Lepirudin

Lepirudin is a recombinant hirudin which is used as anticoaggulant in patients with heparin-induced thrombocytopenia who require parenteral antithrombotic treatment. Lepirudin is being invastigated in arterial thrombo-embolic disorders such as angina and MI (myocardial infarction).


Brands
Adult Dose
Dose: 150 mcg/kg of body weight
Single Dose: 150 (150)
Frequency: As recommended.
Route: IV
Instructions: Followed after initial dose
Neonatal
Paedriatic
Characteristics
Lepirudin also known as Hirudin, Hirudin. . It is of Semi Synthetic origin. . The Molecular Weight of Lepirudin is 6979.50. It is weakly acidic drug.
Contraindications
Lepirudin is contraindicated in conditions like Pregnancy,Breast feeding.
Effects
The severe or irreversible adverse effects of Lepirudin, which give rise to further complications include Bleeding, Hematoma, Hematoma, Hypersensitivity.Lepirudin produces potentially life-threatening effects which include Intracranial hemorrhages. which are responsible for the discontinuation of Lepirudin therapy.The signs and symptoms that are produced after the acute overdosage of Lepirudin include Bleeding complications.The symptomatic adverse reactions produced by Lepirudin are more or less tolerable and if they become severe, they can be treated symptomatically, these include Fever, Hematuria, Allergic reactions, Rectal bleeding, Anemia.
Indications
Lepirudin is primarily indicated in conditions like Endometrial thinning before intra-uterine surgery.
Interactions
No data regarding the interactions of Lepirudin was found.
Interfrence
Risks
Drug should not be given to Paediatrics, and Pregnant Mothers.If prescribing authority justifies the benefits of the drug against the possible damages he/she should reevaluate them and consult the reference material and previous studies.
Storage
Warnings
Renal impairment; hepatic impairment; recent bleeding or risk of bleeding including recent puncture of large vessels, organ biopsy, recent major surgery, stroke, haemorrhagic diathesis, severe uncontrolled hypertension, bacterial endocarditis; determine activated partial thromboplastin time 4 hrs after start of treatment (or after infusion rate altered) and at least once daily thereafter.
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