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Emla cream Information: Product Origin: EU (Turkey)

This product is able to be sourced and supplied at excellent prices because of favourable cross border currency conversions. All products are authentic brand names and will include a product information insert in English.

Medical Information:

Emla cream contains two active ingredients, lidocaine (previously known as lignocaine in the UK) and prilocaine. These are both a type of medicine called a local anaesthetic. They are used to numb areas that would otherwise feel pain.

Pain is caused by the stimulation of pain receptors at the ends of nerves. The stimulation causes sodium to enter the nerve ending, which causes an electrical signal to build up in the nerve. When this electrical signal is big enough, it passes along the nerve to the brain, where the signal is interpreted as pain.

Lidocaine and prilocaine work by temporarily blocking this pathway of pain signals along nerves. They do this by stopping the sodium entering the nerve ending at the site of the pain. This prevents an electrical signal building up and passing along the nerve fibres to the brain.

When Emla cream is applied to the skin, the lidocaine and prilocaine prevent pain signals passing from that area to the brain and so numb the skin. This means otherwise painful procedures can be performed without causing pain.

The cream can be used to temporarily numb the surface of the skin before procedures such as injections, taking blood samples and minor skin surgery. The cream is applied in a thick layer underneath a dressing for at least one hour (at least two hours for procedures on large areas, eg split skin grafting) and up to five hours before the procedure. Your doctor, pharmacist or nurse will either apply the cream, or show you how much to use and where to apply it. This will depend on the procedure that will be performed. The dressing is removed just before the medical procedure starts. You can get dressings to use with the cream from your pharmacist or doctor.

Under the supervision of a medical professional, the cream may also be used to temporarily numb the genitals in adults before the removal of genital warts (no dressings required for this use). The cream is applied five to ten minutes before this procedure starts.

What is it used for?

Temporarily numbing the surface of the skin before potentially painful procedures such as injections, taking blood and minor skin surgery.

Temporarily numbing the genitals in adults before the removal of genital warts (only under the supervision of a medical professional).

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Qty Name Price Order
25/25mg/g 5 x 5gm Tubes Emla cream /Generic Lidocaine, Prilocaine ASTRA ZENECA $62.56

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FAQ
Q:What is self-medication with Emla cream?
A:Self-medication is the treatment of common health problems with Emla cream especially designed and labeled for use without medical supervision and approved as safe and effective for such use.

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Highlights

Flupenthixol
Flupenthixol is a potent, relatively non-sedating, neuroleptic drug of the thioxanthene class. In low to moderate dosages (up to 100mg/2 weeks) flupenthixol is non-sedating, while a sedative effect may be expected when higher doses are administered. Flupenthixol shows antipsychotic effects in patients with schizophrenia. It may be of benefit in patients with flat or depressed affect. In low doses, Psytixol possesses disinhibiting and mood elevating properties. Flupenthixol dose-dependently increases the serum prolactin levels. The decanoic acid esterification of flupenthixol results in the slow release of the drug from the oily solution at the injection site with consequent prolongation of duration of action. The onset of action usually occurs in the range of 24 to 72 hours after injection and the improvement of symptoms continues for two to four weeks. A pre-injection serum concentration of 2-8 nmol/L is recommended for maintenance treatment of schizophrenic patients with a low - moderate degree of illness. However, there is considerable variation in the individual response of patients to flupenthixol decanoate and its use for maintenance therapy requires careful supervision. The maximal serum concentration is reached at the end of the first week after injection. Estimates of half-life varied considerably between studies; elimination is prolonged, in the order of three weeks to three months and probably reflects release of the active compound from the depot.

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