Pricing
Prices are indicative MRP and may vary by pharmacy. Trend compares against the last recorded price.
সব দামের পরিবর্তন →ইঙ্গিত ও ব্যবহার
Danlene এর জন্য নির্দেশিত:
ডোজ নির্দেশিকা
শুধুমাত্র নির্দেশিকা তথ্য
প্রদর্শিত ডোজগুলি সরকারি উৎসের সাধারণ নির্দেশিকা। ব্যক্তিগতকৃত ডোজের জন্য সর্বদা আপনার ডাক্তার বা ফার্মাসিস্টের পরামর্শ নিন।
Adults:
For use in chronic spasticity, adults: the following gradual titration schedule is suggested. Some patients will not respond until a higher daily dosage is achieved. Each dosage level should be maintained for seven days to determine the patient's response. If no further benefit is observed at the next higher dose, the dosage should be decreased to the previous lower dose. The starting dose is 25 mg twice per day, and it can be increased by 25 to 50 mg per day each week. The maximum accepted dosage is 400 mg per day. Paediatric patients: the following gradual titration schedule is suggested. Some patients will not respond until a higher daily dosage is achieved. Each dosage level should be maintained for seven days to determine the patient's response. If no further benefit is observed at the next higher dose, the dosage should be decreased to the previous lower dose. Give 0.5 mg/kg once daily for seven days, then 0.5 mg/kg 3 times daily for 7 days, then 1 mg/kg 3 times daily for 7 days, then 2 mg/kg 3 times a day. Therapy with a dose 4 times daily may be necessary for some individuals. For malignant hyperthermia, preoperatively: administer 4 to 8 mg/kg/day of oral Dantrolene in 3 or 4 divided doses for one or two days prior to surgery, with the last dose given approximately 3 to 4 hours before the scheduled surgery with a minimum of water. Post crisis follow-up: oral Dantrolene should also be administered following a malignant hyperthermia crisis, in doses of 4 to 8 mg/kg per day in four divided doses, for a one to three day period to prevent recurrence of the manifestations of malignant hyperthermia.
পার্শ্বপ্রতিক্রিয়া
The most common side effects of Relaxo are drowsiness, dizziness, weakness, a general feeling of being unwell, tiredness, and diarrhoea. These are usually short-lived, tend to occur early in treatment, and can often be avoided by starting on a low dose and increasing it gradually until the right regimen is found. Diarrhoea may be severe and may require Relaxo to be stopped for a time. If diarrhoea returns when Relaxo is restarted, treatment should probably be stopped permanently.
সতর্কতা ও নিষেধাজ্ঞা
Warnings & Precautions
Because Relaxo can damage the liver with long-term use, treatment should be stopped if no benefit is seen within 45 days. Patients should be warned not to drive or take part in hazardous work while taking Relaxo. Care is needed when tranquilizers are given at the same time. Relaxo may cause a photosensitivity reaction, so patients should be warned about sunlight exposure while taking it. It is important to recognize that fatal and non-fatal liver disorders of an idiosyncratic or hypersensitivity type may occur with Relaxo treatment. When starting Relaxo, liver function tests (SGOT, SGPT, alkaline phosphatase, total bilirubin) should be done to set a baseline or to find out whether liver disease is already present. Liver function tests (e.g., SGOT or SGPT) should be repeated at appropriate intervals during treatment. In some patients these values have returned to normal despite continued treatment; in others they have not. If symptoms suggesting hepatitis appear together with abnormal liver function tests or jaundice, Relaxo should be stopped. When caused by Relaxo and detected early, these liver abnormalities have typically returned to normal after the drug was stopped. Relaxo has been restarted in a few patients who developed clinical and/or laboratory evidence of liver cell injury. Restarting should be attempted only in patients who clearly need Relaxo, and only after the earlier symptoms and laboratory abnormalities have cleared. The patient should be admitted to hospital and the drug restarted at very small, gradually increasing doses. Laboratory monitoring should be frequent, and the drug should be withdrawn immediately at any sign that the liver is affected again. Relaxo should be used with particular caution in women and in patients over 35 years of age, as drug-induced, potentially fatal liver cell disease appears more likely in these groups. It should also be used with caution in patients with impaired lung function, in patients with severely impaired heart function due to heart muscle disease, and in patients with a history of liver disease or abnormal liver function.
নিষেধাজ্ঞা
Active liver disease, such as hepatitis or cirrhosis.