Entecavir STELLA

Entecavir STELLA Thận trọng

entecavir

Nhà sản xuất:

Stellapharm
Thông tin kê toa chi tiết tiếng Anh
Special Precautions
Lactic acidosis and severe hepatomegaly with steatosis, including fatal cases, have been reported with the use of nucleoside analogues alone or in combination with antiretrovirals.
Severe acute exacerbations of hepatitis B have been reported in patients who have discontinued anti-hepatitis B therapy, including entecavir. Hepatic function should be monitored closely with both clinical and laboratory follow-up for at least several months in patients who discontinue anti-hepatitis B therapy. If appropriate, initiation of anti-hepatitis B therapy may be warranted.
Dosage adjustment of entecavir is recommended for patients with a creatinine clearance <50 ml/min, including patients on hemodialysis or CAPD.
The safety and efficacy of entecavir in liver transplant recipients are unknown. If entecavir treatment is determined to be necessary for a liver transplant recipient who has received or is receiving an immunosuppressant that may affect renal function, such as cyclosporine or tacrolimus, renal function must be carefully monitored both before and during treatment with entecavir.
Effects on ability to drive and use machines: No studies on the effects on the ability to drive and use machines have been performed. Dizziness, fatigue and somnolence are common side effects which may impair ability to drive and use machines.
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