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"name": "nimodipine 60 mg",
"description": "When looking for an effective medication for specific neurological and blood vessel-related conditions, Nimodipine 60 mg is a widely prescribed treatment known for its role in improving blood flow to the brain. Healthcare professionals commonly recommend this medicine for patients requiring specialized management of cerebral blood vessel complications.\n\nIf you are researching Nimodipine 60 mg, understanding its uses, benefits, dosage, safety profile, and purchasing considerations can help you make an informed decision. This comprehensive guide covers everything you need to know before buying or using Nimodipine 60 mg.\n\nWhat Is Nimodipine 60 mg?\n\nNimodipine 60 mg is a prescription medication that belongs to a class of drugs called calcium channel blockers. Unlike many calcium channel blockers that primarily affect the heart and peripheral blood vessels, nimodipine is specially designed to target blood vessels in the brain.\n\nIt is most commonly used to reduce the risk of brain damage caused by decreased blood flow following certain neurological events. By relaxing and widening cerebral blood vessels, nimodipine helps maintain adequate oxygen and nutrient delivery to brain tissue.\n\nBecause of its specialized action, Nimodipine 60 mg should only be used under medical supervision and according to prescribed treatment guidelines.\n\nComposition of Nimodipine 60 mg\n\nEach tablet contains:\n\nIngredient\tStrength\nNimodipine\t60 mg\n\nThe active ingredient works by controlling the movement of calcium into smooth muscle cells of blood vessels, helping them remain relaxed and open.\n\nHow Does Nimodipine 60 mg Work?\n\nNimodipine acts by blocking calcium channels located in the smooth muscle cells lining blood vessel walls.\n\nMechanism of Action\nCalcium normally enters vascular smooth muscle cells.\nThis calcium causes blood vessels to contract.\nNimodipine blocks calcium entry.\nBlood vessels relax and widen.\nImproved blood flow reaches brain tissues.\n\nThe unique property of nimodipine is its high affinity for cerebral arteries. This makes it particularly valuable in neurological settings where maintaining adequate cerebral circulation is critical.\n\nBy reducing blood vessel constriction, Nimodipine 60 mg helps support oxygen delivery and may lower the risk of complications associated with reduced cerebral blood flow.\n\nUses of Nimodipine 60 mg\n\nHealthcare providers may prescribe Nimodipine 60 mg for the management of conditions involving cerebral circulation.\n\nCommon Medical Uses\n1. Prevention of Cerebral Vasospasm\n\nNimodipine is widely used to prevent narrowing of brain blood vessels after certain neurological events.\n\n2. Support of Brain Blood Flow\n\nThe medication helps improve circulation in cerebral arteries and supports oxygen supply to brain tissues.\n\n3. Neurological Care Protocols\n\nIn specialized hospital settings, nimodipine may form part of comprehensive neurological treatment plans.\n\n4. Reduction of Ischemic Complications\n\nBy maintaining adequate blood flow, the medication may help reduce complications associated with restricted cerebral circulation.\n\nAlways follow your doctor's recommendations regarding the exact purpose and duration of treatment.\n\nKey Benefits of Nimodipine 60 mg\nImproved Cerebral Blood Flow\n\nThe primary benefit of Nimodipine 60 mg is its ability to enhance blood circulation within the brain.\n\nTargeted Action\n\nUnlike many other calcium channel blockers, nimodipine specifically affects cerebral blood vessels.\n\nNeuroprotective Support\n\nMaintaining adequate blood flow helps support brain tissue function and recovery.\n\nWell-Established Clinical Use\n\nNimodipine has been extensively studied and is commonly included in neurological treatment protocols worldwide.\n\nReliable Therapeutic Effect\n\nWhen taken as prescribed, Nimodipine 60 mg provides consistent therapeutic support for cerebral vascular health.\n\nWhy Choose Nimodipine 60 mg?\n\nMany healthcare professionals choose nimodipine because of its unique brain-selective properties.\n\nAdvantages Include:\nSpecifically targets cerebral arteries\nSupports healthy blood circulation in the brain\nProven clinical history\nPrescription-based safety monitoring\nWidely recognized neurological therapy\nSuitable for structured treatment protocols\n\nPatients searching for Nimodipine 60 mg online often prioritize quality, authenticity, and professional medical guidance when purchasing this medication.\n\nDosage and Administration\n\nThe dosage of Nimodipine 60 mg depends on individual medical needs and physician recommendations.\n\nGeneral Guidelines\nTake exactly as prescribed.\nSwallow the tablet with water.\nFollow scheduled dosing intervals.\nDo not exceed the prescribed dose.\nContinue treatment for the full duration recommended by your healthcare provider.\nImportant Instructions\nAvoid self-adjusting the dosage.\nDo not stop treatment abruptly unless advised by your doctor.\nInform your physician about all medications you are taking.\n\nBecause dosing schedules may vary, always rely on professional medical advice.\n\nPossible Side Effects of Nimodipine 60 mg\n\nLike all prescription medicines, Nimodipine 60 mg may cause side effects in some individuals.\n\nCommon Side Effects\nHeadache\nDizziness\nFlushing\nNausea\nFatigue\nLow blood pressure\nLess Common Side Effects\nRapid heartbeat\nSwelling of extremities\nGastrointestinal discomfort\nLightheadedness\nSeek Medical Attention If You Experience\nSevere allergic reactions\nSignificant drop in blood pressure\nDifficulty breathing\nSevere dizziness or fainting\n\nMost side effects are manageable and should be discussed with your healthcare provider.\n\nSafety Precautions\n\nBefore using Nimodipine 60 mg, discuss your complete medical history with your doctor.\n\nInform Your Physician If You Have:\nLiver disease\nLow blood pressure\nHeart conditions\nKidney disorders\nHistory of medication allergies\nPregnancy and Breastfeeding\n\nConsult your healthcare provider regarding the use of Nimodipine 60 mg during pregnancy or breastfeeding.\n\nDrug Interactions\n\nCertain medications may interact with nimodipine, including:\n\nBlood pressure medications\nAntifungal drugs\nAntibiotics\nAnti-seizure medications\nCertain heart medications\n\nAlways provide a complete medication list to your healthcare professional.\n\nHow to Store Nimodipine 60 mg\n\nProper storage helps maintain the medication's effectiveness.\n\nStorage Guidelines\nStore at room temperature.\nKeep away from direct sunlight.\nProtect from moisture.\nKeep out of reach of children.\nStore in original packaging whenever possible.\n\nDo not use expired medication.\n\nBuying Nimodipine 60 mg Online\n\nWhen purchasing Nimodipine 60 mg online, prioritize safety and authenticity.\n\nWhat to Look For\nLicensed pharmacy or supplier\nGenuine product sourcing\nPrescription verification\nSecure payment methods\nProper packaging\nCustomer support availability\nBuyer Checklist\n\n✔ Verify product strength (60 mg)\n\n✔ Check manufacturing details\n\n✔ Confirm prescription requirements\n\n✔ Review storage recommendations\n\n✔ Ensure sealed packaging upon delivery\n\nChoosing a reputable supplier helps ensure product quality and patient safety.\n\nConclusion\n\nNimodipine 60 mg is a specialized calcium channel blocker designed to support healthy cerebral blood flow. Its targeted action on brain blood vessels makes it an important medication in neurological care and vascular management protocols.\n\nWhether you are researching treatment options or planning to purchase Nimodipine 60 mg with a valid prescription, understanding its benefits, dosage guidelines, precautions, and potential side effects is essential. Always use this medication under the supervision of a qualified healthcare professional to achieve the best possible outcomes.\n\nHigh-Ranking FAQs (Google Search & Voice Search Optimized)\nWhat is Nimodipine 60 mg used for?\n\nNimodipine 60 mg is primarily used to improve blood flow in the brain and help prevent complications related to cerebral blood vessel narrowing under medical supervision.\n\nHow does Nimodipine 60 mg work?\n\nIt blocks calcium entry into blood vessel muscle cells, allowing cerebral arteries to relax and improving blood circulation to brain tissues.\n\nIs Nimodipine 60 mg a blood thinner?\n\nNo. Nimodipine is not a blood thinner. It is a calcium channel blocker that relaxes blood vessels.\n\nCan Nimodipine 60 mg lower blood pressure?\n\nYes. Nimodipine may lower blood pressure as part of its blood vessel-relaxing effects.\n\nHow long should I take Nimodipine 60 mg?\n\nThe duration of treatment depends on your medical condition and your doctor's recommendations.\n\nCan I take Nimodipine 60 mg with food?\n\nFollow your physician's instructions regarding food intake and dosing schedules for optimal results.\n\nWhat are the most common side effects of Nimodipine 60 mg?\n\nCommon side effects include headache, dizziness, nausea, flushing, fatigue, and low blood pressure.\n\nIs Nimodipine 60 mg available without a prescription?\n\nNo. Nimodipine 60 mg is generally a prescription-only medication and should be used under medical supervision.\n\nCan elderly patients use Nimodipine 60 mg?\n\nYes, but dosage and monitoring should be determined by a healthcare professional based on individual health conditions.\n\nWhere can I buy genuine Nimodipine 60 mg online?\n\nYou should purchase Nimodipine 60 mg only from reputable and licensed pharmacies that provide authentic prescription medications and proper product information.",
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"description": "Nefopam Hydrochloride 30 mg Tablets – Effective Pain Management for Acute and Chronic Pain\nNefopam Hydrochloride 30 mg Tablets\n\nNefopam Hydrochloride 30 mg Tablets are a non-opioid analgesic medication used for the management of moderate to severe pain. They provide effective pain relief without the respiratory depression and dependency risks commonly associated with opioid medications. Nefopam works through a unique mechanism in the central nervous system, making it a valuable option for patients who require pain control following surgery, injury, or certain chronic pain conditions.\n\nHealthcare professionals often prescribe Nefopam Hydrochloride 30 mg Tablets as part of a comprehensive pain management plan. The medication helps improve comfort, mobility, and quality of life by reducing pain intensity and supporting faster recovery.\n\nWhat Are Nefopam Hydrochloride 30 mg Tablets?\n\nNefopam Hydrochloride is a centrally acting analgesic that belongs to a class of non-opioid pain-relieving medicines. Unlike traditional anti-inflammatory drugs, Nefopam primarily works within the central nervous system to reduce pain perception.\n\nThe medication is commonly used when effective pain relief is required but opioid use is undesirable or needs to be minimized. Nefopam Hydrochloride 30 mg Tablets are suitable for various pain conditions and are often used in hospitals and clinical settings as well as for outpatient pain management.\n\nComposition\n\nEach tablet contains:\n\nNefopam Hydrochloride 30 mg\n\nThe active ingredient is carefully formulated to provide reliable analgesic effects and support pain control in a wide range of clinical situations.\n\nHow Nefopam Hydrochloride 30 mg Tablets Work\n\nNefopam acts on the central nervous system by influencing neurotransmitters involved in pain signaling.\n\nIts mechanism includes:\n\nInhibition of pain signal transmission in the brain and spinal cord\nModulation of serotonin, norepinephrine, and dopamine pathways\nReduction of pain perception without causing significant respiratory depression\nSupport for effective pain control without opioid-related dependency concerns\n\nThis unique action makes Nefopam a useful option for patients requiring non-opioid pain management.\n\nUses of Nefopam Hydrochloride 30 mg Tablets\n\nNefopam Hydrochloride 30 mg Tablets are prescribed for various painful conditions.\n\n1. Postoperative Pain Management\n\nThe medication is commonly used after surgical procedures to reduce pain and improve patient comfort during recovery.\n\nBenefits:\nHelps control moderate to severe postoperative pain\nReduces discomfort during healing\nSupports faster recovery and mobility\n2. Musculoskeletal Pain\n\nNefopam may be prescribed for painful musculoskeletal conditions affecting muscles, ligaments, and joints.\n\nCommon conditions include:\nMuscle injuries\nSprains and strains\nBack pain\nNeck pain\n3. Trauma and Injury-Related Pain\n\nPatients experiencing pain after accidents or injuries may benefit from Nefopam therapy.\n\nIt may help with:\nSoft tissue injuries\nFracture-related discomfort\nSports injuries\n4. Chronic Pain Management\n\nIn selected patients, Nefopam can be incorporated into long-term pain management strategies under medical supervision.\n\nConditions may include:\nChronic musculoskeletal pain\nPersistent pain syndromes\nNeuropathic pain adjunct therapy\n5. Cancer-Related Pain Support\n\nNefopam may be used alongside other analgesics in comprehensive pain management plans for cancer patients.\n\n6. Pain Associated with Medical Procedures\n\nHealthcare providers may use Nefopam to manage pain before or after certain medical procedures.\n\nKey Benefits of Nefopam Hydrochloride 30 mg Tablets\nEffective Pain Relief\n\nNefopam provides reliable relief from moderate to severe pain, helping patients perform daily activities more comfortably.\n\nNon-Opioid Analgesic\n\nUnlike opioids, Nefopam offers pain control without the same level of dependency risk.\n\nAdvantages include:\nLower addiction potential\nReduced respiratory depression risk\nUseful alternative when opioids are unsuitable\nSupports Postoperative Recovery\n\nEffective pain management allows patients to move more comfortably after surgery and may contribute to improved recovery outcomes.\n\nCentrally Acting Mechanism\n\nNefopam targets pain pathways within the central nervous system, providing a unique approach to pain control.\n\nImproved Quality of Life\n\nBy reducing pain intensity, patients often experience:\n\nBetter physical function\nImproved sleep quality\nEnhanced daily productivity\nGreater overall comfort\nCan Be Used in Multimodal Pain Management\n\nNefopam is frequently included in combination pain-management strategies to improve treatment outcomes while reducing reliance on stronger analgesics.\n\nWho May Benefit from Nefopam Hydrochloride 30 mg Tablets?\n\nThis medication may be suitable for:\n\nAdults experiencing moderate to severe pain\nPost-surgical patients\nIndividuals with musculoskeletal injuries\nPatients requiring non-opioid pain management\nThose recovering from trauma or injury\nPatients requiring adjunctive chronic pain treatment\n\nA healthcare professional will determine whether Nefopam is appropriate based on the patient's medical condition and treatment goals.\n\nRecommended Dosage\n\nThe dosage of Nefopam Hydrochloride 30 mg Tablets should always be determined by a qualified healthcare provider.\n\nGeneral Administration Guidelines\nTake exactly as prescribed.\nSwallow the tablet with water.\nFollow the prescribed treatment schedule.\nDo not exceed the recommended dose.\nContinue treatment only for the duration advised by your physician.\n\nDosage may vary depending on pain severity, patient age, and overall health condition.\n\nSide Effects of Nefopam Hydrochloride 30 mg Tablets\n\nLike all medications, Nefopam may cause side effects in some individuals.\n\nCommon Side Effects\nNausea\nSweating\nDry mouth\nDizziness\nHeadache\nIncreased heart rate\nNervousness\n\nThese effects are generally mild and temporary.\n\nLess Common Side Effects\nBlurred vision\nDifficulty sleeping\nTremors\nFatigue\nDigestive discomfort\nRare but Serious Side Effects\n\nSeek immediate medical attention if you experience:\n\nSevere allergic reactions\nDifficulty breathing\nSignificant palpitations\nSevere confusion\nConvulsions or seizures\nPrecautions and Warnings\n\nBefore using Nefopam Hydrochloride 30 mg Tablets, discuss your medical history with your healthcare provider.\n\nUse with Caution in Patients with:\nHeart disease\nLiver impairment\nKidney disorders\nGlaucoma\nUrinary retention problems\nSeizure disorders\nPregnancy and Breastfeeding\n\nThe use of Nefopam during pregnancy or breastfeeding should only occur under medical supervision after careful evaluation of risks and benefits.\n\nDriving and Operating Machinery\n\nNefopam may cause dizziness or drowsiness in some patients.\n\nAvoid:\n\nDriving\nOperating heavy machinery\nActivities requiring full alertness\n\nuntil you know how the medication affects you.\n\nDrug Interactions\n\nInform your healthcare provider about all medications you are taking.\n\nPotential interactions may occur with:\n\nAntidepressants\nSedatives\nCentral nervous system depressants\nAnticholinergic medications\nOther pain-relieving medicines\n\nProfessional medical guidance helps minimize interaction risks.\n\nStorage Instructions\n\nTo maintain product quality:\n\nStore in a cool, dry place.\nProtect from direct sunlight.\nKeep away from moisture.\nStore below the recommended temperature.\nKeep out of reach of children.\nFrequently Asked Questions (FAQs)\nWhat is Nefopam Hydrochloride 30 mg Tablets used for?\n\nIt is used for the management of moderate to severe pain, including postoperative pain, injury-related pain, and certain chronic pain conditions.\n\nIs Nefopam an opioid?\n\nNo. Nefopam is a non-opioid analgesic that works through central nervous system pathways.\n\nCan Nefopam help after surgery?\n\nYes. It is commonly prescribed for postoperative pain management and recovery support.\n\nDoes Nefopam cause addiction?\n\nNefopam has a significantly lower dependency risk compared to opioid pain medications when used as prescribed.\n\nHow quickly does Nefopam work?\n\nPain relief may begin relatively soon after administration, though individual responses can vary.\n\nCan elderly patients use Nefopam?\n\nIt may be used in older adults under close medical supervision, with dosage adjustments when necessary.\n\nWhy Choose Nefopam Hydrochloride 30 mg Tablets?\n\nNefopam Hydrochloride 30 mg Tablets offer an effective, non-opioid approach to pain management. Their unique mechanism of action helps control pain while reducing concerns associated with opioid medications. The medication is widely used for postoperative recovery, injury-related discomfort, and selected chronic pain conditions.\n\nKey advantages include:\n\nEffective moderate to severe pain relief\nNon-opioid formulation\nCentrally acting analgesic action\nSupports postoperative recovery\nLower risk of respiratory depression\nUseful in multimodal pain management strategies\nHelps improve patient comfort and quality of life\nConclusion\n\nNefopam Hydrochloride 30 mg Tablets are a trusted non-opioid analgesic option for managing moderate to severe pain. By acting on central pain pathways, they provide effective pain relief while helping reduce dependence on opioid medications. Whether used for postoperative recovery, musculoskeletal injuries, trauma-related pain, or selected chronic pain conditions, Nefopam supports improved comfort, mobility, and overall well-being.",
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"name": "nebivolol 5mg cilnidipine 10mg",
"description": "Nebivolol 5mg + Cilnidipine 10mg Tablets—Complete Guide\nA fixed-dose combination antihypertensive for effective blood pressure control. Understand how it works, who it's for, dosage, and safety before you buy.\n\nDrug Class\nBeta-blocker + Calcium Channel Blocker\nStrength\nNebivolol 5mg / Cilnidipine 10mg\nRoute\nOral (tablet)\nSchedule\nRx Only\nWhat is this combination?\nUnderstanding nebivolol 5mg + cilnidipine 10mg\nNebivolol 5mg + cilnidipine 10mg is a fixed-dose combination tablet prescribed for the management of hypertension (high blood pressure) in adults. It pairs two complementary mechanisms into one convenient pill, making it a popular choice when single-drug therapy proves insufficient for adequate blood pressure control.\n\nThis combination is widely preferred by cardiologists when patients need better BP reduction with fewer pills, improved tolerability, and protection of vital organs such as the heart and kidneys. If your doctor has prescribed this tablet, you're likely being treated for stage 1 or stage 2 hypertension, with or without associated cardiovascular risk factors.\n\nThis is not an over-the-counter product. Always use nebivolol + cilnidipine tablets only under the supervision of a licensed physician. Self-medication or dose changes without medical advice can be dangerous.\nHow it works\nMechanism of action — dual-pathway blood pressure control\nThe effectiveness of this combination lies in how its two active ingredients target blood pressure through different pathways simultaneously:\n\nNebivolol 5mg\nA third-generation cardioselective beta-1 blocker. It slows the heart rate, reduces the force of cardiac contraction, and lowers cardiac output. Uniquely, nebivolol also releases nitric oxide, causing blood vessel relaxation — a property not seen in older beta-blockers. This makes it better tolerated and less likely to cause sexual dysfunction or cold extremities.\nCilnidipine 10mg\nAn N/L-type calcium channel blocker. Unlike conventional CCBs (e.g., amlodipine), cilnidipine blocks both L-type and N-type calcium channels. N-type blockade in the sympathetic nervous system reduces norepinephrine release, leading to smoother, more sustained BP reduction with significantly less ankle swelling — a common complaint with older CCBs.\nTogether, these agents provide additive antihypertensive effect while offsetting each other's side effects. Nebivolol reduces tachycardia that CCBs can sometimes cause, while cilnidipine's vasodilatory effect complements nebivolol's cardiac output reduction.\n\nIndications\nWho is Nebivolol 5 mg and Cilnidipine 10 mg prescribed for?\nThis combination is indicated for adults with hypertension who are not adequately controlled on monotherapy. It is especially suited for patients who have:\n\nCondition:\tWhy this combination is preferred\nHypertension with high heart rate\tNebivolol slows heart rate while cilnidipine controls peripheral resistance\nHypertension with diabetes\tMetabolically neutral; does not worsen glucose tolerance or lipid profile\nHypertension with CKD / proteinuria:\tCilnidipine's N-type blockade reduces glomerular pressure and protein leakage\nHypertension with coronary artery disease\tNebivolol provides cardioprotection and anti-anginal effect\nAmlodipine-related ankle edema\tSwitching to cilnidipine substantially reduces pedal edema due to N-type blockade\nUncontrolled BP on single antihypertensive\tCombination adds complementary mechanisms without increasing pill burden\n\nosage & Administration\nHow to take nebivolol 5 mg + cilnidipine 10mg\nThe standard recommended dose is one tablet once daily, preferably at the same time each day — most commonly in the morning with or without food. Your physician may adjust the dose based on your blood pressure response and individual tolerability.\n\nDo not crush, chew, or split the tablet unless your doctor advises. If you miss a dose, take it as soon as you remember, but skip it if it is almost time for the next dose. Never double up on doses. Swallowing the tablet whole with water is the preferred method of administration.\n\nDo not stop taking this medication abruptly. Sudden discontinuation of nebivolol (a beta-blocker) can trigger rebound hypertension or even angina in patients with underlying coronary disease. Always taper under medical guidance.\n\nCommon and serious side effects to know\nLike all medicines, nebivolol + cilnidipine can cause side effects, though not everyone experiences them. Knowing what to watch for helps you respond promptly.\n\nSide effect\tFrequency\tWhat to do\nHeadache, dizziness\tCommon (early phase)\tUsually resolves in 1–2 weeks; avoid sudden posture changes\nFatigue, tiredness\tCommon\tMonitor; often improves after dose adjustment\nAnkle swelling (pedal edema)\tLess common than with amlodipine\tReport if worsening; may require dose review\nBradycardia (slow heart rate)\tUncommon\tSeek medical advice if heart rate <50 bpm\nNausea, stomach upset\tUncommon\tTake after meals to minimise\nBronchospasm\tRare\tStop immediately; seek emergency care if breathlessness\nSevere hypotension\tRare\tEmergency — seek immediate medical attention.\n\nWhen should this combination not be used?\nImportant safety information\nThis tablet is contraindicated in: cardiogenic shock, decompensated heart failure, severe bradycardia (<60 bpm), sick sinus syndrome, second- or third-degree AV block (without pacemaker), severe hepatic impairment, known hypersensitivity to nebivolol or cilnidipine, pregnancy, and breastfeeding.\n\nUse with caution in patients with asthma or COPD (nebivolol has some beta-2 activity at higher doses), peripheral vascular disease, diabetes mellitus (may mask hypoglycemic symptoms), and in elderly patients prone to falls due to postural hypotension.\n\nAlways inform your doctor of all medications you are currently taking. Clinically significant interactions exist with other antihypertensives, NSAIDs, digoxin, antidiabetic agents, and CYP2D6 inhibitors (e.g., fluoxetine, paroxetine), which can raise nebivolol plasma levels.\n\n\n\n\n",
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"description": "Proceftazo 1125 is a powerful combination antibiotic injection containing Ceftriaxone and Tazobactam, formulated to treat a wide range of serious bacterial infections. This combination enhances antibacterial effectiveness by not only killing bacteria but also preventing resistance mechanisms that often reduce the impact of standard antibiotics.\n\nProceftazo 1125 is commonly administered in hospitals or clinical settings for moderate to severe infections requiring immediate and effective treatment.\n\nWhat is Proceftazo 1125 Injection?\n\nProceftazo 1125 is a dual-action antibiotic therapy that combines:\n\nCeftriaxone (1000 mg approx.) – a third-generation cephalosporin antibiotic that kills bacteria by disrupting their cell wall formation.\nTazobactam (125 mg approx.) – a beta-lactamase inhibitor that protects Ceftriaxone from bacterial enzymes that can inactivate it.\n\nTogether, they create a highly effective formulation that works against resistant and difficult-to-treat bacterial strains.\n\nUses of Proceftazo 1125 Injection\n\nProceftazo 1125 is widely prescribed for treating various bacterial infections, including:\n\n1. Respiratory Tract Infections\nPneumonia\nBronchitis\nLung abscess\n2. Urinary Tract Infections (UTIs)\nComplicated UTIs\nKidney infections\n3. Skin and Soft Tissue Infections\nCellulitis\nWound infections\nAbscesses\n4. Intra-Abdominal Infections\nPeritonitis\nGastrointestinal infections\n5. Bone and Joint Infections\nOsteomyelitis\nSeptic arthritis\n6. Bloodstream Infections\nSepsis and bacteremia\n7. Gynecological Infections\nPelvic inflammatory disease\n\nProceftazo 1125 is especially useful in treating infections caused by resistant bacteria, making it a reliable choice in critical care settings.\n\nHow Proceftazo 1125 Works\n\nThe combination of Ceftriaxone and Tazobactam provides a dual mechanism of action:\n\nCeftriaxone attacks and destroys bacterial cell walls, leading to bacterial death.\nTazobactam inhibits beta-lactamase enzymes produced by bacteria, which would otherwise neutralize Ceftriaxone.\n\nThis synergistic action ensures:\n\nBroader antibacterial coverage\nIncreased effectiveness against resistant strains\nFaster infection control\nKey Benefits of Proceftazo 1125 Injection\n1. Broad-Spectrum Antibiotic Coverage\n\nProceftazo 1125 is effective against a wide range of Gram-positive and Gram-negative bacteria.\n\n2. Enhanced Resistance Protection\n\nThanks to Tazobactam, this injection overcomes bacterial resistance mechanisms, making treatment more effective.\n\n3. Rapid Action\n\nBeing an injectable formulation, it works quickly, making it ideal for severe or life-threatening infections.\n\n4. Trusted in Hospital Settings\n\nFrequently used in intensive care units (ICUs) and emergency care for serious infections.\n\n5. Reduced Risk of Treatment Failure\n\nThe combination therapy lowers the chances of antibiotic resistance and relapse.\n\n6. Convenient Dosing\n\nUsually administered once or twice daily depending on the severity of infection.\n\nDosage and Administration\nProceftazo 1125 is administered via intramuscular (I.M.) or intravenous (I.V.) injection.\nDosage depends on:\nType and severity of infection\nPatient’s age and weight\nKidney and liver function\n\n⚠️ Always administered by a healthcare professional. Do not self-inject.\n\nPossible Side Effects of Proceftazo 1125\n\nWhile generally well-tolerated, some patients may experience side effects:\n\nCommon Side Effects\nPain or swelling at injection site\nDiarrhea\nNausea or vomiting\nRash\nModerate Side Effects\nAllergic reactions\nElevated liver enzymes\nHeadache or dizziness\nSerious Side Effects (Rare)\nSevere allergic reactions (anaphylaxis)\nBlood disorders\nClostridium difficile-associated diarrhea\nKidney or liver dysfunction\nWhen to Seek Medical Attention\n\nSeek immediate medical help if you experience:\n\nDifficulty breathing\nSevere rash or itching\nPersistent diarrhea\nYellowing of skin or eyes\nUnusual bleeding\nPrecautions and Warnings\nInform your doctor if you have allergies to cephalosporins or penicillin.\nUse cautiously in patients with kidney or liver disorders.\nNot recommended for premature infants or newborns without medical advice.\nAlcohol consumption should be avoided during treatment.\nDrug Interactions\n\nProceftazo 1125 may interact with:\n\nBlood thinners\nOther antibiotics\nDiuretics\nCalcium-containing IV solutions\n\nAlways inform your doctor about all medications you are taking.\n\nStorage Instructions\nStore below 25°C\nProtect from light and moisture\nKeep out of reach of children\nConclusion\n\nProceftazo 1125 Injection (Ceftriaxone & Tazobactam) is a highly effective, broad-spectrum antibiotic designed to combat serious and resistant bacterial infections. Its dual-action formula ensures enhanced bacterial killing and protection against resistance, making it a trusted choice in hospitals and critical care settings.\n\nWith its rapid action, wide applicability, and strong clinical effectiveness, Proceftazo 1125 plays a crucial role in modern infection management. However, it should always be used under strict medical supervision to ensure safety and effectiveness.",
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"name": "tiapride hydrochloride tablets",
"description": "TIAPRADE 50 tablets, containing Tiapride Hydrochloride 50mg, offer targeted relief for behavioral disorders and movement issues. This atypical antipsychotic helps manage symptoms like agitation and dyskinesia effectively.\n\nProduct Description\nTIAPRADE 50 is a prescription medication featuring Tiapride Hydrochloride as its active ingredient, each tablet delivering precisely 50mg of this compound. Manufactured to high pharmaceutical standards, these tablets are designed for oral administration, typically taken with water after meals to enhance absorption and minimize stomach upset. Tiapride belongs to the class of selective dopamine D2 and D3 receptor antagonists, distinguishing it from typical antipsychotics by its lower risk of extrapyramidal side effects. This makes TIAPRADE 50 particularly suitable for vulnerable populations, including the elderly.\n\nThe tablets are compact, film-coated for easy swallowing, and come in blister packs that protect against moisture and light. As a non-sedating option in many cases, TIAPRADE 50 supports daily functioning without excessive drowsiness, aligning with modern psychiatric care needs. For SEO optimization targeting “Tiapride Hydrochloride Tablets” or “TIAPRADE 50 uses,” this product stands out for its versatility in treating neuropsychiatric conditions.\n\nKey Uses and Applications\nTIAPRADE 50 excels in managing a range of psychiatric and neurological conditions rooted in dopamine imbalance. Primarily, it treats schizophrenia by controlling negative symptoms such as social withdrawal, lack of emotion, and poor concentration, helping patients reintegrate into society.\n\nIt is highly effective for behavioral disorders, including agitation, aggression, and impulsivity, especially in elderly patients with dementia or alcohol withdrawal syndrome. Clinically, TIAPRADE 50 addresses dyskinesia—involuntary movements of limbs or face—often linked to Parkinson's disease or long-term antipsychotic use. Other applications include Tourette's syndrome, tics, chorea in Huntington's disease, and even acute alcohol dependence delirium tremens.\n\nIn hospital settings, such as during COVID-19-related agitation, TIAPRADE 50 has shown promise due to its favorable safety profile. Dosage typically starts at 100-200mg three times daily (2-4 tablets of TIAPRADE 50), adjustable up to 600mg/day based on severity, age, and response. Full effects may take 4-6 weeks, so consistent use under medical supervision is essential.\n\nHow TIAPRADE 50 Works\nTIAPRADE 50 modulates dopamine activity in the brain's limbic system, blocking overactive D2 receptors without strongly affecting other neurotransmitters like serotonin or histamine. This selective action reduces psychotic symptoms, calms agitation, and suppresses abnormal movements while preserving cognitive function.\n\nUnlike broader antipsychotics, Tiapride's mechanism minimizes motor side effects, making it ideal for long-term dyskinesia management. It stabilizes mood swings in mania or schizophrenia, promoting clearer thinking and emotional balance. Patients often report improved sleep patterns and reduced anxiety within days, though optimal benefits build gradually.\n\nFor “Tiapride Hydrochloride Tablets mechanism,” this targeted dopamine inhibition underpins its efficacy across disorders, supported by decades of clinical data.\n\nKey Benefits\nTIAPRADE 50 delivers multifaceted benefits, enhancing quality of life for those with psychiatric challenges.\n\nRapid Symptom Control: Quickly reduces agitation and aggression, vital for elderly care or acute episodes.\n\nLow Extrapyramidal Risk: Unlike older antipsychotics, it rarely causes stiffness or tremors, ideal for dyskinesia patients.\n\nElderly-Friendly: Mild sedation profile supports geriatric use without impairing mobility or cognition.\n\nVersatile for Comorbidities: Effective in alcohol withdrawal, tics, and schizophrenia, reducing polypharmacy needs.\n\nImproved Daily Functioning: Boosts social engagement, attention, and emotional expression in psychosis.\n\nStudies affirm its tolerability, with many patients tolerating doses up to 600 mg daily long-term. Benefits extend to headache relief in some neurological cases and better outcomes in Tourette's management.\n\nBenefit\tTarget Condition\tAdvantage Over Alternatives\nAgitation Reduction\tElderly Behavioral Disorders\tLess sedation than benzodiazepines \nDyskinesia Control\tParkinson's-Related\tMinimal motor worsening \nNegative Symptom Relief\tSchizophrenia\tPreserves cognition \nWithdrawal Support\tAlcohol Dependence\tSafer in delirium tremens \nPotential Side Effects\nWhile generally well-tolerated, TIAPRADE 50 may cause mild, transient side effects that resolve with time or dose adjustment.\n\nCommon effects include drowsiness, dizziness, headache, insomnia, fatigue, and agitation—often fading after the first week. Less frequent are tremor, increased salivation, vertigo, orthostatic hypotension (dizziness on standing), and emotional blunting.\n\nRarely, overdose risks low blood pressure, sedation, or convulsions; seek immediate help if suspected. Avoid abrupt cessation to prevent rebound symptoms. Most resolve without intervention, but persistent issues warrant medical review.\n\nContraindications and Precautions\nDo not use TIAPRADE 50 if you have prolactinoma, pheochromocytoma, severe kidney/liver disease, heart conditions, convulsions history, or allergies to Tiapride. It's contraindicated in pregnancy, breastfeeding, children under 15, and those with epilepsy.\n\nPrecautions include monitoring prolactin levels, blood pressure, and liver function. Avoid alcohol, as it amplifies sedation. Drive cautiously until the effects are known. Drug interactions with antihypertensives or CNS depressants require dose tweaks.\n\nDosage Guidelines\nStart with 50-100mg (1-2 TIAPRADE 50 tablets) three times daily, post-meals. Maximum 600mg/day for adults; elderly may need lower doses (300mg/day). Adjust per response, not exceeding 4-6 weeks without reassessment. Swallow whole; store below 30°C.\n\nConclusion\nTIAPRADE 50 (Tiapride Hydrochloride Tablets 50 mg) stands as a reliable, SEO-highlighted solution for agitation, dyskinesia, schizophrenia, and behavioral disorders, balancing efficacy with safety. Its dopamine-selective action delivers key benefits like symptom control and preserved function, outweighing manageable side effects for suitable patients. Consult your doctor to integrate TIAPRADE 50 into your care plan for optimal mental health outcomes—empowering calmer, more productive lives.",
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"name": "Lactulose Enema 20%",
"description": "Maintaining a healthy digestive system is essential for overall well-being. Constipation, especially chronic or severe cases, can significantly affect quality of life and may lead to complications if left untreated. LACTUSMOOTH ENEMA, formulated with Lactulose Enema 20% w/v, is a clinically trusted solution designed to provide rapid and effective relief from constipation and related conditions. It works gently yet efficiently, making it suitable for patients requiring immediate bowel evacuation or management of specific medical conditions.\n\nWhat is LACTUSMOOTH ENEMA?\n\nLACTUSMOOTH ENEMA is a rectal preparation containing Lactulose 20% w/v, a synthetic disaccharide widely used as an osmotic laxative. Unlike oral laxatives, this enema formulation delivers the medication directly into the rectum, ensuring faster action and targeted relief. It is particularly useful in cases where oral administration is not feasible or when quick bowel clearance is required.\n\nLactulose works by drawing water into the bowel, softening stools and stimulating bowel movement without causing harsh irritation.\n\nHow Does Lactulose Enema Work?\n\nLactulose is not digested in the small intestine. Instead, it reaches the colon unchanged, where it is broken down by beneficial gut bacteria into organic acids such as lactic acid and acetic acid. This process:\n\nIncreases osmotic pressure in the colon\nPulls water into the bowel\nSoftens hardened stools\nStimulates natural bowel movement\n\nAdditionally, it helps reduce ammonia absorption in the gut, making it beneficial in certain liver-related conditions like hepatic encephalopathy.\n\nUses of LACTUSMOOTH ENEMA\n\nLACTUSMOOTH ENEMA is prescribed in a variety of medical situations, including:\n\n1. Treatment of Severe Constipation\n\nIt provides fast relief from acute or chronic constipation, especially when oral laxatives fail or are unsuitable.\n\n2. Bowel Cleansing Before Procedures\n\nUsed before surgeries, colonoscopy, or diagnostic procedures to ensure the bowel is completely cleared.\n\n3. Management of Hepatic Encephalopathy\n\nHelps reduce blood ammonia levels by promoting its excretion through stool, thereby supporting liver health.\n\n4. Fecal Impaction\n\nEffective in softening and removing impacted stool in the rectum.\n\n5. Post-Surgical Bowel Care\n\nAssists in maintaining smooth bowel movements after surgeries, especially abdominal or rectal procedures.\n\nKey Benefits of LACTUSMOOTH ENEMA\n✔ Fast-Acting Relief\n\nSince it is administered rectally, it works quicker than oral laxatives, often producing results within a short time.\n\n✔ Gentle on the Intestines\n\nUnlike stimulant laxatives, lactulose works naturally without causing irritation or dependency.\n\n✔ Effective Stool Softening\n\nHelps soften hard stools, making bowel movements painless and comfortable.\n\n✔ Dual Action in Liver Disorders\n\nReduces ammonia absorption, aiding in the treatment of hepatic encephalopathy.\n\n✔ Suitable for Various Patient Groups\n\nCan be used in elderly patients, bedridden individuals, and those unable to take oral medications.\n\n✔ Non-Habit Forming\n\nDoes not cause dependency when used as directed by a healthcare professional.\n\nDirections for Use\nUse as directed by a physician.\nThe enema is usually administered rectally using the provided applicator.\nThe patient is advised to lie on their side during administration.\nRetain the solution for as long as possible to achieve maximum effectiveness.\n\nNote: Proper hygiene and correct administration technique are essential for best results.\n\nSide Effects of LACTUSMOOTH ENEMA\n\nLike all medications, LACTUSMOOTH ENEMA may cause some side effects, although not everyone experiences them.\n\nCommon Side Effects:\nMild abdominal discomfort\nBloating or gas\nRectal irritation\nCramping\nLess Common Side Effects:\nDiarrhea (if overused)\nElectrolyte imbalance\nNausea\nSerious Side Effects (Rare):\nSevere abdominal pain\nPersistent diarrhea\nDehydration\n\nIf any severe or persistent symptoms occur, medical attention should be sought immediately.\n\nPrecautions and Warnings\nUse only under medical supervision.\nNot recommended for patients with intestinal obstruction unless advised by a doctor.\nUse cautiously in patients with diabetes, as lactulose contains sugars.\nAvoid overuse to prevent electrolyte imbalance.\nMaintain adequate hydration during treatment.\n\nPregnant and breastfeeding women should consult a healthcare provider before use.\n\nStorage Instructions\nStore in a cool and dry place.\nKeep away from direct sunlight.\nDo not freeze.\nKeep out of reach of children.\nWhy Choose LACTUSMOOTH ENEMA?\n\nIn today’s fast-paced lifestyle, digestive issues like constipation are becoming increasingly common. LACTUSMOOTH ENEMA stands out as a reliable, safe, and effective solution due to its:\n\nClinically proven formulation\nRapid onset of action\nGentle and non-irritating mechanism\nVersatile usage in multiple conditions\n\nIt is especially beneficial in hospital settings and for home care patients requiring immediate relief.\n\nConclusion\n\nLACTUSMOOTH ENEMA (Lactulose Enema 20% w/v) is a highly effective and dependable treatment for constipation, bowel cleansing, and hepatic encephalopathy management. Its osmotic action ensures gentle yet efficient relief without causing dependency or harsh side effects. Whether used for acute constipation or as part of a broader medical treatment plan, it delivers consistent and safe results.",
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"name": "ferric carboxymaltose injection",
"description": "RUDIX FCM IV is a sterile intravenous iron formulation containing Ferric carboxymaltose, designed for the rapid and effective treatment of iron deficiency and iron deficiency anemia (IDA). It is specifically developed for patients who require fast iron replenishment, cannot tolerate oral iron supplements, or have conditions where oral iron therapy is ineffective.\n\nIron deficiency remains one of the most common nutritional deficiencies worldwide, affecting women, children, patients with chronic diseases, and individuals recovering from surgery. RUDIX FCM IV provides a modern, safe, and convenient approach to restoring iron stores efficiently under medical supervision.\n\nProduct Overview\n\nProduct Name: RUDIX FCM IV\n\nGeneric Name: Ferric Carboxymaltose Injection\n\nDosage Form: Intravenous injection / infusion\n\nRoute of Administration: IV use only\n\nIndication: Treatment of iron deficiency and iron deficiency anemia\n\nRUDIX FCM IV is formulated using advanced iron-carbohydrate complex technology that allows controlled and gradual release of iron into the bloodstream. This reduces the risk of free iron toxicity while ensuring effective replenishment of hemoglobin levels and iron stores.\n\nWhat is Ferric Carboxymaltose?\n\nFerric carboxymaltose is a next-generation intravenous iron complex. Unlike traditional iron salts, it allows the administration of larger single doses in a shorter duration, reducing the need for multiple hospital visits. The iron core is tightly bound within a carbohydrate shell, enabling controlled release and minimizing adverse reactions compared to older IV iron formulations.\n\nOnce administered, iron from ferric carboxymaltose is taken up by the body's iron-binding proteins and transported to the bone marrow, where it supports red blood cell production and improves hemoglobin levels.\n\nUses of RUDIX FCM IV\n\nRUDIX FCM IV is indicated in the following medical conditions:\n\n1. Iron Deficiency Anemia (IDA)\n\nUsed when oral iron therapy is ineffective, poorly tolerated, or when rapid correction of anemia is required.\n\n2. Chronic Kidney Disease (CKD)\n\nPatients with CKD often experience anemia due to reduced erythropoietin production and iron deficiency. IV iron helps restore iron levels efficiently.\n\n3. Postpartum Anemia\n\nWomen who experience significant blood loss during childbirth may require quick iron restoration.\n\n4. Heavy Menstrual Bleeding\n\nFor women with chronic blood loss leading to iron deficiency.\n\n5. Gastrointestinal Disorders\n\nConditions such as inflammatory bowel disease (IBD), celiac disease, or gastric surgery can impair iron absorption, making IV iron therapy necessary.\n\n6. Pre- and Post-Surgical Patients\n\nPatients undergoing major surgeries may require rapid iron replenishment to improve recovery.\n\nKey Benefits of RUDIX FCM IV\n✔ Rapid Iron Replenishment\n\nAllows administration of high doses in a single sitting, helping patients recover faster compared to oral supplements.\n\n✔ Improved Patient Compliance\n\nFewer hospital visits are required due to the ability to deliver larger doses in one infusion.\n\n✔ Better Tolerability\n\nLower incidence of gastrointestinal side effects compared to oral iron therapy.\n\n✔ Controlled Iron Release\n\nThe stable iron-carbohydrate complex reduces the risk of free iron reactions.\n\n✔ Suitable for Multiple Patient Groups\n\nSafe for use in adults with various underlying medical conditions under medical supervision.\n\n✔ Clinically Proven Effectiveness\n\nHelps improve hemoglobin levels, replenish iron stores, and reduce fatigue and weakness associated with anemia.\n\nDosage and Administration\n\nRUDIX FCM IV should be administered only by qualified healthcare professionals in a clinical setting. The dosage depends on:\n\nPatient’s body weight\n\nHemoglobin level\n\nSeverity of iron deficiency\n\nUnderlying medical condition\n\nIt may be given as a slow intravenous injection or diluted in saline for infusion. Monitoring during and after administration is recommended to ensure patient safety.\n\nPossible Side Effects\n\nLike all medications, RUDIX FCM IV may cause side effects, although not everyone experiences them.\n\nCommon Side Effects:\n\nHeadache\n\nNausea\n\nDizziness\n\nInjection site reactions\n\nFlushing\n\nLess Common but Serious Reactions:\n\nHypersensitivity reactions\n\nHypotension (low blood pressure)\n\nAllergic reactions\n\nShortness of breath\n\nPatients should be monitored during infusion. Immediate medical attention is required if signs of severe allergic reactions occur.\n\nPrecautions and Warnings\n\nShould not be used in patients with known hypersensitivity to ferric carboxymaltose.\n\nNot recommended in patients with iron overload disorders such as hemochromatosis.\n\nUse cautiously in patients with liver dysfunction.\n\nPregnancy and lactation use should be evaluated by a healthcare provider.\n\nMust be administered in facilities equipped to manage anaphylactic reactions.\n\nStorage Instructions\n\nStore at controlled room temperature.\n\nProtect from light.\n\nDo not freeze.\n\nKeep out of reach of children.\n\nWhy Choose RUDIX FCM IV?\nRUDIX FCM IV stands out due to its high-quality formulation, safety profile, and effectiveness in treating iron deficiency anemia. It offers healthcare providers a reliable option for rapid correction of iron deficiency while minimizing patient inconvenience.\n\nIts ability to deliver higher doses in fewer sessions makes it a preferred choice in hospitals, nephrology clinics, gynecology practices, and surgical recovery units.\nConclusion\nIron deficiency anemia can significantly impact quality of life, causing fatigue, weakness, reduced immunity, and impaired cognitive function. Timely correction is essential to restore overall health and vitality.",
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"name": "Tedizolid Phosphate 200 mg ",
"description": "TEDIZOLINE 200 is a state-of-the-art pharmaceutical formulation containing Tedizolid Phosphate 200 mg, representing a significant advancement in the treatment of serious bacterial skin infections. This next-generation oxazolidinone antibiotic offers a powerful solution for patients battling acute bacterial skin and skin structure infections (ABSSSI), including those caused by methicillin-resistant Staphylococcus aureus (MRSA) and other resistant bacterial strains. Developed to address the growing challenge of antibiotic resistance, TEDIZOLINE 200 provides healthcare professionals with an effective therapeutic option when conventional antibiotics may fall short.\nThe active ingredient, Tedizolid Phosphate, functions as a prodrug that is rapidly converted in the body to its active form, tedizolid. This sophisticated mechanism ensures optimal bioavailability and targeted antibacterial action. Each tablet of TEDIZOLINE 200 delivers a precise 200 mg dose, carefully calibrated to provide maximum efficacy while minimizing the risk of adverse effects. The medication is available in convenient oral tablet form, offering flexibility in treatment administration and improving patient compliance compared to intravenous-only alternatives.\nClinical Applications and Therapeutic Uses\nTEDIZOLINE 200 is specifically indicated for the treatment of acute bacterial skin and skin structure infections caused by susceptible strains of various gram-positive bacteria. These infections include cellulitis, major cutaneous abscesses, and wound infections that require systemic antibiotic therapy. The medication demonstrates exceptional efficacy against problematic pathogens including Staphylococcus aureus (both methicillin-susceptible and methicillin-resistant strains), various Streptococcus species, and Enterococcus faecalis.\nHealthcare providers prescribe TEDIZOLINE 200 when patients present with complicated skin infections characterized by significant inflammation, purulent discharge, or systemic signs of infection such as fever and elevated white blood cell counts. The medication is particularly valuable in hospital settings where antibiotic-resistant organisms pose significant treatment challenges, though it is equally effective for outpatient management of appropriate cases.\nThe standard treatment duration with TEDIZOLINE 200 is notably shorter than many traditional antibiotics, typically requiring only six days of therapy. This abbreviated course represents a significant advantage, potentially improving patient adherence, reducing the risk of developing resistance, and minimizing healthcare costs while maintaining excellent clinical outcomes.\nKey Benefits and Therapeutic Advantages\nSuperior Antimicrobial Potency: TEDIZOLINE 200 exhibits exceptional bactericidal activity against resistant gram-positive organisms, making it a frontline weapon against infections that have failed to respond to first-line antibiotics. Its unique mechanism of action—inhibiting bacterial protein synthesis by binding to the 23S ribosomal RNA of the 50S subunit—prevents bacteria from producing essential proteins necessary for survival and reproduction.\nShortened Treatment Duration: Unlike conventional antibiotics that may require ten to fourteen days of therapy, TEDIZOLINE 200 achieves comparable or superior outcomes with just six days of treatment. This condensed regimen reduces the pill burden for patients, improves treatment completion rates, and decreases the opportunity for resistance development.\nFlexible Administration Options: The medication offers both oral and intravenous formulations with nearly identical bioavailability, allowing seamless transitions between routes of administration. This flexibility enables early hospital discharge with continuation of oral therapy at home, reducing healthcare costs and improving patient comfort and quality of life.\nOnce-Daily Dosing Convenience: TEDIZOLINE 200's pharmacokinetic profile supports convenient once-daily administration, simplifying treatment schedules and enhancing patient compliance. The sustained therapeutic levels achieved with this dosing frequency ensure continuous antibacterial activity throughout the treatment course.\nReduced Drug Interaction Profile: Compared to its predecessor oxazolidinone antibiotics, TEDIZOLINE 200 demonstrates minimal interactions with dietary tyramine and requires less stringent dietary restrictions. Additionally, it exhibits reduced potential for serotonin syndrome, offering improved safety when used in patients taking certain antidepressants or other serotonergic medications.\nProven Clinical Efficacy: Extensive clinical trials have demonstrated that TEDIZOLINE 200 achieves cure rates comparable to or exceeding those of vancomycin and linezolid, the traditional gold standards for treating MRSA infections. These studies confirm both the non-inferiority and, in some parameters, the superiority of tedizolid phosphate in treating complicated skin infections.\nPotential Side Effects and Safety Considerations\nWhile TEDIZOLINE 200 is generally well-tolerated, patients and healthcare providers should be aware of potential adverse effects. The most commonly reported side effects include nausea, headache, diarrhea, and vomiting, which typically manifest as mild to moderate in severity and often resolve without intervention.\nGastrointestinal disturbances affect approximately five to ten percent of patients, with nausea being the most frequent complaint. Taking the medication with food may help minimize these symptoms without compromising absorption. Headaches occur in a similar percentage of patients and usually respond well to over-the-counter analgesics.\nMore serious but less common adverse effects include myelosuppression, manifesting as decreased blood cell counts. Although TEDIZOLINE 200 demonstrates less bone marrow suppression than older oxazolidinones, monitoring of complete blood counts is recommended for treatment courses extending beyond the standard six days or in patients with pre-existing hematologic conditions.\nPeripheral and optic neuropathy have been reported with prolonged oxazolidinone use, though the shorter treatment duration of TEDIZOLINE 200 substantially reduces this risk. Patients should report any vision changes, numbness, tingling, or weakness in extremities promptly to their healthcare provider.\nClostridium difficile-associated diarrhea can occur with virtually any antibiotic, including TEDIZOLINE 200. Patients experiencing severe, persistent, or bloody diarrhea during or following treatment should seek immediate medical attention.\nHypersensitivity reactions, though rare, may occur and can range from mild rash to severe anaphylaxis. Any signs of allergic reaction warrant immediate discontinuation and appropriate medical intervention.\nConclusion\nTEDIZOLINE 200 represents a significant therapeutic advancement in the management of acute bacterial skin and skin structure infections, particularly those involving antibiotic-resistant organisms. Its potent antimicrobial activity, convenient once-daily dosing, shortened treatment duration, and improved safety profile compared to earlier oxazolidinones make it an invaluable addition to the antimicrobial arsenal. The medication addresses critical unmet needs in infectious disease management, offering effective treatment options when traditional antibiotics prove insufficient.",
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"name": "Misoprostol Tablet 200 mcg",
"description": "MISOPIRATE 200 is a pharmaceutical preparation containing Misoprostol 200 mcg, a synthetic prostaglandin E1 analogue that has revolutionized women's healthcare and gastrointestinal treatment protocols. This medication represents a critical therapeutic option in modern medicine, offering solutions for conditions ranging from gastric ulcer prevention to obstetric and gynecological applications. Each tablet of MISOPIRATE 200 is precisely formulated to deliver consistent therapeutic benefits while maintaining strict quality standards.Misoprostol, the active ingredient in MISOPIRATE 200, was initially developed for protecting the gastric lining but has since become indispensable in reproductive healthcare. The medication works by mimicking natural prostaglandins in the body, which are hormone-like substances that regulate various physiological processes including gastric acid secretion, cervical ripening, and uterine contractions.Mechanism of ActionMISOPIRATE 200 functions through multiple pathways depending on the clinical indication. In the gastrointestinal system, it reduces gastric acid secretion by directly inhibiting parietal cells in the stomach lining. Simultaneously, it enhances the production of protective mucus and bicarbonate, creating a defensive barrier against acid-induced damage. This dual action makes it exceptionally effective in preventing and treating peptic ulcers, particularly those induced by nonsteroidal anti-inflammatory drugs (NSAIDs).In obstetric and gynecological applications, MISOPIRATE 200 acts on prostaglandin receptors in the uterus and cervix. It causes the cervix to soften and dilate while stimulating rhythmic uterine contractions. These properties make it valuable for medical management of early pregnancy complications, labor induction, and postpartum hemorrhage prevention.Clinical Uses and ApplicationsGastric Protection: MISOPIRATE 200 serves as a prophylactic agent for individuals requiring long-term NSAID therapy who are at elevated risk for developing gastric or duodenal ulcers. Patients with rheumatoid arthritis, osteoarthritis, or chronic pain conditions who depend on NSAIDs benefit significantly from concurrent misoprostol therapy.Peptic Ulcer Treatment: The medication accelerates healing of existing gastric ulcers by reducing acid exposure and promoting mucosal regeneration. Treatment typically spans four to eight weeks, depending on ulcer severity and individual response.Medical Management of Early Pregnancy Loss: Under strict medical supervision, MISOPIRATE 200 is utilized for managing incomplete miscarriage or missed abortion, offering a non-surgical alternative that many women prefer for emotional and practical reasons.Labor Induction: In hospital settings, healthcare providers may use MISOPIRATE 200 to ripen the cervix and initiate labor when medically indicated, such as in cases of post-term pregnancy or maternal health concerns.Postpartum Hemorrhage Prevention: The medication's ability to promote uterine contractions makes it valuable in preventing excessive bleeding after childbirth, particularly in resource-limited settings.Key Benefits of MISOPIRATE 200Effective Gastric Protection: MISOPIRATE 200 provides superior protection against NSAID-induced gastric damage compared to many alternatives. Clinical studies demonstrate up to 80% reduction in serious gastrointestinal complications among high-risk patients using preventive misoprostol therapy.Non-Invasive Medical Option: For women facing early pregnancy complications, MISOPIRATE 200 offers a medical alternative to surgical procedures, preserving privacy, reducing healthcare costs, and eliminating surgical risks such as anesthesia complications or uterine perforation.Rapid Onset of Action: The medication demonstrates quick absorption and onset, with effects typically beginning within 30 minutes to two hours, allowing for predictable therapeutic outcomes.Cost-Effectiveness: Compared to surgical interventions or hospitalization for complications, MISOPIRATE 200 represents an economical treatment option, making essential healthcare more accessible to diverse populations.Versatile Clinical Applications: The medication's multiple therapeutic uses make it a valuable tool across different medical specialties, from gastroenterology to obstetrics.Stable Formulation: MISOPIRATE 200 maintains stability across various storage conditions, improving accessibility in regions with limited refrigeration infrastructure.Potential Side Effects and Adverse ReactionsWhile MISOPIRATE 200 is generally well-tolerated, users should be aware of possible side effects:Gastrointestinal Disturbances: Diarrhea occurs in approximately 15-40% of patients, typically mild and self-limiting. Abdominal cramping, nausea, and flatulence are also common, particularly during initial treatment phases.Uterine Effects: Women of reproductive age may experience menstrual irregularities, heavier menstrual flow, or intermenstrual spotting. Uterine cramping is expected when the medication is used for obstetric purposes.Vascular Symptoms: Some patients report headaches, dizziness, or hot flashes, though these are generally transient and mild in nature.Allergic Reactions: Though rare, hypersensitivity reactions including skin rashes, itching, or more serious anaphylactic responses can occur and require immediate medical attention.Serious Complications: When used inappropriately for pregnancy termination outside medical supervision, serious complications including incomplete abortion, severe bleeding, infection, or rupture can occur. This underscores the critical importance of medical oversight.Important Precautions and ContraindicationsMISOPIRATE 200 is absolutely contraindicated during pregnancy when the intention is to continue the pregnancy, as it can cause miscarriage or severe fetal abnormalities. Women of childbearing potential must use reliable contraception during treatment. The medication should not be used by individuals with known allergy to prostaglandins or those with inflammatory bowel disease without careful medical evaluation.Patients with cardiovascular disease, cerebrovascular conditions, or poorly controlled hypertension require careful monitoring when using MISOPIRATE 200. The medication may interact with antacids containing magnesium, potentially exacerbating diarrhea.Dosage and Administration GuidelinesDosing of MISOPIRATE 200 varies significantly based on the clinical indication. For gastric protection, typical regimens involve 200 mcg taken two to four times daily with meals. For obstetric uses, dosing protocols are highly specific and must be determined by qualified healthcare providers based on individual circumstances, gestational age, and medical history.The medication should be taken with food to minimize gastrointestinal side effects. Tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed otherwise by a healthcare provider.ConclusionMISOPIRATE 200 represents a significant therapeutic advancement in both gastroenterology and reproductive healthcare. Its dual capacity to protect the gastric mucosa and influence uterine function makes it an invaluable medication across multiple clinical scenarios. The proven efficacy in preventing NSAID-induced ulcers has prevented countless cases of serious gastrointestinal bleeding, while its role in women's healthcare has expanded access to safe, effective medical management options.",
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