Rentylin - General Information
A methylxanthine derivative that inhibits phosphodiesterase and affects blood rheology. It improves blood flow by increasing erythrocyte and leukocyte flexibility. It also inhibits platelet aggregation. Rentylin modulates immunologic activity by stimulating cytokine production. [PubChem]
Pharmacology of Rentylin
Rentylin, a synthetic dimethylxanthine derivative structurally related to theophylline and caffeine, is used in the treatment of peripheral vascular diseases and in the management of cerebrovascular insufficiency, sickle cell disease, and diabetic neuropathy.
Rentylin for patients
Although a causal relationship has not been established, there have been reports of bleeding and/or prolonged prothrombin time in patients treated with TRENTAL with and without anticoagulants or platelet aggregation inhibitors. Patients on Warfarin should have more frequent monitoring of prothrombin times, while patients with other risk factors complicated by hemorrhage (e.g., recent surgery, peptic ulceration) should have periodic examinations for bleeding including hematocrit and/or hemoglobin. Concomitant administration of TRENTAL and theophylline-containing drugs leads to increased theophylline levels and theophylline toxicity in some individuals. Such patients should be closely monitored for signs of toxicity and have their theophylline dosage adjusted as necessary. TRENTAL has been used concurrently with antihypertensive drugs, beta blockers, digitalis, diuretics, antidiabetic agents, and antiarrhythmics, without observed problems. Small decreases in blood pressure have been observed in some patients treated with TRENTAL; periodic systemic blood pressure monitoring is recommended for patients receiving concomitant antihypertensive therapy. If indicated, dosage of the antihypertensive agents should be reduced.
No information provided.
Additional information about Rentylin
Rentylin Indication: For the treatment of patients with intermittent lameness or immobility arising from chronic occlusive arterial disease of the limbs.
Mechanism Of Action: Rentylin inhibits erythrocyte phosphodiesterase, resulting in an increase in erythrocyte cAMP activity. Subsequently, the erythrocyte membrane becomes more resistant to deformity. Along with erythrocyte activity, pentoxifylline also decreases blood viscosity by reducing plasma fibrinogen concentrations and increasing fibrinolytic activity.
Drug Interactions: Aminophylline Rentylin increases the effect and toxicity of theophylline
Dyphylline Rentylin increases the effect and toxicity of theophylline
Theophylline Rentylin increases the effect and toxicity of theophylline
Oxtriphylline Rentylin increases the effect and toxicity of theophylline
Anisindione Rentylin increases the anticoagulant effect
Dicumarol Rentylin increases the anticoagulant effect
Acenocoumarol Rentylin increases the anticoagulant effect
Warfarin Rentylin increases the anticoagulant effect
Food Interactions: Not Available
Generic Name: Pentoxifylline
Synonyms: Not Available
Drug Category: Free Radical Scavengers; Vasodilator Agents; Radiation-Protective Agents; Hematologic Agents; Hemorrheologic Agents
Drug Type: Small Molecule; Approved
Absorption: Not Available
Toxicity (Overdose): LD50=1385 mg/kg(orally in mice)
Protein Binding: 70%
Biotransformation: Not Available
Half Life: 0.4-0.8 hours
Dosage Forms of Rentylin: Tablet, extended release Oral
Chemical IUPAC Name: 3,7-dimethyl-1-(5-oxohexyl)purine-2,6-dione
Chemical Formula: C13H18N4O3
Pentoxifylline on Wikipedia: https://en.wikipedia.org/wiki/Pentoxifylline
Organisms Affected: Humans and other mammals