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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 • Prolia 60mgbelongs 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 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 OsteolyticBone Metastases of Solid Tumors : • 120mg subcutaneously every 4 weeks • Injection of drug should be done in upper arm, upper thigh or abdomen
MECHANISM • Denosumablinked to RANKL, a protein which is specific for the formation, function and survival of osteoclasts, the cells necessary for bone resorption. • Denosumabprohibits 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 Proliapharmacokinetics with duration was noticed upon multiple dosing of 60 mg SC administered once every 6 months. Pharmacokinetics of Proliawill not affected by the binding antibodies formation. • Half-life is 25.4 days.
PRECAUTION • Proliainjection 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 Proliatreatment do not breastfeed your infants.
DRUG INTERACTION • No formal drug-drug interaction with denosumabduring trials. • When interacting with some anticancer drug, orthopedic drugs, vaccines will lead to risk of adverse effects can be increased CONTRAINDICATION • Proliais contraindicated in patients having Hypocalcemia, Pregnancy, Hypersensitivity
LACTATION • Prolia60mg 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.
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
Contact Us • phone No :9987711567 • Email :info@myapplepharma.com website • https://myapplepharma.com/prolia-60mg.php