Примери за използване на Denosumab на Английски и техните преводи на Български
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The active substance is denosumab.
Denosumab, an aid for patients with osteoporosis.
Another medicine containing denosumab.
It is unknown whether denosumab is excreted in human milk.
XGEVA 120 mg solution for injection denosumab.
Prolia(denosumab)- Summary of product characteristics- M05BX04.
Prescription drugs listed.Substance:"Denosumab".
The pharmacokinetics of denosumab is not expected to be affected by hepatic impairment.
Prolia 60 mg solution for injection in pre-filled syringe denosumab.
The carcinogenic potential of denosumab has not been evaluated in long-term animal studies.
You should not take Prolia together with another medicine containing denosumab.
The cumulative incidence at one year was 1.1% for denosumab and 0.6% for zoledronic acid, respectively.
Denosumab is a monoclonal antibody, which together with the RANKL protein prevents bone destruction.
In clinical trials,musculoskeletal pain was very common in both denosumab and placebo groups.
By attaching to RANKL and blocking it, denosumab reduces the formation and activity of the osteoclasts.
Denosumab is also used to treat giant cell tumor of the bone that cannot be removed by surgery.
It is especially important that you tell your doctor if you are being treated with another medicine containing denosumab.
Duration of the treatment with Prolia(denosumab)- efficiency, results from clinical researches and metaanalysis.
Denosumab is a fully human monoclonal antibody that targets receptor activator for nuclear factor κB ligand(RANKL).
In clinical trials,musculoskeletal pain was very common in both the denosumab and zoledronic acid treatment groups.
The safety and efficacy of denosumab have not been studied in patients with hepatic impairment(see section 5.2).
The optimal total duration of antiresorptive treatment for osteoporosis(including both denosumab and bisphosphonates) has not been established.
Denosumab is a human monoclonal IgG2 antibody produced in a mammalian cell line(CHO) by recombinant DNA technology.
That year also saw positive clinical trial results for its denosumab, a drug that would rake in $2.7 billion in revenue by 2015.
During denosumab treatment, patients should be advised to report new or unusual thigh, hip, or groin pain.
Treatment should be initiated in women with a low risk for deep vein thrombosis for whom bisphosphonates or denosumab are not appropriate.
Concurrent use of bisphosphonates or denosumab has been found to reduce the incidence of fractures in patients treated with Xofigo.
Calcium levels were transiently decreased andparathyroid hormone levels transiently increased in ovariectomized monkeys treated with denosumab.
Symptoms of hypocalcaemia in denosumab clinical studies included paraesthesias or muscle stiffness, twitching, spasms and muscle cramps.
Patients being treated with XGEVA should not be treated concomitantly with other denosumab containing medicinal products(for osteoporosis indications).