Drugs – Medical Products
Cisapride is a medication historically used to treat certain gastrointestinal disorders, particularly gastroesophageal reflux disease (GERD) and certain motility disorders of the gastrointestinal tract. It belongs to a class of drugs known as prokinetic agents, and its primary action is to enhance the movement of the muscles in the digestive tract.
Rabeprazole sodium is a proton-pump inhibitor that suppresses gastric acid secretion by blocking acid (proton) pump within gastric parietal cells. It is indicated in short-term treatment in healing and symptomatic relief of duodenal ulcers and erosive or ulcerative gastroesophageal reflux disease (GERD); maintaining healing and reducing relapse rates of heartburn symptoms in patients with GERD; and treatment of daytime and nighttime heartburn and other symptoms associated with GERD; long-term treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome and in combination with amoxicillin and clarithromycin to eradicate Helicobacter pylori. The most potent suppressors of gastric acid secretion are inhibitors of the gastric H+K+-ATPase (proton pump).
The stability of palonosetron hydrochloride at concentrations of 5 and 30 micrograms/mL was assessed in polyvinyl chloride bags of the following 4 infusion solutions: glucose 5%, sodium chloride 0.9%, glucose 5% in sodium chloride 0.45%, and glucose 5% in lactated Ringer’s solution. All solutions were considered to be physically and chemically stable for at least 48 hours at room temperature exposed to light, and for 14 days under refrigeration. As for Ondansetron, although no dosage reduction is considered necessary in hepatic impairment.
Imodium Instant Melts is a medicine which is used to treat sudden short-lived (acute) attacks of diarrhoea in adults and children aged 12 years and over. It can also be used to treat diarrhoea associated with Irritable Bowel Syndrome (IBS) in adults aged 18 years and over after your doctor has diagnosed you are suffering from this condition.
The stability of roxatidine acetate hydrochloride in parenteral nutrition solutions was influenced by storage temperature and amino acid content and composition. Unlike cimetidine roxatidine does not appear to affect cytochrome P450, and therefore is considered to have little effect on the metabolism of other drugs. However, like other H2-antagonists its effects on gastric pH may alter the absorption of some other drugs.
Antisecretory drugs are used in the treatment and prophylaxis of peptic ulcer disease (below) some are also employed in other disorders associated with gastric hyperacidity such as gastro-oesophageal reflux disease and dyspepsia (below). Histamine H2-receptor antagonists (H2-antagonists), which act by blocking histamine H2-receptors on gastric parietal cells, thereby antagonising the normal stimulatory effect of endogenous histamine on gastric acid production. Those described in mis site include cimeti-dine, famotidine, nizatidine, and ranitidine.
This medicine can be taken by adults aged 18 years and over. However, some people should not take this medicine or should seek the advice of their pharmacist or doctor first. Driving and using machines: On rare occasions this medicine may cause drowsiness.
BP 2008 (Carbenoxolone Sodium). A white or pale cream-coloured, hygroscopic powder. Freely soluble in water sparingly soluble in alcohol practically insoluble in chloroform and in ether.
Sparingly soluble in water very soluble in acid solutions. Sparingly soluble in water and in alcohol slightly soluble in dichloromethane soluble in methyl alcohol.
The name of your tablet is Janumet. It contains two different medicines called sitagliptin and metformin. They work together to control blood sugar levels in patients with a form of diabetes called ‘type 2 diabetes mellitus’.
Duphalac contains a medicine called lactulose. This belongs to a group of medicines called laxatives. Duphalac is used to treat constipation.
Bismuth compounds are chemical compounds that contain bismuth as one of their elements. Bismuth is a heavy metal often used in various applications, including medicine, cosmetics, and electronics. Some common bismuth compounds include bismuth subsalicylate, used in medications for treating digestive issues, and bismuth oxychloride, used in cosmetics for its pearly appearance.
A white oryellowish crystalline powder. Freely soluble in water very slightly soluble in dehydrated alcohol practically insoluble in dichloromethane slightly soluble in methyl alcohol.
Sulfasalazine is a compound of a sulfonamide, sulfapyridine, with 5-aminosalicylic acid (mesalazine). Its activity is generally considered to lie in the 5-aminosalicylic acid moiety, which is released in the colon by bacterial metabolism, although intact sulfasalazine has some anti-inflammatory properties in its own right.
Treatment for heartburn (reflux oesophagitis and oesophageal reflux disease). For adults, the usual dose is omeprazole 20 mg once a day for 4 weeks.
Lansoprazole is a proton pump inhibitor (PPI) medication that reduces stomach acid production. By reducing stomach acid, lansoprazole is effective in treating gastroesophageal reflux disease (GERD), peptic ulcers, and other acid-related disorders.
Alizapride is well absorbed from the gastrointestinal tract. It is mainly excreted unchanged in the urine and has an elimination half-life of about 3 hours.
Irritable bowel syndrome (IBS) is a disorder of the lower gastrointestinal tract characterized by symptoms such as diarrhea, diarrhea alternating with constipation, abdominal cramping and pain, gas and bloating, and mucus in the stool. IBS is one of the most common medical disorders in the U.
Urogastrone is a polypeptide first isolated from human urine. Two forms have been identified, p and y urogastrone.
US licensed product information states that, once reconstituted and diluted as directed in sodium chloride 0.9%, a solution of fosaprepitant meglumine is stable for 24 hours at room temperature (at or below 25°). Fosaprepitant is aprodrug of the antiemetic aprepitant, which is a neurokinin-1 receptor antagonist.