Drug Detail:Pentoxifylline (Pentoxifylline [ pen-tox-i-fi-leen ])
Drug Class: Miscellaneous coagulation modifiers
Drug Detail:Pentoxifylline (Pentoxifylline [ pen-tox-i-fi-leen ])
Drug Class: Miscellaneous coagulation modifiers
400 mg orally 3 times a day. If adverse effects develop, reducing the dose to 400 mg twice a day is recommended.
Creatine Clearance 10 to 50 mL/min:
400 mg orally twice a day. If adverse effects develop, reducing the dose to 400 mg once a day is recommended.
Creatine Clearance less than 10 mL/min:
400 mg orally once a day. Further dosage reduction may be required such as 200 mg once daily but current products (extended or controlled release; unscored) may require adaptation to 400 mg once every other day.
Note: Pentoxifylline is not eliminated unchanged in the urine; however, the pharmacologically active metabolite may accumulate in patients with renal impairment and add to pharmacologic and toxic effects.
400 mg orally twice a day. If adverse effects develop, reducing the dose to 400 mg once a day is recommended.
In patients with both renal and liver dysfunction, the dose should be reduced to 400 mg orally once a day.
Patients with impaired renal and/or liver function should be monitored closely for adverse effects.
Safety and effectiveness have not been established in pediatric patients (less than 18 years of age).
Limited data suggest that pentoxifylline is moderately dialyzed during hemodialysis. Therefore, doses should follow hemodialysis sessions.
Pentoxifylline is preferably given with meals to decrease gastric irritation. Pentoxifylline should be given for at least 8 weeks to determine efficacy.