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"description": "TELAVINCE 300 is a high-quality antiviral medication containing Tenofovir Disoproxil Fumarate 300 mg, specifically formulated for the effective management of HIV-1 infection and chronic Hepatitis B in adults and adolescents. Manufactured under strict pharmaceutical standards, TELAVINCE 300 offers consistent, potent, and clinically proven antiviral action, helping to suppress viral replication and improve immune function.\n\nTenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor (NtRTI). It works by interfering with the enzyme reverse transcriptase, which is essential for viral replication in HIV and Hepatitis B viruses. By inhibiting this enzyme, TELAVINCE 300 reduces the amount of virus in the body, helping to prevent further immune system damage and liver complications.\n\n \nKey Indications:\n \n\nTELAVINCE 300 is indicated for:\n\nHIV-1 Infection: In combination with other antiretroviral agents for the treatment of HIV-1 in adults and adolescents (aged 12 years and older, weighing at least 35 kg).\n\nChronic Hepatitis B: For the treatment of chronic hepatitis B virus infection in adults and adolescents with compensated liver disease and evidence of active viral replication.\n\n \nMechanism of Action:\n \nTenofovir Disoproxil Fumarate is a prodrug of tenofovir, which, once absorbed and metabolized in the body, is converted into tenofovir diphosphate, the active form. Tenofovir diphosphate acts as a competitive inhibitor of reverse transcriptase, incorporating itself into the viral DNA chain and causing premature chain termination. This process disrupts the life cycle of the virus, significantly reducing its ability to multiply and spread.\n\n \nDosage and Administration:\n \n\nRecommended Dose for Adults and Adolescents (≥12 years, ≥35 kg): One tablet (300 mg) once daily, preferably with food.\n\nFor HIV Treatment: Administer in combination with other antiretroviral medications as per the treatment regimen.\n\nFor Chronic Hepatitis B: Monotherapy or as part of combination therapy, depending on patient condition and physician's assessment.\n\nDosage adjustments may be required in patients with renal impairment. Close monitoring is recommended for patients with existing kidney disease.\n\n \nKey Benefits of TELAVINCE 300:\n \n\nPotent Antiviral Action: Rapid and sustained suppression of HIV and HBV replication.\nOnce-Daily Dosing: Improves patient compliance and treatment adherence.\n\nBacked by Clinical Research: Proven efficacy in managing viral load and improving immune markers (CD4 count).\n\nTrusted Quality: Manufactured under GMP-certified facilities with stringent quality control processes.\n\nPart of First-Line Therapy: Recommended in various national and international treatment guidelines for HIV and Hepatitis B.\n\n \nSafety and Precautions:\n \n\nRenal Monitoring: Tenofovir may affect kidney function. Routine renal function tests are recommended before and during treatment.\n\nBone Mineral Density: Long-term use may reduce bone mineral density. Consider monitoring in patients at risk of osteopenia or osteoporosis.\n\nHepatic Flare: Discontinuation of therapy in hepatitis B patients may result in severe acute exacerbations. Liver function should be closely monitored post-treatment.\n\nLactic Acidosis and Hepatomegaly: Rare but serious side effects. Patients presenting symptoms such as abdominal pain, fatigue, or difficulty breathing should seek immediate medical attention.\n\n \n\nPossible Side Effects:\n \n\nMost patients tolerate TELAVINCE 300 well. However, some may experience:\n\nNausea\n\nDiarrhea\n\nHeadache\n\nFatigue\n\nRash\n\nDizziness\n\nDecreased bone mineral density\n\nRenal impairment (in rare cases)\n\nIf any side effects persist or worsen, consult a healthcare professional immediately.\n\n \nStorage Instructions:\n \n\nStore in a cool, dry place below 30°C.\n\nProtect from light and moisture.\n\nKeep out of reach of children.\n\n \n\nWhy Choose TELAVINCE 300?\n \n\nTELAVINCE 300 offers a dependable, clinically validated solution for the long-term management of HIV and Hepatitis B. With its once-daily dosing and proven effectiveness, TELAVINCE 300 is an ideal choice for patients and healthcare providers looking for quality, safety, and therapeutic reliability. It is manufactured by a trusted name in healthcare, ensuring every tablet meets global pharmaceutical standards.\n\n \nDisclaimer:\n \n\nThis product description is for informational purposes only and is not a substitute for professional medical advice. Always consult your doctor or healthcare provider before starting any medication.",
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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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"description": "CONARIS SB 65 is a powerful antifungal medication specifically formulated to treat a variety of fungal infections. With its active ingredient, Itraconazole (65 mg), this medication is effective against both superficial and systemic fungal infections, providing comprehensive relief for individuals suffering from these conditions. Whether you're dealing with skin infections, nail infections, or more severe systemic issues, CONARIS SB 65 is designed to help restore your health and well-being.\n\n \nKey Benefits:\n \n\nBroad-Spectrum Antifungal Activity: CONARIS SB 65 effectively targets various fungi, including those responsible for conditions like athlete's foot, ringworm, and nail fungus.\n\nFast-Acting Formula: The formulation is designed to provide rapid relief from symptoms, helping to alleviate itching, redness, and discomfort associated with fungal infections.\n\nSystemic Treatment: In addition to treating superficial infections, Itraconazole can penetrate deep tissues, making CONARIS SB 65 suitable for systemic fungal infections.\n\nWell-Tolerated: Many patients tolerate CONARIS SB 65 well, with a low incidence of side effects, allowing for effective treatment without significant discomfort.\n\nConvenient Dosage Form: The formulation is easy to take, making it suitable for patients of all ages who require antifungal treatment.\n\n \nHow Does It Work?\n \n\nItraconazole works by inhibiting an enzyme called lanosterol 14-alpha demethylase, which is crucial for the conversion of lanosterol to ergosterol in fungal cell membranes. Ergosterol is essential for maintaining the integrity and fluidity of fungal cell membranes. By disrupting ergosterol synthesis, Itraconazole compromises the fungal cell membrane, leading to cell death and effectively clearing the infection. This mechanism makes CONARIS SB 65 an effective choice for treating both superficial and systemic fungal infections.\n\n \nDirections for Use:\n \n\nDosage: The recommended dosage of CONARIS SB 65 is one capsule (65 mg of Itraconazole) taken orally, once a day, or as directed by a healthcare professional.\n\nAdministration: It is advisable to take the capsule with a full glass of water, preferably after a meal to enhance absorption.\n\nDuration of Treatment: Treatment duration may vary depending on the type and severity of the infection. It is essential to complete the full course as prescribed, even if symptoms improve, to prevent recurrence.\n\nConsult Your Doctor: Always consult a healthcare professional for personalized dosing instructions based on your medical history and specific condition.\n\n \nSide Effects:\n \n\nWhile CONARIS SB 65 is generally well-tolerated, some individuals may experience side effects. Common side effects include:\n\nNausea: Mild stomach upset or nausea may occur, particularly when the medication is taken on an empty stomach.\n\nHeadache: Some users may report mild headaches during treatment.\n\nDizziness: Occasionally, patients may experience dizziness or lightheadedness.\n\nLiver Function: In rare cases, Itraconazole may affect liver function. Regular monitoring through blood tests may be necessary, especially in patients with pre-existing liver conditions.",
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"description": "Fabrical D3 6L \nCholecalciferol Vitamin D3 (600,000IU) Injection\nIntroduction\nFabrical D3 6L is a potent vitamin D3 (Cholecalciferol) injection, providing 600,000 IU per dose. This high-dose formulation is designed to address severe vitamin D deficiency and support overall bone health. It is particularly useful for individuals who cannot achieve adequate vitamin D levels through oral supplements or dietary intake.\n\nComposition\n\nCholecalciferol (Vitamin D3) 600,000 IU: A fat-soluble vitamin essential for the absorption of calcium and phosphorus in the body, playing a crucial role in maintaining bone health and calcium homeostasis.\nMechanism of Action\nCholecalciferol (Vitamin D3) undergoes hydroxylation in the liver to form 25-hydroxyvitamin D, which is then converted in the kidneys to its active form, calcitriol (1,25-dihydroxyvitamin D). Calcitriol enhances the intestinal absorption of calcium and phosphorus, supports bone mineralization, and modulates immune function.\n\nIndications\nFabrical D3 6L is indicated for:\n\nSevere Vitamin D Deficiency: To rapidly correct low levels of vitamin D.\nOsteoporosis: To support bone health and prevent fractures.\nHypocalcemia: To assist in the treatment of low calcium levels due to hypoparathyroidism or other conditions.\nRickets and Osteomalacia: To treat and prevent bone disorders caused by vitamin D deficiency.\nMalabsorption Syndromes: In conditions like Crohn’s disease, celiac disease, and bariatric surgery where vitamin D absorption is impaired.\nDosage and Administration\n\nAdult Dosage: Typically, a single dose of 600,000 IU is administered intramuscularly. The frequency of administration depends on the severity of deficiency and the patient's response to treatment.\nAdministration: The injection should be administered by a healthcare professional. It is important to monitor serum calcium and vitamin D levels during treatment to avoid hypercalcemia and vitamin D toxicity.\nSide Effects\nCommon side effects may include:\n\nPain at the injection site\nMild gastrointestinal disturbances (nausea, vomiting)\nFatigue\nHeadache\nMore severe side effects can include:\n\nHypercalcemia (high calcium levels), which may present with symptoms like weakness, confusion, increased thirst and urination, and abdominal pain.\nHypervitaminosis D, resulting from excessive vitamin D intake.\nPrecautions\n\nHypercalcemia: Patients should be monitored for signs of elevated calcium levels.\nKidney Function: Use with caution in patients with renal impairment as vitamin D metabolism and excretion may be affected.\nPregnancy and Lactation: High doses of vitamin D should be used under medical supervision during pregnancy and lactation.\nDrug Interactions\n\nThiazide Diuretics: May increase the risk of hypercalcemia when used with vitamin D.\nAntiepileptic Drugs: Some antiepileptics may decrease vitamin D levels.\nGlucocorticoids: May reduce the effectiveness of vitamin D by impairing calcium absorption.\nConclusion\nFabrical D3 6L, with its high-dose Cholecalciferol (600,000 IU), provides an effective treatment for severe vitamin D deficiency and related conditions. Its ability to rapidly restore adequate vitamin D levels makes it an essential therapeutic option for individuals with significant deficiencies or those who have difficulty absorbing vitamin D. As with any high-dose supplementation, it is critical to use this medication under the guidance of a healthcare professional to ensure safety and efficacy, with regular monitoring to prevent potential side effects such as hypercalcemia and vitamin D toxicity.\nFor further information: \nEMAIL: info@sterispharma.com / contact@sterispharma.com \n CALL/WHATSAPP: 7877551268, 7849827488 \n Order NOW\n",
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"description": "SLIM BOOST CTSTAT 60 \nCetilistat (60mg)\nIntroduction\nSLIM BOOST CTSTAT 60 is a weight management medication containing Cetilistat (60mg), an oral lipase inhibitor designed to assist in weight reduction in individuals with obesity. By inhibiting the digestion and absorption of dietary fats, Cetilistat helps reduce caloric intake, promoting weight loss when used in conjunction with a reduced-calorie diet and appropriate physical activity.\n\nComposition\n\nCetilistat (60mg): A novel lipase inhibitor that targets gastrointestinal lipases, crucial enzymes for fat digestion.\nMechanism of Action\nCetilistat works by inhibiting pancreatic lipase, an enzyme necessary for the breakdown of triglycerides in the intestine. When lipase activity is blocked, triglycerides from the diet are not hydrolyzed into absorbable free fatty acids and monoglycerides. Instead, undigested triglycerides are excreted, reducing the overall caloric intake and aiding weight loss.\n\nIndications\nSLIM BOOST CTSTAT 60 is indicated for:\n\nObesity Management: To assist in weight reduction for obese patients with a body mass index (BMI) of 30 or higher.\nWeight Loss for Overweight Patients: With a BMI of 27 or higher who also have risk factors such as diabetes, hypertension, or dyslipidemia.\nDosage and Administration\n\nRecommended Dosage: The typical dosage is 60mg taken three times daily with or up to one hour after meals containing fat.\nAdministration: It should be taken with water and in conjunction with a nutritionally balanced, reduced-calorie diet that contains approximately 30% of calories from fat. Adherence to dietary recommendations is crucial to minimize gastrointestinal side effects and enhance weight loss efficacy.\nSide Effects\nCommon side effects may include:\n\nGastrointestinal issues such as oily spotting, flatulence with discharge, fecal urgency, fatty/oily stool, increased defecation, and fecal incontinence.\nAbdominal pain or discomfort\nDiarrhea\nNausea\nThese side effects are typically related to the drug's mechanism of action and can often be managed by adhering to the recommended dietary guidelines.\n\nPrecautions\n\nChronic Malabsorption Syndrome: Cetilistat should not be used in patients with chronic malabsorption syndrome.\nCholestasis: It is contraindicated in patients with cholestasis (a condition where bile flow from the liver is blocked).\nFat-Soluble Vitamins: Cetilistat may impair the absorption of fat-soluble vitamins (A, D, E, and K). It is recommended to take a multivitamin supplement at least 2 hours before or after taking Cetilistat.\nDrug Interactions\n\nCyclosporine: Concomitant use may decrease cyclosporine levels; it should be administered 2 hours before or after Cetilistat.\nWarfarin: Close monitoring of anticoagulant effects is necessary when co-administered, as Cetilistat may affect vitamin K absorption.\nFat-Soluble Vitamins and Supplements: Ensure adequate intake of vitamins A, D, E, and K by taking a multivitamin supplement.\nConclusion\nSLIM BOOST CTSTAT 60, with its active ingredient Cetilistat, offers an effective solution for weight management in obese and overweight individuals. By inhibiting fat absorption, it helps reduce caloric intake, contributing to weight loss when combined with a balanced, reduced-calorie diet and regular physical activity. It is essential to use this medication under the guidance of a healthcare professional to ensure safe and effective weight loss while minimizing potential side effects and nutrient deficiencies. Always adhere to dietary recommendations and monitor for any adverse effects to achieve the best outcomes with SLIM BOOST CTSTAT 60.\nFor further information: \nEMAIL: info@sterispharma.com / contact@sterispharma.com \n CALL/WHATSAPP: 7877551268, 7849827488 \n Order NOW\n",
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"description": "CEFEXOTIME DICLOXA \nCefixime (200mg), Dicloxacillin ER (500mg)\nIntroduction\nCEFEXOTIME DICLOXA is a potent antibiotic combination therapy that includes Cefixime (200mg) and Dicloxacillin ER (500mg). This medication is designed to combat a broad spectrum of bacterial infections, leveraging the synergistic effects of both antibiotics to enhance efficacy.\n\nComposition\n\nCefixime (200mg): A third-generation cephalosporin antibiotic known for its broad-spectrum activity against Gram-positive and Gram-negative bacteria. It works by inhibiting bacterial cell wall synthesis, leading to cell lysis and death.\nDicloxacillin ER (500mg): An extended-release form of dicloxacillin, a penicillinase-resistant penicillin. It is particularly effective against penicillinase-producing staphylococci and works by inhibiting cell wall synthesis.\nMechanism of Action\n\nCefixime: It binds to penicillin-binding proteins (PBPs) within the bacterial cell wall, disrupting the cross-linking of peptidoglycan chains necessary for cell wall strength and rigidity, resulting in cell lysis.\nDicloxacillin: It similarly binds to PBPs, preventing the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, which is crucial for maintaining cell wall integrity.\nIndications\nCEFEXOTIME DICLOXA is indicated for the treatment of various bacterial infections, including:\n\nRespiratory tract infections (e.g., bronchitis, pneumonia)\nUrinary tract infections (UTIs)\nSkin and soft tissue infections\nOtitis media\nSinusitis\nBone and joint infections\nDosage and Administration\nThe typical dosage for adults is one tablet taken twice daily, with or without food. The duration of treatment depends on the severity and type of infection, usually ranging from 7 to 14 days. It is essential to complete the full course of therapy to prevent the development of antibiotic-resistant bacteria.\n\nSide Effects\nCommon side effects may include:\n\nGastrointestinal disturbances (nausea, vomiting, diarrhea)\nAllergic reactions (rash, itching, anaphylaxis in severe cases)\nPseudomembranous colitis\nHepatic dysfunction (elevated liver enzymes)\nHematologic effects (eosinophilia, neutropenia)\nRenal toxicity (in rare cases)\nPrecautions\n\nAllergy: Patients with a history of allergic reactions to cephalosporins, penicillins, or any other beta-lactam antibiotics should use this medication with caution.\nRenal Impairment: Dose adjustment may be necessary for patients with renal dysfunction.\nPregnancy and Lactation: The safety of this medication in pregnant and breastfeeding women has not been fully established. It should only be used if clearly needed and prescribed by a healthcare provider.\nDrug Interactions\n\nProbenecid: May increase blood levels of Cefixime.\nWarfarin: Concomitant use can enhance anticoagulant effects, increasing the risk of bleeding.\nMethotrexate: Cefixime may reduce renal clearance of methotrexate, increasing its toxicity.\nOral Contraceptives: Antibiotics may reduce the efficacy of oral contraceptives, suggesting the need for additional contraceptive measures.\nConclusion\nCEFEXOTIME DICLOXA, with its combination of Cefixime and Dicloxacillin, provides a robust treatment option for various bacterial infections. Its broad-spectrum efficacy, combined with the extended-release formulation, ensures a potent and convenient antibiotic therapy. As with all antibiotics, it is crucial to use this medication as prescribed and complete the full course to prevent the emergence of resistant bacteria and achieve optimal therapeutic outcomes. Always consult with a healthcare professional before starting any new medication.\nFor further information: \nEMAIL: info@sterispharma.com / contact@sterispharma.com \n CALL/WHATSAPP: 7877551268, 7849827488 \n Order NOW\n\n",
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