Примери за използване на Pegfilgrastim mundipharma на Английски и техните преводи на Български
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How to use Pegfilgrastim Mundipharma.
Pegfilgrastim Mundipharma is injected subcutaneously.
How to store Pegfilgrastim Mundipharma.
Pegfilgrastim Mundipharma has not been tested in pregnant women.
Other medicines and Pegfilgrastim Mundipharma.
Why is Pegfilgrastim Mundipharma authorised in the EU?
What you need to know before you use Pegfilgrastim Mundipharma.
Do not use Pegfilgrastim Mundipharma if.
Unless your doctor directs you otherwise, you must stop breast-feeding if you use Pegfilgrastim Mundipharma.
Pegfilgrastim Mundipharma is a biosimilar medicinal product.
If you develop or are likely to develop cancers of the blood,you should not use Pegfilgrastim Mundipharma, unless instructed by your doctor.
What is Pegfilgrastim Mundipharma and what is it used for?
Accidental exposure to freezing temperatures for two periods of less than 72 hours each does not adversely affect the stability of Pegfilgrastim Mundipharma.
Pegfilgrastim Mundipharma is for use in adults aged 18 and over.
Do not shake Pegfilgrastim Mundipharma vigorously as this may affect its activity.
Pegfilgrastim Mundipharma contains the active substance pegfilgrastim. .
Your doctor has given you Pegfilgrastim Mundipharma to encourage your bone marrow(part of the bone which makes blood cells) to produce more white blood cells that help your body fight infection.
Pegfilgrastim Mundipharma contains the active substance pegfilgrastim. .
Pegfilgrastim Mundipharma 6 mg solution for injection in pre-filled syringe.
What Pegfilgrastim Mundipharma contains- The active substance is pegfilgrastim. .
Pegfilgrastim Mundipharma left at room temperature for more than 96 hours should be discarded.
Pegfilgrastim Mundipharma may be used if it is accidentally frozen for two periods of less than 72 hours each.
Pegfilgrastim Mundipharma may be exposed to room temperature(not above 30º C) for a maximum single period of up to 96 hours.
Pegfilgrastim Mundipharma has a highly similar structure, purity and biological activity to Neulasta and is distributed in the body in the same way.
Pegfilgrastim Mundipharma is given as a single dose of 6 mg injected under the skin at least 24 hours after the end of each cycle of chemotherapy.
Pegfilgrastim Mundipharma can only be obtained with a prescription and treatment should be started and supervised by a doctor who has experience in the treatment of cancer or blood disorders.
What Pegfilgrastim Mundipharma looks like and contents of the pack Pegfilgrastim Mundipharma is a clear, colourless solution for injection in a pre-filled syringe(6 mg/0.6 mL).
Because Pegfilgrastim Mundipharma is a biosimilar medicine, the studies on effectiveness andsafety of pegfilgrastim carried out with Neulasta do not all need to be repeated for Pegfilgrastim Mundipharma.
Pegfilgrastim Mundipharma is not intended for use in patients with the blood cancer chronic myeloid leukaemia or with myelodysplastic syndromes(conditions in which large numbers of abnormal blood cells are produced, which can develop into leukaemia).
Pegfilgrastim Mundipharma is a medicine used in cancer patients to help with neutropenia(low levels of neutrophils, a type of white blood cell), which is a common side effect of cancer chemotherapy and can leave patients vulnerable to infections.