion, under 1% of the dose is excreted as unchanged cyclosporine.

Pregnancy & Breastfeeding use

Pregnancy category C. There are no adequate and well-controlled studies of Tianke ophthalmic emulsion in pregnant women. It should be administered topregnant women if clearly needed. Tianke is known to be excreted in human milk following systemic administration but excretion in human milk after topical treatment has not been investigated.

Although blood concentrations are undetectable after topical administration of Tianke ophthalmic emulsion, caution should be exercised when it isadministered to a nursing woman.

Contraindication

Tianke is contraindicated in patients with active ocular infections and in patients with known or suspected hypersensitivity to any of the ingredients in the formulation.

Acute Overdose

No information provided

Interaction with other Medicine

No information provided

Storage Condition

Keep out of the reach of children. Keep in a cool and dry place, away from light. Do not use more than 4 weeks after opening

Innovators Monograph

You find simplified version here Tianke

Tianke contains Cyclosporine see full prescribing information from innovator Tianke Monograph, Tianke MSDS, Tianke FDA label

FAQ

What is Tianke used for?

Tianke is a calcineurin inhibitor, used as an immunosuppressant medication. Tianke is used together with other medicines to prevent the body from rejecting a transplanted organ (eg, kidney, liver, or heart).

How safe is Tianke?

Tianke is a very strong medicine. It can cause side effects that can be very serious, such as kidney problems. It may also decrease the body's ability to fight infections. You and your doctor should talk about the benefits of this medicine as well as the risks of using it.

How does Tianke work?

Tianke works by suppressing the immune system's responses. By reducing the immune response, Tianke prevents the immune system from attacking healthy tissues. In the same way, it prevents the body from treating a transplanted organ as foreign matter.

What are the common side effects of Tianke?

Common side effects of Tianke are include shaking, headache, dizziness, unusual growth of body hair, nausea/vomiting, diarrhea, stomach upset, or flushing. If any of these effects last or get worse, tell your doctor or pharmacist promptly. Unusual growth and swelling of the gums may occur.

Is Tianke safe during pregnancy?

Animal reproduction studies have shown an adverse effect on the fetus and there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks.

Is Tianke safe during breastfeeding?

Women taking Tianke are not advised to breast feed because Tianke is excreted in milk at concentrations similar to those in blood.

Can I drink alcohol with Tianke?

There is no particular reason for you to avoid alcohol while taking Tianke.

Can I drive after taking Tianke?

Do not drive, use machinery, or do anything that needs alertness until you can do it safely. Limit alcoholic beverages. Talk to your doctor if you are using marijuana (cannabis). This medication may contain alcohol.

When is the best time to take Tianke?

Tianke should be taken with food to decrease stomach upset, but may be taken on an empty stomach. Tianke should be taken at the same time each day.

How often is Tianke taken?

The starting dose is usually 15 mg per kg of body weight per day. This is taken as a single dose 4 to 12 hours before organ transplantation and continued after transplantation as directed by your doctor.

How long does Tianke take to work?

Tianke may take from three to four months to reach optimal control.

What is the half life of Tianke?

Half-Life 8.4 to 27 hours. The time to peak blood Tianke concentrations ranges from 1.5 to 2 hours following oral administration of cyclosporine oral solution USP modified.

Can I stop Tianke suddenly?

You should consult your doctor before you stop taking this medicine or before you change the amount for any reason. You may become ill if you stop taking this medicine suddenly. You may want to take Tianke with some food if the medicine upsets your stomach.

What happens when I stop taking Tianke?

Your body may reject your transplanted organ or your symptoms of RA or psoriasis may return.

Does Tianke make my hair grow?

Tianke can potently induce hair growth in humans.

Is Tianke hard on kidneys?

Tianke is a very strong medicine. It can cause side effects that can be very serious, such as kidney problems. It may also decrease the body's ability to fight infections.

Does Tianke cause anxiety?

Tianke can increased anxiety-related behavior.

Who should not take Tianke?

You should not use Tianke if you are allergic to it. You may not be able to use Tianke if you have: kidney disease; untreated or uncontrolled high blood pressure; or any type of cancer.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happen if I overdose on Tianke?

Symptoms of a Tianke overdose include: vomiting. fatigue. rapid heart rate, or tachycardia. Overdosages of Tianke can cause liver and kidney toxicity. It can also increase people's risk of certain types of cancer, especially lymphoma and skin cancer.

Can Tianke affect my kidneys?

Tianke is a very strong medicine. It can cause side effects that can be very serious, such as kidney problems. It may also decrease the body's ability to fight infections.

Can Tianke affects my liver?

Liver injury was common in patients receiving Tianke. These abnormalities are usually self-limited and asymptomatic but may cause diagnostic difficulty if a preexisting liver disease is present.

Does Tianke affect heart rate?

Tianke did not affect heart rate but contractility (+dp/dtmax) tended to decrease, although not significantly.

*** Taking medicines without doctor's advice can cause long-term problems.
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