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Recombinant Human Protein ST2, also known as IL-1 R4 and T1, is an Interleukin-1 receptor family glycoprotein that contributes to Th2 immune responses (1, 2). Soluble ST2(sST2) is a member of the interleukin 1(IL-1) receptor family existing in blood. And it has been already confirmed to have capacity of capturing IL-33, inhibiting IL-33/ST2 signal transferring, and rise significantly in mechanical overloading cardiac cells. As a result, soluble ST2 can be detected in the blood when heart failure or chronic heart failure exacerbation, or heart muscle can not expand and contract because of cicatrization caused by AMI. Specification Of Human Recombinant ST2 Protein Source: E.coli Purification: Affinity purified. Concentration: 1.4mg/ml Buffer: 10mMpbs, PH=7.4, 1mm EDTA,0.1% SKL,0.2%NaN3 Preservative: 0.2%NaN3 Storage & Shelf life: Store at -20C for 3 years. Avoid multiple freeze/thaw cycles. Application Of Human Recombinant ST2 Protein Suitable for use as a standard in immunoassay, immunogen for antisera production, and tracer for iodination. Each laboratory should determine an optimum working titer for use in its particular application. More information about in vitro diagnostic market, please visit our website. If you need in vitro diagnostics, please contact us.

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H.pylori infects more than half the people in the world. The prevalence of the infection varies among countries and among different groups within the same country. The prevalence rate in the United State suggests an incidence of infection of 2%. The lifetime prevalence of peptic ulcer disease is about 12% in men and 9% in women. Studies have found that more than 90% of patients with duodenal ulcer and 80% of patients with gastric ulcer are infected with helicobacter pylori breath test kit detects the presence of H.pylori antigens in stool specimens. Expected values for any given population should be determined for each laboratory. The positivity rate of any given laboratory may vary depending on geographic location, ethnic group, and living environment. Features Of H.pylori Test Kit This h pylori test kit is for qualitative detection of H. pylori antigen in stool sample and dose not indicate the quantity of the antigens. This h pylori test kit is for in vitro diagnostic use only. This h pylori test kit result should be used only to evaluate with patient with signs and symptoms of gastrointestinal disease. A definitive clinical diagnosis should only be made by the physician after all clinical and laboratory finding have been evaluated. Principle Of H.pylori Test Kit H. pylori Antigen Rapid Test Kit simplified as h pylori kit, is a sandwich solid phase immunochromatographic assay. To perform the test, an aliquot of diluted stool sample is added to the sample well of the test cassette. The sample flows through a label pad containing H. pylori antibody coupled to redcolored colloidal gold. If the sample contains H. pylori antigens, the antigen will bind to the antibody coated on the colloidal gold particles to form antigen-antibody-gold complexes. These complexes move on the nitrocellulose membrane by capillary action toward the test line region on which H. pylori specific antibodies are immobilized. If you want to buy h pylori test kit, please contact us. More information about in vitro diagnostics market, please visit our website. As one of in vitro diagnostics companies, we also have various types of ivd products for sale, anything you need, leave us a message.

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Hepatitis C Virus (HCV) is a small, enveloped, positive-sense, single- stranded RNA Virus. HCV is now known to be the major cause of parenterally transmitted non-A, non-B hepatitis. Antibody to HCV is found in over 80% of patients with well-documented non-A, non-B hepatitis. Conventional methods fail to isolate the virus in cell culture or visualize it by electron microscope. Cloning the viral genome has made it possible to develop serologic assays that use recombinant antigens. Features Of HCV Test Kit Compared to the first generation HCV EIAs using single recombinant antigen, multiple antigens using recombinant protein and/or synthetic peptides have been added in new serologic tests to avoid nonspecific cross-reactivity and to increase the sensitivity of the HCV antibody tests. Rapid hcv test kits (Whole Blood/Serum/Plasma), also known as hepatitis c test kit or hep c test kit, is a rapid test to qualitatively detect the presence of antibody to HCV in a whole blood, serum or plasma specimen. The test utilizes colloid gold conjugate and recombinant HCV proteins to selectively detect antibody to HCV in whole blood, serum or plasma.There combinant HCV proteins used in the test kit are encoded by the genes for both structural (nucleocapsid) and non- structural proteins.The HCV Rapid Test Kit (Serum / Plasma/ Whole Blood) is a rapid chromatographic immunoassay for the qualitative detection of antibody to Hepatitis C Virus in whole blood, serum or plasma. Convenient and quick to perform at-home hepatitis c test. Material Of HCV Test Kit Materials Provided: 1. 25 Individual sealed pouches, each containing: Test device Desiccant pouch Extraction tubes 2. One extraction buffer in a dropper bottle (6mL): 0.01M phosphate buffer saline (PBS). Material Required But Not Provided: Timer If you want to know more about hcv rapid test price and hcv rapid test kit procedure, please contact us. As one of hcv test kit manufacturers, we will provide more high quality ivd test kits for customers, anything you need, leave us a message. More information about ivd diagnostics, please contact us.

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Rapid test for ebola (Colloidal gold method) is intended for the qualitative detection of ebola antigens from Nose swabs. This rapid test for ebola is intended to be used as an aid in the diagnosis of ebola, secretion of patients, and the incubation period of infection is 2-21 days. All the infected patients had high fever, headache, sore throat, weakness and muscle pain. Then there's vomiting, abdominal pain, diarrhea. Within two weeks after the onset of the disease, the virus overflowed, leading to internal and external bleeding, blood coagulation, necrotic blood quickly spread to all organs of the body, patients eventually appear oral, nasal and anal bleeding and other symptoms, patients can die within 24 hours. In about 1500 confirmed Ebola cases, the mortality rate is as high as 88% We have ebola test kit for sale, if you have needs, contact us. As one of in vitro diagnostics companies, we also have various types of ivd raw materials for sale, anything you need, leave us a message.

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Dengue virus is an enveloped, single-stranded, positive-sense RNA virus that comprises four related but distinct serotypes (Den 1, 2, 3, and 4). The virus is transmitted by mosquitoes of the daytime-biting Stegomyia family, principally Aedes aegypti and Aedes albopictus. Today, more than 2.5 billion people living in the areas of tropical Asia, Africa, Australia and the Americas are at risk for dengue infection. An estimated 100 million cases of dengue fever and 250,000 cases of life- threatening dengue hemorrhagic fever occur annually on a worldwide basis. Serological detection is a common method for the diagnosis of infection with dengue virus. IgM anti-dengue virus starts to appear at 3 days after initial exposure and remains in circulation for about 30- 60 days. IgG anti-dengue virus is raised at around 7 days, peaks at 2-3 weeks and persists for the duration of life4-6. Detection of antigens released during virus replication in the infected patient show very promising results; it enables diagnosis from the first day after the onset of fever up to day 9 once the clinical phase of the disease is over, thus, allowing early detection and prompt treatment. Features of dengue duo rapid test kit The Dengue Ag NS1-IgM/IgG rapid test detects IgG and IgM anti-dengue virus and circulating dengue antigen in one test within 20 minutes. This dengue rapid test kit is user-friendly, does not require cumbersome laboratory equipment and requires minimal staff training. The Dengue NS1+IgM/IgG Combo rapid test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG anti– dengue virus, IgM anti-dengue virus and dengue antigen (Dengue Ag) in human serum, plasma or whole blood. It is intended to be used by professionals as a screening test and as an aid in the diagnosis of infection with dengue virus. Any reactive specimen with the Dengue Ag NS1-IgM/IgG rapid test must be confirmed with alternative testing method(s). Precautions Of Dengue Test Kit 1. For in vitro diagnostic use and professional use only. 2. Read the package insert instruction before use the kit. 3. Do not use beyond the expiration date which appears on the package label. 4. Do not open the sealed pouch, unless ready to conduct the assay 5. Bring all reagents to room temperature (15°C-30°C) before use. 6. Haemolized blood may be used for the testing, but do not take precipitants. 7. Wear protective clothing and disposable gloves while assaying samples. Wash hands thoroughly after performing the test. 8. Handle all specimens as if they contain infectious agents. When the assay procedure is completed, dispose of specimens carefully after autoclaving them for at least one hour. Alternatively, they can be treated with 0.5 to 1% solution of sodium hypochlorite for one hour before disposal. 9. Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled. 10. Read result after 30 minutes may give erroneous results. 11. Do not perform the test in a room with strong air flow, an electric fan or strong air-conditioning. 12. As with all diagnostic tests, a definitive clinical diagnosis should not be based on the results of a single test, but should only be made by the physician after all clinical and laboratory findings have been evaluated. 13. Excess sample volume (>5µL) can give false positives Now the dengue ns1 price is affordable, if you want to buy dengue test kit, please contact us. If you need ivd in vitro diagnostic, please leave us a message. More types of in vitro diagnostic products, please visit our website.

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Cardiac Biomarkers List Positive cardiac markers are substances that are released into the blood when the heart is damaged or stressed. Tests of these markers are used to help diagnose acute coronary syndrome (ACS) and cardiac ischemia, conditions associated with insufficient blood flow to the heart. The main markers of myocardial injury were troponin T, troponin I, creatine kinase isoenzyme mass (CK MB) and myoglobin. Troponin is composed of three subunits. Product NameCatalog #SourceFormat Purification Concentration LotRecombinant CK- MM ProteinPDF DownloadL4C00703E. ColiPurified Liquid MW: 43KDPurified>85%3mg/mlL20200301Purified D-dimmer AntigenPDF DownloadL4C00801Human serumAffinity purified5mg/mlL20200501Recombinant Troponin CPDF DownloadL4C01301E. Coli20mM TrisHCl buffer (pH 8.0) , 5% Trehalose, 1mMEDTA>85% by SDS-PAGE1.1mg/mlL20200901Purified cTnI ProteinRecombinant cTnI ProteinPDF DownloadL4C00102Expressed in E. coliPurifiedPurified, >90% pure by SDS-PAGE1.1 mg/ml (Roche ECLIA)L20200901Recombinant MYO AntigenPDF DownloadL4C00402Expressed in E. coliPurified, >85% pure by SDS-PAGE1.5mg/ml (activity Concentration)L20201201Recombinant NT-PRO-BNP ProteinPDF DownloadL4C00302E. coliPurified, Liquid>85% pure (SDS-PAGE)1 mg/ml (Roche ECLIA)L20200101Human Recombinant ST2 ProteinPDF DownloadL4C01501E.coliAffinity purified1.1mg/mlL20201101 Advantages Of Cardiac Marker Test Myocardial injury markers are increasingly becoming the markers of screening, monitoring, follow-up and prognosis of myocardial injury such as MI and AMI. Myocardial projects, mature antigens, and gradually perfect antibodies. Cardiac Markers Meaning Myoglobin is the best early marker for myocardial injury.CTnI / cTnT was unanimously rated by the American and European Heart Association as a highly specific and sensitive diagnostic marker for acute myocardial infarction.The sensitivity and specificity of CK mbmass detection are much higher than CK-MB activity. Therefore, when cTnI or cTnT detection is not carried out, CK mbmass can be used to assist clinical diagnosis. It is close to troponin in the diagnosis of acute coronary syndrome and the evaluation of the degree of myocardial injury, as well as in sensitivity and specificity. If you want to know more about cardiac biomarkers in myocardial infarction and cardiac markers test name, please visit our website. Now the cardiac marker test price is affordable, if you have needs or buy recombinant protein, please contact us. As one of in vitro diagnostics companies, we have many in vitro diagnostics examples, if you want to know more information, please leave us a message.

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Soprano Ice Version Diode Laser System 808nm or 755nm+808nm+1064nm for your option. Professional choice for dermatologist Applications： Fo , r any unwanted hairs on areas of face, arms, armpits, chest, back, bikini, legs and etc. (including light, blond and thin hairs) Working Principle: Diode laser hair removal technology is based on the selective dynamics of light and heat. The laser goes through the skin surface to reach the root of hair follicles; light can be absorbed and converted into heat damaged hair follicle tissue, so that hair loss regeneration without injury surrounding tissue. Slight pain, easy operation, the most safe, technology for permanent hair removal now. It is performed using gold standard 808nm or Triple- wavelength(755nm+808nm+1064nm) diode laser technology, with energy penetrates deep into the dermis with high average power and a rapid 10 pulse-per-second repetition rate to heat the hair shaft and hair follicle, rather than destroy the oxygen organization around hair follicle. Meanwhile, contacting surface cooling technology applied on the Sapphire tip can eliminate the heat effect attributed to optical energy, greatly improving both the treatment performance and safety. Technical Specifications: Laser Type Diode Laser Laser Stacks Power 600W(800W for your option) Wavelength (Spectrum) 808nm/Triple-wavelength-755nm+808nm+1064nm Ener , gy Density (Fluence) 1-100J/cm² (Continuously adjustable) Spot Size 12*20mm² (standard),12*35mm² (for option) Pulse Repetition Rate 1-10Hz Pulse Duration 10-300ms Pulses Single Cooling • Continuous Sapphire contact cooling(-5℃~1℃) • Air cooling • Closed water circulation cooling • TEC Semi-conductor cooling Stand-by Working Continuously for 20 hours Display 10.4" True Color LCD Touch Screen Electrical Requirements 110/230VAC, 15/20A max., 50/60Hz Net Weight 65kgs Dimensions (WxDxH) 400*620*1100 mm

Minimum Order: 1 bags

Kaufen Sie Nembutal Espana / bestellen Sie Nembutal Nembutal (Pentobarbital -Natrium) erhältlich Pentobarbital wird kurzfristig als Beruhigungsmittel zur Behandlung von Schlafstörungen oder zum Einschlafen bei Operationen eingesetzt. Pentobarbital wird auch als Notfallbehandlung bei Anfällen eingesetzt. Wir handeln mit Pulver, Lösung (oral und injizierbar) und Tabletten. Unsere Preise sind eine der besten und wir bieten eine sehr gute Qualität. Für weitere Informationen und wenn Sie Rat suchen, besuchen Sie bitte unsere Website oder senden Sie uns eine E-Mail. Webseite: https://www.euthagroup.org Email: ... info@euthagroup.org Bestellen / Kaufen Nembutal Online kaufen nembutal, Nembutal kaufen ohne Rezept, nembutal kaufen deutschland, nembutal kaufen schweiz, nembutal® kaufen, Nembutal kaufen Berlin, Nembutal Pentobarbital kaufen, Nembutal online kaufen, Kaufen Sie Nembutal Belgien

independently developed by Beilu Pharma for the treatment of generalized anxiety disorder (GAD). It is a unique anti-GAD Chinese medicine approved by NMPA. The clinical efficacy of Jiuweizhenxin Granules in treating GAD is equivalent to that of Paroxetine tablets, but the adverse reactions of Jiuweizhenxin Granules are significantly lower than that of Paroxetine. Clinical research results show that taking Jiuweizhenxin Granules alone for 6 weeks can significantly improve the anxiety symptoms of patients and improve the quality of life with continuous use. Features Of anti anxiety traditional Chinese medicine-Jiuweizhenxin Granules Product name: Jiuweizhenxin Granules Ingredients: Ginseng(rhizome-removed), Wild jujube seed, Schisandra Chinensis, Poria cocos, polygala, rhizoma corydalis, Radix Asparagi, Cooked rehmannia root, cinnamon Specification: 6g/ bag Indication: Nourishing heart and tonifying spleen: the product is intended for generalized anxiety disorder, syndrome of deficiency of both heart and spleen, symptoms of unrelieved thoughtfulness and excessive worries, insomnia, dreaminess and palpitations. Benefiting vital energy and soothing the nerves: small and wiry pulse or deep thready pulse, sallow complexion, pale tongue with thin white coating, dizziness, sweating, frequent sighs, loss of appetite, fatigue weariness. Dosage and Administration: Administered with warm water, 1 bag each time, three times a day. Adverse Reactions: Occasionally dry mouth, hazy vision, increased constipation, nausea and vomiting, diarrhoea, inappetence or anorexia, abdominal distension, bitter mouth, gastric pain, somnolence, agrypnia, tremor, headache, wooziness, lipothymia, electrocardiogram abnormal, palpitations, tachycardia, ALT increased, white blood cells decreased, and menstrual disorders. Shelf life: 36 months The Effect of Jiuweizhenxin Granules Jiuweizhenxin Granules is a modern Chinese patent medicine approved by NMPA to treat anxiety disorders. The ingredients of Jiuweizhenxin Granules are Ginseng(rhigome-removed), Wild jujube seed, Schisandra Chinensis, Poria cocos, polygala, rhizoma corydalis, Radix Asparagi, Cooked Rehmannia root, cinnamon. The anti-anxiety effect is definite, especially for physical anxiety such as diarrhoea, headache, dizziness, and insomnia. It has a unique overall regulating effect. As one of the effective anti-anxiety drugs on the market, Jiuweizhenxin Granules can significantly improve anxiety and depression symptoms. If combined medication can significantly improve depression symptoms compared with the single medication group, the combination of Jiuweizhenxin Granules and duloxetine can significantly improve the clinical efficacy. Not only that, Jiuweizhenxin Granules can significantly improve the symptoms of insomnia in patients with insomnia. After taking Jiuweizhenxin Granules for 4 weeks, the time to fall asleep, sleep time, sleep quality, daytime dysfunction and total sleep score is better than the treatment before 【Note】Use with caution in patients with abnormal cardiac and liver functions and leukopenia.

Minimum Order: 20 square metres

Repaglinide tablets are non-sulfonylurea insulin secretion agents and are used to treat patients with type 2 diabetes. Repaglinide tablets were listed in China in 2000, and it is a Class B drug in the National Medical Insurance List. Repaglinide tablets have been listed as a drug for diabetic patients with renal insufficiency by many guidelines at home and abroad. Product name: Repaglinide Tablets Characteristic: White or off-white tablet Specification: repaglinide 0.5 tablet×30 tablets, repaglinide 0.5mg×60 tablets. Indications： It is used for type 2 diabetes (non-insulin-dependent) patients whose hyperglycemia cannot be effectively controlled by diet control, weight loss and exercise. When metformin alone cannot effectively control hyperglycemia, Repaglinide tablets can be combined with metformin. Treatment should start from the adjuvant treatment of diet control and exercise to reduce blood sugar during meals. Specifications of Repaglinide Tablets: 0.5mg Usage and Dosage，Adverse reactions，Contraindications，Precautions： , Please refer to the package insert. Medicine Interactions: Some drugs are known to affect glucose metabolism. Therefore, doctors should consider possible drug interactions. In vitro studies have shown that the metabolism of Repaglinide is affected by CYP2C8 and CYP3A4. Repaglinide was found to be a substrate for active liver uptake (organic anion transporter OATP1B1). Data from clinical studies carried out in healthy volunteers show that CYP2C8 is the main enzyme in the metabolism of Repaglinide, while CYP3A4 has limited effects. But if the effect of CYP2C8 is inhibited, the effect of CYP3A4 will be relatively enhanced. Therefore, the metabolism and clearance of Repaglinide may be changed due to the inhibition or induction of cytochrome P450. Therefore, extreme caution should be exercised when using CYP2C8 and CYP3A4 inhibitors simultaneously with Repaglinide. Drugs that inhibit OATP1B1 (such as cyclosporine) may increase the plasma concentration of Repaglinide. ( For more details, please refer to the package insert.) Storage: Similar to the storage of glimepiride tablets, tab repaglinide should also be shaded, sealed, kept in a dry place. Packaging: Aluminum plastic packaging, 15 pills/plate , 2 plates/box; 15 pills/plate, 4 plates/box, 15 pills/plate, 6 plates/box Beilu is a professional contrast media manufacturer, we provide repaglinide 0.5 mg tablet, ct contrast media and etc. Want to know more? Please contact us.

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Iohexol Injection is a non-ionic Contrast Media. Compared with a traditional ionic Contrast Media, Iohexol Injection has an excellent molecular structure and it can greatly improve user safety and significantly reduce adverse reactions. The iodinated contrast agent has excellent clinical feedback and good imaging results. In 1998, Iohexol Injection was launched as Beilu's 1st iodinated Contrast Media. Product name: Iohexol Injection Generic name: Iohexol Injection Type: Injectable Contrast Media for CT/X-ray Ingredients: Iohexol Specification: (1) 20 ml: 6 gI (2) 50 ml: 15 gI (3) 75 ml: 22.5 gI (4) 100 ml: 30 gI (5) 20 ml: 7 gI (6) 50 ml: 17.5 gI (7) 100 ml: 35 gI Administration: For injection or oral use of iodinated contrast Adverse reactions: See the details from the package insert Shelf life: 36 months Indications of Iohexol Injection The omnipaque iohexol is an X-ray contrast agent. It can be used for angiocardiography, arteriography, urography, enhanced CT examination inclduing cervical, thoracic and lumbar myelography, CT cisternography following intrathecal injection (i.e., an injection into the subarachnoid space); arthrography, endoscopic retrograde cholangiopancreatography (ERCP), herniography or fistulography, hysterosalpingography, sialography, percutaneous transhepatic cholangiography (PTC), sinography, gastroenterography, T-tube angiography, etc. Precautions of Iohexol Injection General precautions for the use of nonionic-monomer contrast agent: 1. Special attention should be paid to patients with allergies, asthma and adverse reactions to iodinated contrast agents. Prophylactic medications such as steroids and H1/H2 histamine receptor antagonists may be considered for these patients. 2. The risk of serious reactions related to this type of CT contrast agent is low. However, iodinated contrast agents can provoke anaphylactoid reactions or other allergic reactions. Therefore, first aid measures should be trained in advance, and necessary rescue drugs and devices should be prepared for possible serious reactions. 3. In view of the low accuracy of pre-test in predicting allergic reactions caused by nonionic contrast agents and the possibility that the pre-test itself may lead to serious allergic reactions, it is not recommended to use pretest to predict iodine allergic reactions. 4. Venous access should be kept smooth throughout the X-ray examination. 5. In the in-vitro tests, the effect of nonionic contrast agents on the coagulation system is lighter than that of ionic contrast agents. During angiography, great care should be taken in the intravascular technical procedures, and the catheter should be irrigated with heparinized saline from time to time to reduce the thrombosis and embolism related to the technical procedures. 6. Patients, especially patients with multiple myeloma, diabetes, renal insufficiency, infants and young children, and the elderly, must be appropriately hydrated before and after the use of contrast agent. Electrolyte disturbance and hemodynamic disorders are common in infants (< 1 year old), particularly neonates. Special attention should be paid to patients with serious heart diseases and pulmonary arterial hypertension because they are prone to developing hemodynamic disorders and cardiac rhythm disturbances. 7. Patients with acute encephalopathy, brain tumour or history of epilepsy should be prevented from seizures, and special attention should be paid to them. The risks of seizures and neurologic reactions are significantly increased in patients with alcohol or drug abuse. Transient hearing loss or deafness occurs in a few patients after myelography, which is possibly caused by a decrease in CSF pressure after lumbar puncture. 8. In view of the high risks of acute renal failure after the use of contrast agent, special attention should be paid to patients with pre-existing renal impairment and diabetes and patients with atypical globulinemia (multiple myelomatoses and Waldenstrom macroglobulinemia). 9. Preventive actions include: Identify patients with high-risk factors. Ensure patients are appropriately hydrated and, if necessary, the infusion may be maintained intravenously prior to examination until the contrast agent is cleared from the kidneys. Avoid any nephrotoxic agent, oral gallbladder contrast agent, surgery for arterial occlusion, renal angioplasty or other major surgeries that increase the renal burden until the contrast agent is cleared. Repeat radiographic testing is delayed until renal function returned to the pre-examination level. To prevent lactic acidosis, the level of serum creatinine must be determined before intravascular injection of iodinated contrast agent into diabetic patients taking metformin. For patients with abnormal serum creatinine/renal function, metformin must be discontinued and the examinations with contrast agent must be postponed until after 48 hours of discontinuation. Metformin should be reused only after renal function and serum creatinine level are constant. In some emergency cases of patients with abnormal or unknown renal function, the physician must assess both advantages and disadvantages of using contrast agent and take precautions, such as discontinuation of metformin, adequate hydration of patients, testing of renal functions, and careful observation of symptoms of lactic acidosis. There is a potential risk of transient hepatic dysfunction. Special attention should be paid to patients with serious hepatic and renal insufficiency due to significantly longer time to clear contrast agent. Hemodialysis patients may receive the examinations with contrast agents. Immediate hemodialysis is not necessary after the injection of contrast agent because there is no evidence showing that hemodialysis can protect patients with renal impairment from contrast-induced nephropathy. Iodinated contrast agents may exacerbate symptoms of myasthenia gravis. Patients with pheochromocytoma should be treated with α-blockers to prevent hypertensive crisis in interventional procedures. Special attention should also be paid to patients with hyperthyroidism. Patients with multinodular goitre may develop hyperthyroidism after using iodinated contrast agents. The possibility of transient hypothyroidism in preterm infants after using contrast agents should be clearly recognized. Contrast media extravasation (CME) occasionally causes localized pain or oedema, which gradually subsides without sequelae. However, inflammation and even tissue necrosis may occasionally occur. Routine treatment is to elevate the affected limb and cold-compress at local sites. Surgical decompression is required in case of compartment syndrome. This type of Iohexol contrast agent should be drawn into the barrel before use. Each vial is for single use only, and the unused portion should be discarded. Beilu is a professional contrast media manufacturing companies, we provide ct contrast medium, iohexol package insert, omnipaque package insert and etc. Want to know more? Please contact us.

Minimum Order: 20 square metres

Glimepiride Tablets is a sulfonylurea hypoglycemic drug that can be used in combination with insulin. In 2001, Glimepiride tablets (Dibei), as the first hypoglycemic product of Beilu Pharma, was first listed in China and belongs to the second class of national new drugs. Product name: Glimepiride Tablets Specifications: glimepiride 1 mg×30 tablets；glimepiride 2 mg×15 tablets； glimepiride 2mg×30 tablets Characteristics: White tablet Indications : As one of the oral antidiabetic drugs produced by Beilu Pharma, our glimepiride tablets are only suitable for type 2 diabetes that cannot fully control blood sugar through diet control, exercise therapy and weight loss. Glimepiride tablets are not suitable for type 1 diabetes (for example, the treatment of diabetic patients with a history of ketoacidosis), diabetic ketoacidosis or Treatment of pre-diabetic coma or coma. Usage and Dosage: Please refer to the package insert Adverse reactions, Contraindications, Precautions: Please refer to the package insert. Storage: Shade, seal, and keep in a dry place. Packaging: Aluminum plastic packaging, 15 pills/plate, 1 plate/box; 15 pills/plate, 2 plates/box. Shelf life: 24 months Advantages of Glimepiride Tablets Double effect directly hit the hypoglycemic core Double effect: Glimepiride tablets can promote insulin secretion and improve insulin resistance. At the same time, it can improve the two major pathophysiological abnormalities of insulin secretion and insulin resistance in patients with type 2 diabetes. Efficiently reduce postprandial blood glucose, fasting blood glucose and glycosylated haemoglobin Glimepiride tablets monotherapy can comprehensively reduce FPG PPG and HbA1c in newly diagnosed T2DM patients Combination therapy, such as combined metformin, acarbose, etc., has a more significant overall hypoglycemic effect Less hypoglycemia, less weight impact, high safety Short-term treatment, the risk of glimepiride hypoglycemia is only 1/3 of that of Glibenclamide Long-term treatment, the risk of glimepiride hypoglycemia is only 1/7of that of Glibenclamide Glimepiride has a small impact on the weight of T2DM patients Once a day to improve patient compliance If the patient's compliance is poor, Glimepiride tablets should be selected, once a day. Beilu is a professional contrast media manufacturing companies, we provide gadolinium contrast media, glimepiride 2mg tablets, glimepiride package insert and etc. Want to know more? Please contact us.

Minimum Order: 20 square metres

Ferric Ammonium Citrate Effervescent Granules was launched in 2004. It is an oral magnetic resonance contrast agent/media approved by NMPA in the market, which is a safe and effective double contrast media product with the advantages of convenient use and good safety. This ammonium iron citrate can significantly improve the images quality of MRCP and MRU, and can also be used as a positive contrast agent for the digestive tract. Product name: Ferric Ammonium Citrate Effervescent Granules Type: Oral MRI Contrast Media Ingredients: Ferric ammonium citrate Specification: 3g: 0.6g（Fe 129mg), 6g: 1.2g（Fe 258mg） Posology and method of administration: Oral Adverse reactions: Foreign clinical data reported that after using this MRI contrast medium, 0.1-0.5% of patients has diarrhea, 0.1% had nausea, vomiting, and decreased appetite, and a very small number of patients has stomach discomfort and bloating. All the above symptoms can be eliminated by themselves. Shelf life: 24 months Indications of Ferric Ammonium Citrate Effervescent Granules Used for magnetic resonance abdominal imaging, angiography of the digestive tract (stomach duodenum and jejunum). Precautions of Ferric Ammonium Citrate Effervescent Granules Use with caution in the following patients: patients with the gastrointestinal tract such as peptic ulcer, ulcerative colitis, local enteritis, etc. The stool appearing black after administration is a normal phenomenon. During the ferric ammonium citrate uses, false-positive for occult blood may occur. Beijing beilu pharmaceutical co ltd is a professional contrast media manufacturing companies, we provide contrast medium, mri contrast medium and etc. Want to know more? Please contact us.

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CAS No.: 67-43-6 Molecular formula: C₁₄H₂₃N₃O₁₀ Molecular weight: 393.35 Quality standard: CP Characteristics: White powder Content (HPLC): ≥99.0% Packing: 2.5KG/ drum Storage: Protected from light, sealed tightly Beijing beilu pharmaceutical co ltd is a professional contrast media manufacturing companies, we provide ct contrast agent, mri contrast medium, dtpa diethylenetriaminepentaacetic acid and etc. Want to know more? Please contact us.

Minimum Order: 20 square metres