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Name/scientific name |
ELOSULFASE ALFA
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Self-financed or subsidized by the Hospital Authority |
Hospital Authority Drug Formulary
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Indications |
Mock syndrome type IVA
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body system |
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Elosulfase alfa is a drug used to treat people with mucopolysaccharidosis type IVA. This disease is a rare genetic disorder that causes a lack of a specific enzyme in the body, which affects the body's metabolism of polysaccharides. Irosufasalfa is a synthetic enzyme that can help supplement the enzymes deficient in the patient's body, thereby improving symptoms and slowing down the progression of the disease. Patients usually receive this medication through an intravenous injection.
Patients may experience some minor side effects, such as redness, swelling or pain at the injection site while receiving irosuvastat alfa. While using this medication, patients should follow their doctor's recommendations and dosage instructions and receive regular medical monitoring. If you have any discomfort or questions, patients should check with your doctor immediately. The use of erosufasalfa must be done under professional medical supervision to ensure safe and effective treatment of patients with mucopolysaccharidosis type IVA.
Instructions for use: ELOSULFASE ALFA is usually given by intravenous injection and needs to be administered by a professional medical professional. Before injection, check whether the solution is clear and particle-free, and avoid turbidity or precipitation. The injection speed should be controlled at no more than 2 ml per minute. During the injection, the patient should remain quiet and avoid sudden movements.
Dosing Guidelines: For adult patients, the recommended starting dose is 2 mg/kg body weight per week, divided into three doses per week. Depending on the patient's specific condition and severity of illness, the physician may adjust the dose, but each adjustment should not exceed 2 mg/kg per week. For pediatric patients, the dosage needs to be determined according to age and weight, usually starting from 1 mg/kg per week, and can also be adjusted according to the condition. During use, the patient's response and condition changes should be regularly monitored to ensure efficacy and safety.
ELOSULFASE ALFA is a medicine used to treat Mucopolysaccharidosis Type IVA (MPS IVA). Its side effects include fever, headache, skin redness, muscle pain, nausea and vomiting. Some patients may also experience allergic reactions such as rash, difficulty breathing and swelling of the throat. If serious side effects occur, such as severe allergic reaction or heart problems, you should stop taking the medicine immediately and seek medical help. Before seeing your doctor, remember to discuss your medical conditions and other medications with your doctor to make sure ELOSULFASE ALFA is the right treatment option for you.
ELOSULFASE ALFA is a drug used to treat mucopolysaccharidoses, but there are some contraindications to its use. First, people who are allergic to ELOSULFASE ALFA or any of its ingredients should avoid using this medication to avoid a serious allergic reaction. Second, women who are pregnant or breastfeeding should consult their doctor before using this drug because the effects of this drug on the fetus or baby have not been determined. In addition, patients with major heart problems or respiratory problems should avoid using ELOSULFASE ALFA to avoid worsening of their condition. When using this drug, patients should strictly follow the doctor's recommendations and prescribed dosage, and should not increase or decrease the dosage or discontinue treatment without authorization. In summary, people with a history of allergies, pregnant women, breastfeeding women, or people with heart or respiratory problems should avoid using ELOSULFASE ALFA and consult a professional doctor before use.
Elosulfase alfa is used to treat patients with MPS IVA (Mucopolysaccharidosis Type IVA, also known as Morquio A syndrome). Patients should strictly follow their doctor's instructions when using this medication and receive regular monitoring and evaluation. If you have any unusual reactions or symptoms, tell your doctor immediately.
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Pregnant women should avoid the use of Lisopril Acetate Silica as there are currently insufficient studies to confirm its safety. Pregnant women with mucopolysaccharide storage disease who need treatment should try to choose other alternative therapies or drugs. If you are pregnant or planning to become pregnant, you should consult your doctor first to assess the risks and benefits before deciding whether to use Lisopip Acetate Silicone Protein.
During pregnancy, doctors may recommend that pregnant women with mucopolysaccharide storage disease try to control symptoms of the disease to reduce risks to the mother and fetus. The medication regimen should be adjusted according to the doctor's advice and monitored regularly to ensure the therapeutic effect and safety during pregnancy.
In summary, pregnant women who suffer from mucopolysaccharide storage disease during pregnancy should use Lisopril acetate silica with caution and treatment under the guidance of a doctor to ensure the health and safety of the mother and fetus.
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