Eldepryl - antiparkinsonian agent. The MAO-B selective inhibitor, participating in dopamine metabolism, etc. catecholamines. Dopamine metabolism, the return capture oppresses at the level of presynaptic nerves, promoting thereby increase in its concentration in kernels of extrapyramidal system, etc. parts of a brain.
Enalapril is prescribed at various forms of arterial hypertension, including renovascular hypertensia, and also as a part of a combination therapy of chronic heart failure. Enalapril - anti-hypertensive drug, the mechanism of its action is connected with reduction of education from angiotensin I of angiotensin II which decrease leads to direct reduction of release of Aldosteronum.
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Eldepryl Product Description
Drug Uses
Eldepryl is an antiparkinson drug, which inhibits the reuptake of dopamine and enhances its concentration in the brain. Eldepryl is used for treatment of patients with Parkinson's disease. Clinical studies have demonstrated that Eldepryl, used during the early stages of Parkinson's disease, helps patients maintain the working ability and go without levodopa for a longer time.
The combination therapy of Eldepryl with levodopa strengthens and extends the levodopa action. Therefore, the drug is prescribed to those patients, who show poor clinical efficacy to levodopa/carbidopa therapy. The recommended daily dose makes 10 mg of Eldepryl, divided into two doses (5 mg in the morning and 5 mg in the evening).
If Eldepryl is indicated in combination with levodopa, the dose of levodopa is recommended to be reduced by an average of 30% in three days of application. It has been found that the higher doses of Eldepryl do not increase the therapeutic effect, and even may cause the development of side effects.
Missed Dose
If you found out that you had forgotten to take a dose of Eldepryl, take it as soon as possible. If you’ve remembered about the missed dose of the antiparkinsonian agent just before the next dose, skip the missed dose of Eldepryl, do not double the next one and return to a normal scheduled dose.
More Information
Antiparkinson medication Eldepryl is recommended to be taken during a meal (breakfast and dinner). The daily dose of the antiparkinson drug should not be adjusted, if Eldepryl is used in patients with impaired liver and kidney function. Alcoholic beverages are recommended to be avoided during the treatment of Parkinson's disease.
Storage
Eldepryl should be stored at room temperature, not exceeding 25°C in the original package. A container with Eldepryl tablets should be kept tightly closed, away from children and pets.
Eldepryl Safety Information
Warnings
Patients are recommended to adhere to a prescribed dosage regimen and to avoid taking a daily dose exceeding 10mg, since the risk of non-selective inhibition of MAO is increased. Despite that there is no data on Eldepryl impact on the melanoma development in patients with Parkinson's disease, periodic skin examinations are recommended and the recommendations on the antiparkinson drug application should be complied. Clinical studies have demonstrated that Eldepryl in combination with levodopa, may significantly lower the blood pressure in patients with cardiovascular diseases.
Disclaimer
Information about Parkinson's disease, contained in the review of Eldepryl, shall not be considered to substitute for the neurologist’s medical advice. The online pharmacy shall not be responsible for any kind of damage, caused by incorrect use of the information on antiparkinsonian agent Eldepryl.
Eldepryl Side Effects
Usually, Eldepryl is well-tolerated. All undesirable effects, which may be caused by this antiparkinsonian agent, are mild. Most common undesirable effects, which can be met during the therapy with Eldepryl include headache, hallucinations, dizziness, sleeping disorders, nausea, stomatitis and confusion. Some undesirable effects, observed in patients during Eldepryl therapy, may require the antiparkinsonian agent use to be stopped. These undesirable effects include depression, arrhythmia, delusions, syncope, angina pectoris and hypertension.
In case of an arterial hypertension of Atacand causes dose-dependent long lowering of arterial pressure. Anti-hypertensive action happens due to decrease in system peripheric resistance without reflex increase in heart rate. Instructions on serious or strengthened hypotension after taking of the first dose or Withdrawal Effect after termination of treatment are absent.
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Betapace - beta adrenoblocker, antiarrhytmic medicine. It is taken for treatment of ventricular arrhythmia, tachycardia, supraventricular arrhythmia, tachycardia at thyrotoxicosis, angina of effort, especially at combination with tachyarrhythmias, arterial hypertension, hypertrophic cardiomyopathy, prolapse of the mitral valve, prevention and treatment of myocardial infarction at stable condition of the patient.
Caduet consists of Amlodipine besylate and atorvastatin calcium. Caduet has a double mechanism of action; action of amlodipin as dihydropyridinic antagonist of calcium and for suppression of atorvastatin HMG-CoA reductase. It is taken for prevention of cardiovascular events at patients with hypertension, with three concurrent factors of cardiovascular risk, with cholesterol level from normal to moderately raised, without clinical manifestations of ischemic heart disease and also when according to the existing recommendations about treatment the combined use of amlodipin and low dose of atorvastatin is deemed appropriate.
Cardizem, derivative benzothiazepine, has anti-anginal, antiarrhytmic and hypotensive effect. It is prescribed at arterial hypertension: after myocardial infarction, at patients with accompanying stenocardia when beta adrenoblockers, are contraindicative at patients with diabetic nephropathy, in cases when ACE inhibitors are contraindicated; angina of effort, Prinzmetal's angina; prevention of a coronary spasm when carrying out a coronary angiography or operation of aortocoronary shunting.
Claritin prevents development and facilitates the course of allergic reactions. Possesses antiallergic, antipruritic, antiexudative action. Reduces permeability of capillaries, controls oedemata of tissues, removes spasms of smooth muscles. It is prescribed at allergic rhinitis, conjunctivitis, pollinosis, urticaria fever, angioedema, pruritic dermatosis; pseudo-allergic reactions, caused by release of histamine; allergic reactions at stings of insects.
Exelon drug for treatment of Alzheimer's disease with poorly and moderately expressed dementia. By the principle of action of Exelon it is the Selection inhibitor of acetylcholinesterase of a brain.
Fosamax - drug for treatment of Paget disease, osteoporosis at women in a postmenopause, osteoporosis at men, a hypercalcemia at malignant tumors. Active alendronate ingredient - non-hormonal specific inhibitor of an osteoclastic bone resorption, suppresses osteoclasts. Taking of Fosamax stimulates bone formation, recovers positive balance between a resorption and recovery of a bone, progressively increases the mineral density of bones, promotes formation of a normal bone tissue with normal histologic structure.
Glucophage - guanyl guanidine, hypoglycemic medicine for peroral takein. At patients with a diabetes mellitus reduces concentration of glucose in blood by oppression of gluconeogenesis in a liver, reduction of absorption of glucose from GIT and increase of its utilization in tissues. Stabilizes or reduces a body weight.
Haldol antipsychotic remedy, butyrophenone derivative. It has a powerful antipsychotic effect, moderate sedation. The mechanism of antipsychotic action of haloperidol is associated with the blockade of dopamine receptors in the mesocortex and limbic system.
BCCC; a derivative of diphenylalkylamine. Has antianginal, anti-arrhythmic and hypotensive effect. The antianginal effect is associated with both direct action on the myocardium and with the effect on peripheral hemodynamics. It is prescribed with stenocardia, supraventricular tachycardia, sinus tachycardia, ciliary tachyarrhythmia, atrial flutter, atrial extrasystole, arterial hypertension, GOKMP, primary hypertension in the "small" circle of the circulation.
Anticholinesterase agent; having a cholinesterase effect through a reversible acetylcholinesterase inhibition and enhancing the action of acetylcholine. Improves neuromuscular transmission, increases the motility of the gastrointestinal tract, increases the tone of urinary bladder, bronchi, the secretion of exocrine glands. Prescribed for myasthenia gravis, postoperative intestinal atony, atonic constipation, bladder atony, post-traumatic movement disorders; flaccid paralysis; residual explication of polio, encephalitis, violation of emptying the bladder after gynecological surgery and childbirth.
A blocker of H1-histamine receptors of the first generation, derived from ethanolamine; eliminates the effects of histamine, mediated through this type of receptors. Promotes the local anaesthesia (when intaken, there is a short numbing of the mucous membranes in the mouth) - only in high doses, it blocks m-cholinergic receptors in the central nervous system, has sedative, hypnotic, antiemetic and antiparkinsonian effects. The therapeutic indications include: allergic conjunctivitis, allergic rhinitis, chronic urticaria, pruritic dermatoses, dermatographism, serum sickness.
An antispasmodic drug, which removes pain and reduces the tone of smooth muscles: gastrointestinal tract, biliary tract, uterus, it also relaxes the detrusor (direct antispasmodic and m-anticholinergic effect). Increases bladder capacity, reduces the frequency of detrusor contractions, hinders urination. Well tolerated when appointed for a long term. Used in neurogenic bladder (including detrusor hyperreflexia, multiple sclerosis or spina bifida), urinary incontinence (of idiopathic origin), nocturnal enuresis (in children older than 5 years).
Pirfenex shows anti- fibrosing and anti-inflammatory properties in many systems in vitro and in animal models of pulmonary fibrosis (the fibrosis induced by bleomycin and transplantation). Assigned to adults suffering the idiopatic pulmonary fibrosis.
A lipid-lowering agent. Reversibly inhibits HMG-COA reductase, inhibits the cholesterol synthesis at the stage of mevinolinic acid and moderately reduces its intracellular concentration. The indications for the drug use include: primary hypercholesterolemia mainly of IIa and IIb types, under the ineffective diet treatment in patients with increased risk of coronary atherosclerosis, hypercholesterolemia combined with hypertriglyceridemia; prevention of coronary artery disease. The drug decreases the risk of myocardial infarction, the need for revascularization of the myocardium, deaths from cardiovascular system diseases.
The anti-malarial drug from the group of 8-aminohinolina derivatives. It is characterized by intercalation with DNA plasmodia, leading to disruption of nucleic acids synthesis. It demonstrates high activity against exo-erythrocytic forms of all types of malaria, including primary tissue and para- erythrocyte forms. Particularly active against primary tissue forms of Plasmodium falciparum.
Antidepressant. Strengthens the central adrenergic and serotonergic transfer. Used for the treatment of depressions including anhedonia, psychomotor retardation, insomnia, early awakening, weight loss, loss of interest in life, suicidal thoughts and mood swings.
Starlix - an oral synthetic hypoglycemic drug. A medicine based on nateglinide for the treatment of diabetes, which helps to control blood sugar levels. This medicine helps your body to react better to the insulin produced by your pancreas.
Starlix is used in conjunction with diet and exercise to improve blood sugar control in adults with type 2 diabetes mellitus.
Zetia contains ezetrol as an active ingredient, which is a selective representative of a new class of lipid-lowering drugs that reduce the absorption of cholesterol in the intestine, including cholesterol from plant fats.
Zithromax - antibiotic of a wide spectrum of action. Antibiotic-azalide, a representative of a new subgroup of macrolide antibiotics. In the focus of inflammation it has a bactericidal effect. For the active ingredient of Zithromax, Azithromycin, all the gram-positive cocci (except those bacteria which are resistant to erythromycin) are susceptible.
Tadacip - an Indian brand, whose main chemical element is tadalafil, which is also a principal part of Cialis pills. It's been created by Cipla Ltd. with a more lucrative cost in comparison to Cialis made by the brand-maker Eli Lilly.
Suhagra If one has difficulties with a masculine power, we’d suggest buying Suhagra® a drug of an Indian enterprise, named Cipla, founded back in 1937. It is an exact Viagra® copy, a well-known worldwide medical mean targeted to eliminate the ED problems. Still, Suhagra® is not a Generic Drug. It is a completely independent brand pharmaceutical product that has been verified by all needed health organizations in developed countries. One can buy Suhagra® in 180 countries around the globe. This is an evidence of the reliability and safety of the good.
Astelin belongs to antihistamines which purpose is to block histamines in the human organism. It’s a spray that deletes nasal congestion, itching, and sneezing. The medicine is effective in case of infection, inflammation, and allergic reaction which result in itching, stuffy, and runny nose. Medics usually prescribe it for adults and children above five (in case of seasonal allergy) and above twelve (in case of vasomotor rhinitis that constricts and dilates a vein, artery, or capillary in the nasal cavity).
Atorlip-5 is a drug which purpose is to lower the level of so-called bad cholesterol in the human organism. Its amount is identified due to the blood testing. The accumulation of low-density lipoprotein can lead to atherosclerosis. As the result, arteries are getting narrow causing cardiovascular complications as strokes, heart attacks, hypertonia, and peripheral artery disease. Liver fat can be also reduced thanks to the drugs. The other benefit is that the medicine increases the level of high-density lipoprotein.
Combined oral contraceptives block the action of gonadotropins. The first effect of these drugs is aimed to inhibit ovulation. The drug leads to modifications in cervical mucus. Thus, it is strenuous for sperm to pass to the uterine cavity and affect the uterine lining, thereby reducing the possibility of implementation. It helps to prevent pregnancy. Moreover, oral contraceptives prevent pregnancy and have a number of advantages. They have an impact on the cycle of menses and it becomes regular. The amount of blood loss at the time of menstruation is shorter as well as the loss of iron, dysmenorrhea is rare.
Lovegra is Sildenafil and given to women to increase genital blood flow in order to obtain vaginal compliance and boost libido in women.
Tadalafil is phosphodiesterase type 5 inhibitor and has similar actions to the other phosphodiesterase type 5 inhibitors such as Sildenafil Citrate.
Zhewitra 20 mg is made of Sunrise remedies which is a generic pill of the patent medicine Levitra. It contains Vardenafil HCL in the composition of 20 mg. In India, the sunrise cure is a fast-growing manufacturer, exporter & provider of Pharmaceutical and Herbal Formulations including Herbal Remedies, Cosmetics & Ayurvedic devising.
It also deals in Allopathic formulations in the form of pills, medicine, water, and Topical sections as per international acceptance levels.
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Dapoxetine is used as a treatment for premature ejaculation.