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Selegiline

Apomorphine, cabergoline, and Selegiline may be considered to reduce off time (Level C). Studies have shown that the Selegiline transdermal system (STS) does not significantly affect sensitivity to ingested tyramine, unlike tranylcypromine, which markedly increases sensitivity.

Other names for this medication:
Selegiline, Eldepryl, Anipryl, Carbex, Comenter, Deprenyl, Jumex, Niar, Segan, Selecom, Selegilina, Selegos, Selerin, Selgene, Selgian, Selgin, Selgina, Zelapar,

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Transdermal selegiline comes as a patch to apply to the skin. It is usually applied once a day and left in place for 24 hours. Remove your old selegiline patch and apply a new patch at around the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Use transdermal selegiline exactly as directed. Do not apply more patches or apply patches more often than prescribed by your doctor.

Your doctor may start you on a low dose of transdermal selegiline and gradually increase your dose, not more often than once every 2 weeks.

Transdermal selegiline controls depression but does not cure it. Your condition may begin to improve after you have used transdermal selegiline for one week or longer. However, you should continue to use transdermal selegiline even if you feel well. Do not stop using transdermal selegiline without talking to your doctor.

Apply selegiline patches to dry, smooth skin anywhere on your upper chest, your back (between your neck and your waist), your upper thigh, or the outer surface of your upper arm. Choose an area where the patch will not be rubbed by tight clothing. Do not apply selegiline patches to skin that is hairy, oily, irritated, broken, scarred, or calloused.

After you apply a selegiline patch, you should wear it all the time until you are ready to remove it and put on a fresh patch. If the patch loosens or falls off before it is time to replace it, try to press it back in place with your fingers. If the patch cannot be pressed back on, dispose of it and apply a fresh patch to a different area. Replace the fresh patch at your regularly scheduled patch change time.

Do not cut selegiline patches.

While you are wearing a selegiline patch, protect the patch from direct heat such as heating pads, electric blankets, heat lamps, saunas, hot tubs, and heated water beds. Do not expose the patch to direct sunlight for very long.

To use the patches, follow these steps:

  1. Choose the area where you will apply the patch. Wash the area with soap and warm water. Rinse off all of the soap and dry the area with a clean towel.
  2. Open the protective pouch and remove the patch.
  3. Peel the first piece of liner off the sticky side of the patch. A second strip of liner should remain stuck to the patch.
  4. Press the patch firmly onto your skin with the sticky side down. Be careful not to touch the sticky side with your fingers.
  5. Remove the second strip of protective liner and press the rest of the sticky side of the patch firmly against your skin. Be sure that the patch is pressed flat against the skin with no bumps or folds and that it is firmly attached.
  6. Wash your hands with soap and water to remove any medicine that may have gotten on them. Do not touch your eyes until you have washed your hands.
  7. After 24 hours, peel the patch off slowly and gently. Fold the patch in half with the sticky sides together and dispose of it safely, so that is out of reach of children and pets. Children and pets can be harmed if they chew on, play with, or wear used patches.
  8. Wash the area that was under the patch with mild soap and warm water to remove any residue. If necessary, you can use baby oil or a medical adhesive removal pad to remove residue that will not come off with soap and water. Do not use alcohol, nail polish remover, or other solvents.
  9. Apply a new patch to a different area immediately by following steps 1 to 6.

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Size estimation and magnification error in radiographic imaging: implications for classification of arteriovenous malformations. The absence of a strong bystander effect may limit, on one hand, the overall utility of the cyp4B1 systems for cancer gene therapy. Roles of human hepatic cytochrome P450s 2C9 and 3A4 in the metabolic activation of diclofenac. Our present findings indicate that suggestion reduces Stroop effects in HSIs.

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Cost effectiveness of external hip protectors in the hospital setting: a modeling study. Ultrasound-assisted pseudodigestion for toxic metals determination in fish muscles followed by electrothermal atomic absorption spectrophotometry: multivariate strategy. Einstein gravity coupled to a massless scalar field in arbitrary spacetime dimensions.

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These components can be integrated with information management systems to form the basis for a work-station for diagnostic pathology. This feature can be utilized to transport increased amounts of glutamine into damaged podocytes. Blood gene expression profiling in pediatric systemic lupus erythematosus and systemic juvenile idiopathic arthritis: from bench to bedside. TNF-like weak inducer of apoptosis (TWEAK) is a member of the tumor necrosis factor (TNF) cytokine superfamily which regulates a number of cellular responses, including inflammation and proliferation. An epidemiological relationship between these patients could be neither established nor disproved.

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We experienced the rare case of an elderly woman with uncorrected tetralogy of Fallot. The structure shows a densely packed core region from about 15 to 55 A in radius, where a pair of concentric tubular features of high density is present without well-defined subunit boundaries, and an outer part from 55 to 115 A, where the subunits are mostly well separated from each other. The expression of flaA gene was verified by various immunological methods, including western blotting, enzyme-linked immunosorbent assay (ELISA) and immunogold electron microscopy (IEM). In the first 10 years Gleason score was the single most important predictor of death. We present a 73-year-old man with a cystic sebaceous neoplasm on his arm, clinically not associated with Muir-Torre syndrome.

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The molecular anatomy of spontaneous germline mutations in human testes. Second, the electron properties, such as density and energy, are typically combined in a linear fashion to reproduce those for the entire molecular system, which makes the overall computation scale linearly with the size of the system. In the HIV patient, the echography allows an specific initial diagnostic assessment, being able in most of the patients with abdominal manifestations to diagnose the causal pathology. Having support people as participants also helped during pregnancy, birth, and child care. The focus will be on idiopathic pulmonary fibrosis (idiopathic usual interstitial pneumonia), nonspecific interstitial pneumonia, cryptogenic organizing pneumonia, and acute interstitial pneumonia.

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The protein-DNA binding mode prediction was introduced to help improve DNA-binding residues prediction. Are model organisms aberrations, or are the first steps in speciation easier than they seem?

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Based on these observations, fungal antigens should exist which mediate such protective immunoreactions and have in part already been identified. We have designed and tested a set of five miniature nested magnetic shields constructed of high-permeability material, with external volumes for the individual shielding layers ranging from 0.01 to 2.5 cm(3). The distribution of endogenous epidermal growth factor after small bowel resection suggests increased intestinal utilization during adaptation. Psychoanalytic discoveries concerning the psychogenesis of objectivity in perception and thought support the correspondence theory of truth and provide, in addition, an answer to the third party critique of correspondence.

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