Cilostazol - reversibly oppresses aggregation of thrombocytes caused by various incentives, surpassing in this respect Аspirin, Dipiridamolum, Тiclopidine and Pentoxifylline. It also inhibits formation of arterial blood clots and proliferation of smooth muscle cells, possesses vasodilating action.
Cilostazol
| Package | pill | Total price | Save | Order |
|---|---|---|---|---|
| 100mg × 30 Pills | $1.22 | $36.48 + Bonus - 4 Pills | - | Add to cart |
| 100mg × 60 Pills | $0.99 | $59.28 + Bonus - 4 Pills | $13.80 | Add to cart |
| 100mg × 90 Pills | $0.91 | $82.08 + Bonus - 7 Pills | $27.90 | Add to cart |
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Cilostazol product description
Cilostazol is an antiplatelet drug that increases intracellular cAMP content in platelets, selectively inhibits type 3 phosphodiesterase, thereby lessens the platelet aggregate ability. According to experimental data, cilostazol suppresses the synthesis of DNA and inhibits the growth of smooth muscle cells, in addition, it has a vasodilating action. These properties of cilostazol allowed us to advise it for the prevention of restenosis after implantation of metallic uncoated stents. Cilostazol is consumed to eliminate the functional limitations of the limbs that arise from cramping pains with the insufficient circulation. So, in case of the Charcot syndrome, this medical remedy allows patients to walk much longer without feeling much discomfort.
Cilostazol safety information
This pharmaceutical product should be taken on an empty stomach, at least 30 minutes before or two hours after a meal. The maximum effect of the remedy may appear only after 12 weeks of its proper reception, although often the signs of the successful healing with the medicine are palpable earlier. Immediately stop taking this medical remedy if bleeding occurs from the eyes. Also, you should seek an advice if you have got bruises during the therapy. If the patient needs to undergo surgery, then the drug should be withdrawn 5 days before the surgery. If it is administered in parallel with the other chemicals, which are thinning the blood or lowering blood pressure, as well as with inhibitors or inducers of CYP 3A4, CYP 2C19 or CYP 3A4 substrates, it is necessary to exercise extra caution. If during therapy, the patient has a sore throat or hyperthermia, a laboratory test should be carried out for pathological changes. In case of such changes, the medical care with Cilostazol should be discontinued immediately.
Contraindications
If the patient underwent a surgery on coronary vessels in the last half of the year, then Cilostazol should be assigned.
Cilostazol is not received if the patient has detected to have any of the following condition: hypersensitivity to the basic substance or to any component of this pharmaceutical product, any known tendency to bleeding (eg, gastric or duodenal ulcer in the acute stage, recent hemorrhagic stroke), congestive heart failure, moderate or severe hepatic insufficiency , severe renal failure.
The very medical preparation is not prescribed for the therapy of pregnant women and children since there are no data on studies of possible negative consequences.
Cilostazol side effects
From the side of the nervous system: a headache, dizziness.
From the side of the cardiovascular system: palpitation, tachycardia, angina pectoris, arrhythmia, ventricular extrasystoles.
On the part of the respiratory tract: rhinitis, pharyngitis.
On the part of the gastrointestinal tract: diarrhea, nausea, vomiting, dyspepsia, flatulence, abdominal pain, impaired excrement.
On the part of the skin: rash, itching.
Common disorders: chest pain, bruises, asthenia.
The antibiotic produced by Streptomyces lincolniensis, has a bacteriostatic effect. Suppresses protein synthesis of bacteria due to reversible binding to the 50S subunit of ribosomes, disrupts the formation of peptide bonds.
It is active against gram-positive cocci Streptococcus spp., including Streptococcus pneumoniae); Haemophilus influenzae; Bacillus anthracis, Mycoplasma spp., Bacteroides spp., Corynebacterium diphtheriae, Clostridium perfringens, Clostridium tetani.
A drug for the prevention and treatment of HIV infection. An antiviral agent, which competitively blocks the reverse transcriptase and selectively inhibits the replication of viral DNA.
Diflucan - antifungal medicine, possesses highly specific action, inhibiting activity of enzymes of fungus. It is taken at systemic lesions caused by fungus including meningitis, sepsis, infections of lungs and skin as at patients with a normal immune response, and at patients with various forms of immunosuppression.
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.
Cialis Professional - effective tablets for improvement of erection. They begin to work in 15 minutes from the moment of taking and actions for 36 hours. They can cause not less than 10, but no more than 16 erections. The medicine increases duration of sexual intercourse. The tablets are successfully used for reduction of time for recovery of erection after ejaculation.
stimulant of the intestinal peristalsis. Motillium is assigned in cases of: distention, overeating, vomiting, heartburn, flatulence, a feeling of overflow of the stomach.
Methocarbamol – a muscle relaxant used to treat muscle spasms and pain. Its action is to block pain nerve impulses sent to the brain. The mechanism of action is not completely clear. The drug has no direct effect on skeletal muscles. It's likely that its effect is associated with sedative properties.
Trecator SC - an anti-TB drug (antituberculous), contains Ethionamide as a basic substance, the drug is prescribed for the treatment of multidrug-resistant type of tuberculosis, with the mycobacterium tuberculosis susceptible to it.
Olanzapine is an antipsychotic drug (neuroleptic). It is shown in schizophrenia in adults, psychotic disorders, bipolar affective disorder in adults, depressive states.
The local application of Rogaine 2 has a stimulating effect on hair growth in men and women with androgenetic alopecia. In clinical studies, it is reported that Regain stimulates hair growth and stops it falling out in cases when it begins to fall from the top (men) or in the middle part (women). The stimulation of hair growth begins approximately 4 months after using the product. After the withdrawal of the drug, the growth of new hair stops. In patients with normal or high blood pressure, a local use of the medicine was not accompanied by common side effects.
Finpecia - potent pharmaceutical agent aimed to cure an illness named alopecia, of an androgenic as well as a hereditary genesis. Moreover, it stops the manifestation of various maladies deteriorating the advancement of the follicles and other difficulties connected with baldness.
Uroxatral - Alfuzosinis an active substance, as an antagonist of the α1 adenogenetic receptor, this drug relaxes the muscles of the prostate and the bladder. Used in the treatment of benign prostatic hyperplasia (BPH). Reduces pressure in the urethra and reduces resistance to urine flow, eases urination and eliminates dysuria.
Coumadin is a drug that promotes blood thinning in the veins. Within a short period of application, anticoagulant reduces viscous blood consistency and lowers the risk of blood clots. The drug is prescribed only after laboratory blood tests when certain symptoms are detected. Independent use of tablets is prohibited, only a doctor may establish the need for taking the drug. Thrombosis is a disease that is characterized by the formation of blood clots. In case of delayed treatment, this disease may cause disorders of oxygen metabolism in the blood and embolism.
Voveran SR is the special formulation of Voveran, developed for the suspended release of its active ingredients and, consequently, a prolonged period of action. Apart from this feature, it has no notable characteristics differentiating it from the original medicine – an analgesic that provides satisfying results in the treatment of moderate pain syndromes. It helps with a wide range of painful conditions allowing patients to stop the pain before it grows stronger or control it in case of chronic joint diseases. In general, the new form provides better results in particular in the treatment of prolonged pain.
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.