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"description": "The STERIS DPI DEVICE is a modern, user-friendly Dry Powder Inhaler (DPI) designed to deliver respiratory medication directly to the lungs in a highly efficient and portable form. Inhalation therapy plays a critical role in the management of chronic respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). The DPI device simplifies this process by delivering the drug in the form of a dry powder without the need for coordination between actuation and inhalation, making it ideal for patients of all ages.\n\nWhat is a DPI Device?\nA Dry Powder Inhaler (DPI) is a medical device used to deliver therapeutic medication directly into the lungs. Unlike traditional inhalers that use propellants to push the drug into the lungs, DPI devices rely on the patient’s own inhalation power to disperse and inhale the powdered drug effectively. Essentially, a DPI device is a tool that administers medication in dry powder form to the lungs, providing quick and targeted respiratory relief.\n\nDPI Full Form: Dry Powder Inhaler\n\nUses of STERIS DPI DEVICE\nThe STERIS DPI DEVICE is commonly used in the treatment and management of respiratory diseases such as:\n\nAsthma\n\nChronic Obstructive Pulmonary Disease (COPD)\n\nBronchitis\n\nAllergic airway conditions\n\nIt helps deliver medication directly to the airways, ensuring faster action and reduced systemic side effects compared to oral treatments.\n\nHow It Works\nWhen the patient inhales through the mouthpiece, the device uses the airflow to disperse the dry powder into fine particles, allowing it to reach deep into the lungs. The inhaled medication begins working quickly to open airways, reduce inflammation, or treat infection, depending on the formulation used with the DPI.\n\nSide Effects of Dry Powder Inhaler Use\nWhile the STERIS DPI DEVICE itself is safe and user-friendly, some medications delivered via DPI may cause minor side effects such as:\n\nDry throat or mouth\n\nHoarseness\n\nCough\n\nIrritation in the throat\n\nFungal infections in the mouth (if corticosteroids are used and mouth is not rinsed after use)\n\nThese side effects can often be minimized with proper usage and hygiene.\n\nPrecautions Before Using STERIS DPI DEVICE\nAlways read the instructions carefully before first-time use.\n\nMake sure the device is clean and free from moisture.\n\nInhale deeply and forcefully to ensure proper medication delivery.\n\nDo not exhale into the device, as moisture can affect the powder's consistency.\n\nStore in a dry, cool place away from direct sunlight.\n\nAlways rinse your mouth after using corticosteroid-based powders.\n\nAdvantages of STERIS DPI DEVICE\nPropellant-free and eco-friendly\n\nPortable and compact design for daily use\n\nNo coordination required between inhalation and actuation\n\nDelivers medication effectively with minimal effort\n\nEasy-to-use, even for elderly or pediatric patients\n\nConclusion\nThe STERIS DPI DEVICE is a highly effective solution for individuals suffering from chronic or acute respiratory disorders. By delivering medication directly to the lungs in a dry powder form, it ensures fast relief, greater bioavailability, and improved patient compliance. Whether you’re managing asthma or COPD, this DPI device offers a dependable and convenient way to breathe easier every day.",
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"name": "FLUTICATONE VILO 200",
"description": "FLUTICATONE VILO 200 is a combination inhalation therapy containing Fluticasone Furoate (200 mcg), a potent corticosteroid, and Vilanterol (25 mcg), a long-acting beta2-adrenergic agonist (LABA). This fixed-dose inhalation powder is specially formulated to manage and prevent symptoms associated with chronic obstructive pulmonary disease (COPD) and asthma, helping patients breathe more easily and maintain better lung function.\n\nThis combination works synergistically—Fluticasone Furoate reduces inflammation and swelling in the airways, while Vilanterol relaxes the airway muscles, offering long-lasting bronchodilation. The once-daily dosing improves compliance and ensures consistent therapeutic effects throughout the day.\n\nWhat is Fluticasone Furoate and Vilanterol Powder for Inhalation?\nFluticasone Furoate and Vilanterol Powder for Inhalation is a prescription combination medication used for long-term maintenance treatment of asthma and COPD. It is not a rescue medicine and should not be used to relieve sudden breathing problems.\n\nFluticasone Furoate 200 mcg: A highly effective corticosteroid that helps to reduce inflammation in the lungs.\n\nVilanterol 25 mcg: A bronchodilator that keeps airways open by relaxing muscles around them for up to 24 hours.\n\nUses of Fluticasone Furoate and Vilanterol Powder for Inhalation\nLong-term treatment of moderate to severe asthma in adults and adolescents.\n\nMaintenance treatment of chronic obstructive pulmonary disease (COPD) including chronic bronchitis and emphysema.\n\nReduces the frequency of asthma attacks and COPD exacerbations.\n\nImproves overall lung function, quality of life, and exercise capacity in chronic airway diseases.\n\nKeyword integrated: fluticasone furoate and vilanterol powder for inhalation uses\n\nSide Effects of Fluticasone Furoate and Vilanterol Powder for Inhalation\nWhile FLUTICATONE VILO 200 is generally well-tolerated, it may cause some side effects in certain individuals, especially during the initial phase of therapy. Common and less frequent side effects may include:\n\nHeadache\n\nHoarseness or voice changes\n\nSore throat\n\nCough or throat irritation\n\nFungal infection in the mouth (oral thrush)\n\nIncreased heart rate or palpitations\n\nMuscle cramps\n\nDizziness\n\nRespiratory tract infections\n\nSerious but rare effects include allergic reactions, paradoxical bronchospasm, and increased risk of pneumonia in COPD patients.\n\nKeyword integrated: fluticasone furoate and vilanterol powder for inhalation side effects\n\nPrecautions Before Using\nDo not use FLUTICATONE VILO 200 for acute asthma or COPD attacks. Always carry a fast-acting inhaler.\n\nInform your doctor if you have a history of heart disease, hypertension, thyroid problems, liver disorders, or tuberculosis.\n\nRinse your mouth after each use to avoid oral thrush.\n\nUse the inhaler as prescribed, and do not exceed the recommended dose.\n\nNot recommended for use in children under 12 years unless prescribed.\n\nInform your healthcare provider if you are pregnant, planning pregnancy, or breastfeeding.\n\nDrug Interactions\nCertain medications may affect the way FLUTICATONE VILO 200 works or increase the risk of side effects. Consult your doctor if you are taking:\n\nBeta-blockers (e.g., atenolol, propranolol)\n\nDiuretics (may increase the risk of hypokalemia)\n\nMAO inhibitors or tricyclic antidepressants (can enhance the effect of Vilanterol)\n\nAntifungal or antiviral medications (e.g., ketoconazole, ritonavir) that may increase corticosteroid levels\n\nOther long-acting beta agonists (LABAs) or inhaled corticosteroids\n\nWhat drugs interact with Fluticasone Furoate and Vilanterol?\nFluticasone Furoate and Vilanterol may interact with:\n\nStrong CYP3A4 inhibitors (like ritonavir, itraconazole) leading to increased steroid effects\n\nBeta-adrenergic blockers which may reduce the efficacy of vilanterol\n\nXanthine derivatives, diuretics, or digoxin, which may lead to heart rhythm disturbances when combined\n\nConclusion\nFLUTICATONE VILO 200 offers an effective, once-daily treatment for asthma and COPD by combining the anti-inflammatory power of Fluticasone Furoate 200 mcg and the long-acting bronchodilation of Vilanterol 25 mcg. It not only helps maintain clear airways but also improves your overall breathing comfort and quality of life. For optimal results, use the inhaler consistently and under your healthcare provider’s guidance.",
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"description": "TOPBETA GM Cream is a topical dermatological preparation specially formulated to treat a range of inflammatory and infectious skin disorders. It combines the potent anti-inflammatory action of Clobetasol Propionate, the antimicrobial efficacy of Neomycin Sulphate, and the antifungal power of Miconazole Nitrate. This makes it particularly effective in treating skin conditions where infection and inflammation coexist, such as infected eczema, fungal dermatitis, intertrigo, and athlete’s foot.\n\nKey Ingredients\nClobetasol Propionate: A strong corticosteroid that helps reduce inflammation, redness, itching, and skin irritation. It works by suppressing inflammatory chemicals in the skin.\n\nNeomycin Sulphate: A broad-spectrum antibiotic that kills or inhibits bacteria commonly responsible for secondary skin infections.\n\nMiconazole Nitrate: A powerful antifungal agent that disrupts fungal cell membranes, making it effective against yeast and dermatophyte infections.\n\nKey Benefits\nRelieves itching, swelling, and redness associated with inflammatory skin conditions\n\nTreats fungal and bacterial infections of the skin\n\nPrevents secondary infections in damaged or sensitive skin areas\n\nPromotes faster healing and restoration of normal skin\n\nIdeal for mixed infections where both fungi and bacteria are present\n\nHow Does It Work?\nTOPBETA GM Cream works through a synergistic mechanism:\n\nClobetasol Propionate suppresses the skin’s inflammatory response, helping to reduce the signs and symptoms of dermatitis, eczema, and allergic reactions.\n\nNeomycin Sulphate targets and destroys bacteria on the skin surface, preventing infections from spreading or worsening.\n\nMiconazole Nitrate acts on the fungal cell wall, stopping the growth and spread of fungi, helping resolve fungal infections at the source.\n\nTogether, these ingredients provide a comprehensive therapeutic effect against inflammation, bacterial infection, and fungal overgrowth.\n\nDirections for Use\nClean and dry the affected area thoroughly before application.\n\nApply a thin layer of the cream to the affected skin.\n\nGently massage until it is fully absorbed.\n\nUse twice daily or as directed by a healthcare professional.\n\nAvoid covering the treated area with bandages or dressings unless instructed.\n\nWash hands after application unless treating the hands.\n\nSide Effects\nAlthough well tolerated in most cases, some users may experience:\n\nMild burning or stinging at the site of application\n\nSkin thinning or dryness with prolonged use\n\nRedness, itching, or hypersensitivity reactions\n\nRare allergic responses such as rash or swelling\n\nDiscontinue use and consult a healthcare provider if any serious or persistent side effects occur.\n\nPrecautions\nFor external use only\n\nAvoid contact with eyes, nose, mouth, and mucous membranes\n\nNot recommended for use on broken or highly sensitive skin unless prescribed\n\nDo not use for extended periods without medical advice\n\nKeep out of reach of children\n\nConsult a doctor before use during pregnancy or breastfeeding\n\nConclusion\nTOPBETA GM Cream offers an effective, convenient, and targeted treatment for skin conditions involving infection and inflammation. With the combined strength of Clobetasol Propionate, Neomycin Sulphate, and Miconazole Nitrate, it provides fast relief from symptoms while addressing the root causes. Ideal for short-term use under medical guidance, it helps restore skin health, comfort, and protection.",
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"description": "GLIMITERIS MV1 0.2 is an advanced fixed-dose combination (FDC) medication designed for adults with Type 2 Diabetes Mellitus (T2DM) who require more than lifestyle modifications or single/dual therapy to maintain optimal blood sugar levels. This innovative formulation brings together the power of three well-established antidiabetic agents—Glimepiride (1 mg), Voglibose (0.2 mg), and Metformin Hydrochloride SR (500 mg)—to provide comprehensive glycemic control.\n\nIt is particularly effective for patients struggling with postprandial hyperglycemia, fasting glucose regulation, and HbA1c reduction, making it a preferred choice in cases of poorly controlled diabetes.\n\n \n\nMechanism of Action\nThe therapeutic benefit of GLIMITERIS MV1 0.2 comes from the unique synergy of its three components, each targeting different aspects of glucose metabolism:\n\n1. Glimepiride (1 mg) – Sulfonylurea\nStimulates insulin secretion by activating pancreatic beta cells.\n\nProvides a long-lasting effect with comparatively lower hypoglycemia risk than older sulfonylureas.\n\nHelps reduce both fasting and postprandial glucose levels.\n\n2. Voglibose (0.2 mg) – Alpha-Glucosidase Inhibitor\nDelays the breakdown and absorption of carbohydrates in the intestine.\n\nMinimizes post-meal glucose spikes (PPBG).\n\nActs locally in the gut and has minimal systemic absorption, which reduces systemic side effects.\n\n3. Metformin Hydrochloride SR (500 mg) – Biguanide\nDecreases hepatic glucose production (gluconeogenesis).\n\nImproves peripheral insulin sensitivity, enhancing glucose uptake in muscles.\n\nDoes not cause hypoglycemia on its own.\n\nThe sustained-release (SR) formulation ensures extended control and reduces gastrointestinal side effects.\n\n \n\nIndications\nGLIMITERIS MV1 0.2 is indicated for:\n\nAdults with Type 2 Diabetes Mellitus.\n\nPatients inadequately controlled with monotherapy or dual therapy.\n\nManagement of fasting and postprandial hyperglycemia.\n\nLong-term HbA1c reduction as part of a comprehensive diabetes care plan.\n\n \n\nKey Benefits\n✅ Comprehensive Blood Sugar Control – Acts on fasting, post-meal, and long-term HbA1c levels.\n✅ Postprandial Spike Management – Voglibose effectively controls carbohydrate-induced sugar surges.\n✅ Reduced Pill Burden – Combines three medicines into a single tablet.\n✅ Lower Hypoglycemia Risk – Metformin and Voglibose balance out Glimepiride’s insulin-secreting effect.\n✅ Weight Management Support – Metformin may promote modest weight loss or prevent weight gain.\n✅ Improved Tolerability – SR formulation of Metformin enhances gastrointestinal comfort.\n\n \n\nDosage and Administration\nRecommended dose: One tablet once or twice daily with meals, or as directed by the physician.\n\nAdministration tips:\n\nTake with the first bite of a main meal to maximize Voglibose’s effect.\n\nSwallow whole with water; do not crush or chew the SR tablet.\n\nDose adjustments: Based on blood sugar monitoring, clinical response, and renal/hepatic function.\n\n \n\nContraindications\nGLIMITERIS MV1 0.2 is not suitable for patients with:\n\nType 1 diabetes or diabetic ketoacidosis.\n\nSevere renal impairment (eGFR <30 mL/min/1.73 m²).\n\nHepatic dysfunction.\n\nSevere gastrointestinal diseases.\n\nHistory of lactic acidosis.\n\nHypersensitivity to Glimepiride, Voglibose, or Metformin.\n\nPregnancy and lactation (unless strictly advised by a physician).\n\n \n\nWarnings and Precautions\nHypoglycemia: Risk is higher when combined with other antidiabetics or with missed meals.\n\nLactic Acidosis: A rare but life-threatening effect of Metformin—renal function monitoring is essential.\n\nGI Side Effects: Voglibose and Metformin may cause bloating, flatulence, or diarrhea (usually temporary).\n\nVitamin B12 Monitoring: Long-term Metformin use may reduce B12 absorption.\n\nLiver and Kidney Function: Regular monitoring is recommended for safe long-term use.\n\n \n\nAdverse Effects\nCommon:\nGlimepiride: Mild hypoglycemia, dizziness, slight weight gain.\n\nVoglibose: Gas, abdominal discomfort, mild diarrhea.\n\nMetformin SR: Nausea, bloating, metallic taste, loose stools.\n\nRare but Serious:\nLactic acidosis (from Metformin).\n\nSevere hypoglycemia (especially if meals are skipped).\n\nAllergic reactions such as rash, itching, or swelling.\n\nElevated liver enzymes.\n\nSeek medical attention if symptoms such as rapid breathing, confusion, severe fatigue, or muscle pain occur.\n\n \n\nDrug Interactions\nIncreased hypoglycemia risk: With insulin, beta-blockers, and sulfonylureas.\n\nReduced Metformin efficacy: With corticosteroids, estrogens, and diuretics.\n\nLactic acidosis risk: Higher with alcohol or iodinated contrast agents. ",
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"name": "SACUSMART 200",
"description": "Description: \nSACUSMART 200 is a combination medicine containing Sacubitril (97 mg) and Valsartan (103 mg), specifically designed to manage chronic heart failure with reduced ejection fraction (HFrEF). This dual-acting therapy is classified as an angiotensin receptor neprilysin inhibitor (ARNI) and is widely prescribed to reduce the risk of cardiovascular death and hospitalization in patients with heart failure.\n\nHeart failure is a progressive condition where the heart cannot pump blood efficiently to meet the body’s needs. SACUSMART 200 improves the efficiency of the heart by relaxing blood vessels, reducing fluid retention, and lowering strain on the heart, helping patients live a better and longer life.\n\n \nWhat is SACUSMART 200?\n \n\nSACUSMART 200 is a highly effective heart failure medication that combines two active components:\n\nSacubitril (97 mg) – a neprilysin inhibitor that increases levels of natriuretic peptides, leading to vasodilation, sodium excretion, and reduced stress on the heart.\n\nValsartan (103 mg) – an angiotensin II receptor blocker (ARB) that relaxes blood vessels, lowers blood pressure, and prevents harmful effects of angiotensin II.\n\nTogether, these mechanisms make SACUSMART 200 a superior alternative to traditional ACE inhibitors or ARBs alone in treating chronic heart failure.\n\n \nUses of SACUSMART 200\n \n\nSACUSMART 200 is prescribed for:\n\nChronic heart failure with reduced ejection fraction (HFrEF)\n\nReducing risk of hospitalization due to worsening heart failure\n\nImproving survival rates in patients with heart failure\n\nEnhancing exercise tolerance and quality of life in long-term heart failure management\n\n \nBenefits of SACUSMART 200\n \n\nDual action with neprilysin inhibition + ARB effect for comprehensive heart protection\n\nProven to reduce mortality and hospitalization risk in heart failure patients\n\nImproves symptoms such as breathlessness, fatigue, and swelling\n\nHelps patients regain better physical stamina and daily activity levels\n\nLong-term use significantly contributes to improved quality of life\n\n \nPossible Side Effects of SACUSMART 200\n \n\nWhile SACUSMART 200 is effective and generally well tolerated, some patients may experience:\n\nLow blood pressure (hypotension)\n\nIncreased blood potassium levels (hyperkalemia)\n\nDizziness or light-headedness\n\nKidney function changes\n\nCough\n\nRarely, serious allergic reactions or angioedema (swelling of face, lips, or throat)\n\nImmediate medical attention is required if severe swelling, difficulty breathing, or fainting occurs.\n\n \nPrecautions Before Using SACUSMART 200\n \n\nDo not use if you are allergic to sacubitril, valsartan, or other ARBs\n\nAvoid if you have taken an ACE inhibitor within the last 36 hours due to the risk of angioedema\n\nNot recommended for patients with a history of hereditary angioedema\n\nCaution in patients with severe kidney or liver disease\n\nPregnant and breastfeeding women should avoid this medicine due to harmful effects on the baby\n\nAlways monitor blood pressure, kidney function, and potassium levels while on this treatment\n\n \nDrug Interactions\n \n\nSACUSMART 200 may interact with:\n\nACE inhibitors – should not be combined, risk of angioedema\n\nPotassium supplements or potassium-sparing diuretics – risk of high potassium\n\nNSAIDs (e.g., ibuprofen, naproxen) – may reduce kidney function\n\nLithium – risk of lithium toxicity\n\nDiuretics – may increase the risk of low blood pressure\n\nAlways inform your doctor about all medicines, supplements, or herbal products you are taking before starting SACUSMART 200.\n\n \nConclusion\n \n\nSACUSMART 200 (Sacubitril 97 mg & Valsartan 103 mg) is a breakthrough treatment in managing chronic heart failure with reduced ejection fraction (HFrEF). By combining neprilysin inhibition and angiotensin receptor blockade, it not only reduces symptoms but also significantly lowers the risk of hospitalization and death, improving both longevity and quality of life.\n\nFor patients living with heart failure, SACUSMART 200 offers a scientifically proven and clinically superior solution to regain control over their health and live a more fulfilling life.",
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"name": "RIFAXEMANIA 400",
"description": "RIFAXEMANIA 400 contains Rifaximin 400 mg, a special type of antibiotic that works mainly in the intestines. Unlike many other antibiotics that get absorbed into the bloodstream, rifaximin stays in the digestive tract, making it highly effective for infections and conditions related to the gut while minimizing unwanted effects on the rest of the body.\n\nIt belongs to the rifamycin class of antibiotics and is particularly useful for reducing harmful bacteria in the intestines, restoring gut balance, and improving digestive health. Doctors commonly prescribe it for traveler’s diarrhea, irritable bowel syndrome with diarrhea (IBS-D), and hepatic encephalopathy.\n\nUses of RIFAXEMANIA 400\n\nRIFAXEMANIA 400 is recommended for:\n\nTraveler’s Diarrhea: Effective against non-invasive strains of Escherichia coli.\n\nHepatic Encephalopathy: Helps reduce the recurrence of confusion and related symptoms by lowering the production of toxins such as ammonia in the gut.\n\nIrritable Bowel Syndrome with Diarrhea (IBS-D): Provides relief from abdominal pain, bloating, and frequent loose stools.\n\nSmall Intestinal Bacterial Overgrowth (SIBO): Often prescribed off-label for managing bacterial imbalance in the small intestine.\n\nPrevention of gut-related complications in chronic liver disease.\n\nSide Effects of RIFAXEMANIA 400\n\nMost people tolerate RIFAXEMANIA 400 well because of its local action in the intestines. However, like any medication, some side effects may occur, such as:\n\nNausea or vomiting\n\nHeadache or dizziness\n\nAbdominal pain, bloating, or gas\n\nConstipation or diarrhea (rare)\n\nTiredness or weakness\n\nRash, itching, or other mild allergic reactions\n\nSerious side effects are rare but may include severe diarrhea, persistent abdominal cramps, or signs of allergy such as swelling and breathing difficulty. If these occur, medical help should be sought immediately.\n\nPrecautions Before Using RIFAXEMANIA 400\n\nPatients should keep in mind the following precautions:\n\nDo not use if you are allergic to rifaximin, rifampin, or other rifamycin antibiotics.\n\nAvoid self-medication if you have fever, bloody stools, or severe abdominal pain, as these may indicate a more serious illness.\n\nPatients with advanced liver problems should take the medicine under close medical supervision.\n\nSafety during pregnancy and breastfeeding has not been fully established—consult a doctor before use.\n\nComplete the prescribed course, even if symptoms improve early, to avoid recurrence.\n\nNot meant for viral infections like flu or the common cold.\n\nDrug Interactions\n\nThough rifaximin is minimally absorbed, some drug interactions may occur:\n\nWarfarin or other anticoagulants: May require monitoring of blood clotting.\n\nOther antibiotics: Combining with multiple antibiotics may reduce effectiveness.\n\nCyclosporine and similar drugs: May increase rifaximin levels in the body.\n\nOral contraceptives: Effectiveness may be lowered; consider additional contraception.\n\nAlways share your full list of medications, supplements, or herbal products with your doctor before starting RIFAXEMANIA 400.\n\nConclusion\n\nRIFAXEMANIA 400 (Rifaximin 400 mg) is a trusted and effective choice for managing gastrointestinal conditions like traveler’s diarrhea, IBS-D, hepatic encephalopathy, and bacterial overgrowth syndromes. Its unique property of acting directly in the intestines ensures high effectiveness with fewer systemic side effects.\n\nFor best results, patients should use RIFAXEMANIA 400 only under medical guidance, follow the recommended dosage, and complete the prescribed course.",
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"name": "FLUTICATONE PROP NASAL SPRAY",
"description": "Fluticasone Nasal Spray IP is a widely prescribed medication for managing nasal allergies, sneezing, runny nose, and nasal congestion. Marketed under the trusted brand name FLUTICATONE PROP NASAL SPRAY, it provides fast and effective relief from seasonal and perennial allergic rhinitis. Patients suffering from chronic nasal blockage, sinus discomfort, or persistent sneezing often find fluticasone nasal spray as one of the most reliable treatments. With its targeted action, it works directly in the nasal passages to reduce inflammation, making breathing easier and improving overall comfort.\n\nWhat is Fluticasone Nasal Spray IP?\n\nFluticasone belongs to the class of corticosteroids, which are powerful anti-inflammatory agents. When delivered as a nasal spray, it works locally in the nose to reduce swelling, mucus production, and irritation caused by allergens such as dust, pollen, or pet dander.\n\nUnlike oral medications, fluticasone nasal spray acts directly at the site of the problem, providing long-lasting relief with fewer systemic side effects. FLUTICATONE PROP NASAL SPRAY is therefore a safe, convenient, and effective option for patients struggling with allergic symptoms.\n\nUses of Fluticasone Nasal Spray\n\nThe uses of fluticasone nasal spray cover a wide range of allergic and nasal conditions, such as:\n\nRelief from seasonal allergies (hay fever).\n\nControl of perennial allergic rhinitis (year-round symptoms).\n\nReduction of nasal congestion and swelling.\n\nManagement of sneezing, itching, and runny nose.\n\nSupporting patients with sinus discomfort due to allergy-related inflammation.\n\nFor many patients, using FLUTICATONE PROP NASAL SPRAY daily provides consistent relief and helps restore normal breathing.\n\nDosage and How to Use\n\nThe usual recommended dose for adults is one to two sprays in each nostril once daily, or as directed by a doctor.\n\nChildren’s dosage should always be determined by a healthcare provider.\n\nShake the spray bottle gently before each use.\n\nClear nasal passages before spraying for best absorption.\n\nUse consistently for maximum benefit, as the full effect may take a few days.\n\nSide Effects of Fluticasone Nasal Spray\n\nMost patients tolerate fluticasone nasal spray well. However, some may experience mild side effects, including:\n\nDryness or irritation in the nose or throat.\n\nNosebleeds.\n\nMild headache.\n\nSneezing immediately after use.\n\nRarely, changes in sense of taste or smell.\n\nSevere side effects are uncommon, but if patients experience persistent nosebleeds, vision changes, or difficulty breathing, they should consult a doctor immediately.\n\nPrecautions Before Using\n\nBefore starting FLUTICATONE PROP NASAL SPRAY, patients should take the following precautions:\n\nInform the doctor if you have recent nasal surgery or injury.\n\nUse with caution if you have asthma, tuberculosis, or immune system problems.\n\nPregnant and breastfeeding women should use only under medical advice.\n\nAvoid exceeding the recommended dose to prevent unwanted side effects.\n\nRegular monitoring may be advised for patients on long-term use.\n\nDrug Interactions\n\nFluticasone nasal spray may interact with other medicines. Patients should inform their doctor if they are taking:\n\nStrong antifungal medicines (like ketoconazole).\n\nCertain HIV medications (ritonavir, cobicistat).\n\nOther steroid medications.\n\nProper medical guidance ensures safe and effective use without harmful interactions.\n\nWhy Choose Steris Healthcare?\n\nWhen it comes to safe and effective medicines, Steris Healthcare is a name patients and doctors trust. By choosing FLUTICATONE PROP NASAL SPRAY, you get:\n\nA high-quality formulation designed for fast allergy relief.\n\nStrict quality control standards to ensure safety and effectiveness.\n\nA product trusted by healthcare professionals across India.\n\nA patient-centric approach where comfort and results are prioritized.\n\nSteris Healthcare continues to provide advanced solutions in healthcare, making treatments more reliable and accessible for patients.",
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"description": "MAGRAL 160 is a pharmaceutical medication containing megestrol acetate 160 mg, a synthetic progestin known for its potent antineoplastic and appetite-stimulating properties. This drug is primarily prescribed to manage significant health challenges such as unexplained weight loss, anorexia, and cachexia, especially in patients suffering from chronic conditions like cancer or AIDS. Additionally, megestrol acetate functions as a hormone therapy agent employed in the treatment of certain hormone-sensitive malignancies. Its dual action both supports tumor management and improves patients' nutritional status by stimulating appetite and promoting weight gain, thereby enhancing overall quality of life. The drug is regarded as a crucial option in oncology and palliative care for managing complex conditions related to hormone-dependent cancers and severe wasting syndromes.\n\nWhat is MAGRAL 160?\nMAGRAL 160 is an oral medication formulated with megestrol acetate 160 mg, a synthetic progestin hormone derivative. It works primarily by modulating hormone receptors and altering hormone levels that influence the growth of hormone-responsive tumors such as breast and endometrial cancers. Apart from its antineoplastic action, it stimulates appetite by acting on the hypothalamic centers responsible for hunger, helping patients suffering from severe weight loss regain a healthy appetite and weight.\n\nUses of MAGRAL 160\n\nTo treat hormone-dependent cancers, specifically advanced breast cancer and endometrial cancer.\n\nTo stimulate appetite and promote weight gain in patients experiencing anorexia, cachexia, or unexplained severe weight loss related to chronic illnesses like cancer or AIDS.\n\nTo manage wasting syndromes that lead to malnutrition and significant weight loss.\n\nTo serve as an antineoplastic agent in hormone-sensitive malignancies.\n\nIn short, MAGRAL 160 is primarily used to treat anorexia and cachexia or serious unexplained weight loss and is also used as an antineoplastic agent to treat certain types of malignancy.\n\nSide Effects of MAGRAL 160\n\nWeight gain (often desirable but can be excessive)\n\nFluid retention and edema (swelling)\n\nNausea and vomiting\n\nDiarrhea or constipation\n\nVaginal bleeding or spotting in women\n\nFatigue, weakness, and insomnia\n\nHeadache and dizziness\n\nIncreased risk of blood clots (deep vein thrombosis or pulmonary embolism)\n\nHormonal imbalances, such as decreased sex hormone levels, which can lead to sexual dysfunction or bone density loss\n\nAllergic reactions including rash or itching\n\nPatients should report severe or unusual symptoms, especially signs of blood clots such as limb swelling, chest pain, or sudden shortness of breath, immediately to their healthcare provider.\n\nPrecautions before Using MAGRAL 160\n\nInform your doctor if you are pregnant, breastfeeding, or planning to conceive as MAGRAL 160 is contraindicated in pregnancy.\n\nDisclose any history of blood clots, cardiovascular diseases, liver or kidney impairment.\n\nPatients with diabetes should monitor blood sugar closely as megestrol acetate may cause hyperglycemia.\n\nAvoid sudden discontinuation without medical advice to prevent potential hormonal withdrawal effects.\n\nRegular monitoring is required, including hormone levels and blood tests, to assess efficacy and safety during treatment.\n\nUse cautiously in patients at risk for deep vein thrombosis or pulmonary embolism due to increased clotting risks.\n\nDrug Interactions: What Drugs Interact with MAGRAL 160?\n\nCYP3A4 enzyme inducers (e.g., rifampin, phenytoin) may reduce the effectiveness of megestrol acetate by increasing its metabolism.\n\nConcurrent use with blood thinners (anticoagulants) requires careful monitoring as MAGRAL 160 might influence clotting parameters.\n\nCombining with drugs that affect hormonal pathways, such as other hormonal therapies or corticosteroids, may alter treatment outcomes.\n\nInteractions with diabetes medications might necessitate dose adjustment due to potential effects on blood sugar control.\n\nCareful medical supervision is necessary when used with immunosuppressants or other chemotherapy agents to avoid additive side effects or altered drug levels.\n\nConclusion\nMAGRAL 160, containing megestrol acetate 160 mg, is a clinically validated medication widely used to manage complex conditions such as hormone-dependent cancers as well as severe weight loss due to anorexia and cachexia. Its unique ability to act both as an antineoplastic agent and an appetite stimulant makes it invaluable in improving patient outcomes, nutritional status, and overall quality of life. Patients prescribed MAGRAL 160 should adhere strictly to their healthcare provider’s instructions and report any adverse effects promptly. This medication should always be used under medical supervision to ensure optimal benefits and minimize risks.",
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