Fluconazole belongs to a group of medications known as antifungals. More on Body and Health.

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Fluconazole belongs to a group of medications known as antifungals. It is most commonly used to treat fungal infections of the mouth thrush, esophagus the tube that takes food from the throat to the stomach, lungs, urinary tract, and vagina yeast infection. It works by preventing the fungi that are causing infection from reproducing and the infection from continuing. The fungi then die off, causing the infection to clear. It is also used to treat cryptopcoccal meningitis and prevent the recurrence of cryptococcal meningitis in people with acquired immunodeficiency syndrome AIDS, and to decrease the risk of candidiasis infection in people undergoing bone marrow transplants who are treated with chemotherapy or radiation therapy. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Do not stop taking this medication without consulting your doctor. Do not give this medication to anyone else, even if they have the same symptoms as you do. It can be harmful for people to take this medication if their doctor has not prescribed it. Fluconazole must be taken for at least 2 weeks after the symptoms of the infection resolve to prevent the infection from returning.

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UK Edition. This teva fluconazole 50mg is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. This includes any possible side effects not listed in this leaflet. See section 4.

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Fluconazole, commonly known as Diflucan, is an teva fluconazole 50mg drug used for the treatment of both systemic and superficial fungal infections in a variety of tissues. It was initially approved by the FDA in This drug is an azole antifungal, in the same drug family as ketoconazole and itraconazole. Fluconazole has many advantages over the other antifungal drugs including the option of oral administration. The side effect profile of this drug is minimal.

This receptor is found at the neuromuscular junction. It is a protein consisting of five subunits, two α and one each of β, γ and δ, which are arranged in the membrane around the channel. Acetylcholine binds to the α subunits. Thus, each receptor has two binding sites and both must be occupied for the receptor to be activated. Receptors for some other neurotransmitters, for example gamma-aminobutyric acid and glutamate, are believed to be similar.

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Examples of osmotic laxatives used prior to imaging are magnesium citrate and magnesium sulphate. Lactulose is a disaccharide with a similar action. Polyethylene glycol is an osmotic laxative used for bowel cleansing (see below). Although only small amounts of these drugs are absorbed, osmotic laxatives should not be used in patients with poor renal function because of the risk of magnesium accumulation. High concentrations of magnesium in the body can interfere with the function of calcium ions in the heart, skeletal muscle and the central nervous system.

Substances transported by the same transport system compete with each other and the more slowly a drug is transported the more effective it is at inhibiting the transport of another. A well-documented historical example of this is the competition between penicillin and probenecid. Penicillin is a drug that is approximately eliminated by a kidney transport system. This was a disadvantage in the days when penicillin was expensive and difficult to produce, because its action was prematurely terminated unless high doses were given. Penicillin used to be administered together with probenecid. Probenecid is slowly transported by the same system and therefore considerably reduces the elimination of penicillin.

According to the protein theory, the site of action is a hydrophobic region of cellular proteins, possibly receptors or proteins involved in transmitter release. Interaction with general anaesthetic would result in reduction in the excitability of the cell and inhibition of nerve transmission. This could be through potentiation of neurotransmitter release at inhibitory synapses or by inhibition at excitatory synapses. Gamma-aminobutyric acid (GABA) is an inhibitory neurotransmitter and glutamate is an excitatory neurotransmitter in the brain. Intravenous general anaesthetics at least seem to work by enhancing the effects of GABA or blocking the effects of glutamate.

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