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当前位置:药品说明书与价格首页 >> 糖尿病 >> Ⅱ型糖尿病 >> 药物临床研究及应用 >> 默克糖尿病新药Janumet获准在欧盟国家上市

默克糖尿病新药Janumet获准在欧盟国家上市

2008-07-24 17:40:29  作者:  来源:互联网  浏览次数:254  文字大小:【】【】【
简介:据英国媒体22日报道,美国默克公司的糖尿病复方新药Janumet当天获准在欧盟27个成员国上市。 这种药物含有西他列汀和盐酸二甲双胍两种成分,可以解决Ⅱ型糖尿病患者3个关键的病症,即胰岛素缺乏、胰岛素 ...
据英国媒体22日报道,美国默克公司的糖尿病复方新药Janumet当天获准在欧盟27个成员国上市。
 
    这种药物含有西他列汀和盐酸二甲双胍两种成分,可以解决Ⅱ型糖尿病患者3个关键的病症,即胰岛素缺乏、胰岛素流失和葡萄糖过剩,从而有效降低患者的血糖水平。与单独服用盐酸二甲双胍药物相比,Janumet可以更有效降低Ⅱ型糖尿病患者体重增加和发生低血糖的风险。
 
    去年4月,美国食品和药物管理局批准Janumet在美国上市。到目前为止,这种药物已在全球50多个国家和地区获得上市批准。
 
    糖尿病分为Ⅰ型糖尿病、Ⅱ型糖尿病和妊娠期糖尿病。Ⅰ型糖尿病患者体内只能产生少量或不能产生胰岛素;Ⅱ型糖尿病又称成年发病型糖尿病,特点是胰岛素抵抗,即自体能够产生胰岛素,但细胞无法对它作出反应;妊娠期糖尿病是指妇女妊娠怀孕期间患上糖尿病
Janumet

Sitagliptin + metformin HCl in one tablet

Company:

Merck

Pharmacologic class:

Antihyperglycemic (dipeptidyl peptidase-4 inhibitor (DPP-4) + biguanide)

Active ingredient:

Sitagliptin 50mg, metformin (as HCl) 500mg; tabs.

Also:

JANUMET 50mg/1000mgb>

Indication:

Adjunct to diet and exercise to improve glycemic control in patients with type 2 diabetes who are not adequately controlled on metformin or sitagliptin alone or in patients already being treated with the combination of sitagliptin and metformin.

Pharmacology:

Janumet combines the two antihyperglycemic agents sitagliptin and metformin. Sitagliptin, a DPP-4 inhibitor, increases and prolongs the activity of incretins, hormones that play a role in the regulation of glucose homeostasis. Metformin, a biguanide, reduces endogenous hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization.

Clinical trials:

There have been no clinical efficacy studies conducted with Janumet, however, bioequivalence of Janumet with coadministered sitagliptin and metformin tablets was demonstrated.

Adults:

Individualize. Take twice daily with meals. Previously on metformin alone: initially 50mg twice daily of sitagliptin plus metformin dose. Previously on metformin 850mg twice daily: start with 50mg/1000mg twice daily. Previously on sitagliptin alone: initially 50mg/500mg twice daily; may increase to 50mg/1000mg twice daily. Previously on sitagliptin and metformin: switch on a mg/mg basis. Max 100mg sitagliptin/2000mg metformin per day.

Children:

<18 yrs: not recommended.

Contraindications:

Renal disease or dysfunction. Metabolic acidosis, ketoacidosis. Concomitant intravascular iodinated contrast agents (suspend during and for 48 hours after use). Type 1 diabetes.

Precautions:

Confirm normal renal function before starting and monitor (esp. in elderly). Avoid if clinical or lab evidence of hepatic disease. Discontinue if lactic acidosis, ketoacidosis, renal impairment, shock, acute MI, acute CHF, sepsis, or hypoxemia occurs. May need to suspend therapy during periods of stress or if dehydration occurs or before surgery. Monitor hematology (esp. serum Vit. B12 in susceptible patients). Elderly, debilitated, malnourished, deficient caloric intake, adrenal or pituitary insufficiency, or alcohol intoxication: increased risk of hypoglycemia. Pregnancy (Cat.B). Nursing mothers.

Interactions:

Cationic drugs eliminated by renal tubular secretion (eg, amiloride, digoxin, morphine, procainamide, quinine, quinidine, ranitidine, triamterene, trimethoprim, vancomycin), furosemide, nifedipine, cimetidine: may increase metformin levels. Avoid excessive alcohol intake (potentiates effects of metformin on lactate). Monitor digoxin. Diuretics, steroids, estrogens, oral contraceptives, phenothiazines, phenytoin, thyroid products, nicotinic acid, sympathomimetics, calcium channel blockers, isoniazid, others that may cause hyperglycemia. β-blockers may mask hypoglycemia.

Adverse reactions:

Nasopharyngitis, GI disturbances, asthenia, headache; lactic acidosis (rare, half of the cases are fatal).

责任编辑:p53


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