Monday, October 10, 2016

Ethanolamine Oleate Injection BP (UCB Pharma Ltd)





1. Name Of The Medicinal Product



Ethanolamine Oleate Injection (monoethanolamine oleate). Solution for injection.


2. Qualitative And Quantitative Composition



Oleic acid 4.23% w/v



Ethanolamine 0.910% w/v



For excipients see 6.1.



3. Pharmaceutical Form



Solution for injection.



5 ml neutral glass ampoule containing a clear solution.



4. Clinical Particulars



4.1 Therapeutic Indications



The injection is recommended for use as a sclerosing agent in the treatment of small, uncomplicated varicose veins in the lower extremities.



4.2 Posology And Method Of Administration



Ethanolamine Oleate is administered by slow intravenous injection.



Adults Including The Elderly



The product is used only as a sclerosant and injected directly into the varicose vein. A dose of 2 to 5ml, divided between 3 or 4 sites, administered by slow injection into empty isolated segments of vein.



Children



The product is not recommended for use in children.



4.3 Contraindications



Inability to walk, acute phlebitis, oral contraceptive use, obese legs, known hypersensitivity to Ethanolamine Oleate or benzyl alcohol. Superficial thrombophlebitis and deep vein thrombosis in the region of the varicose veins. Marked arterial, cardiac or renal disease. Uncontrolled metabolic disorders such as diabetes mellitus. Patients with local or systemic infections.



4.4 Special Warnings And Precautions For Use



Care should be taken to ensure that the injection does not leak into perivenous tissue which could cause sloughing, ulceration and in severe cases, necrosis.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



None known.



4.6 Pregnancy And Lactation



Safety during pregnancy has not been established. Use in pregnancy is not recommended.



4.7 Effects On Ability To Drive And Use Machines



None known.



4.8 Undesirable Effects



Burning, cramping sensation, urticaria. Allergic reactions and anaphylaxis have been reported following use of sclerosing agents.



4.9 Overdose



Acute nephrotoxicity has been reported in two patients given 15-20ml of a solution containing 5% Ethanolamine with 2% Benzl Alcohol.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



ATC Code: C05B B 01; sclerosing agent for local injection.



Ethanolamine Oleate is an irritant. An injection of Ethanolamine Oleate into a vein irritates the intimal endothelium resulting in the formation of a thrombus. The thrombus occludes the vein and fibrous tissue develops resulting in a permanent obliteration of the vein.



5.2 Pharmacokinetic Properties



Ethanolamine Oleate is a locally acting agent. Absorption from the site of administration is not anticipated as its mode of action is to cause a permanent obstruction in the vein.



5.3 Preclinical Safety Data



None.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Benzyl alcohol



Water for Injection



6.2 Incompatibilities



Not applicable.



6.3 Shelf Life



36 months.



6.4 Special Precautions For Storage



Do not store above 25°C. Keep the ampoule in the outer carton.



6.5 Nature And Contents Of Container



5 ml Neutral Glass (Type 1) Ampoules.



6.6 Special Precautions For Disposal And Other Handling



The product is used only as a sclerosant and injected directly into the varicose vein.



7. Marketing Authorisation Holder



UCB Pharma Limited



208 Bath Road



Slough



Berkshire



SL1 3WE



UK



8. Marketing Authorisation Number(S)



PL 0039/5671R



9. Date Of First Authorisation/Renewal Of The Authorisation



27 March 1987 / 26 May 1994 / 27 May 1999



10. Date Of Revision Of The Text



June 2005





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