Buy Tracrium ampoules 10 mg/ml, 5 ml, 5 pcs
  • Buy Tracrium ampoules 10 mg/ml, 5 ml, 5 pcs

Tracrium [Atracurium besylate]

GlaxoSmithKline
774 Items
2019-09-19
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$61.19
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Clinical Pharmacology

Tracrium is a highly selective non-depolarizing muscle relaxant. It is a competitive antagonist of the acetylcholine receptor postsynaptic membrane. Causes temporary relaxation of skeletal muscles, incl. respiratory.

Indications

It is used as one of the components for general anesthesia for intubation of the trachea and relaxation of skeletal muscles during surgical procedures, mechanical ventilation, and also for mechanical ventilation in intensive care units.

Composition

1 ml contains:

Active substance: Atracuria besyat 10 mg.

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Tracrium [Atracurium besylate]

Dosage and Administration

Adults and children over 1 month in order to relax the skeletal muscles, Trakrium is injected intravenously in a jet at a dose of 300-600 mcg / kg (which provides relaxation of the skeletal muscles for 15-35 minutes). Tracheal intubation can usually be performed within 90 seconds after intravenous administration of a dose of 500-600 mcg / kg. For prolongation of the complete neuromuscular blockade, the drug is administered additionally IV the jet at a dose of 100-200 mg / kg. The introduction of additional doses is not accompanied by cumulative effects. Spontaneous recovery to 95% occurs after 35 minutes.
After the initial bolus dose of 300-600 mcg / kg has been administered, a continuous intravenous infusion can be performed at a rate of 300-600 mcg / kg / h to maintain neuromuscular blockade during long-term surgical interventions.
Tracrium can be administered by infusion at recommended doses for coronary artery bypass surgery. The neuromuscular blockade created by Trakrium can be quickly removed with medium therapeutic doses of anticholinesterase agents (for example, neostigmine, edrofonii) with prior or subsequent administration of atropine. In hypothermia conditions (at a patient's body temperature of 25-26 ° C), the recommended doses of Trakrium should be reduced by 2 times.
When used in the intensive care unit (ICU) After the initial bolus dose of 300-600 mcg / kg has been administered, Trakrium can be used to maintain neuromuscular blockade by continuous infusion at a rate of 11 to 13 mcg / kg / min (650-780 mcg / kg / h). The spontaneous recovery of neuromuscular conductivity after Tracrium infusion in patients in the intensive care unit does not depend on the duration of drug administration. Spontaneous recovery can be expected within 60 minutes. Gaps in the 32-108 min were observed in clinical practice.
Patients with impaired renal and / or liver function at any stages, including terminal, Trakrium can be entered in the recommended doses.
Patients with cardiovascular diseases the initial dose of Trakrium should be administered within 60 seconds.
Elderly patients Trakrium can be used in the lowest recommended doses and reduce the rate of administration.

Adverse reactions

Since the cardiovascular system: possible transient arterial hypotension.

On the part of the respiratory system: rarely, bronchospasm (may be associated with increased histamine release).

From the side of the central nervous system: extremely rarely - convulsions (patients in the intensive care unit who received Trakrium in combination with other drugs; these patients usually had comorbidities that predisposed to the convulsive syndrome - traumatic brain injury, brain edema, viral encephalitis, hypoxic encephalopathy, uremia). Clinical trials did not reveal a correlation between the plasma concentration of the metabolite atrakuria besilate - laudonazin and convulsive syndrome.

Allergic reactions: extremely rarely - anaphylactic reactions (with the introduction of Trakrium with one or more anesthetics).

Other: possible hyperemia of the skin.

Contraindications

Hypersensitivity to the drug.

Drug interactions

The neuromuscular blockade caused by Trakrium can be enhanced by using such means for inhalation anesthesia as halothane, isoflurane, enflurane.
With the introduction of Tracrium, as well as other non-depolarizing muscle relaxants, the severity of neuromuscular blockade and / or its duration may increase with the simultaneous use of certain antibiotics (aminoglycosides, polymyxins, spectinomycin, tetracyclines, lincomycin, clindamycin), antiarrhythmic drugs (propranolol, calcinicin, tetracyclines, lincomycin, clindamycin), antiarrhythmic drugs (propranolol, tetracyclines, lincomycin, clindamycin), antiarrhythmic drugs (propranolol, tetracyclines, lincomycin, clindamycin) lidocaine, procainamide, quinidine), diuretics (furosemide and possibly mannitol, thiazide diuretics, acetazolamide), magnesium sulfate, ketamine, lithium salts, ganglioblokatorov (trimetafa n, hexametonium).
Occasionally, some drugs may enhance or unmask latently flowing myastenia gravis or cause myasthenic syndrome, which can lead to increased sensitivity to Trakrium. Such drugs include various antibiotics, beta-blockers (propranolol, oxprenolol), antiarrhythmic drugs (procainamide, quinidine), antirheumatic drugs (chloroquine, D-penicillamine), trimetafan, chlorpromazine, steroids, phenytoin and lithium preparations.
In patients receiving long-term anticonvulsant drugs, the onset and shorter duration of neuromuscular blockade caused by Trakrium may be later.
The introduction of other non-depolarizing muscle relaxants in combination with Trakrium can cause a more pronounced neuromuscular blockade than could be expected with the introduction of an equivalent total dose of Tracrium. The synergistic effect may vary depending on the combination of drugs.
Depolarizing muscle relaxants should not be administered to increase the duration of the neuromuscular blockade caused by non-depolarizing muscle relaxants, since This can lead to the development of a long and complex blockade, which is difficult to eliminate with anticholinesterase agents.
Pharmaceutical Interaction
In alkaline solutions inactivation of Trakrium occurs, therefore it cannot be mixed in the same syringe with thiopentone or any other alkaline solution.
Tracrium is compatible with the following infusion solutions: 0.9% sodium chloride solution; 5% glucose solution; ringer's solution; 0.18% sodium chloride solution with 4% glucose solution for intravenous administration; Hartman solution.

Pregnancy and Lactation

Use of the drug during pregnancy is possible only when the intended benefit to the mother outweighs the potential risk to the fetus.
In obstetric practice, Trakrium can be used as a muscle relaxant for caesarean section, because At the recommended doses of atracuria, besylate does not penetrate the placenta at clinically significant concentrations.
It is not known whether Atracurium besylate is released and its metabolites in breast milk.

Special instructions

Trakrium paralyzes the respiratory and other skeletal muscles, without affecting the human mind. In this regard, the drug should be used only in combination with adequate general anesthesia, under the control of an experienced anesthesiologist, and if funds are available for carrying out endotracheal intubation and mechanical ventilation.
Tracrium can promote the release of histamine (like other muscle relaxants). Therefore, care should be taken when administering it to patients with a known hypersensitivity to histamine.
At the recommended doses, Trakrium has no significant vagal or ganglion blocking action and is not contraindicated in bradycardia associated with the use of many anesthetics or vagal stimulation during surgery.
It is recommended to monitor the neuromuscular function when selecting an individual dosing regimen of Trakrium.
Patients with myastenia gravis, other neuromuscular diseases and severe electrolyte disorders may experience increased sensitivity to Trakrium (as well as to other muscle relaxants).
Patients with the risk of a significant reduction in blood pressure, for example, in hypovolemia, the administration of Trakrium should be carried out for 60 seconds.
Data from experimental and clinical studies indicate that Trakrium does not cause malignant hyperthermia.
Patients with burns may develop Trakrium resistance and may require an increase in dose, depending on the period elapsed since the time of the burn and the area of ​​the burn surface.
After insertion of Tracrium into the peripheral vein or when other drugs are injected into the same needle or cannula, the infusion system should be flushed with an adequate amount of saline.

Overdosage

Symptoms: prolonged myoplegia (and its possible consequences).

Treatment: IVL under positive pressure until spontaneous respiration is restored. It is necessary that the patient was under the influence of sedatives. When the first signs of spontaneous recovery of neuromuscular function appear, it can be accelerated by administering anticholinesterase drugs in combination with atropine.

  • Brand name: Tracrium
  • Active ingredient: Atracurium besylate
  • Dosage form: Injection
  • Manufacturer: GlaxoSmithKline
  • Country of Origin: Great Britain

Studies and clinical trials of Atracurium besylate (Click to expand)

  1. Separation of cis-cis, cis-trans and trans-trans isomers of (±)-atracurium besylate and cis and trans isomers of its major quaternary decomposition products and related impurity by reversed-phase high-performance liquid chromatography
  2. Determination of atracurium besylate in human plasma
  3. Atracurium besylate in paediatric anaesthesia
  4. The use of atracurium besylate for laparoscopy
  5. Neuromuscular blockade in myasthenia gravis with atracurium besylate
  6. Neuromuscular blockade in dystrophia myotonica with atracurium besylate
  7. Weight-determined dosage of atracurium besylate
  8. A comparison of the infusion pharmacokinetics and pharmacodynamics of cisatracurium, the 1R-cis 1′R-cis isomer of atracurium, with atracurium besylate in healthy patients
  9. Neuromuscular blockade with atracurium besylate in a patient with myasthenia gravis
  10. Pharmacokinetics of atracurium besylate in the pig after a single i.v. injection
  11. Effect of intraurethral administration of atracurium besylate in male cats with urethral plugs
  12. Dose-response relationship of atracurium besylate in the halothaneana-esthetised pig
  13. Atracurium besylate: Does it have a place in the helicopter drug box?
  14. Directly Coupled Chiral HPLC−NMR and HPLC−CD Spectroscopy as Complementary Methods for Structural and Enantiomeric Isomer Identification:  Application to Atracurium Besylate
  15. Pharmacokinetics and Neuromuscular Blocking Effects of Atracurium Besylate and Two of Its Metabolites in Patients with Normal and Impaired Renal Function
  16. Pharmacokinetics of 1R-cis 1'R-cis atracurium besylate (51W89) and plasma laudanosine concentrations in health and chronic renal failure
  17. Effect of urethral infusion of atracurium besylate on manual bladder expression in dogs and cats with spinal cord injuries: a randomised trial
  18. PHARMACOKINETICS OF ATRACURIUM BESYLATE IN HEALTHY PATIENTS (AFTER A SINGLE I.V. BOLUS DOSE)
  19. Use of Atracurium Besylate to Arrest Fetal Activity During Intrauterine Intravascular Transfusion
  20. Clinical Evaluation of Atracurium Besylate Requirement for a Stable Muscle Relaxation During Surgery
  21. The Effects of Atracurium Besylate (Tracrium??) on Intracranial Pressure and Cerebral Perfusion Pressure
  22. Clinical Pharmacology of Atracurium Besylate (BW 33A)
  23. HISTAMINE-RELEASING POTENCIES OF ATRACURIUM BESYLATE (BW 33A), METOCURINE, AND d-TUBOCURARINE

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