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Prolia 60mg dose belongs to novel, fully human IgG2 monoclonal antibody especially to receptor activator of nuclear factor kappa-B ligand (RANKL), restrain bone resorption markers in patients with a difference of metastatic tumors and is being examined in multiple clinical trials for the inhibition and treatment of bone metastases.<br>
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Prolia 60mg | Prolia 60mg Injections | denosumab Apple pharmaceuticals Prolia 60mg | Prolia 60mg Injections | denosumab 60mg | denosumab Injections Prolia 60mg | Prolia 60mg Injections Prolia 60mg belongs to novel, fully human IgG2 monoclonal antibody especially to receptor activator of nuclear factor kappa-B ligand (RANKL), restrain bone resorption markers in patients with a difference of metastatic tumors and is being examined in multiple clinical trials for the inhibition and treatment of bone metastases. Chemically, it exists of 2 heavy and 2 light chains. Each light chain contains of 215 amino acids. Each heavy chain contains of 448 amino acids with 4 intramolecular disulfides. PRESCRIBED FOR
Treatment for patients having postmenopausal women with osteoporosis at high risk for fracture. Treatment for patients with increase bone mass in men at more risk for fracture getting androgen deprivation therapy for non-metastatic prostate cancer. Treatment for patients having to increase bone mass in women at more risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer. DOSAGE For adult : Osteoporosis : 60mg SC (subcutaneously) once every 6 months Injection of drug should be done in upper arm, upper thigh or abdomen Giant Cell Tumor of bone : 120mg SC, every 4 weeks with additional 120mg doses on days 8 and 15 of the 1st month treatment Injection of drug should be done in upper arm, upper thigh or abdomen
Osteolytic Bone Metastases of Solid Tumors : 120mg subcutaneously every 4 weeks Injection of drug should be done in upper arm, upper thigh or abdomen Hypercalcemia : Dose of 120mg Prolia tablet given SC, every 4 weeks with additional 120mg doses on days 8 and 15 of the 1st month treatment Injection of drug should be done in upper arm, upper thigh or abdomen Dosage and administration in pediatric : 13 years and older and 45kg or more Giant Cell Tumor of bone: Dose of 120mg Prolia tablet given SC, every 4 weeks with additional 120mg doses on days 8 and 15 of the 1st month treatment OVERDOSE: Prolia overdose has no overdose. If occurs seek to emergency department and call poison control MECHANISM Denosumab linked to RANKL, a protein which is specific for the formation, function and survival of osteoclasts, the cells necessary for bone resorption. Denosumab prohibits osteoclast formation, function and survival hence, reducing bone resorption and raising bone mass and strength of the bone. ADME
Peak plasma concentration: 6.75mcg/mL Tmax : 10days Without aggregation in Prolia pharmacokinetics with duration was noticed upon multiple dosing of 60 mg SC administered once every 6 months. Pharmacokinetics of Prolia will not affected by the binding antibodies formation. Half-life is 25.4 days. PRECAUTION • Before to start treatment with Prolia, discuss with the doctor about any other regimens you are using (including over-the-counter drugs, vitamins, or herbal remedies). Do not take aspirin or products containing aspirin unless your doctor permits this. • Prolia injection may improve the negative effects of immuno-suppressants. Especially the risk for serious infections may be increased. Inform your doctor of any immuno-suppressive drugs you early consume. • Not to receive any type of vaccination without your doctor's consultation while admonishing denosumab. • Use in pregnancy only if benefit to mother outweighs risk to fetus. Consult with doctor before the treatment • During Prolia treatment do not breastfeed your infants. DRUG INTERACTION
No formal drug-drug interaction with denosumab during trials. When interacting with some anticancer drug, orthopedic drugs, vaccines will lead to risk of adverse effects can be increased CONTRAINDICATION Prolia is contraindicated in patients having Hypocalcemia, Pregnancy, Hypersensitivity LACTATION Prolia 60mg is excreted into human milk is not known. Since possible for severe side effects occurs in nursing infants from Prolia 60mg injection, a decision should be considered that to discontinue nursing or discontinue the drug by giving preference of the importance of the drug to the mother.
STORAGE Store at 2℃ to 8℃ in the original container, avoid freeze Before to administration keep at room temperature Prolia protect from direct light and heat. MISSED DOSE Take the dose immediately before next dose duration, then left off the missed dose and continue regular schedule.Avoid taking double dose at same time. Please consult the doctor for further information. SIDE EFFECTS Common side effects for the patient taking Prolia 60mg as follows : Fatigue, Muscle weakness, Phosphorus level reduced in blood, Nausea Less common side effects for patients taking Prolia: Dyspnea, Hypocalcemia, Cough, Arthralgia, Limb pain, Eczema, Headache
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