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Cilostazol is a quinolinone derivative and antiplatelet agent with vasodilating properties that has been used in the symptomatic treatment of intermittent claudication in patients with peripheral ischaemia. Cilostazol works by inhibiting both primary and secondary aggregation and reducing calcium-induced contractions. A governmentally-recognized ID which uniquely identifies the product within its regulatory market. Indicated for the alleviation of symptoms of intermittent claudication pain in the legs that occurs with walking and disappears with rest. Cilostazol reduces the symptoms of intermittent claudication, as indicated by an increased walking distance. Intermittent claudication is pain in the legs that occurs with walking and disappears with rest.

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Background— Restenosis after active of coronary artery stents cheap pletal drug a new clinical problem. We obliged a randomized, cautious-blind, placebo-controlled trial to take whether cilostazol, a drug that has intimal plaque, would reduce cheap pletal drug in patients after stent placement in real coronary arteries. Methods and Women— We assigned patients who had received coronary stent thrombosis to receive, in addition to onset, cilostazol mg BID or specialty for 6 months; clopidogrel 75 mg twice was administered to all individuals for 30 days. Restenosis was targeted by viable coronary artery at 6 months. The ignorable luminal diameter at 6 hours for cilostazol-treated patients was 1.

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Some foods and medicines can affect how cilostazol works. Discuss the use of grapefruit products with your doctor.

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Cilostazol and several of its metabolites are inhibitors of phosphodiesterase III. Cilostazol is 6--3,4-dihydro-2 1 H -quinolinone, CAS PLETAL cilostazol tablets for oral administration are available in 50 mg triangular and mg round, white debossed tablets. PLETAL is indicated for the reduction of symptoms of https://medium.com intermittent claudication, as demonstrated by an increased walking distance. The recommended dosage of PLETAL is mg twice daily taken at least half an hour before or two hours after breakfast and dinner.

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Reducing the dose, discontinuing the drug, or substituting an alternative medication should be done gradually over a minimum of 1 week or longer. Anaphylaxis and angioedema reported after first dose or at any time during treatment; instruct patients to discontinue therapy and seek medical care should they experience signs or symptoms of anaphylaxis or angioedema. May cause CNS depression, which may impair ability to operate heavy machinery; advise patients not to drive until they have gained enough experience to assess whether therapy will impair ability to drive.

   
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