Tranexamic Acid BP
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CYKLOKAPRON® Pharmacia & Upjohn Tranexamic Acid Antifibrinolytic Agent

Action and Clinical Pharmacology: Tranexamic acid produces an Antifibrinolytic effect by competitively inhibiting the activation of plasminogen to plasmin. It is also a weak noncompetitive inhibitor of plasmin. These properties make possible its clinical use as an Antifibrinolytic in the treatment of both general and local fibrinolytic hemorrhages. It has an action mechanism similar to, but about 10 times more potent in vitro than that of epsilon aminocaproic acid (EACA).

Absorption from the human gastrointestinal tract is not complete (40%).

Tranexamic acid binds considerably more strongly than EACA to both the strong and weak sites in the plasminogen molecule in a ratio corresponding to the difference in potency between the compounds. The pharmacological significance of the binding to these different sites has not yet been evaluated.

Tranexamic acid does not bind to serum albumin. The plasma protein binding that seems to be fully accounted for by its binding to plasminogen, appears to be negligible at therapeutic plasma levels of 5 to 10 mg/L.

Possible routes of biotransformation are acetylation or deamination followed by oxidation or reduction. After oral administration approximately 50% of the parent compound, 2% of the deaminated dicarboxylic acid, and 0.5% of the acetylated product are excreted.

Tranexamic acid is eliminated by glomerular filtration, excretion being about 30% at 1 hour, 55% at 3 hours, and 90% at 24 hours after i.v. administration of 10 mg/kg. After oral administration of 10 to 15 mg/kg, excretion was 1% at 1 hour, 7% at 3 hours, and 39% at 24 hours.

I.V. administration of 10 mg/kg gave plasma concentrations of 18.3 µg, 9.6 µg, and 5 µg/ml 1, 3 and 5 hours after the injection.

When administered 36 to 48 hours before surgery in 4 doses of 10 to 20 mg/kg an antifibrinolytically active concentration (10 µg/mL) of tranexamic acid remained up to 17 hours in the tissues investigated, and up to 7 to 8 hours in the serum.

Tranexamic acid crosses the placenta. After an i.v., injection of 10 mg/kg the concentration can rise to about 30 µg/mL of fetal serum.

Tranexamic acid also passes over into the breast milk during lactation in concentrations 1/100 of the corresponding serum levels.

After both oral and i.v. administration tranexamic acid passes into the semen and inhibits its fibrinolytic activity, but without affecting the motility of the spermatozoa.

The ability of tranexamic acid to cross the blood-brain barrier has been demonstrated when administered to patients with ruptured intracranial aneurysms.

Tranexamic acid diffuses rapidly to the joint fluid and to the synovial membrane. In the joint fluid, the same concentration was obtained as in the serum. The biological half-life in the joint fluid was about 3 hours.

Three hours after a single oral dose of 25 mg/kg, the peak serum level was 15.4 g/L and the aqueous humour level was 1.6 g/L.

 
 
Indications and Clinical Uses:
Hereditary angioneurotic edema. Increased local fibrinolysis when the diagnosis is indicative of hyperfibrinolysis, as with conization of the cervix, dental extraction in patients with coagulopathies (in conjunction with antihemophilic factor) epistaxis, hyphema, and menorrhagia (hypermenorrhea).

Contra-Indications: Patients with a history or risk of thrombosis should not be given tranexamic acid, unless at the same time it is possible to give treatment with anticoagulants. The preparation should not be given to patients with acquired disturbances of color vision. If disturbances of color vision arise during the course of treatment, the administration of the preparation should be discontinued. tag_WarningWarnings

Manufacturers' Warnings In Clinical States: For patients who are to be treated for several weeks with tranexamic acid an ophthalmic checkup is advisable (sharpness of vision, color vision, fundus, field of vision, etc.) if possible, before treatment is initiated and regularly during treatment.

Pregnancy: The safety of tranexamic acid during pregnancy has not yet been established. No harmful effects have been reported.

A woman with fibrinolytic bleeding in the fourth month of pregnancy was treated with tranexamic acid for a total of 64 days. The total dose was 256 g. The delivery occurred spontaneously in the 30th week of pregnancy and was normal in all other respects. The infant was healthy.

In a case of threatened placental abruption that was prevented by giving tranexamic acid, the patient had already lost two children in connection with placental abruption. In the 26th week of her third pregnancy bleeding occurred, indicating abruption. Pathological proteolysis with predominant activation of the fibrinolytic system was established. Between the 26th and 33rd week of pregnancy about 250 g of tranexamic acid were given, both i.v. and orally. The bleeding was arrested and a healthy child was delivered by Caesarean section.

Tranexamic acid crosses over to the fetus. After an i.v., injection of 10 mg/kg the concentration can reach a level of about 30 µg/mL fetal serum. Fibrinolytic activity is very high in neonates. It is not known for certain whether a reduction of this activity during the first hours of life is harmful. Kullander and Nilsson who have wide experience with tranexamic acid in connection with childbirth have observed no negative effect on the infants.
 
 
Precautions: Care should be taken in cases of renal insufficiency due to the risk of accumulation, and where there is pronounced hematuria from the upper urinary tract, since in isolated cases obstacles to passage have been observed in the tract.

Renal Insufficiency: In patients with serum creatinine concentrations of 120 to 250 µmol/L, 15 mg orally or 10 mg i.v. tranexamic acid/kg body weight twice daily. At serum creatinine levels of 250 to 500 µmol/L the dosage should be 15 mg orally or 10 mg i.v. /kg body weight at 24-hour intervals and at serum creatinine levels of 500 µmol/L or more the same dose should be given at intervals of 48 hours between doses.

Tranexamic acid therapy is not indicated in hematuria caused by diseases of the renal parenchyma. Intravascular precipitation of fibrin frequently occurs in these conditions and may aggravate the disease. In addition, in cases of massive renal hemorrhage of any cause, Antifibrinolytic therapy carries the risk of clot retention in the renal pelvis.

Lactation: Tranexamic acid is secreted in the mother's milk at a concentration only a hundredth of the corresponding serum levels. The investigators are of the opinion that tranexamic acid can be given during lactation without risk to the child.

Adverse Reactions: Gastrointestinal symptoms (nausea, vomiting, and diarrhea) occur but disappear when the dose is reduced. Isolated cases of dizziness or reduced blood pressure have been reported.

To be observed by reason of experimental findings in animals: In the dog, retinal changes have been observed after long-term administration of large doses of tranexamic acid and in the cat, after i.v. injection of 250 mg/kg/day for 14 days. Such changes have not been obtained in the rat, where the maximum tolerated dose has been administered. No retinal changes have been reported or observed at ophthalmic checkups of patients treated with Cyklokapron for several weeks or months.

Symptoms and Treatment of Overdose: Symptoms: There is no known case of over dosage of tranexamic acid in humans. Symptoms may be nausea and vomiting, orthostatic symptoms and hypotension.

Treatment: REG>Initiate vomiting, institute gastric lavage and charcoal therapy.
 
 
Dosage and Administration:
Conization of the cervix: 2 to 3 tablets every 8 to 12 hours, 12 days postoperatively.

Epistaxis: 2 to 3 tablets every 8 to 12 hours for 10 days.

Hyphema: 2 to 3 tablets every 8 to 12 hours for 7 days.

Dental surgery in patients with coagulopathies: 2 hours before the operation, Factor VIII and Factor IX should be given as well as Cyklokapron, 25 mg orally or 10 mg i.v/kg body weight. After the operation, 25 mg/kg of tranexamic acid is given orally 3 to 4 times a day for 6 to 8 days. After the operation, the patient does not generally require further substitution therapy.

Administer tranexamic acid solution for injection by slow i.v. injection over a period of at least 5 minutes. For i.v. infusion, the tranexamic acid solution for injection may be mixed with electrolyte solutions, carbohydrate solutions, and Aminosol and dextran solutions. Heparin may be added to tranexamic acid solution for injection. Cyklokapron solution for injection should not be mixed with blood and infusion solutions containing penicillin.

Menorrhagia (hypermenorrhea): 2 to 3 tablets 3 to 4 times a day for several days. Tranexamic acid treatment should only be started when copious bleeding has begun.

Hereditary Angioneurotic Edema: Some patients can sense the onset of attacks and are best treated intermittently with 2 to 3 tablets 2 to 3 times a day for several days. Others should be treated continuously with this dose.

Children: Dosage should be calculated according to body weight at 25 mg/kg, 2 to 3 times a day.

Availability And Storage: Injection: Each ampul contains: tranexamic acid BP 100 mg/mL. Ampuls of 5 and 10 mL. Packages of 10.

Tablets: Each white, film-coated, capsule-shaped tablet, with CY engraved in arcs, contains tranexamic acid 500 mg. Tartazine-free. Bottles of 100. (Shown in Product Recognition Section)
 
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