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Dantrolene 20mg vial(丹曲林钠粉末注射剂[DANTRIUM仿制药])
药店国别  
产地国家 美国 
处 方 药: 是 
所属类别 20毫克/瓶 6瓶/盒 6盒/箱 
包装规格 20毫克/瓶 6瓶/盒 6盒/箱 
计价单位: 箱 
生产厂家中文参考译名:
US WORLD MEDS
生产厂家英文名:
US WORLD MEDS
该药品相关信息网址1:
http://www.drugs.com/pro/dantrium.html
该药品相关信息网址2:
该药品相关信息网址3:
原产地英文商品名:
DANTROLENE SODIUM(DANTRIUM GENERIC) 20mg/vial 6vials/box 6boxes/case
原产地英文药品名:
Dantrolene Sodium
中文参考商品译名:
丹曲林钠(DANTRIUM仿制药) 20毫克/瓶 6瓶/盒 6盒/箱
中文参考药品译名:
丹曲林钠
曾用名:
简介:

 

部份中文丹曲林钠处方资料(仅供参考)
丹曲洛林(Dantrolene)是治疗恶性高热的特效药物。治疗的可能机制是通过抑制肌质网内钙离子释放,在骨骼肌兴奋-收缩耦联水平上发挥作用,使骨骼肌松弛。
在使用丹曲洛林治疗时,应尽早静脉注射丹曲洛林,以免循环衰竭后,因骨骼肌血流灌注不足,导致丹曲洛林不能到达作用部位而充分发挥肌松作用。
该药具有乏力、恶心及血栓性静脉炎等副作用 。
INDICATIONS AND CLINICAL USE: 
Dantrium (dantrolene sodium) Intravenous is indicated in the management of malignant hyperthermia crisis
As soon as the crisis is recognized (i.e., tachycardia, tachypnea, central venous desaturation, central venous hypercarbia, metabolic acidosis, fever, skeletal muscle rigidity or cyanosis and mottling of the skin) cooling procedures should be instituted and Dantrium Intravenous administered.  If anesthetic agents are being administered they should be promptly discontinued.  It is also important that appropriate supportive measures be instituted for treatment of the physiologic and metabolic abnormalities.  Dantrium Intravenous, when given early in the malignant hyperthermia crisis, has caused abrupt lowering of body temperature, correction of the respiratory and/or metabolic acidosis, decrease of the heart rate, stabilization of blood pressure, and disappearance of the rigidity and/or fasciculations.  Patients who received Dantrium Intravenous during the crisis had less evidence of muscle destruction as shown by serum creatinine phosphokinase measurements than those treated by other measures.
CONTRAINDICATIONS: 
There are no known contraindications when Dantrium (dantrolene sodium) Intravenous is used during an acute malignant hyperthermia crisis.
WARNINGS: 
General: The use of dantrolene sodium intravenous in the management of malignant hyperthermia crisis is not a substitute for previously known supportive measures.  These measures must be individualized, but it will usually be necessary to discontinue the suspect triggering agents, attend to increased oxygen requirements, manage the metabolic acidosis, institute cooling when necessary, monitor urinary output, and monitor for electrolyte imbalance. Please see complete warnings and full prescribing information for further information.
ADVERSE REACTIONS: The more serious reactions reported with repeated doses of oral Dantrium (dantrolene sodium) as a muscle relaxant have been hepatitis, seizures and pleural effusions with pericarditis. Cases of fatal hepatitis have been reported in patients who had received Dantrium for sixty days or longer. Symptomatic hepatitis and laboratory evidence of liver dysfunction have also been reported in a number of patients receiving Dantrium as a muscle relaxant. Acneiform skin reactions have also been infrequently reported. For a list of adverse reactions reported with the use of Dantrium as a muscle relaxant, please consult the Product Monograph for Dantrium Capsules.
The administration of intravenous dantrolene sodium to human volunteers is associated with loss of grip strength and weakness in the legs, as well as subjective central nervous system complaints.
Based upon data in human volunteers, it will sometimes be appropriate to tell patients who receive dantrolene sodium intravenous that decrease in grip strength and weakness of leg muscles, especially walking down stairs, can be expected postoperatively. In addition, symptoms such as “lightheadedness” may be noted. Since some of these symptoms may persist for up to 48 hours, patients must not operate an automobile or engage in other hazardous activity during this time. Caution is also indicated at meals on the day of administration because difficulty swallowing and choking have been reported. Caution should be exercised in the concomitant administration of tranquilizing agents.
AVAILABILITY:  Dantrium Intravenous is available in 70 mL vials containing a sterile lyophilized mixture of 20 mg dantrolene sodium, 3000 mg mannitol, and sufficient sodium hydroxide to yield a pH of approximately 9.5 when reconstituted.  These are not multiple dose vials.  Available in cartons of 6 vials.
Dantrium Intravenous is available only for use in hospitals or in dental clinics that are equipped to provide the necessary supportive measures used in the treatment of the malignant hyperthermia crisis.
Carton of 6 vials  

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