Gadobutrol Injection/API
In 2020, Beilulaunched its macrocyclic Contrast Media- Gadobutrol Injection, it is gadolinium-based non-ionic Contrast Media, a paramagnetic Contrast Media used in various parts of the body lesion (including the brain and spinal cord) MRI imaging and angiography examination. Its macrocyclic nature ensures it is well-tolerated with a good safety profile for MRI Contrast. As a professional contrast media manufacturer,Beilu can provide you with the high concentration gadobutrol gadovistthat leads to a better image with lower volume. We also provide DTPA acid with high quality.
Product name: GadobutrolInjection
Generic name: Gadobutrol Injection
Type: Injectable Contrast Media for MRI, Macrocyclic Contrast Media
Ingredients: Gadobutrol
Specification:gadovist 7.5 ml: 4.5354 g
Administration: Intravenous administration only.
Adverse reactions: See the details from the package insert.
Shelf life: 24 months
Indication of Gadopentetate Dimegumine Injection
Magnetic resonance imaging of the central nervous system (brain and spinal cord), abdomen, chest, pelvis, limbs and other human organs and tissues.
Precautions of Gadopentetate Dimegumine Injection
- gadobutrol injection usesso as to prevent tissue pain.
- gadovist dose, follow the relevant safety regulations in magnetic resonance imaging.
Current evidence shows that after repeated use of GBCAs, trace amounts of gadolinium can remain in the brain and other body tissues. Research reports have shown that multiple uses of GBCAs can increase the intensity of brain signals, especially in the dentate nucleus and globus pallidus. Currently, there are more reports about linear GBCAs and fewer reports about macrocyclic GBCAs. Animal experiments have shown that the amount of gadolinium deposited after repeated use of linear GBCAs is higher than that of repeated use of macrocyclic.
The clinical significance of brain gadolinium deposition is unclear.
In order to minimize the potential risks associated with gadolinium deposition in the brain, it must be used in strict accordance with the indications and approved doses. It is recommended to use the lowest approved dose that meets the requirement of diagnosis and perform a careful benefit-risk assessment and patient informed communication before repeated administration.
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