Buy Tachocomb Other 2.5x3.0x0.5 cm, 1 pc.
  • Buy Tachocomb Other 2.5x3.0x0.5 cm, 1 pc.

Tachocomb®

Takeda GmbH
Dosage form
Brand & Manufacturer
Package Size
$161.25
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Clinical Pharmacology

hemostatic agent.

ATX code: B02BC07.

Pharmacological properties

Pharmacodynamics.
Tachocomb® is an absorbent hemostatic agent for local use.
Tachocomb® consists of a collagen sponge coated on one side with components of fibrin glue (highly concentrated fibrinogen and thrombin), which promotes blood coagulation. Upon contact with a bleeding wound or other body fluids, coagulation factors contained in the covering layer are released and thrombin converts fibrinogen into fibrin.

Pharmacokinetics
In the body components of the sponge Tachocomb® subjected to enzymatic cleavage within 3 to 6 weeks.
A special manufacturing and sterilization process ensures maximum safety of viruses and bacteria in the contents of the sponge.

Indications

Tachocomb® it is usually indicated in cases where bleeding, as well as biliary, lymphatic, fluid and air fistulas cannot be controlled by traditional methods or when the expected results of these methods are insufficient
TACHOCOMB is used to achieve hemostasis and the “gluing” of tissues, especially during surgical interventions on parenchymal organs (for example, liver, spleen, pancreas, kidneys, lungs, adrenal glands and thyroid, lymph nodes). The drug can also be used to stop bleeding in surgical interventions in the field of ENT surgery, gynecology, urology, vascular surgery, traumatology, etc.
Tachocomb® It can also be used for prophylactic purposes in the case of lymphatic, biliary and fluid fistulas.
Tachocomb® can be used to create a tightness for surgical interventions on the lungs.

Composition

1 cm2 sponge Tachocomb® contains:
Active ingredients: fibrinogen 5.5 mg, thrombin 2 ME
Excipients: albumin, arginine hydrochloride, collagen, sodium chloride, sodium citrate, riboflavin.

Description
The sponge is almost white with a yellow coating on one side.

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Tachocomb®

Dosage and Administration

Tachocomb® should be applied to surgical wound surfaces under sterile conditions.
Before applying the sponge Tachocomb®and the wound surface should be as clean as possible (for example, from blood, disinfectants and other fluids).
The side covered with coagulation factors and marked in yellow color, put on the wound surface and press for 3-5 minutes. When applying sponge Tachocomb®and on sufficiently wet wound surfaces, no additional moistening of the sponge is required. In the case of
Tachocomb®and on dry wound surfaces, the sponge should be moistened with saline to achieve a complete connection with the dry areas of the wound surface.
Moisturized sponge Tachocomb®and should be used immediately!
The size and number of sponge Tachocomb®and depend on the size of the wound surface. The edges of the wound should be covered with a sponge for 1-2 cm. If more than one sponge is required to close the wound surface, then when applying it to the wound their edges should overlap each other. Using sterile scissors, you can cut out sponges of the required size both before and after application to the wound surface. Unused sponge fragments must be destroyed.

Adverse reactions

Possible increase in body temperature.

Contraindications

Hypersensitivity to Tachocomb Sponge Components®.

Drug interactions

Interaction with other drugs is not installed.

Overdosage

There are no reports of overdose cases. Since the content of active ingredients is very small, overdose incidence when applying
Tachocomb®but virtually impossible.

  • Brand name: Taflotan
  • Active ingredient: Collagen, Fibrinogen, Thrombin
  • Dosage form: Sponge
  • Manufacturer: Takeda GmbH
  • Country of Origin: Japan

Studies and clinical trials of Tachocomb (Click to expand)

  1. Watertightness and Effectiveness of a Fibrinogen-Based Collagen Fleece (TachoComb®) in Neurosurgery
  2. Staple Line Reinforcement with Fleece-Coated Fibrin Glue (TachoComb) After Thoracoscopic Bullectomy for the Treatment of Spontaneous Pneumothorax
  3. Successful continuation of pregnancy after repair of a midgestational uterine rupture with the use of a fibrin-coated collagen fleece (TachoComb) in a primigravid woman with no known risk factors
  4. Randomised Controlled Trial to Evaluate the Efficacy of TachoComb H Patches in Controlling PTFE Suture–hole Bleeding
  5. Sutureless Repair With TachoComb Sheets for Oozing Type Postinfarction Cardiac Rupture
  6. Use of TachoComb in laparoscopic myomectomy
  7. Off-pump suture repair of left ventricular rupture utilizing TachoComb®sheet: a case report and literature review
  8. Tachocomb used in endoscopic surgery
  9. Efficacy and safety of topical application of human fibrinogen/thrombin-coated collagen patch (TachoComb) for treatment of air leakage after standard lobectomy
  10. Fibrinogen/thrombin-based collagen fleece (TachoComb(R)) promotes regeneration in pulmonary arterial injury
  11. The efficacy of TachoComb on reducing postoperative complications after tonsillectomy in children
  12. Effect of fibrin-coated collagen fleece (TachoComb) on pain and bleeding after adenotonsillectomy in children
  13. Pulmonary middle lobe fixation using TachoComb in patients undergoing right upper lobectomy with complete oblique fissure
  14. Haemostatic Fleece (TachoComb®) to Prevent Intrapleural Adhesions after Thoracotomy: A Rat Model
  15. Influence of TachoComb® in Comparison to Local Hemostyptic Agents on Epidural Fibrosis in a Rat Laminectomy Model
  16. Induratio penis plastica: Histologische und mechanische Ergebnisse der plastischen Defektdeckung mittels TachoComb®
  17. Alternative Treatment of Induratio Penis Plastica with a Collagen Sponge Bonded with a Tissue-Bonding Agent (TachoComb®)
  18. Use of a Fibrinogen/Thrombin-Based Collagen Fleece (TachoComb, TachoSil) With a Stapled Closure to Prevent Pancreatic Fistula Formation Following Distal Pancreatectomy
  19. Comparison Between TachoComb and TachoSil for Surgical Hemostasis in Arterial Bleeding: An Animal Experimental Study
  20. Comparison of TachoSil and TachoComb in patients undergoing liver resection—a randomized, double-blind, non-inferiority trial

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