'low glycemic index foods'

Composition : Esomeprazole 40mg Esomeprazole intravenous (IV) is a prescription proton pump inhibitor (PPI) medication used for short-term treatment of gastroesophageal reflux disease (GERD) with erosive esophagitis or for reducing risk of rebleeding of gastric or duodenal ulcers following therapeutic endoscopy. INDICATIONS Chronic Gastritis Gastric Bleeding Gastro Esophageal Reflux Disease (GERD) Gastric Rebleeding Gastric Surgery Peptic Ulcer

Composition : Esomeprazole 40mg + Levosulpiride 75mg Esomeprazole : A proton pump inhibitor (PPI) that reduces stomach acid production. This creates a less acidic environment in the stomach, which helps relieve symptoms of GERD like heartburn and acid reflux and promotes healing of peptic ulcers. Levosulpiride : A prokinetic agent that works differently than Domperidone, which is sometimes used in similar combinations. Levosulpiride works by: Increasing the tone and contractions of the stomach muscles, helping to move food through the digestive system more efficiently. Slightly increasing the pressure in the lower esophageal sphincter (LES), the muscular valve between the esophagus and stomach. This can help prevent stomach acid from flowing back up into the esophagus. INDICATIONS Chronic Gastritis Gastric Bleeding Gastro Esophageal Reflux Disease (GERD) Gastric Rebleeding Gastric Surgery Peptic Ulcer

Composition : Piperacillin 4 gm + Tazobactam 0.5 gm Piperacillin : Belongs to a class of antibiotics called penicillins. Works by interfering with the bacteria's cell wall formation, preventing them from growing and multiplying. Tazobactam : A beta-lactamase inhibitor. Does not directly kill bacteria but protects Piperacillin from being broken down by certain enzymes produced by bacteria (beta-lactamase) that can render antibiotics ineffective. This allows Piperacillin to function effectively against a broader range of bacteria. INDICATIONS Intra Abdominal Infections Lower Respiratory Tract Infections Pelvic Inflammatory Disease Pre-Operative Prophylaxis Secondary Infections

Composition : Cefuroxime 250mg. (As Cefuroxime Axetil) It is a cephalosporin antibiotic Excellent activity against wide spectrum of bacterial Infections Low incidence of resistance Higher penetration in tissues INDICATIONS: ENT infections RTIs UTIs SSTIs Gonorrhoea

Composition : Cefuroxime 500mg. (As Cefuroxime Axetil) It is a cephalosporin antibiotic Excellent activity against wide spectrum of bacterial Infections Low incidence of resistance Higher penetration in tissues INDICATIONS: ENT infections RTIs UTIs SSTIs Gonorrhoea

Composition : Cefuroxime 500mg + Clavulanic Acid 125mg Cefuroxime : This is a cephalosporin antibiotic. Antibiotics work by killing or stopping the growth of bacteria. Cefuroxime targets a broad spectrum of bacteria commonly causing infections. Clavulanic Acid : This is a beta-lactamase inhibitor. It doesn't directly kill bacteria, but it helps to protect Cefuroxime from being broken down by certain enzymes produced by bacteria. This allows Cefuroxime to work more effectively against bacteria that are resistant to some antibiotics. INDICATIONS: Upper respiratory tract infections Lower respiratory tract infections Skin and skin structure infections Urinary tract infections

Composition : Ceftriaxone 1000 mg + Tazobactam 125 mg Ceftriaxone : Belongs to a class of antibiotics called third-generation cephalosporins. Works by interfering with the bacteria's cell wall formation, preventing them from growing and multiplying. This ultimately kills the bacteria. Tazobactum : A beta-lactamase inhibitor. Doesn't directly kill bacteria itself. Protects Ceftriaxone from being broken down by certain enzymes produced by bacteria (beta-lactamase) that can render antibiotics ineffective. This allows Ceftriaxone to function effectively against a broader range of bacteria, especially those resistant to other antibiotics. INDICATIONS Septicemia Meningitis Peritonitis UTIs RTIs SSTIs Endometritis

Composition : Etoricoxib 90 mg Highly selective cox II inhibitors. Superior gastrointestinal tolerability. Effective in osteoarthritis (OA) pain than diclofenac. Rapid & durable treatment effects in patients with OA of the knee of hip. Delivers rapid & powerful relief of excruciating pain with anti-inflammatory power similar to indomethacin in acute gouty arthritis. INDICATIONS Gout Spondylitis Acute Low Back Pain Rheumatoid Arthritis Osteoarthritis Post Surgical Pain Management

Composition: Paracetamol (as immediate release) 325 mg + Paracetamol (as sustained release) 675 mg. Paracetamol: This is the main pain-relieving and fever-reducing ingredient. It works by blocking the body's production of certain chemicals that cause pain and fever. Immediate release: This portion of the paracetamol is not coated and dissolves quickly in your stomach. This allows for faster absorption into the bloodstream, providing pain relief within 15-30 minutes. Sustained release: This portion of the paracetamol is coated in a special way that allows for a slower release into the bloodstream. This provides pain relief that lasts for several hours (typically 4-6 hours) after taking the tablet. INDICATIONS Analgesic Antipyretic Fever Pain relief Mild to moderate pain