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"name": "Sucralfate Tinidazole and Povidone Iodine Ointment",
"description": "Sucralfate, Tinidazole, and Povidone Iodine Ointment is an advanced multi-action topical formulation designed to promote rapid wound healing, prevent infection, and enhance tissue regeneration. This combination therapy is widely used in dermatology, surgery, gynecology, and general wound management due to its broad-spectrum antimicrobial activity and strong healing-supportive characteristics. Each active ingredient plays a unique and complementary role, making this ointment highly effective in managing acute and chronic wounds, ulcers, burns, and infected skin lesions.\n\nAt the core of the formulation, Sucralfate acts as a protective barrier over damaged tissues. It binds to proteins at the wound site, forming a protective layer that shields the area from external irritants and bacterial contamination. This barrier not only promotes faster healing but also enhances tissue regeneration by stimulating growth factors and improving blood supply to the injured surface.\n\nTinidazole, a potent antiprotozoal and antibacterial agent, further strengthens the formulation by targeting anaerobic bacteria and protozoa commonly responsible for wound infections. Its inclusion helps reduce microbial load, prevent secondary infections, and create an ideal environment for clean and complication-free healing.\n\nFinally, Povidone Iodine, a trusted antiseptic, provides broad-spectrum germicidal action against bacteria, fungi, viruses, and spores. It effectively reduces wound contamination, minimizes odor, and prevents colonization of harmful microorganisms. Together, these ingredients create a synergistic effect that supports comprehensive wound management.\n\nProduct Uses\n\nThis ointment is commonly prescribed for:\n\nDiabetic foot ulcers\nHelps control infection while promoting tissue repair in complex ulcers.\n\nPressure sores and bedsores\nProvides protection and healing acceleration for chronic wounds.\n\nBurns (first and second degree)\nPrevents infection and reduces healing time.\n\nMinor cuts, abrasions, and skin injuries\nIdeal for daily wound care and minor trauma.\n\nPost-surgical wounds\nHelps prevent infection and supports clean healing.\n\nInfected wounds or skin lesions\nEffective against wounds contaminated with anaerobic bacteria or other pathogens.\n\nGynecological wound care\nMay be used for episiotomy care or infected perineal wounds under medical supervision.\n\nKey Benefits\n1. Broad-Spectrum Antimicrobial Protection\n\nThe combination of Tinidazole and Povidone Iodine provides robust defense against bacteria, fungi, protozoa, and viruses, significantly reducing infection risk.\n\n2. Accelerated Healing and Tissue Regeneration\n\nSucralfate forms a protective layer that maintains moisture balance, promotes granulation tissue formation, and speeds up recovery.\n\n3. Reduced Inflammation and Discomfort\n\nBy minimizing bacterial load and shielding damaged tissues, the ointment helps reduce redness, swelling, and pain.\n\n4. Ideal for Complex and Chronic Wounds\n\nEspecially effective for ulcers, burns, and infected wounds where multiple layers of treatment are needed.\n\n5. Odor Control in Infected Wounds\n\nPovidone Iodine’s antimicrobial action helps reduce foul odor associated with infected or necrotic tissue.\n\n6. Safe and Well-Tolerated\n\nWhen used as directed, this combination ointment is suitable for a wide range of patients, including those with difficult-to-heal wounds.\n\nPossible Side Effects\n\nWhile generally safe, some individuals may experience:\n\nMild skin irritation or redness\n\nBurning or stinging sensation at the application site\n\nDryness or peeling of skin\n\nAllergic reactions (rare), such as rash or itching\n\nTemporary discoloration of skin due to Povidone Iodine\n\nSensitivity reactions in iodine-allergic individuals\n\nPatients with thyroid disorders, severe burns, or extensive wounds should use Povidone Iodine-containing products only under medical guidance.\n\nConclusion\n\nSucralfate, Tinidazole, and Povidone Iodine Ointment stands out as a highly effective and versatile wound-care solution. Its triple-action design—protective, antimicrobial, and regenerative—makes it ideal for managing complicated wounds, preventing infection, and supporting faster, cleaner healing. Whether used for chronic ulcers, burns, surgical wounds, or everyday skin injuries, this formulation offers a reliable and scientifically supported approach to comprehensive wound management. With its blend of protection, infection control, and healing enhancement, it remains a valuable tool for both healthcare professionals and patients seeking superior wound-care outcomes.",
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"name": "Gabapentin and Lidocaine Hydrochloride Gel ",
"description": "Gabapentin and Lidocaine Hydrochloride is a specialized combination therapy primarily used to manage neuropathic pain—pain resulting from nerve damage, irritation, or dysfunction. This blend unites two highly effective agents: gabapentin, an anticonvulsant widely used for nerve-related pain, and lidocaine hydrochloride, a fast-acting local anesthetic that numbs nerve signals in targeted areas. Together, they deliver both systemic and localized pain relief, making the product ideal for patients seeking comprehensive control of chronic or acute neuropathic symptoms.\n\nThis combination may appear in different formulations, such as topical creams, patches, or oral gabapentin used alongside lidocaine topical therapy. The synergistic action makes it especially beneficial for individuals who do not achieve adequate relief from a single medication. By addressing pain through two different mechanisms—central nerve modulation (gabapentin) and peripheral nerve numbing (lidocaine)—this combination delivers a balanced approach to pain management with reduced need for stronger systemic medications.\n\nGabapentin works by calming overactive nerve signals in the central nervous system. It binds to calcium channels in the brain and spinal cord, reducing the abnormal firing responsible for neuropathic discomfort. Lidocaine, on the other hand, blocks sodium channels in peripheral nerves, preventing pain signals from traveling to the brain. Together, they create a powerful relief profile suitable for various nerve-related conditions.\n\nUses of Gabapentin and Lidocaine Hydrochloride\n\nThis combination is commonly recommended for patients dealing with complex nerve pain. Typical uses include:\n\n1. Neuropathic Pain\n\nIdeal for conditions such as:\n\nPeripheral neuropathy\n\nDiabetic neuropathy\n\nChemotherapy-induced neuropathy\n\nPost-surgical nerve pain\n\n2. Postherpetic Neuralgia (PHN)\n\nPatients recovering from shingles often experience burning, sharp, or stabbing nerve pain. Lidocaine patches offer localized relief, while gabapentin reduces the intensity of nerve signaling.\n\n3. Sciatica and Radicular Pain\n\nWhen pain radiates from the spine to the legs or arms due to nerve compression, this combination offers both deep and surface-level relief.\n\n4. Fibromyalgia\n\nGabapentin may reduce widespread nerve sensitivity, while lidocaine provides targeted relief in high-pain areas.\n\n5. Localized Musculoskeletal or Joint Pain With Nerve Involvement\n\nLidocaine can temporarily numb sensitive regions, while gabapentin addresses chronic nerve irritation.\n\nKey Benefits\n1. Dual-Action Pain Relief\n\nGabapentin works internally to stabilize nerve activity, while lidocaine provides immediate external numbing. This dual approach addresses pain from both ends.\n\n2. Reduced Need for Strong Systemic Painkillers\n\nMany patients experience significant relief without relying on opioids or sedatives.\n\n3. Rapid Onset from Lidocaine\n\nTopical lidocaine begins relieving pain within minutes by blocking peripheral nerve transmission.\n\n4. Long-Term Nerve Modulation from Gabapentin\n\nGabapentin’s central action builds gradually, offering sustained reduction of chronic nerve pain with consistent use.\n\n5. Versatile Application\n\nThe combination can be tailored to individual needs—oral gabapentin for long-term control and lidocaine patches or gel for targeted, immediate comfort.\n\n6. Improved Daily Function\n\nBy reducing constant nerve irritation, patients often regain mobility, sleep quality, and overall comfort.\n\nPossible Side Effects\nGabapentin Side Effects\n\nCommon:\n\nDizziness\n\nDrowsiness\n\nFatigue\n\nMild swelling in the legs\n\nCoordination problems\n\nLess common but important:\n\nMood changes\n\nBlurred vision\n\nDifficulty concentrating\n\nLidocaine Hydrochloride Side Effects\n\nCommon:\n\nSkin redness or irritation\n\nTemporary numbness\n\nMild burning or itching at application site\n\nRare but serious:\n\nAllergic reactions\n\nIrregular heartbeat (with excessive use)\n\nSystemic toxicity if large amounts are absorbed\n\nPatients should follow dosing instructions carefully and avoid applying lidocaine to broken skin unless instructed.\n\nConclusion\n\nThe combination of Gabapentin and Lidocaine Hydrochloride represents a powerful and effective solution for individuals struggling with neuropathic pain. By blending the internal nerve-calming effects of gabapentin with the fast-acting local numbing properties of lidocaine, this therapy covers multiple pain pathways simultaneously. It offers significant relief for conditions such as diabetic neuropathy, shingles-related pain, nerve compression syndromes, and chronic nerve-related disorders.",
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"name": "Ginkgo Biloba Extract and Piracetam Tablets ",
"description": "Ginkgo Biloba Extract & Piracetam Tablets is a scientifically formulated neuroprotective and cognitive-enhancing combination designed to support memory, concentration, and brain function. It combines two powerful agents — Ginkgo Biloba, a time-tested herbal extract known for its circulation-enhancing and antioxidant properties, and Piracetam, a well-researched nootropic compound that enhances neuronal communication and cognitive performance.\n\nTogether, these two active ingredients work synergistically to improve cerebral blood flow, increase oxygen and nutrient delivery to the brain, and enhance mental clarity and alertness. The formulation is widely prescribed as a neurotonic and cognitive enhancer for individuals experiencing memory decline, age-related cognitive impairment, or neurological disorders such as dementia, Alzheimer’s disease, and cerebrovascular insufficiency.\n\nComposition\n\nEach film-coated tablet typically contains:\n\nGinkgo Biloba Extract (Standardized to contain 24% Flavone Glycosides & 6% Terpene Lactones) – 40 mg or 60 mg\n\nPiracetam – 800 mg\n\nExcipients – q.s.\n\nThe tablets are designed for oral administration, offering convenient dosage and high bioavailability.\n\nMechanism of Action\n1. Ginkgo Biloba Extract\n\nGinkgo Biloba, derived from the leaves of the ancient Ginkgo tree, is rich in flavonoids and terpenoids, which possess antioxidant, vasodilatory, and neuroprotective properties. It acts through several mechanisms:\n\nImproves microcirculation: Enhances blood flow to brain tissues by reducing blood viscosity and promoting vasodilation.\n\nAntioxidant action: Neutralizes free radicals that cause oxidative stress, protecting neurons from damage.\n\nIncreases neurotransmitter activity: Supports the release and uptake of acetylcholine and serotonin, improving mood and memory.\n\nReduces platelet aggregation: Improves oxygen supply to the brain and minimizes risk of ischemic injury.\n\n2. Piracetam\n\nPiracetam is a nootropic (cognitive enhancer) that improves neuronal efficiency and communication between brain cells.\nIts mechanism includes:\n\nEnhancing neuronal plasticity: Facilitates the transmission of impulses across synapses, improving learning and memory.\n\nImproving cerebral blood flow and metabolism: Enhances glucose utilization and oxygen consumption in the brain.\n\nProtecting neurons: Increases membrane fluidity and stabilizes nerve cells against hypoxic or oxidative damage.\n\nTogether, Ginkgo Biloba and Piracetam complement each other to enhance mental performance, protect neural structures, and improve cerebral function.\n\nUses and Indications\n\nGinkgo Biloba Extract & Piracetam Tablets are indicated for the following conditions:\n\nCognitive Decline and Memory Disorders:\n\nImproves memory, focus, and concentration in elderly individuals or those with mild cognitive impairment.\n\nDementia and Alzheimer’s Disease:\n\nUsed as supportive therapy to slow progression of degenerative brain disorders and enhance daily functioning.\n\nCerebrovascular Insufficiency:\n\nBeneficial in cases of reduced blood flow to the brain, helping alleviate symptoms like dizziness, headache, and mental fatigue.\n\nPost-Stroke Rehabilitation:\n\nEnhances neurological recovery and helps restore cognitive function after ischemic brain injury.\n\nVertigo and Tinnitus (Ringing in the Ears):\n\nImproves inner ear circulation, reducing dizziness and balance-related issues.\n\nLearning Disorders and Attention Deficits:\n\nImproves attention span and memory recall in both adults and children.\n\nNeuroprotective Supplement for Elderly:\n\nMaintains brain vitality and helps prevent age-related cognitive decline.\n\nKey Benefits\n\nEnhances Memory and Concentration:\nThe synergistic effect of Ginkgo Biloba and Piracetam improves synaptic transmission and neuroplasticity, enhancing learning, focus, and recall.\n\nBoosts Cerebral Circulation:\nGinkgo Biloba improves microcirculation within brain tissues, ensuring efficient delivery of oxygen and glucose to neurons.\n\nProtects Against Neurodegeneration:\nThe powerful antioxidant activity of flavonoids and terpenes from Ginkgo Biloba helps neutralize harmful free radicals, delaying age-related brain cell damage.\n\nImproves Cognitive Function in Dementia:\nClinical studies have shown improved cognition, mood, and behavior in patients with Alzheimer’s and vascular dementia with this combination.\n\nRestores Energy and Mental Clarity:\nPiracetam enhances brain metabolism and ATP synthesis, combating mental fatigue and promoting alertness.\n\nAids Recovery After Stroke or Brain Injury:\nEnhances neural regeneration, oxygen utilization, and cerebral function in post-stroke rehabilitation.\n\nReduces Dizziness, Vertigo, and Tinnitus:\nGinkgo’s vasodilatory and anti-platelet properties improve blood flow to the inner ear and brain, alleviating these symptoms.\n\nSafe and Well-Tolerated:\nNon-sedating, non-addictive, and suitable for long-term use under medical supervision.\n\nDosage and Administration\n\nAdults: One tablet two or three times daily, or as directed by a physician.\n\nElderly Patients: Dosage may be adjusted according to tolerance and medical condition.\n\nChildren: Use only if prescribed by a doctor.\n\nTablets should be swallowed whole with water, preferably after meals to avoid gastrointestinal discomfort.\n\nPrecautions and Warnings\n\nMedical Supervision Required: Should only be used under the guidance of a healthcare professional, especially for elderly patients or those on multiple medications.\n\nBleeding Disorders: Ginkgo Biloba may increase bleeding risk; avoid in patients with clotting disorders or those taking anticoagulants.\n\nSurgery: Discontinue use at least two weeks before scheduled surgery to minimize bleeding risk.\n\nEpilepsy: Piracetam may lower the seizure threshold; caution advised in epileptic patients.\n\nPregnancy and Lactation: Safety not well established; use only if prescribed by a doctor.\n\nDriving or Operating Machinery: Some individuals may experience dizziness or drowsiness; caution advised.\n\nPossible Side Effects\n\nWhile generally safe, Ginkgo Biloba Extract & Piracetam Tablets may cause mild, transient side effects in some users. These typically resolve upon dosage adjustment or discontinuation.\n\nCommon Side Effects:\n\nHeadache or mild dizziness\n\nNausea or stomach discomfort\n\nNervousness or restlessness\n\nInsomnia (if taken late in the day)\n\nLess Common Side Effects:\n\nAllergic skin rash or itching\n\nGastrointestinal upset\n\nPalpitations or rapid heartbeat\n\nMild bleeding (nosebleed, bruising) in sensitive individuals\n\nTremors (rare, usually at higher doses)\n\nSeek medical help immediately if severe allergic reactions, confusion, or unusual bleeding occur.\n\nDrug Interactions\n\nAnticoagulants and Antiplatelet Agents (e.g., Warfarin, Aspirin): May increase bleeding risk.\n\nNSAIDs (e.g., Ibuprofen): Combined use may enhance bleeding tendency.\n\nAntiepileptic Medications: Use with caution as Piracetam may affect seizure control.\n\nHerbal Supplements (e.g., Garlic, Ginseng): May potentiate anticoagulant effects.\n\nStorage and Handling\n\nStore below 30°C, protected from moisture and direct sunlight.\n\nKeep out of reach of children.\n\nDo not use tablets past the expiry date or if the blister pack is damaged.\n\nConclusion\n\nGinkgo Biloba Extract & Piracetam Tablets represent a powerful blend of herbal wisdom and modern neuroscience, formulated to promote optimal brain function and long-term cognitive health. By enhancing blood circulation to the brain, protecting neurons from oxidative damage, and improving neurotransmitter activity, this combination supports memory, focus, and mental agility across all age groups.\n\nIdeal for individuals suffering from age-related memory loss, stress-induced mental fatigue, or neurological disorders, this formulation provides comprehensive neuroprotection and cognitive enhancement in a safe, well-tolerated form.",
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"name": "Nicorandil Tablets 5mg",
"description": "Nicorandil Tablets 5 mg is a vasodilatory anti-anginal medication widely prescribed for the management and prevention of angina pectoris (chest pain) associated with coronary artery disease (CAD). Angina results from an imbalance between the heart’s oxygen demand and supply due to restricted blood flow in the coronary arteries. Nicorandil offers a dual mechanism of action — acting both as a nitrate-like vasodilator and a potassium channel opener, making it unique among anti-anginal agents.\n\nBy improving oxygen delivery to the myocardium and reducing cardiac workload, Nicorandil 5 mg Tablets provide effective relief from anginal pain and reduce the frequency and severity of ischemic episodes. It is also beneficial in preventing future attacks, improving exercise tolerance, and enhancing the overall quality of life in patients with chronic stable angina.\n\nComposition\n\nEach tablet contains:\n\nNicorandil IP – 5 mg\n\nExcipients – q.s.\n\nNicorandil tablets are available in film-coated form to ensure stability, easy swallowing, and optimal absorption. They are manufactured in compliance with Good Manufacturing Practices (GMP) standards to ensure safety, purity, and efficacy.\n\nPharmacological Action / Mechanism of Action\n\nNicorandil exhibits a dual mechanism that makes it distinct among anti-anginal drugs:\n\nNitrate-Like Effect:\nNicorandil acts as a nitric oxide (NO) donor. Nitric oxide activates guanylate cyclase, increasing cyclic GMP (cGMP) levels in vascular smooth muscle. This leads to relaxation of blood vessels, particularly veins and large arteries, thereby reducing preload and afterload on the heart. This nitrate-like activity lowers myocardial oxygen demand.\n\nPotassium Channel Opening Effect:\nNicorandil opens ATP-sensitive potassium (KATP) channels in vascular smooth muscle, resulting in arteriolar vasodilation. This increases coronary blood flow and improves oxygen supply to ischemic heart tissues.\n\nTogether, these effects reduce cardiac workload, enhance coronary perfusion, and prevent anginal pain by correcting the oxygen supply-demand mismatch in the heart muscle.\n\nUses and Indications\n\nNicorandil Tablets 5 mg are indicated for the treatment and prevention of angina pectoris in adults, particularly:\n\nChronic Stable Angina:\n\nHelps reduce the frequency and severity of chest pain associated with exertion or emotional stress.\n\nProphylaxis of Angina Attacks:\n\nUsed regularly to prevent anginal episodes, especially in patients with known coronary artery disease.\n\nAdjunct Therapy in Ischemic Heart Disease (IHD):\n\nCan be used alongside beta-blockers, calcium channel blockers, or antiplatelet drugs for enhanced symptom control and long-term protection.\n\nImprovement of Exercise Tolerance:\n\nReduces the likelihood of anginal pain during physical activity, enabling patients to perform daily tasks comfortably.\n\nIn some clinical cases, Nicorandil is also considered for post-myocardial infarction recovery, as it improves coronary perfusion, although this is at the discretion of a cardiologist.\n\nDosage and Administration\n\nRecommended Starting Dose: 5 mg to 10 mg twice daily.\n\nMaintenance Dose: May be increased gradually to 10–20 mg twice daily, depending on clinical response and tolerance.\n\nThe tablets should be swallowed whole with water, preferably at the same times each day.\n\nNicorandil should not be stopped abruptly; dosage tapering is recommended to avoid rebound angina.\n\nAlways follow the dosage instructions provided by the physician.\n\nKey Benefits\n\nDual Mechanism for Comprehensive Relief:\nCombines nitrate-like and potassium channel-opening properties for both arterial and venous dilation, providing superior protection against anginal attacks.\n\nImproves Coronary Blood Flow:\nDilates coronary arteries, increasing oxygen delivery to ischemic myocardial tissues.\n\nReduces Cardiac Workload:\nBy decreasing preload (venous return) and afterload (arterial resistance), Nicorandil minimizes the heart’s oxygen consumption.\n\nRapid Onset of Action:\nNicorandil acts within a short duration, offering quick relief from anginal discomfort.\n\nPrevents Future Angina Episodes:\nRegular use helps maintain steady control of chest pain, improving exercise capacity and quality of life.\n\nCompatible with Other Cardiac Medications:\nCan be safely used alongside antiplatelet agents, beta-blockers, ACE inhibitors, and statins as part of comprehensive cardiac care.\n\nFavorable Safety Profile:\nCompared to nitrates, Nicorandil carries a lower risk of tolerance development, making it suitable for long-term therapy.\n\nEnhances Myocardial Protection:\nNicorandil’s KATP channel activation provides additional cardioprotective effects by improving microvascular blood flow and limiting ischemic damage during stress.\n\nPrecautions and Warnings\n\nAlthough Nicorandil is generally well-tolerated, certain precautions are advised:\n\nHypotension:\nNicorandil may cause a drop in blood pressure due to vasodilation. Caution is advised in patients with hypotension or dehydration.\n\nConcurrent Use with Nitrates:\nShould not be used together with other nitrate medications to avoid severe hypotension.\n\nOral or Gastrointestinal Ulcers:\nRarely, Nicorandil may cause ulcerations in the mouth, intestines, or skin. Treatment should be discontinued if ulceration occurs.\n\nPatients with Low Blood Volume:\nUse cautiously in individuals with hypovolemia or those on diuretics.\n\nDriving and Machinery:\nDizziness or light-headedness may occur; avoid driving until effects are known.\n\nPregnancy and Lactation:\nShould be used only if prescribed by a physician when the potential benefits outweigh the risks.\n\nPossible Side Effects\n\nNicorandil is generally safe but may cause some side effects, particularly at the start of therapy or with higher doses. Common and rare adverse reactions include:\n\nCommon Side Effects:\n\nHeadache (due to vasodilation)\n\nFlushing or warmth sensation\n\nDizziness or light-headedness\n\nNausea or mild stomach upset\n\nFatigue or weakness\n\nLess Common / Rare Side Effects:\n\nHypotension (low blood pressure)\n\nPalpitations or tachycardia\n\nMouth ulcers, anal ulcers, or skin ulceration (uncommon but serious — discontinue if occurs)\n\nRash or allergic reaction\n\nVisual disturbances (rare and usually reversible)\n\nIf any severe reaction or persistent discomfort occurs, medical attention should be sought promptly.\n\nDrug Interactions\n\nAvoid concomitant use with nitrates or phosphodiesterase type-5 inhibitors (e.g., Sildenafil, Tadalafil), as it may cause a dangerous fall in blood pressure.\n\nCaution with antihypertensive drugs or diuretics, which may enhance hypotensive effects.\n\nAlcohol consumption can potentiate dizziness or hypotension and should be limited.\n\nStorage and Handling\n\nStore below 30°C, protected from moisture and direct sunlight.\n\nKeep out of reach of children.\n\nDo not use tablets past the expiry date or if the packaging is damaged.\n\nConclusion\n\nNicorandil Tablets 5 mg offer a modern and effective approach to managing angina pectoris, providing reliable relief through their dual-action mechanism. By combining nitrate-like vasodilation with potassium channel opening, Nicorandil ensures both oxygen supply improvement and reduction of cardiac workload — the cornerstone of angina management.\n\nIt is well-tolerated, fast-acting, and suitable for long-term therapy, making it a preferred choice for patients with chronic stable angina. Regular use under medical supervision helps reduce the frequency of chest pain, improve physical endurance, and enhance the overall quality of life in individuals with coronary artery disease.",
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"name": "Paracetamol Infusion ip",
"description": "Paracetamol Infusion IP is a sterile, non-pyrogenic, and clear solution of Paracetamol (Acetaminophen) formulated for intravenous administration. It is primarily used for the management of pain and fever when oral or rectal routes are not suitable, such as in hospitalized or post-operative patients. Recognized as one of the most widely used analgesic and antipyretic medications, Paracetamol Infusion IP offers rapid onset of action, consistent therapeutic effects, and excellent patient tolerance.\n\nThis formulation ensures precise and controlled delivery of Paracetamol directly into the bloodstream, allowing for faster relief and improved bioavailability compared to oral administration.\n\nComposition\n\nEach 100 mL of Paracetamol Infusion IP typically contains:\n\nParacetamol IP – 1000 mg (1% w/v)\n\nExcipients – as required for stability and isotonicity\n\nWater for Injection – q.s. to 100 mL\n\nThe infusion is usually supplied in ready-to-use glass or plastic bottles or flexible bags, ensuring sterility and ease of use in hospital settings.\n\nMechanism of Action\n\nParacetamol (acetaminophen) exerts its therapeutic effects primarily through central inhibition of prostaglandin synthesis. Unlike nonsteroidal anti-inflammatory drugs (NSAIDs), Paracetamol has minimal peripheral anti-inflammatory activity, making it a safer option for patients with gastrointestinal or platelet-related concerns.\n\nThe drug acts by:\n\nInhibiting the cyclooxygenase (COX) enzymes, particularly COX-3, within the central nervous system, thereby reducing the synthesis of prostaglandins responsible for fever and pain.\n\nModulating the endocannabinoid system and serotonergic pathways, enhancing its analgesic potential.\n\nAs a result, Paracetamol Infusion IP provides effective fever reduction (antipyretic) and pain relief (analgesic) without significant gastrointestinal irritation or bleeding risks.\n\nIndications and Uses\n\nParacetamol Infusion IP is indicated for:\n\nManagement of Fever (Pyrexia):\n\nReduces elevated body temperature in adults and children.\n\nSuitable for patients unable to take oral medication due to nausea, vomiting, or unconsciousness.\n\nRelief of Mild to Moderate Pain:\n\nEffective in conditions like headaches, dental pain, menstrual cramps, and musculoskeletal pain.\n\nCommonly used as part of multimodal pain management after surgical procedures.\n\nPost-Operative and Trauma Pain:\n\nProvides fast, reliable pain relief in surgical recovery and trauma cases where oral medication is not feasible.\n\nAdjunct Therapy:\n\nCan be used alongside opioids to enhance analgesic effect and reduce opioid requirements.\n\nDosage and Administration\n\nAdults and adolescents (>50 kg): 1 g every 6 hours, not exceeding 4 g per day.\n\nAdults and adolescents (<50 kg): Dose adjusted based on body weight, typically 15 mg/kg every 6 hours.\n\nChildren (≥10 kg): 15 mg/kg per dose every 6 hours.\n\nThe infusion should be administered over 15 minutes, using aseptic technique. Paracetamol Infusion should not be mixed with other drugs in the same IV line unless compatibility is established.\n\nKey Benefits\n\nRapid Onset of Action:\nIntravenous administration ensures faster absorption and onset of relief compared to oral or rectal forms.\n\nHigh Bioavailability:\nSince it bypasses gastrointestinal metabolism, almost the entire dose reaches systemic circulation, providing consistent therapeutic effect.\n\nConvenience in Critical Care:\nIdeal for patients who are unconscious, post-surgery, or unable to tolerate oral medications.\n\nSafe and Well-Tolerated:\nHas minimal gastrointestinal side effects and no significant effect on platelets or renal function when used within the recommended dose range.\n\nEffective Multimodal Pain Relief:\nEnhances pain control when combined with opioids, allowing reduced opioid dosage and minimizing associated risks.\n\nStable Formulation:\nThe isotonic and sterile composition ensures patient safety, stability, and reduced risk of contamination.\n\nSuitable for Broad Patient Demographics:\nCan be used in adults, elderly patients, and children under proper medical supervision.\n\nPrecautions and Warnings\n\nWhile Paracetamol Infusion IP is generally safe, the following precautions should be observed:\n\nLiver Impairment:\nUse with caution in patients with hepatic insufficiency, chronic alcoholism, or pre-existing liver disease, as Paracetamol is primarily metabolized in the liver.\n\nRenal Impairment:\nDosage adjustment may be required in severe renal dysfunction.\n\nAvoid Overdose:\nExceeding the recommended dose can lead to severe liver toxicity and, in extreme cases, hepatic failure.\n\nDrug Interactions:\nConcomitant use with other Paracetamol-containing medications increases risk of overdose.\nCaution when used with hepatotoxic drugs or alcohol.\n\nPregnancy and Lactation:\nGenerally considered safe when used under medical supervision, though benefits should outweigh potential risks.\n\nPossible Side Effects\n\nAlthough rare and usually mild, Paracetamol Infusion IP may cause:\n\nAllergic Reactions:\nSkin rash, itching, urticaria, or swelling.\n\nHypotension:\nA transient drop in blood pressure may occur during infusion in some patients.\n\nLiver Toxicity:\nOverdose or prolonged use can lead to hepatocellular injury or elevated liver enzymes.\n\nInjection Site Reactions:\nMild pain, redness, or inflammation at the infusion site.\n\nBlood Disorders (Very Rare):\nThrombocytopenia or leukopenia may occur in extremely rare cases.\n\nIf any severe reaction such as jaundice, persistent vomiting, or allergic swelling occurs, medical attention should be sought immediately.\n\nStorage and Handling\n\nStore below 30°C, protected from light and freezing.\n\nDo not use if the solution appears cloudy or contains particles.\n\nSingle-use only; discard any unused portion after opening.\n\nConclusion\n\nParacetamol Infusion IP stands as a trusted, fast-acting, and safe intravenous formulation of one of the most widely used analgesic and antipyretic agents worldwide. Its ability to deliver rapid and predictable pain and fever relief makes it invaluable in hospitals, emergency care, and post-surgical settings.\n\nWith its favorable safety profile, high efficacy, and compatibility with multimodal pain management strategies, Paracetamol Infusion IP continues to be a first-line choice for clinicians seeking a reliable and well-tolerated solution for pain and fever management.",
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"description": "Sitagliptin 50 mg, Metformin Hydrochloride 1000 mg, and Glimepiride 2 mg is a triple-combination oral anti-diabetic medication formulated to achieve optimal blood sugar control in adults with Type 2 Diabetes Mellitus (T2DM). This unique blend brings together three complementary agents — Sitagliptin (a DPP-4 inhibitor), Metformin (a biguanide), and Glimepiride (a sulfonylurea) — that work through distinct mechanisms to enhance glucose regulation, improve insulin sensitivity, and support overall metabolic balance.\n\nThis advanced combination therapy is prescribed when monotherapy or dual therapy fails to achieve adequate glycemic control. It helps reduce both fasting plasma glucose (FPG) and postprandial glucose (PPG) levels, promoting stable long-term glycemic management.\n\nUses of Sitagliptin + Metformin + Glimepiride\n\nThis fixed-dose combination is primarily indicated for the management of Type 2 Diabetes Mellitus in adults. It is especially beneficial for patients whose blood sugar levels remain uncontrolled despite treatment with Metformin and Glimepiride or Metformin and Sitagliptin alone.\n\nIts main objectives include:\n\nControlling elevated blood glucose levels in adults with Type 2 diabetes\n\nReducing the risk of diabetes-related complications such as neuropathy, nephropathy, and cardiovascular diseases\n\nSupporting better insulin utilization by the body\n\nComplementing diet, exercise, and lifestyle modification to maintain optimal glycemic balance\n\nMechanism of Action\n\nEach component of this combination plays a vital role in maintaining blood sugar control:\n\nSitagliptin (50 mg) – A Dipeptidyl Peptidase-4 (DPP-4) inhibitor that enhances the activity of incretin hormones. These hormones stimulate insulin release and suppress glucagon production when blood glucose levels rise, thereby improving post-meal glucose control.\n\nMetformin Hydrochloride (1000 mg) – A biguanide that lowers glucose production in the liver and increases the body’s sensitivity to insulin. It also decreases intestinal glucose absorption, making it an essential first-line therapy in diabetes management.\n\nGlimepiride (2 mg) – A sulfonylurea that stimulates pancreatic beta cells to release more insulin, especially when blood glucose levels are high. It works synergistically with Metformin and Sitagliptin for more effective glycemic control.\n\nKey Benefits\n\nTriple Mechanism for Superior Control:\nBy combining three potent agents, the medication addresses multiple pathways of glucose regulation—insulin secretion, insulin sensitivity, and hepatic glucose output—resulting in comprehensive and consistent control of blood sugar levels.\n\nEffective Glycemic Stability:\nThe combination helps maintain target HbA1c levels and reduces both fasting and post-meal glucose spikes without significant weight gain when used with proper diet and exercise.\n\nReduced Risk of Diabetic Complications:\nLong-term blood sugar control minimizes the risk of complications such as kidney disease, vision problems, nerve damage, and heart conditions associated with uncontrolled diabetes.\n\nConvenient Fixed-Dose Formulation:\nCombining three medications into a single tablet simplifies dosing schedules, improves patient adherence, and reduces pill burden, which is crucial for long-term treatment success.\n\nImproved Insulin Efficiency:\nEnhances the body's natural insulin response and glucose metabolism, allowing for smoother daily energy levels and reduced fatigue associated with hyperglycemia.\n\nPossible Side Effects\n\nWhile this combination is generally well tolerated, some patients may experience side effects, especially at the beginning of therapy. Common and rare side effects include:\n\nHypoglycemia (low blood sugar): More likely when meals are skipped or during excessive physical exertion. Symptoms include sweating, dizziness, and rapid heartbeat.\n\nGastrointestinal disturbances: Such as nausea, vomiting, diarrhea, abdominal discomfort, or loss of appetite (mostly due to Metformin).\n\nHeadache or Weakness: Usually mild and transient.\n\nAllergic reactions: Rarely, rash or itching may occur.\n\nLactic Acidosis (rare but serious): A potential complication of Metformin, particularly in patients with kidney impairment or excessive alcohol consumption.\n\nWeight gain: Mild weight gain may occur due to Glimepiride’s insulin-enhancing effect.\n\nPrecautions:\n\nRegular monitoring of blood sugar levels and kidney function is essential.\n\nAvoid alcohol and consult a doctor before using this medicine if you have liver or kidney disease.\n\nThe medication should not be used in patients with Type 1 diabetes or diabetic ketoacidosis.\n\nConclusion\n\nThe combination of Sitagliptin 50 mg, Metformin Hydrochloride 1000 mg, and Glimepiride 2 mg represents a powerful and balanced therapy for adults with Type 2 Diabetes Mellitus, especially those requiring triple-drug intervention to achieve desired glycemic control. Its multi-targeted approach ensures effective management of both fasting and postprandial glucose levels, thereby improving long-term metabolic health and reducing the risk of complications.",
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"description": "Tiotropium Bromide and Formoterol Fumarate Inhaler is a combination medication designed to provide long-term relief for patients suffering from chronic respiratory conditions such as Chronic Obstructive Pulmonary Disease (COPD) and asthma. This inhaler combines the bronchodilator properties of tiotropium bromide with the fast-acting benefits of formoterol fumarate, ensuring both immediate and sustained relief from breathing difficulties. By improving airflow in the lungs, this inhaler significantly enhances the quality of life for individuals with obstructive airway diseases.\n\nComposition and Mechanism of Action\nThe inhaler contains two active ingredients:\n\nTiotropium Bromide – a long-acting anticholinergic agent that relaxes the muscles around the airways, preventing bronchospasm and helping to keep the airways open for an extended period.\n\nFormoterol Fumarate – a long-acting beta-2 adrenergic agonist (LABA) that quickly relaxes airway muscles, providing fast relief from shortness of breath and wheezing.\n\nTogether, these agents work synergistically. Tiotropium ensures long-term bronchodilation, while formoterol provides rapid symptom relief, making this inhaler ideal for patients who require both immediate and sustained respiratory support.\n\nUses\nThe Tiotropium Bromide and Formoterol Fumarate Inhaler is primarily used to:\n\nManage Chronic Obstructive Pulmonary Disease (COPD) – Helps reduce the frequency and severity of COPD exacerbations, improving breathing efficiency.\n\nControl Asthma Symptoms – Offers better control of persistent asthma symptoms, particularly in patients who do not respond adequately to standard inhalers.\n\nPrevent Exercise-Induced Bronchospasm – Can be used as part of a preventive regimen for patients prone to exercise-triggered breathing difficulties.\n\nEnhance Overall Lung Function – Improves airflow and oxygen exchange, contributing to better overall respiratory health.\n\nDosage and Administration\nProper usage of the inhaler is critical for maximum effectiveness. The dosage may vary based on your condition and doctor's recommendation. General guidelines include:\n\nTypically, one inhalation twice daily (morning and evening).\n\nShake the inhaler well before each use.\n\nExhale fully, place the mouthpiece in your mouth, and inhale deeply while pressing the inhaler to release the medication.\n\nHold your breath for 10 seconds after inhalation to ensure the medication reaches deep into the lungs.\n\nRinse your mouth with water after use to reduce the risk of oral infections or irritation.\n\nPatients should strictly follow their doctor’s instructions regarding dosage, frequency, and technique, as incorrect use may reduce the medication’s effectiveness.\n\nKey Benefits\n\nDual Action for Immediate and Long-Term Relief – Combines a fast-acting bronchodilator with a long-acting maintenance agent.\n\nReduces Exacerbations – Regular use can significantly lower the risk of flare-ups and hospital visits for COPD or severe asthma patients.\n\nImproves Lung Function – Enhances airflow and oxygen intake, leading to reduced shortness of breath and wheezing.\n\nConvenient Usage – A single inhaler provides both maintenance and symptom relief, reducing the need for multiple medications.\n\nEnhanced Quality of Life – Patients often experience better sleep, increased physical activity tolerance, and improved daily functioning.\n\nSide Effects\nWhile Tiotropium Bromide and Formoterol Fumarate Inhaler is generally well-tolerated, some patients may experience side effects. Common side effects include:\n\nDry mouth or throat irritation\n\nCough or hoarseness\n\nHeadache or dizziness\n\nTremors or mild palpitations\n\nSerious but rare side effects may include:\n\nSevere allergic reactions (rash, swelling, difficulty breathing)\n\nIrregular heartbeat or chest pain\n\nWorsening of respiratory symptoms\n\nPatients should immediately consult a healthcare professional if they experience severe or persistent side effects. Regular follow-up with a doctor is recommended to monitor lung function and adjust the dosage if necessary.\n\nPrecautions\n\nNot recommended for individuals with hypersensitivity to either tiotropium bromide or formoterol fumarate.\n\nShould be used cautiously in patients with cardiovascular diseases, kidney or liver problems, or thyroid disorders.\n\nAvoid sudden discontinuation without consulting your doctor, as this may worsen symptoms.\n\nAlways carry a rescue inhaler for emergency situations, as this inhaler is primarily for maintenance and not for immediate acute attacks.\n\nPrice\nThe price of Tiotropium Bromide and Formoterol Fumarate Inhaler may vary depending on the brand, pack size, and pharmacy. It is advisable to compare prices and check with local pharmacies for the most cost-effective options. Many insurance plans may cover this inhaler under prescription respiratory medications.\n\nConclusion\nTiotropium Bromide and Formoterol Fumarate Inhaler is a highly effective combination treatment for patients suffering from COPD and asthma. By providing both rapid symptom relief and long-term airway maintenance, it helps patients breathe more easily, reduces the frequency of exacerbations, and improves overall quality of life. Proper usage, adherence to prescribed dosage, and monitoring for side effects are essential for achieving the best results. For anyone managing chronic respiratory conditions, this inhaler represents a reliable and convenient treatment option under medical guidance.",
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"name": "Formoterol (6mcg), Fluticasone (250mcg)",
"description": "INH AIRFLOW MAX F250 combines two trusted respiratory agents — Formoterol (6 mcg) and Fluticasone (250 mcg) — in one convenient inhaler. This dual-therapy formulation is designed to deliver both rapid bronchodilation and long-term anti-inflammatory control, helping patients manage asthma and chronic obstructive pulmonary disease (COPD) more effectively.\nManufactured by Steris Healthcare Pvt. Ltd., INH AIRFLOW MAX F250 ensures reliable performance, quality assurance, and enhanced patient compliance.\nKey Indications\nINH AIRFLOW MAX F250 is indicated for:\nAsthma Maintenance Therapy: Provides long-term control of moderate to severe asthma.\nSymptom Relief: Reduces shortness of breath, wheezing, chest tightness, and airway inflammation.\nCOPD Management: Controls chronic respiratory symptoms and reduces the frequency and severity of COPD exacerbations.\nMechanism of Action\nINH AIRFLOW MAX F250 works through two complementary mechanisms:\n1. Formoterol (6 mcg) — Long-Acting Beta Agonist (LABA)\nAction: Relaxes airway smooth muscles for rapid and sustained bronchodilation.\nBenefit: Provides relief within minutes and lasts up to 12 hours.\n2. Fluticasone (250 mcg) — Corticosteroid\nAction: Reduces airway inflammation and prevents swelling of the bronchial walls.\nBenefit: Improves long-term respiratory control and reduces the risk of asthma attacks.\nTogether, these agents ensure both immediate symptom relief and prolonged protection against respiratory flare-ups.\nDosage and Administration\nRecommended Dose: As prescribed by a physician — usually one or two inhalations twice daily.\nRoute: Oral inhalation only.\nTiming: Use at the same time each day for best results.\nTechnique: Shake well before use and rinse mouth after each use to prevent throat irritation or infection.\n⚠️ Always follow your doctor’s instructions. Do not self-adjust or discontinue the medicine without consultation.\nKey Benefits of INH AIRFLOW MAX F250\n Provides dual-action relief — rapid bronchodilation + anti-inflammatory control.\n Ensures better breathing comfort and reduced daily symptoms.\n Prevents asthma and COPD exacerbations, improving long-term lung function.\n Convenient single-inhaler therapy improves adherence and treatment consistency.\n Suitable for chronic use under medical supervision.\nPossible Side Effects\nCommon Side Effects:\nThroat irritation or hoarseness\nMild headache\nTremor or shakiness\nNausea or cough\nSerious but Rare Side Effects:\nRespiratory infections (e.g., pneumonia)\nAllergic reactions (rash, swelling, or difficulty breathing)\nReduced bone density with long-term steroid use\nRinse your mouth after each inhalation to lower the risk of oral thrush or irritation.\nSafety and Precautions\nInform your physician about any heart, liver, or thyroid conditions before starting therapy.\nNot recommended during pregnancy or breastfeeding unless medically advised.\nAvoid exposure to tobacco smoke or environmental irritants.\nRegular lung function monitoring is recommended for long-term users.\nStorage Instructions\nStore below 30 °C, in a cool, dry place away from direct sunlight.\nKeep the inhaler tightly closed and out of reach of children.\nDo not use after the expiry date printed on the label.\nWhy Choose INH AIRFLOW MAX F250\nDeveloped by Steris Healthcare Pvt. Ltd., a trusted leader in respiratory care.\nCombines proven molecules for optimized asthma and COPD management.\nEnsures consistent dosing accuracy and ease of use.\nBacked by clinical reliability and patient-focused innovation.",
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"name": "Sitagliptin Phosphate Monhydrate 64.25 mg, Sitagliptin 50 mg, Metformin Hydrochloride 1000 mg & Glimepirde 1 mg",
"description": "ST GLIPTIN GM is a high-quality, fixed-dose combination oral antidiabetic medication containing Sitagliptin 50 mg, Metformin Hydrochloride 1000 mg, and Glimepiride 1 mg. This triple-combination therapy is specifically formulated to provide effective glycemic control in adults with type 2 diabetes mellitus (T2DM) who require multiple agents to achieve adequate blood sugar control.\nST GLIPTIN GM works through complementary mechanisms to target the core pathophysiological defects of T2DM—insulin resistance, impaired insulin secretion, and increased hepatic glucose output—making it an ideal choice for patients requiring intensified therapy.\nKey Indications:\nST GLIPTIN GM is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus when dual therapy with any two of the individual components (Sitagliptin, Metformin, or Glimepiride) does not provide adequate control.\nMechanism of Action:\nSitagliptin (50 mg):\nA Dipeptidyl Peptidase-4 (DPP-4) inhibitor that enhances the levels of active incretin hormones (GLP-1 and GIP), increasing insulin release and decreasing glucagon secretion in a glucose-dependent manner.\nMetformin Hydrochloride (1000 mg):\nA biguanide that improves insulin sensitivity by decreasing hepatic glucose production and enhancing peripheral glucose uptake.\nGlimepiride (1 mg):\nA sulfonylurea that stimulates pancreatic β-cells to secrete insulin, thereby reducing blood glucose levels.\nThe combination targets multiple metabolic pathways to provide synergistic and sustained blood glucose control.\nDosage and Administration:\nRecommended Dose:\nOne tablet daily, preferably with meals to reduce gastrointestinal side effects.\nIndividualization Required:\nDosage should be tailored based on patient response, renal function, and physician assessment.\nRenal Monitoring:\nBaseline and periodic assessment of renal function is advised, particularly due to the metformin component.\nKey Benefits of ST GLIPTIN GM 50/1000/1:\nTriple Mechanism of Action:\nTargets insulin resistance, insufficient insulin secretion, and excessive hepatic glucose production.\nEnhanced Glycemic Control:\nEffective in achieving and maintaining HbA1c targets.\nOnce-Daily Convenience:\nImproves adherence by reducing pill burden in patients requiring combination therapy.\nWeight Neutral to Modest Reduction:\nMetformin and sitagliptin components support weight neutrality.\nLow Hypoglycemia Risk:\nSitagliptin and metformin carry minimal hypoglycemia risk; however, glimepiride may increase the risk—monitor accordingly.\nSafety and Precautions:\nHypoglycemia:\nMay occur, particularly due to the glimepiride component. Educate patients on recognizing and managing low blood sugar.\nLactic Acidosis:\nA rare but serious complication of metformin. Avoid in patients with significant renal impairment or conditions predisposing to hypoxia.\nRenal Function:\nDose adjustment or discontinuation may be needed based on renal function.\nPancreatitis:\nRare reports with DPP-4 inhibitors like sitagliptin. Discontinue if suspected.\nAllergic Reactions:\nDiscontinue use if hypersensitivity reactions occur.\nPossible Side Effects:\nWhile ST GLIPTIN GM is generally well-tolerated, some patients may experience:\nNausea\nDiarrhea\nHeadache\nHypoglycemia (especially in elderly or with missed meals)\nAbdominal discomfort\nUpper respiratory tract infections\nDizziness\nFlatulence\nIf any side effects persist or worsen, seek immediate medical advice.\nStorage Instructions:\nStore at a temperature below 30°C.\nProtect from moisture and direct sunlight.\nKeep out of reach of children.\nWhy Choose ST GLIPTIN GM 50/1000/1?\nST GLIPTIN GM provides a powerful and synergistic combination of three well-established antidiabetic agents in a single, convenient daily dose. It offers a comprehensive approach to managing type 2 diabetes by addressing multiple metabolic abnormalities with a focus on safety, efficacy, and patient compliance. Manufactured under stringent GMP-certified conditions, ST GLIPTIN GM ensures quality, reliability, and therapeutic confidence for both patients and prescribers.",
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