国家: 马来西亚
语言: 英文
来源: NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)
NIFEDIPINE
Abio Marketing Sdn Bhd
NIFEDIPINE
30tablet Tablets; 28tablet Tablets
CHINA CHEMICAL & PHARMACEUTICAL CO., LTD.
C max (ng/ml) t max (h) 20 ~ 12 ~ 15 * 43 ~ 7 ~ 9 * NIFERIN SR 30MG TABLET COMPOSITION: Each Tablet contains: Nifedipine 30 mg PRODUCT DESCRIPTION: A round tablet with rose-pink film and a small laser orifice on the surface PHARMACOLOGY: Nifedipine is a calcium antagonist of the 1,4-dihydropyridine type. Calcium antagonists reduce the transmembranal influx of calcium ions through the slow calcium channel into the cell. Nifedipine acts particularly on the cells of the myocardium and the smooth muscle cells of the coronary arteries and the peripheral vessels. In the heart nifedipine dilates the coronary arteries, especially the large conductance vessels, even in the free wall segment of partially stenosed areas. Further, nifedipine reduces the vascular smooth muscle tone in the coronary arteries and prevent vasospasm. The end-result is an increased poststenotic blood flow and an increased oxygen supply. Parallel to this, nifedipine reduces the oxygen requirement by lowering peripheral resistance (afterload). With long-term use nifedipine can also prevent the development of new atherosclerotic lesions in the coronary arteries. Nifedipine reduces the smooth muscle tone of the arterioles, thus lowering the increased peripheral resistance and consequently the blood pressure. At the beginning of the nifedipine treatment there may be a transient reflex increase in heart rate and thus in the cardiac output. However, this increase is not enough to compensate for the vasodilation. In addition nifedipine increases sodium and water excretion both in the short-term and long-term use. The blood- pressure-lowering effect of nifedipine is particularly pronounced in hypertensive patients. PHARMACOKINETICS Niferin SR 30mg tablets are formulated to provide nifedipine at an approximately constant rate over 24 hours. Nifedipine is released from the tablet at a zero-order rate by a membrane-controlled, osmotic push-pull process. The delivery rate is independent of gastrointestinal pH or motility. Upon swallowing, the biologically inert 阅读完整的文件