Buy Fermathron Online
How does Fermathron work?
Buy Fermathron Online is a viscosupplement containing sodium hyaluronate used for injection into the synovial joints of patients with mild to moderate osteoarthritis. It can also be used to treat traumatic or degenerative changes to the synovial joint.
Buy Fermathron Online is made up of highly folded, long chained molecules of hyaluronan in the form of sodium hyaluronate. It is made using a patented process of continuous fermentation of the natural bacterium Streptococcus.
The sodium Hyaluronate in Fermathron is highly biocompatible as it is chemically the same as hyaluronate within the body.
As soon as the Fermathron solution is delivered into the synovial joint, it begins lubricating and performing its shock absorbent activities.
What’s in the box?
- 20mg/2ml sterile 1% (w/v) Sodium Hyaluronate in phosphate buffered saline.
- 1 x 2.0ml pre-filled sterile glass syringe packed within a blister packet.
What are the benefits of Fermathron?
Sodium Hyaluronate’s essential properties and pseudo plastic behaviour can be used to :
- Perform shock absorbency properties within the synovial joint
- Lubricate the synovial compartment
How is treatment carried out?
Fermathron is injected 3-5 times on a weekly basis into the synovial compartment. For more severe osteoarthritis treatment to treat more traumatic joints, 5 injections is normal.
Buy Fermathron Online The site of injection must be clean as well as infection free and disease free. Antiseptic can be used to present the site free from contamination. The skin must be dried prior to treatment. Clean the skin around the injection site with antiseptic and allow to dry before the injection is given.
How long will results last for?
5 injections a week can help patients be symptom free for up to 6 months.
Buy Fermathron Online Sodium hyaluronate in the composition is a biopolymer consisting of repeating disaccharide units of D-glucuronic acid and N-acetyl-D-glucosamine (long-chain polysaccharide). It is shown that this biopolymer, synthesized by the bacterium Streptococcus equi, is identical to sodium hyaluronate contained in the human body. The hyaluronan contained in the composition complements the natural hyaluronan contained in the synovial membrane, the amount of which has decreased due to degenerative changes or traumatic injuries of the synovial joint. Sodium hyaluronate is a natural component of the human body.
Fermathron prosthetic synovial fluid and Fermathron Plus prosthetic synovial fluid have a pH similar to that of synovial fluid.
To alleviate pain and stiffness in the knee, hip, ankle and shoulder joints of patients with mild to moderate osteoarthritis resulting from degenerative and traumatic changes in the synovial joint.
Do not enter with inflammation or signs of skin disease at the injection site.
Do not use in patients with known hypersensitivity to sodium hyaluronate.
Use during pregnancy and lactation
Safety of use during pregnancy and lactation has not been established.
Side effects of Fermathron
With intra-articular administration, temporary transient pain and swelling is possible.
In rare cases, an inflammatory reaction, septic arthritis or arthralgia may occur, which may or may not be associated with use.
The compatibility of simultaneous intra-articular administration with other substances has not been tested. Therefore, mixing or simultaneous administration of other intra-articular drugs is not recommended.
Dosage and administration
Injections should be performed only by a physician trained in the appropriate technique.
Before the introduction of the injection site must be treated with an antiseptic.
If there is an articular effusion, it must be aspirated prior to injection.
The contents of the syringe are sterile. The introduction should be made with a sterile needle of an appropriate size (from 18 to 21G / 19 to 20G is recommended) (for Fermathron Plus synovial fluid prosthesis, Fermathron C synovial fluid prosthesis / Fermathron synovial fluid prosthesis, respectively).
The syringe has a Luer Lok ™ connector (6%) for secure attachment of the needle to the syringe.
Dispose of the syringe and needle after a single use.
For patients with mild to moderate osteoarthrosis, it is recommended to inject 2 ml of the drug into the synovial cavity of the knee joint once a week for 1-3 weeks for Fermathron Plus synovial fluid prosthesis, 1-5 weeks for Fermathron synovial fluid prosthesis.
The health care professional should specify the dosage regimen for injection into the synovial space of the hip, ankle and shoulder joints.
It is recommended to perform injections in the hip, ankle and shoulder joints under ultrasound or fluoroscopic control.
The duration of the effect in patients with mild or moderate osteoarthritis of the knee joint is up to 6 months.
The duration of the effect with the introduction of the hip, ankle and shoulder joint has not been established.
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