এই ওষুধে সাশ্রয় করুন
একই সক্রিয় উপাদানের অন্যান্য ব্র্যান্ড
এই ব্র্যান্ডগুলোতে একই সক্রিয় উপাদান আছে (Enzalutamide). একই মাত্রা ও ধরন। বদলানোর আগে আপনার ডাক্তার বা ফার্মাসিস্টের সাথে নিশ্চিত হয়ে নিন।
ইঙ্গিত ও ব্যবহার
Prozenza 40 এর জন্য নির্দেশিত:
ডোজ নির্দেশিকা
শুধুমাত্র নির্দেশিকা তথ্য
প্রদর্শিত ডোজগুলি সরকারি উৎসের সাধারণ নির্দেশিকা। ব্যক্তিগতকৃত ডোজের জন্য সর্বদা আপনার ডাক্তার বা ফার্মাসিস্টের পরামর্শ নিন।
প্রাপ্তবয়স্ক:
The recommended dosage of Enzalutamide is 160 mg administered orally once daily with or without food. Swallow capsules or tablets whole. Do not chew, dissolve, or open the capsules. Do not cut, crush, or chew the tablets.Dosage Modifications for Adverse Reactions: If a patient experiences a ≥Grade 3 or an intolerable adverse reaction, withhold Enzalutamide for one week or until symptoms improve to ≤Grade 2, then resume at the same or a reduced dose (120 mg or 80 mg) if warranted.Strong CYP2C8 Inhibitors: Avoid the coadministration of strong CYP2C8 inhibitors. If the coadministration of a strong CYP2C8 inhibitor cannot be avoided, reduce the Enzalutamide dosage to 80 mg once daily. If the coadministration of the strong inhibitor is discontinued, increase the Enzalutamide dosage to the dosage used prior to initiation of the strong CYP2C8 inhibitor.Strong CYP3A4 Inducers: Avoid the coadministration of strong CYP3A4 inducers. If the coadministration of a strong CYP3A4 inducer cannot be avoided, increase the Enzalutamide dosage from 160 mg to 240 mg orally once daily. If the coadministration of the strong CYP3A4 inducer is discontinued, decrease the Enzalutamide dosage to the dosage used prior to initiation of the strong CYP3A4 induce. Pediatric Use: Safety and effectiveness of Enzalutamide in pediatric patients have not been established.Renal Impairment: No dosage modification is recommended for patients with mild to moderate renal impairment.Hepatic Impairment: No dosage modification is recommended for patients with mild, moderate, or severe hepatic impairment.
পার্শ্বপ্রতিক্রিয়া
The most common adverse reactions (≥10%) that occurred more frequently (≥2% over placebo) in the XTANDI-treated patients are asthenia/fatigue, back pain, hot flush, constipation, arthralgia, decreased appetite, diarrhea, and hypertension.
সতর্কতা ও নিষেধাজ্ঞা
সতর্কতা ও সাবধানতা
Seizure occurred in 0.5% of patients receiving Prozenza. In patients with predisposing factors, seizures were reported in 2.2% of patients. Permanently discontinue Prozenza in patients who develop a seizure during treatment.Posterior reversible encephalopathy syndrome (PRES): Discontinue Prozenza.Hypersensitivity: Discontinue Prozenza.Ischemic Heart Disease: Optimize management of cardiovascular risk factors. Discontinue Prozenza for Grade 3-4 events. Falls and Fractures occurred in 11% and 10% of patients receiving Prozenza, respectively. Evaluate patients for fracture and fall risk, and treat patients with bone-targeted agents according to established guidelines.Embryo-Fetal Toxicity: Prozenza can cause fetal harm and loss of pregnancy. Advise males with female partners of reproductive potential to use effective contraception.