Valentis Pharma is a prominent pharma company incorporated in the year of 2015 Manimajra, Chandigarh. We are operating as a trader, manufacturers, and suppliers of a recommendable range of pharma products. Which includes of quality tested a range of pharmaceutical medicines. We use the finest chemical ingredients. Our company has satisfying customers by providing solutions for third-party contract manufacturing and pharma PCD Franchise.
Valentis Pharma is a group of pharmaceutical companies that formulate and produce innovative Pharmaceutical Capsules. Making of these Capsules is done by utilizing the finest ingredients, in the best possible combination. These Capsules have high effectiveness, longer shelf life, and accurate pH level.
Valentis Pharma is a PCD Pharma Company and is known to be amongst the finest manufacturers and suppliers of the commendable range of pharmaceutical products which includes of quality tested the range of Pharmaceutical Tablets. These Tablets are found in the solid unit dosage form.
Valentis Pharma is a Pharma Franchise, PCD Pharma, and ISO Certified Company that manufacture a wide array of Pharmaceutical Injections. These Injections are WHO-GMP Certified, non-toxic in nature, less side effects and have premium quality ingredients.
Rabeprazole is a PPI that suppresses gastric acid secretion by inhibiting the gastric H+/K+ ATPase at the secretory surface of the gastric parietal cell. Because this enzyme is regarded as the acid (proton) pump within the parietal cell, rabeprazole has been characterized as a gastric proton pump inhibitor. Rabeprazole blocks the final step of gastric acid secretion. Onset of action is 1 hour. Duration 24 hours. Absorption Oral bioavailability is about 52% and peak plasma concentrations are reached about 3.5 hr after oral admin. The median inhibitory effect of rabeprazole on 24 hour gastric acidity is 88% of maximal after the first dose. Domperidone is a dopamine antagonist with anti-emetic properties domperidone does not readily cross the blood-brain barrier. Its anti-emetic effect may be due to a combination of peripheral (gastrokinetic) effects and antagonism of dopamine receptors in the chemoreceptor trigger zone, which lies outside the blood-brain barrier in the area postrema. Studies in man have shown oral domperidone to increase lower esophaegeal pressure, improve antroduodenal motility and accelerate gastric emptying. There is no effect on gastric secretion. In fasting subjects, domperidone is rapidly absorbed after oral administration, with peakplasma concentrations at 30 to 60 minutes. The low absolute bioavailability of oral domperidone (approximately 15%) is due to an extensive first-pass metabolism in the gut wall and liver. Although domperidones bioavailability is enhanced in normal subjects when taken after a meal, patients with gastro-intestinal complaints should take domperidone 15-30 minutes before a meal. Reduced gastric acidity impairs the absorption of domperidone. DOSAGE AND ADMINISTRATION One capsule once daily. INDICATIONS Rabezyme-D is indicated for the relief of symptoms of Dyspepsia GERD Nausea associated with acid peptic disorders Post-operative nausea and vomiting Chronic gastritis
Rabeprazole is a PPI that suppresses gastric acid secretion by inhibiting the gastric H+/K+ ATPase at the secretory surface of the gastric parietal cell. Itopride increases acetylcholine (ACh) concentrations by inhibiting dopamine D2 receptors and acetylcholinesterase. Higher ACh increases GI peristalsis, increases the lower oesophageal sphincter pressure, stimulates gastric motility, accelerates gastric emptying, and improves gastro-duodenal coordination. Special Precautions Itopride should be used with caution because it enhances the action of acetylcholine Rabeprazole should be used with caution in patients with severe hepatic impairment, Pregnancy. Other Drug Interactions Rabeprazole increase elimination T1/2 of digoxin, decreases effects with aminoglutethimide, carbamazepine, phenytoin and rifampin and reduces absorption of ketoconazole and itraconazole. Anticholinergic agents reduces the action of itopride. Rabeprazole + Itopride Side Effects Headache, diarrhoea, dizziness, rash. Potentially Fatal Anaphylaxis, agranulocytosis.
With our rich experience in this domain, we are able to offer V-cob-pg. Our product is meticulously tested on quality factors to guarantee their long shelf life and safe consumption. The offered product is formulated by consuming best grade chemical ingredients according to the predefined guidelines at our highly developed premises. This product is available in different packaging option at competitive rates within a given time frame. Features: High medicinal value Accurate composition No side effects Specifications: pregabalin ip : 75 mg methylcobalamin : 750 mcg packing : 10*1*10 pack : alu-alu
Methylcobalamin is an essential nutrient for neurons and Alpha Lipoic Acid is a powerful antioxidant that protects the neurons from oxidative stress Indications and uses: The trio of Methylcobalarnin, Pyridoxine and Folic Acid helps in bringing down the plasma level of homocysteine, the major risk factor for Atherosclerosis, Alpha Lipoic Acid prevents plaque formation in the arteries by preventing LDL oxidation. Thus this combination reduces the major risk factors for Atherosclerosis Antioxidant Benfotiamine exhibits direct antioxidative capacity and prevents induction of DNA damage in vitro. Inositol is a vitamin-like substance. Inositol is used for diabetic nerve pain, panic disorder, high cholesterol, insomnia,cancer, depression, schizophrenia, Alzheimer's disease, attention deficit-hyperactivity disorder (ADHD), autism, promoting hair growth, a skin disorder called psoriasis, and treating side effects of medical treatment with lithium. Pharmacology: Benfotiamine is a synthetic S-acyl derivative of thiamine (vitamine B1). After absorption, benfotiamine can be dephosphorylated by cells bearing an ecto-alkaline phosphatase to the lipid-soluble S-benzoylthiamine. Benfotiamine should not be confused with allithiamine, a naturally occurring thiamine disulfide derivative with a distinct pharmacological profile. Pharmacokinetics: Benfotiamine is absorbed much better than water-soluble thiamine salts: maximum plasma levels of thiamine are about 5 times higher after benfotiamine, the bioavailability is at maximum about 3,6 times as high as that of thiamine hydrochloride and better than other lipophilic thiamine derivates. Due to its excellent pharmacokinetic profile this combination should be preferred in treatment of relevant indications. Methylcobalamin: Absorption of vitamin 612 from the GI tract may be decreased by aminoglycoside antibiotics, colchicine, extended-release potassium preparations, aminosalicylic acid and its salts, anticonvulsants (e.g., phenytoin, Phenobarbital, primidone), cobalt irradiation of the small bowel, and by excessive alcohol intake lasting longer than 2 weeks. Neomycin-induced malabsorption of vitamin 612 may be increased by concurrent administration of colchicine. Alphalipoic Acid: Alpha lipoic acid may improve blood sugar control, so people with diabetes who are taking medication to lower blood sugar, such as metformin, glyburide, should only take alpha lipoic acid under the supervision of a qualified health professional and have their blood sugar levels carefully monitored. Benefits: The primary use of this antioxidant is as an "anti-AGE" supplement. • Useful in various Neuropathies like Diabetic Neuropathy, Alcoholic Neuropathy, Drug-induced Neuralgia Storage: Store at room temperature, 15-30° C (59-86°F). Keep away from moisture