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{ "products": [ { "_id": "666c0208d89239081848a527", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "STARGAB 300 ", "description": "STARGAB 300 \nGabapentin 300 mg\nIntroduction:\n\nSTARGAB 300 contains Gabapentin, a versatile anticonvulsant and neuropathic pain agent widely used to manage conditions such as epilepsy and neuropathic pain. With a dosage strength of 300mg, STARGAB 300 aims to alleviate symptoms by modulating neurotransmitter release, thereby improving quality of life for patients.\nKey Features and Benefits:\n\nAnticonvulsant Action:\n\nSTARGAB 300 works by stabilizing electrical activity in the brain, making it an effective treatment for various types of seizures in patients with epilepsy. It helps reduce the frequency and severity of seizures, enhancing overall neurological stability.\nNeuropathic Pain Relief:\n\nGabapentin is particularly effective in managing neuropathic pain, which is pain caused by nerve damage. It helps reduce pain sensations, providing relief for conditions such as diabetic neuropathy, postherpetic neuralgia, and spinal cord injury-related pain.\nImproved Sleep Quality:\n\nPatients suffering from chronic pain often experience disrupted sleep. STARGAB 300 can improve sleep quality by alleviating pain, leading to better rest and overall well-being.\nMood Stabilization:\n\nIn addition to its primary uses, Gabapentin has been shown to have mood-stabilizing properties, making it beneficial for patients with mood disorders coexisting with neuropathic pain or epilepsy.\nWell-Tolerated and Safe:\n\nGabapentin is generally well-tolerated, with a favorable safety profile, making STARGAB 300 a reliable option for long-term management of neuropathic pain and seizures.\nDosage and Administration:\n\nInitial Dosage for Epilepsy:\n\nThe recommended starting dose of STARGAB 300 for epilepsy is 300mg once daily on the first day, 300mg twice daily on the second day, and 300mg three times daily on the third day. The dose can be gradually increased based on clinical response and tolerability, with a maintenance dose typically ranging from 900mg to 1800mg per day, divided into three doses.\nInitial Dosage for Neuropathic Pain:\n\nFor neuropathic pain, the initial dose is typically 300mg taken once daily, gradually increasing to 300mg three times daily, based on patient response and tolerability. The maintenance dose may range from 900mg to 3600mg per day, divided into multiple doses.\nAdministration Instructions:\n\nSTARGAB 300 tablets should be taken orally with or without food. It is advisable to take the medication at the same time each day to maintain consistent therapeutic levels in the bloodstream.\nContinued Monitoring:\n\nRegular monitoring of symptoms, pain levels, and potential side effects is essential during STARGAB 300 therapy to ensure therapeutic efficacy and patient safety.\nFor further information: \nEMAIL: info@sterispharma.com / contact@sterispharma.com \n CALL/WHATSAPP: 7877551268, 7849827488 \n Order NOW\nhttps://www.sterisonline.com/product/stargab-300-134312", "price": 155.0, "discountamount": 46.5, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 7, "_keywords": [ "mg", "rest", "life", "food", "brain", "EMAIL", "option", "epilepsy", "seizures", "addition", "symptoms", "severity", "Benefits", "patients", "same time", "first day", "third day", "frequency", "second day", "conditions", "Gabapentin", "medication", "information", "bloodstream", "pain levels", "three doses", "nerve damage", "Introduction", "sterispharma", "initial dose", "tolerability", "primary uses", "chronic pain", "Key Features", "sterisonline", "various types", "CALL/WHATSAPP", "starting dose", "multiple doses", "mood disorders", "patient safety", "Initial Dosage", "dosage strength", "pain sensations", "patient response", "maintenance dose", "clinical response", "Regular monitoring", "overall well-being", "Mood Stabilization", "STARGAB 300 tablets", "STARGAB 300 therapy", "electrical activity", "diabetic neuropathy", "effective treatment", "long-term management", "Continued Monitoring", "therapeutic efficacy", "Anticonvulsant Action", "neuropathic pain agent", "potential side effects", "postherpetic neuralgia", "Improved Sleep Quality", "Neuropathic Pain Relief", "favorable safety profile", "neurotransmitter release", "versatile anticonvulsant", "mood-stabilizing properties", "Administration Instructions", "consistent therapeutic levels", "overall neurological stability", "spinal cord injury-related pain" ], "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 1899, "imageuri": "https://productimages.withfloats.com/actual/666c020b8c6c791fd3b7131b.png", "tileimageuri": "https://productimages.withfloats.com/tile/666c020b8c6c791fd3b7131b.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2024-06-14T08:40:40.129Z", "updatedon": "2026-03-12T09:30:38.275Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM/products/stargab-300-/1899", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "STARGAB 300 ", "category": "NEUROLOGY RANGE", "tags": [ "stargab 300 uses in hindi", "stargab 300 price in hindi", "gabapentin 300mg used for", "gabapentin 300mg dosage", "maximum dosage of gabapentin for nerve pain" ], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": "", "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.001, "isnotforsale": false }, { "_id": "6a460bf90c11f3c74a816c87", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "methylprednisolone sodium succinate for injection usp", "description": "Methylprednisolone Sodium Succinate for Injection USP is a fast-acting corticosteroid administered intravenously or intramuscularly to control severe inflammation, allergic reactions, and autoimmune flare-ups. It works by rapidly suppressing the immune and inflammatory response and is used in hospital or clinical settings for acute conditions such as severe asthma attacks, anaphylaxis, autoimmune disease flares, and spinal cord injury protocols. It is a Schedule H prescription drug administered only under medical supervision.\n\nWhat Is Methylprednisolone Sodium Succinate for Injection USP?\n\nMethylprednisolone Sodium Succinate for Injection USP is a water-soluble, injectable corticosteroid used for rapid control of severe inflammatory, allergic, and autoimmune conditions. It is manufactured to United States Pharmacopeia (USP) standards and is typically administered by a healthcare professional via intravenous (IV) or intramuscular (IM) route when fast, high-potency anti-inflammatory or immunosuppressive action is required — situations where oral steroids act too slowly or oral intake isn't feasible.\n\nHow It Works\n\nMethylprednisolone sodium succinate is a synthetic glucocorticoid that acts rapidly once reconstituted and injected.\n\n\nBinds glucocorticoid receptors – enters cells and binds intracellular receptors that regulate inflammatory gene expression.\nSuppresses inflammatory mediators – reduces production of prostaglandins, leukotrienes, and cytokines responsible for swelling, redness, and pain.\nStabilizes cell membranes – reduces capillary permeability, limiting fluid leakage and tissue swelling at the site of inflammation.\nDampens immune overactivity – suppresses lymphocyte and macrophage activity, calming autoimmune or allergic overreactions.\nDelivers rapid systemic action – because it's water-soluble and given IV/IM, onset of anti-inflammatory effect is significantly faster than oral steroids.\n\n\nClinical Indications\n\nConditionWhy Methylprednisolone Injection Is UsedSevere Allergic Reactions / AnaphylaxisRapidly controls swelling, airway inflammation, and allergic cascadeAcute Asthma Exacerbation / COPD FlareReduces airway inflammation when inhalers alone are insufficientAutoimmune Disease Flares (Lupus, Rheumatoid Arthritis)High-dose pulse therapy to control acute flaresSpinal Cord Injury (acute, under specialist protocol)Used in specific clinical protocols to limit secondary inflammationSevere Dermatologic ReactionsControls widespread inflammatory skin reactionsPost-Transplant / Organ Rejection ManagementUsed as part of immunosuppressive regimens\n\nDosage & Administration\n\nParameterRecommendationTypical Adult Dose10–40 mg IV, may range up to 30 mg/kg in high-dose pulse therapy for specific conditionsRouteIntravenous (IV) injection/infusion or Intramuscular (IM) injectionFrequencyAs directed by the treating physician; often single dose or short tapering courseReconstitutionMust be reconstituted only with the accompanying diluent as per product insert, immediately before useAdministration SettingHospital, clinic, or under direct medical/nursing supervision onlyDurationShort-term acute use unless otherwise directed; long-term use requires specialist monitoring\n\nThis is a Schedule H prescription-only medicine. Dosage must be determined and administered by a qualified healthcare professional.\n\nPrecautions\n\n\nTo be administered only by or under the supervision of a healthcare professional.\nNot for self-administration or home use.\nInform the doctor of any active infections, as corticosteroids can mask symptoms and suppress immune response.\nUse with caution in patients with diabetes, hypertension, peptic ulcer disease, osteoporosis, or psychiatric history.\nAvoid live vaccines during treatment due to immunosuppressive effects.\nPregnant or breastfeeding patients should use only under strict medical guidance.\nAbrupt discontinuation after prolonged use should be avoided; tapering may be required as advised by the physician.\n\n\nPossible Side Effects\n\nMost side effects relate to the drug's systemic corticosteroid action and are monitored by the administering clinician:\n\n\nElevated blood sugar levels\nFluid retention, increased blood pressure\nMood changes, insomnia, or restlessness\nNausea or gastrointestinal discomfort\nIncreased susceptibility to infection\nInjection site reactions\n\n\nSerious side effects requiring immediate medical attention include severe allergic reaction, signs of infection (fever, chills), significant mood or behavioral changes, unusual swelling, or vision disturbances. Because this is administered in a clinical setting, the healthcare team monitors for these actively.\n\nComparison: Methylprednisolone vs. Other Injectable Corticosteroids\n\nDrugRelative PotencyCommon Use CaseRouteMethylprednisolone Sodium SuccinateHighAcute severe inflammation, autoimmune flaresIV/IMHydrocortisone Sodium SuccinateLowerAdrenal insufficiency, milder acute inflammationIV/IMDexamethasone Sodium PhosphateVery HighCerebral edema, severe allergic/inflammatory conditionsIV/IMBetamethasone Sodium PhosphateHighAllergic and inflammatory conditions, fetal lung maturityIV/IMTriamcinolone AcetonideModerate (depot)Localized/intra-articular inflammationIM/Intra-articular\n\nKey Statistics\n\nStatisticData PointSourceOnset of anti-inflammatory action after IV administrationWithin 1–2 hours for measurable effectClinical pharmacology references, USP monographUse in acute severe asthma protocolsRecommended as part of systemic corticosteroid therapy in emergency guidelinesGlobal Initiative for Asthma (GINA) guidelinesHospital use in anaphylaxis managementIncluded as an adjunct in anaphylaxis treatment protocols alongside epinephrineWorld Allergy Organization guidanceHigh-dose pulse therapy applicationUsed in select autoimmune flare protocols under specialist supervisionPublished rheumatology treatment guidelines\n\nExpert Insight\n\n[Insert verified physician or clinical pharmacologist commentary here — Claude has not fabricated a quote. Recommend sourcing a short, attributable statement from a Steris Healthcare medical advisor or a cited clinical guideline before publishing.]\n\nConclusion\n\nMethylprednisolone Sodium Succinate for Injection USP is a high-potency, fast-acting corticosteroid reserved for situations where rapid control of severe inflammation, allergic reaction, or autoimmune flare is essential. Administered only under clinical supervision, it plays a critical role in emergency and hospital-based treatment protocols — from anaphylaxis and acute asthma to autoimmune disease management. As a Schedule H medicine, it must never be self-administered; dosage, route, and duration should always be determined by a qualified physician based on the patient's condition. For pharmacopoeia-grade quality and reliable hospital supply, source this injection through a WHO-GMP certified manufacturer.\n\nPrescription only – consult your doctor.\n\n\nHigh-Ranking FAQs (Google Search & Voice Search Optimized)\n\n1. What is methylprednisolone sodium succinate injection used for?\nIt is used to rapidly control severe inflammation, allergic reactions, and autoimmune flare-ups, such as anaphylaxis, acute asthma attacks, and lupus or rheumatoid arthritis flares. It is administered under medical supervision in hospital or clinical settings.\n\n2. Is methylprednisolone injection a steroid?\nYes, it is a synthetic corticosteroid (glucocorticoid) that works by suppressing inflammatory and immune responses in the body, providing rapid relief in acute, severe conditions.\n\n3. How is methylprednisolone sodium succinate injection given?\nIt is given by a healthcare professional via intravenous (IV) or intramuscular (IM) injection, after being reconstituted with the correct diluent immediately before administration. It is not for self-injection or home use.\n\n4. How fast does methylprednisolone injection start working?\nBecause it is water-soluble and given directly into the bloodstream or muscle, measurable anti-inflammatory effects typically begin within one to two hours of administration.\n\n5. What are the side effects of methylprednisolone injection?\nCommon effects include elevated blood sugar, fluid retention, mood changes, and increased infection risk. These are monitored by the administering healthcare team, and serious reactions are managed promptly in a clinical setting.\n\n6. Is methylprednisolone sodium succinate injection available without a prescription?\nNo. It is a Schedule H prescription-only medicine that must be administered by or under the direct supervision of a qualified healthcare professional.\n\n7. What is the difference between methylprednisolone and dexamethasone injection?\nBoth are injectable corticosteroids, but dexamethasone has a longer duration of action and higher relative potency, while methylprednisolone is often preferred for acute pulse therapy and shorter-acting systemic control. The choice depends on the clinical scenario and physician judgment.\n\n8. Can methylprednisolone injection be used in pregnancy?\nIt may be used in pregnancy only when clearly necessary and under strict medical supervision, as the treating physician will weigh the benefits against potential risks for the specific condition being treated.", "price": 47.0, "discountamount": 19.0, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 1, "_keywords": null, "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 2465, "imageuri": "https://productimages.withfloats.com/actual/6a460bfb9f5529389b8b15b8.png", "tileimageuri": "https://productimages.withfloats.com/tile/6a460bfb9f5529389b8b15b8.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2026-07-02T06:58:01.631Z", "updatedon": "2026-07-02T06:58:01.631Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//methylprednisolone-sodium-succinate-for-injection-usp/2465", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "METHIDENOSOLE 40 INJ", "category": "GENERAL RANGE", "tags": [ "methylprednisolone sodium succinate injection uses", "methylprednisolone sodium succinate injection uses in hindi", "methylprednisolone sodium succinate", "methylprednisolone sodium succinate injection", "inj methylprednisolone sodium succinate", "methylprednisolone sodium succinate uses in hindi", "methylprednisolone sodium succinate for injection", "methylprednisolone sodium succinate injection usp" ], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": null, "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.0, "isnotforsale": false }, { "_id": "6a23ea9077576cb2b8e237ba", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "nefopam hydrochloride 30 mg", "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.", "price": 129.0, "discountamount": 99.0, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 1, "_keywords": null, "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 2439, "imageuri": "https://productimages.withfloats.com/actual/6a23ea940522fa56c444240d.png", "tileimageuri": "https://productimages.withfloats.com/tile/6a23ea940522fa56c444240d.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2026-06-06T09:38:24.458Z", "updatedon": "2026-06-06T09:38:24.458Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//nefopam-hydrochloride-30-mg/2439", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "NAFTIBEST 30", "category": "ORTHOLOGYRANG", "tags": [ "nefopam hydrochloride 30 mg", "nefopam hydrochloride 30", "Nefopam hydrochloride tablets 30 mg uses", "Nefopam 30 mg side effects" ], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": null, "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.0, "isnotforsale": false }, { "_id": "666bff0d4cb45413344ec745", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "Gabapentine 100mg", "description": "STERIS GABAPENTIN 100 \nGabapentine (100mg)\nIntroduction:\n\nSTERIS GABAPENTIN 100 contains Gabapentin, an anticonvulsant and neuropathic pain agent widely used to manage conditions such as epilepsy and neuropathic pain. With a dosage strength of 100mg, STERIS GABAPENTIN 100 aims to alleviate symptoms by modulating neurotransmitter release, thereby improving quality of life for patients.\nKey Features and Benefits:\n\nAnticonvulsant Action:\n\nSTERIS GABAPENTIN 100 works by stabilizing electrical activity in the brain, making it an effective treatment for various types of seizures in patients with epilepsy.\nNeuropathic Pain Relief:\n\nGabapentin is particularly effective in managing neuropathic pain, which is pain caused by nerve damage. It helps reduce pain sensations, providing relief for conditions such as diabetic neuropathy, postherpetic neuralgia, and spinal cord injury-related pain.\nImproved Sleep Quality:\n\nPatients suffering from chronic pain often experience disrupted sleep. STERIS GABAPENTIN 100 can improve sleep quality by alleviating pain, leading to better rest and overall well-being.\nMood Stabilization:\n\nIn addition to its primary uses, Gabapentin has been shown to have mood-stabilizing properties, making it beneficial for patients with mood disorders coexisting with neuropathic pain or epilepsy.\nWell-Tolerated and Safe:\n\nGabapentin is generally well-tolerated, with a favorable safety profile, making STERIS GABAPENTIN 100 a reliable option for long-term management of neuropathic pain and seizures.\nDosage and Administration:\n\nInitial Dosage for Epilepsy:\n\nThe recommended starting dose of STERIS GABAPENTIN 100 for epilepsy is 300mg on the first day, followed by 300mg twice daily on the second day, and 300mg three times daily on the third day. The dose can be gradually increased based on clinical response and tolerability.\nInitial Dosage for Neuropathic Pain:\n\nFor neuropathic pain, the initial dose is typically 100-300mg taken once daily, gradually increasing to 300mg three times daily based on patient response and tolerability.\nAdministration Instructions:\n\nSTERIS GABAPENTIN 100 tablets should be taken orally with or without food. It is advisable to take the medication at the same time each day to maintain consistent therapeutic levels in the bloodstream.\nContinued Monitoring:\n\nRegular monitoring of symptoms, pain levels, and potential side effects is essential during STERIS GABAPENTIN 100 therapy to ensure therapeutic efficacy and patient safety.\nFor further information: \nEMAIL: info@sterispharma.com / contact@sterispharma.com \n CALL/WHATSAPP: 7877551268, 7849827488 \n Order NOW\n", "price": 85.0, "discountamount": 25.5, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 7, "_keywords": [ "rest", "life", "food", "brain", "EMAIL", "300mg", "100mg", "option", "seizures", "addition", "symptoms", "Benefits", "patients", "epilepsy", "third day", "same time", "first day", "medication", "conditions", "second day", "Gabapentine", "information", "bloodstream", "pain levels", "nerve damage", "Introduction", "sterispharma", "initial dose", "tolerability", "chronic pain", "primary uses", "Key Features", "sterisonline", "CALL/WHATSAPP", "various types", "starting dose", "mood disorders", "Initial Dosage", "patient safety", "pain sensations", "dosage strength", "patient response", "clinical response", "Regular monitoring", "Mood Stabilization", "overall well-being", "electrical activity", "effective treatment", "diabetic neuropathy", "Continued Monitoring", "long-term management", "therapeutic efficacy", "Anticonvulsant Action", "Improved Sleep Quality", "neuropathic pain agent", "potential side effects", "postherpetic neuralgia", "Neuropathic Pain Relief", "neurotransmitter release", "favorable safety profile", "Administration Instructions", "mood-stabilizing properties", "STERIS GABAPENTIN 100 therapy", "STERIS GABAPENTIN 100 tablets", "consistent therapeutic levels", "spinal cord injury-related pain" ], "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 1898, "imageuri": "https://productimages.withfloats.com/actual/666bff128c6c791fd3b7123a.png", "tileimageuri": "https://productimages.withfloats.com/tile/666bff128c6c791fd3b7123a.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2024-06-14T08:27:57.94Z", "updatedon": "2026-03-14T10:15:22.493Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//gabapentine-100mg/1898", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "STERIS GABAPENTIN 100 ", "category": "NEUROLOGY RANGE", "tags": [ "normal dosage of gabapentin for nerve pain side ef", "maximum dose of gabapentin for adults", "gabapentin 100mg uses", "gabapentin a high dose", "uses of gabapentin capsules", "gabapentin 100mg" ], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": "", "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.001, "isnotforsale": false }, { "_id": "69da35fd3c63c5c22eae5b2b", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "pregabalin methylcobalamin duloxetine | DULOXTIME 3D 30", "description": "DULOXTIME 3D 30 is a scientifically formulated combination medicine used for the effective management of neuropathic pain and nerve-related disorders. It contains Pregabalin 75 mg, Methylcobalamin 1500 mcg, and Duloxetine 30 mg (Delayed Release), which work synergistically to relieve pain, restore nerve health, and improve overall patient well-being.\nNeuropathic pain arises due to nerve damage caused by conditions such as diabetes, spinal cord injuries, or chronic illnesses. Symptoms often include burning sensation, tingling, numbness, and sharp shooting pain. DULOXTIME 3D 30 is widely prescribed by healthcare professionals in India for its dual benefit of pain relief and nerve repair, making it a reliable and comprehensive treatment option.\n\nUses\n\nDULOXTIME 3D 30 is primarily used for the treatment of:\nDiabetic Neuropathy: Helps control nerve pain caused by prolonged high blood sugar levels\nPeripheral Neuropathy: Reduces tingling, numbness, and burning sensation in hands and feet\nChronic Neuropathic Pain: Provides long-term relief from nerve-related pain conditions\nFibromyalgia: Assists in managing widespread muscle and nerve pain\nSpinal Cord Injury Pain: Improves nerve-related discomfort after spinal damage\nDepression Associated with Pain: Duloxetine helps manage mood disturbances linked with chronic pain\nBenefits\n\nDULOXTIME 3D 30 offers multiple clinical advantages due to its combination therapy:\nEffective Pain Control: Pregabalin calms overactive nerves, reducing pain signals\nNerve Regeneration: Methylcobalamin (Vitamin B12) supports repair and regeneration of damaged nerves\nImproved Mood & Sleep: Duloxetine helps reduce anxiety and depression, improving sleep quality\nComprehensive Treatment: Targets both the cause and symptoms of neuropathic pain\nEnhanced Quality of Life: Reduces discomfort and improves daily functioning\nThis triple-action formula ensures better patient outcomes compared to single-drug therapy.\n\nDosage\n\nThe dosage of DULOXTIME 3D 30 should be taken strictly as per the doctor’s prescription.\nUsually prescribed once daily\nSwallow the capsule whole with water; do not crush or chew\nCan be taken with or without food\nDuration of therapy depends on the severity and response to treatment\nImportant: Do not stop taking the medicine suddenly, as it may lead to withdrawal symptoms. Always consult your doctor before discontinuation.\n\nSide Effects\n\nLike all medicines, DULOXTIME 3D 30 may cause some side effects. Most are mild and temporary:\nCommon Side Effects:\nDizziness or sleepiness\nNausea or vomiting\nDry mouth\nConstipation\nFatigue\nBlurred vision\nSerious Side Effects (Rare):\nMood changes or depression\nSevere allergic reactions\nSwelling of face, lips, or limbs\nDifficulty in breathing\nSeek immediate medical help if any severe or unusual symptoms occur.\n\nPrecautions and Warning\n\nBefore using DULOXTIME 3D 30, keep the following precautions in mind:\nInform your doctor if you have kidney, liver, or heart problems\nAvoid alcohol, as it may increase drowsiness and side effects\nNot recommended during pregnancy and breastfeeding unless advised by a doctor\nAvoid driving or operating machinery due to possible dizziness\nMonitor blood sugar levels regularly in diabetic patients\nInform your doctor about all other medications to prevent interactions\nPatients with a history of depression or suicidal thoughts should be carefully monitored during treatment.\n\nConclusion\n\nDULOXTIME 3D 30 (Pregabalin 75 mg, Methylcobalamin 1500 mcg & Duloxetine 30 mg Delayed Release Capsules) is a trusted and effective solution for managing neuropathic pain and nerve damage. Its unique combination provides comprehensive relief by reducing pain, repairing nerves, and improving mental well-being.\nWhen used under proper medical guidance, DULOXTIME 3D 30 significantly enhances the quality of life for patients suffering from chronic nerve-related conditions. For best results, always follow the prescribed dosage and complete the full course of treatment.", "price": 345.0, "discountamount": 104.0, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 1, "_keywords": null, "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 2377, "imageuri": "https://productimages.withfloats.com/actual/69da35ff835e796becbf992d.png", "tileimageuri": "https://productimages.withfloats.com/tile/69da35ff835e796becbf992d.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2026-04-11T11:52:29.924Z", "updatedon": "2026-04-15T12:58:29.101Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//pregabalin-methylcobalamin-duloxetine-duloxtime-3d-30/2377", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "DULOXTIME 3D 30", "category": "NEUROLOGY RANGE", "tags": [ "pregabalin methylcobalamin duloxetine", "pregabalin methylcobalamin duloxetine capsules uses for nerve pain", "delayed release duloxetine 30 mg how it works in neuropathy", "pregabalin methylcobalamin duloxetine side effects in elderly", "best time to take pregabalin duloxetine combination capsules", "capsule for burning feet nerve pain india", "best medicine for neuropathy with vitamin b12 support", "pregabalin methylcobalamin duloxetine capsules india price", "pregabalin 75 mg duloxetine 30 mg capsules brands india", "buy pregabalin methylcobalamin duloxetine capsules online", "pregabalin 75 mg duloxetine 30 mg price india", "pregabalin duloxetine capsules with prescription delivery" ], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": null, "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.0, "isnotforsale": false }, { "_id": "6990397c160585bfd7038bed", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "Baclofen Sustained Release 30 mg", "description": "BACLOFINE SR 30: Comprehensive Product Guide\nProduct Overview\nBACLOFINE SR 30 is an advanced pharmaceutical formulation containing Baclofen 30 mg in a sustained-release delivery system. This prescription medication represents a significant advancement in the management of muscle spasticity and related neuromuscular conditions. The sustained-release technology ensures consistent therapeutic effects throughout the day, providing patients with improved symptom control and enhanced quality of life.\nBaclofen, the active pharmaceutical ingredient in BACLOFINE SR 30, belongs to a class of medications known as skeletal muscle relaxants and antispasmodic agents. The SR (Sustained Release) formulation is specifically engineered to release the medication gradually over an extended period, maintaining steady blood levels and reducing the frequency of dosing compared to conventional immediate-release formulations.\nMechanism of Action and Therapeutic Use\nBACLOFINE SR 30 works by acting on the central nervous system, specifically targeting GABA-B receptors in the spinal cord and brain. GABA (gamma-aminobutyric acid) is the primary inhibitory neurotransmitter in the nervous system. By stimulating these receptors, Baclofen reduces the excessive nerve signals that cause muscles to contract involuntarily, thereby alleviating spasticity and associated discomfort.\nThe sustained-release technology incorporated in BACLOFINE SR 30 utilizes advanced polymer-based matrices that control the rate at which the active ingredient is released into the bloodstream. This innovative approach ensures that patients receive consistent therapeutic coverage for up to 12-24 hours from a single dose, eliminating the peaks and troughs associated with immediate-release formulations.\nPrimary Indications\nBACLOFINE SR 30 is primarily prescribed for managing muscle spasticity associated with various neurological conditions including multiple sclerosis, spinal cord injuries, cerebral palsy, stroke, brain injuries, and other conditions affecting the central nervous system. The medication is particularly beneficial for patients experiencing painful muscle spasms, stiffness, and involuntary muscle contractions that interfere with daily activities, mobility, and rehabilitation efforts.\nKey Benefits of BACLOFINE SR 30\nExtended Duration of Action\nThe most significant advantage of BACLOFINE SR 30 is its sustained-release formulation, which provides prolonged therapeutic effects. Patients typically require only one or two doses per day, compared to three or four doses with conventional formulations. This extended duration improves medication adherence and provides more consistent symptom control throughout the day and night.\nImproved Symptom Management\nBy maintaining steady blood levels of Baclofen, BACLOFINE SR 30 delivers superior control of muscle spasticity with fewer fluctuations in symptom relief. Patients experience reduced muscle stiffness, decreased frequency and severity of muscle spasms, improved range of motion, and enhanced ability to participate in physical therapy and rehabilitation programs.\nEnhanced Quality of Life\nThe consistent therapeutic effects of BACLOFINE SR 30 translate into meaningful improvements in daily functioning. Patients often report better sleep quality due to reduced nighttime spasms, improved mobility and independence in performing daily activities, reduced pain and discomfort associated with muscle spasticity, and greater participation in social and recreational activities.\nReduced Dosing Frequency\nThe sustained-release technology means fewer doses throughout the day, which simplifies medication regimens and improves compliance, particularly for patients managing multiple medications. This convenience factor is especially valuable for individuals with cognitive impairments or those who require caregiver assistance with medication administration.\nSmoother Therapeutic Response\nUnlike immediate-release formulations that can cause pronounced peaks in drug levels, BACLOFINE SR 30 provides a more gradual and sustained therapeutic effect. This results in reduced risk of dose-related side effects, more stable muscle relaxation throughout the dosing interval, and minimized breakthrough spasticity between doses.\nPotential Side Effects and Considerations\nWhile BACLOFINE SR 30 is generally well-tolerated, patients should be aware of potential side effects. It's important to note that not everyone experiences these effects, and many side effects diminish as the body adjusts to the medication.\nCommon Side Effects\nThe most frequently reported side effects include drowsiness and sedation, which typically occur during initial therapy or dose adjustments. Patients may also experience dizziness, fatigue, weakness, headache, nausea, and constipation. These effects are usually mild to moderate and often resolve within the first few weeks of treatment.\nCentral Nervous System Effects\nSome patients may experience confusion, particularly elderly individuals, difficulty concentrating, insomnia or sleep disturbances, and mood changes. These effects should be monitored and reported to healthcare providers if they persist or worsen.\nCardiovascular and Other Effects\nOccasional side effects may include hypotension (low blood pressure), urinary frequency or retention, dry mouth, and muscle weakness beyond the intended therapeutic effect.\nSerious Considerations\nPatients should seek immediate medical attention if they experience severe allergic reactions, hallucinations or severe confusion, difficulty breathing, severe muscle weakness affecting breathing or swallowing, or signs of overdose including extreme drowsiness, respiratory depression, or seizures.\nImportant Warnings\nBACLOFINE SR 30 should never be discontinued abruptly without medical supervision, as sudden withdrawal can lead to serious complications including seizures, hallucinations, increased spasticity, and other potentially life-threatening symptoms. Dose reduction must be gradual and carefully supervised by a healthcare provider.\nThe medication may cause drowsiness and impair mental alertness, so patients should avoid driving, operating machinery, or engaging in activities requiring full alertness until they understand how the medication affects them. Alcohol and other central nervous system depressants should be avoided or used with extreme caution, as they can potentiate the sedative effects of Baclofen.\nDosage and Administration Guidelines\nBACLOFINE SR 30 should be taken exactly as prescribed by a healthcare provider. The tablets should be swallowed whole and not crushed, chewed, or broken, as this would compromise the sustained-release mechanism and potentially lead to dose dumping. The medication can be taken with or without food, though taking it with food may help reduce gastrointestinal side effects.\nDosage is highly individualized based on the patient's condition, response to treatment, and tolerance. Healthcare providers typically initiate therapy at lower doses and gradually titrate upward to achieve optimal therapeutic effects while minimizing side effects.\nConclusion\nBACLOFINE SR 30 represents a sophisticated therapeutic option for individuals struggling with muscle spasticity and related neuromuscular conditions. The sustained-release formulation offers distinct advantages over conventional immediate-release preparations, including extended duration of action, improved symptom control, reduced dosing frequency, and enhanced patient convenience and compliance.", "price": 245.0, "discountamount": 74.0, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 1, "_keywords": null, "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 2306, "imageuri": "https://productimages.withfloats.com/actual/6990397eb2070251db7032d7.png", "tileimageuri": "https://productimages.withfloats.com/tile/6990397eb2070251db7032d7.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2026-02-14T08:59:40.632Z", "updatedon": "2026-04-28T12:02:50.6Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//baclofen-sustained-release-30-mg/2306", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "BACLOFINE SR 30", "category": "NEUROLOGYRANGE", "tags": [ "baclofen sr 30 mg tablet uses", "what is baclofen sr 30 prescribed for", "baclofen sr 30 mg dosage guide", "baclofen sr 30 mg for back pain", "baclofen sr 30 mg vs regular baclofen", "baclofen sr 30 mg for spinal cord injury", "baclofen sr 30 mg side effects in adults", "is baclofen sr 30 mg addictive", "buy baclofen sr 30 mg online", "baclofen sr 30 mg manufacturer", "baclofen sr 30 mg prescription required", "baclofen sr 30 mg vs baclofen 10 mg" ], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": null, "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.0, "isnotforsale": false }, { "_id": "6662e3b87247ae19c482b97c", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "Enzalutamide 40mg", "description": "Enzalutamide 40 mg capsules represent a breakthrough in targeted therapy for advanced prostate cancer, particularly in metastatic castration-resistant prostate cancer (mCRPC) and metastatic castration-sensitive prostate cancer (mCSPC). This second-generation androgen receptor inhibitor works by disrupting multiple steps in the androgen signaling pathway, offering patients a chance to slow disease progression, reduce tumor burden, and extend survival even after other treatments fail. Administered as a once-daily oral capsule, enzalutamide 40 mg provides four capsules per day (total 160 mg), making it convenient for long-term use in clinical settings where hormone therapy alone proves insufficient.​\n\nPatients often turn to enzalutamide when facing rising PSA levels despite androgen deprivation therapy (ADT), experiencing bone pain, or dealing with cancer spread to lymph nodes or distant sites. Its high affinity for androgen receptors—5-8 times stronger than first-generation antiandrogens like bicalutamide—ensures potent blockade without agonist activity, translating to real-world benefits like delayed chemotherapy needs and improved quality of life during treatment.​\n\nProduct Use and Indications\nEnzalutamide 40 mg primarily treats metastatic castration-resistant prostate cancer (mCRPC) in patients previously treated with docetaxel or progressing despite ADT. The FDA and EMA approvals extend to non-metastatic CRPC (nmCRPC) with high-risk biochemical recurrence and metastatic castration-sensitive prostate cancer (mCSPC) alongside ADT, based on landmark trials like AFFIRM, PREVAIL, PROSPER, and ARCHES.​\n\nKey uses include:\n\nSlowing tumor growth in hormone-refractory stages by inhibiting androgen-driven proliferation.\n\nReducing skeletal-related events like fractures or spinal cord compression in bone metastases.\n\nDelaying progression to chemotherapy in pre-chemotherapy mCRPC, with PREVAIL showing 17-month median radiographic progression-free survival (rPFS) versus 4 months for placebo.​\n\nIn mCSPC, ARCHES trial data demonstrated 61% risk reduction in progression or death when combined with ADT. Clinicians monitor PSA response (≥50% decline in 70-80% of patients) and imaging every 3 months to assess efficacy.​\n\nMechanism of Action\nEnzalutamide 40 mg exerts a threefold blockade on androgen receptor (AR) signaling: it competitively inhibits androgen binding to AR (with affinity rivaling dihydrotestosterone), prevents nuclear translocation of the ligand-receptor complex, and disrupts DNA binding and coactivator recruitment at androgen response elements. This comprehensive inhibition downregulates oncogenes like TMPRSS2-ERG fusion genes common in prostate cancer, inducing apoptosis and halting cell proliferation without lowering systemic testosterone levels.​\n\nUnlike earlier antiandrogens, enzalutamide avoids partial agonist effects, ensuring pure antagonism even in AR-overexpressing tumors. Its active metabolite, N-desmethyl enzalutamide (via CYP2C8), contributes 30% to activity, with steady-state levels achieved in 4 weeks.​\n\nKey Benefits\nExtended Progression-Free Survival: In PREVAIL (pre-chemo mCRPC), median overall survival reached 32.4 months versus 30.2 for placebo; PROSPER (nmCRPC) delayed metastasis by 22 months.​\n\nPSA Response and Tumor Shrinkage: 78% PSA90 response rate; radiographic responses in 29% with measurable disease.​\n\nQuality of Life Preservation: Delays pain progression (hazard ratio 0.40) and chemotherapy (by 17 months), maintaining daily function.​\n\nBone Protection: Reduces fractures by 30% in high-risk patients via AR inhibition in osteoblasts.​\n\nCombination Synergy: Enhances ADT efficacy in mCSPC, cutting death risk by 33% per ARCHES.​\n\nThese benefits position enzalutamide 40 mg as a cornerstone in modern prostate cancer protocols, especially for fit patients tolerating oral therapy.​\n\nSide Effects\nEnzalutamide 40 mg carries a manageable profile, with most effects dose-related and reversible upon discontinuation.\n\nCommon Side Effects\nFatigue/Asthenia (34-50%): Often mild, peaking in first months; rest and nutrition help.\n\nArthralgia/Myalgia (14-21%): Joint/muscle pain managed with NSAIDs.\n\nHot Flashes (20%): Androgen blockade mimic; hydration aids.\n\nHeadache/Dizziness (12-19%): Transient; avoid driving if severe.\n\nHypertension (6-13%): Monitor BP monthly; antihypertensives as needed.\n\nGI Issues (diarrhea 12%, nausea 11%): Antiemetics support compliance.​\n\nSerious Side Effects\nSeizures (0.9%): Highest risk in epileptics or brain mets; EEG baseline, avoid triggers.\n\nPosterior Reversible Encephalopathy (PRES): Rare (<0.1%); headache, confusion—MRI confirms.\n\nFalls/Fractures (15% increased risk): Due to weakness/falls; DEXA scans recommended.\n\nCardiac Events (2-5%): MI/arrhythmias; ECG monitoring in CVD history.\n\nHepatic Injury (1%): ALT/AST elevation; monthly labs first 3 months.​\n\nDiscontinuation occurs in 8-10%; supportive care mitigates most.​\n\nDosage and Administration\nStandard dose: 160 mg (four 40 mg capsules) once daily, with or without food. Swallow intact; no crushing. Adjust for CYP2A4 inducers (e.g., rifampin—increase to 240 mg) or strong inhibitors (reduce to 80 mg). Continue until progression/toxicity; no dose interruptions beyond 28 days without reassessment.​\n\nPrecautions and Monitoring\nContraindicated in pregnancy (teratogenic; absolute contraception for men/ partners). Screen for seizure history; CYP2C8/3A4 interactions (e.g., ketoconazole). Baseline LFTs, PSA, testosterone; imaging q8-12 weeks. Elderly (>75) monitor falls.​\nConclusion\nEnzalutamide 40 mg stands as a transformative therapy, empowering prostate cancer patients with prolonged control over aggressive disease through precise AR inhibition. Balancing robust efficacy—evidenced by landmark trials delaying metastasis and death—with proactive side effect management, it enhances survival and daily living. Patients achieve meaningful milestones, from family events to travel, underscoring its role in personalized oncology. Consult oncologists for integration into care plans, ensuring optimal outcomes in this challenging journey.\nEmail: info@sterispharma.com / contact@sterispharma.com\nCall/WhatsApp: 7877551268, 7849827488\n\n\n\n\n\n\n\n\n", "price": 10781.0, "discountamount": 3235.0, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 7, "_keywords": [ "Call", "Email", "doctor", "product", "fatigue", "WhatsApp", "treatment", "schedules", "ENZULAMIDE", "monitoring", "hot flashes", "information", "sterisonline", "hypertension", "sterispharma", "prostate cancer", "Enzalutamide 40mg", "prescribed dosages", "androgen receptors", "cancer cell growth", "Common side effects", "comprehensive guidance" ], "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 1527, "imageuri": "https://productimages.withfloats.com/actual/667d2a356c582d228f45a098.png", "tileimageuri": "https://productimages.withfloats.com/tile/667d2a356c582d228f45a098.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2024-06-07T10:40:56.587Z", "updatedon": "2026-03-16T08:18:18.117Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//enzalutamide-40mg/1527", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "ENZULAMIDE 40", "category": "Oncology", "tags": [ "enzalutamide 40 mg side effects", "enzalutamide 40 mg brands in india", "enzalutamide 40 mg uses in hindi", "enzalutamide 40 mg dosage", "advanced prostate cancer", "prostate cancer", "metastatic castration-resistant prostate cancer", "enzalutamide 40mg tablets", "enzalutamide 40 mg capsule", "enzalutamide 40mg uses", "enzalutamide 40mg dosage", "enzalutamide 40mg price in india", "enzalutamide 40mg composition", "enzalutamide 40mg working mechanism", "enzalutamide 40mg side effects", "enzalutamide 40mg benefits", "enzalutamide 40mg drug information", "enzalutamide 40mg therapy details", "enzalutamide 40mg oral capsule", "enzalutamide 40mg treatment option", "enzalutamide 40mg pharmaceutical uses", "enzalutamide 40mg branded tablets", "enzalutamide 40mg generic medicine", "enzalutamide 40mg manufacturer in india", "what is enzalutamide 40mg used for", "how enzalutamide 40mg works", "is enzalutamide 40mg safe", "enzalutamide 40mg tablet information", "enzalutamide 40mg dosage guidelines" ], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": "", "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.001, "isnotforsale": false }, { "_id": "662ba161f7fe09029cbf518e", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "Temozolomide 100mg", "description": "TMOZOLMIDE 100\nTemodal 100mg Capsule stands as a cornerstone in oncology, specifically formulated with temozolomide 100mg to combat aggressive brain tumors like glioblastoma multiforme (GBM) and anaplastic astrocytoma. This oral alkylating agent crosses the blood-brain barrier effectively, delivering targeted chemotherapy that disrupts cancer cell DNA replication, halting tumor progression in adults with newly diagnosed or recurrent cases. Patients and caregivers often seek Temodal 100mg for its role in standard-of-care regimens, combining seamlessly with radiotherapy for enhanced survival outcomes in high-grade gliomas.​\n\nManufactured to rigorous standards, Temodal 100mg offers convenient capsule dosing, swallowed whole on an empty stomach to maximize bioavailability. Its proven track record in clinical settings makes it indispensable for neuro-oncology, where timely intervention can extend quality life years amid challenging diagnoses.​\n\nProduct Uses and Mechanism of Action\nTemodal 100mg Capsule primarily treats adult patients with newly diagnosed glioblastoma multiforme alongside radiotherapy, followed by maintenance monotherapy to prevent relapse. It also addresses refractory anaplastic astrocytoma—tumors that progress despite prior therapies—and recurrent malignant gliomas in children over three years, including brainstem glioma and high-grade astrocytoma.​\n\nThe mechanism hinges on temozolomide's rapid conversion to the active metabolite MTIC (5-(3-methyltriazen-1-yl)imidazole-4-carboxamide) at physiological pH, which methylates DNA at O6 and N7 guanine positions. This methylation induces DNA strand breaks during replication, triggering apoptosis in rapidly dividing glioma cells while sparing normal brain tissue to a degree. Unlike intravenous chemotherapies, Temodal 100mg achieves therapeutic CNS concentrations without specialized delivery, ideal for outpatient management.​\n\nIn practice, concomitant phase dosing (75 mg/m² daily with RT for 42 days) transitions to cycles of 150-200 mg/m² on days 1-5 every 28 days, tailored by body surface area and toxicity monitoring. This cyclical approach balances efficacy against cumulative myelosuppression, supporting long-term tumor control.​\n\nKey Benefits of Temodal 100mg Capsule\nTemodal 100mg delivers transformative benefits grounded in landmark trials:\n\nSuperior Survival in GBM: Concomitant temozolomide with RT extends median survival from 12.1 to 14.6 months, with 2-year survival rising from 10% to 26% per pivotal Phase III data.​\n\nMaintenance Therapy Efficacy: Post-RT cycles sustain progression-free survival up to 6-12 months in responders, delaying recurrence in MGMT-methylated tumors.​\n\nConvenient Oral Administration: Eliminates hospital visits, improving compliance for patients undergoing radiotherapy; rapid absorption (peak in 1 hour) ensures consistent exposure.​\n\nBlood-Brain Barrier Penetration: Achieves 30-40% cerebrospinal fluid levels, outperforming many alkylators in CNS malignancies.​\n\nPediatric Applicability: Effective in recurrent pediatric gliomas, with tolerance mirroring adults for ages 3+.​\n\nThese advantages position Temodal 100mg as a first-line essential, particularly for newly diagnosed cases where every month counts toward preserving cognitive function and independence.​\n\nReal-world use extends to off-label scenarios like metastatic melanoma or high-risk meningiomas under specialist oversight, though primary indications remain brain tumors. Its stability in acidic environments enhances reliability during storage and transit.​\n\nSide Effects of Temodal 100mg Capsule\nWhile Temodal 100mg offers life-prolonging potential, its myelotoxic profile demands vigilant hematologic monitoring. Common effects stem from DNA damage in rapidly proliferating bone marrow cells, peaking mid-cycle.​\n\nCommon Side Effects\nHematologic Toxicity: Neutropenia, thrombocytopenia (platelet nadir day 21-28), lymphopenia, and anemia affect 10-20%; febrile neutropenia occurs in vulnerable patients.​\n\nGastrointestinal Issues: Nausea (up to 50%), vomiting, constipation—mitigated by antiemetics like ondansetron taken 30 minutes prior.​\n\nNeurologic Symptoms: Fatigue, headache, ataxia, dizziness, or amnesia-like effects, often transient and RT-attributable.​\n\nOther: Alopecia, anorexia, rash, or elevated liver enzymes resolving post-cycle.​\n\nProphylactic measures like dose delays (if platelets <100 x 10⁹/L or neutrophils <1.5 x 10⁹/L) maintain tolerability; supportive care ensures most complete therapy.​\n\nSerious Side Effects\nRare but critical risks include:\n\nPancytopenia or Aplastic Anemia: Prolonged suppression risking infections or bleeding—mandatory weekly CBCs in early cycles.​\n\nSecondary Malignancies: Myeloid leukemia post-treatment (latency 1-5 years), hepatitis B reactivation.​\n\nOpportunistic Infections: Pneumocystis jirovecii pneumonia (PJP) prophylaxis with TMP-SMX recommended due to grade 3/4 lymphopenia.​\n\nNeurologic Deterioration: Status epilepticus, hemiplegia in advanced disease.​\n\nDiscontinue if non-hematologic CTC grade >2 persists; pregnant women face fetal toxicity—use contraception during and 6 months post-therapy.​\n\nDosage and Administration Guidelines\nInitiate Temodal 100mg at 75 mg/m² daily during RT (up to 49 days), escalating to 150 mg/m² (cycle 1) or 200 mg/m² (subsequent) for 5 days/23 off. Adjust downward for toxicity; hepatic/renal impairment rarely necessitates change unless severe. Capsules (5,20,100,250mg strengths) enable precise BSA-based dosing—e.g., ~100mg capsule for 70kg/m² patients.​\n\nPrecautions and Substitutes\nMonitor pregnancy status; avoid live vaccines. Substitutes include generic temozolomide capsules matching bioequivalence, though Temodal 100mg remains the reference standard. Interactions with valproic acid reduce clearance—increase dose 40% if co-administered.​\n\nConclusion\nTemodal 100mg Capsule empowers patients against glioblastoma's relentless advance, blending potent antineoplastic action with manageable administration for meaningful survival gains. From halting tumor growth via strategic DNA alkylation to fitting seamlessly into multimodal care, it embodies hope amid adversity—always under oncologist guidance to navigate toxicities and optimize outcomes. Embrace informed treatment; lives extend beyond statistics with vigilant care.\nFor further information:\nEmail: info@sterispharma.com / contact@sterispharma.com\nCall/WhatsApp: 7877551268, 7849827488\nBuy Now: \n", "price": 7400.0, "discountamount": 2220.0, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 7, "_keywords": [ "part", "body", "types", "drugs", "class", "nausea", "spread", "growth", "surgery", "fatigue", "vomiting", "capsules", "TMOZOLMIDE", "instructions", "Temozolomide", "cancer cells", "brain tumors", "glioblastoma", "unusual symptoms", "potent medication", "other medications", "radiation therapy", "blood cell counts", "healthcare provider", "Common side effects", "comprehensive treatment plan" ], "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 773, "imageuri": "https://productimages.withfloats.com/actual/662ba164481840e7a7fdadc0.png", "tileimageuri": "https://productimages.withfloats.com/tile/662ba164481840e7a7fdadc0.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2024-04-26T12:43:13.957Z", "updatedon": "2026-03-12T08:07:02.773Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//temozolomide-100mg/773", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "TMOZOLMIDE 100", "category": "NEPHROLOGYRANGE", "tags": [], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": "", "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.001, "isnotforsale": false }, { "_id": "6a7722af7f45a0190eb37920", "fptag": "STERISHEALTHCARE", "merchantname": null, "customwidgets": null, "externalsourceid": null, "name": "Tolperisone Hydrochloride & Paracetamol Tablets", "description": "TOPERITIME P 150/325: Dual-Action Relief for Musculoskeletal Pain and Spasms\nTOPERITIME P 150/325 is a prescription combination therapy formulated to treat acute musculoskeletal discomfort, muscle stiffness, and associated inflammatory pain. By uniting a centrally acting muscle relaxant with a proven analgesic, this film-coated tablet addresses both the neurological and physical aspects of muscle strain, restoring movement and facilitating recovery.\n\nActive Ingredients\nEach film-coated tablet contains:\n\nTolperisone Hydrochloride (150 mg): A muscle relaxant targeting involuntary contractions within the central nervous system.\n\nParacetamol (325 mg): A widely recognized analgesic and antipyretic agent that blocks pain signal transmission.\n\nAvailable in blister packaging and dispensed strictly under a licensed physician's order.\n\nTherapeutic Mechanism\nPainful muscle conditions often create a feedback loop where localized pain triggers involuntary spasms, which in turn exacerbate the pain. TOPERITIME P 150/325 disrupts this cycle through a two-pronged mechanism:\n\nNeuromuscular Regulation: Tolperisone Hydrochloride acts on the spinal cord and brainstem reflexes to inhibit hyperactive nerve impulses driving muscle tension. Unlike traditional skeletal muscle relaxants, it achieves this with minimal central nervous system depression, significantly reducing the likelihood of heavy sedation.\n\nNociceptive Blocking: Paracetamol inhibits prostaglandin synthesis within the central nervous system, raising the body's overall pain threshold and attenuating pain signals originating from injured tissues.\n\nBy simultaneously relaxing tight muscle fibers and dampening pain sensation, the formulation provides comprehensive symptomatic relief.\n\nClinical Indications\nHealthcare professionals may prescribe TOPERITIME P 150/325 for various acute and subacute conditions characterized by pain and hypertonia, including:\n\nAcute muscle spasms and athletic injuries\n\nAcute or chronic lower back pain (lumbago)\n\nCervical spine discomfort and stiff neck\n\nCervical and lumbar spondylosis\n\nFrozen shoulder (adhesive capsulitis)\n\nPost-operative or post-traumatic muscle recovery\n\nGeneralized connective tissue or orthopedic pain\n\nKey Clinical Features\nBalanced Dual Action: Simultaneously targets involuntary contractions and pain sensation.\n\nLow-Sedation Profile: Tolperisone allows patients to maintain daily function without severe daytime drowsiness typical of older relaxants.\n\nEnhanced Mobility: Reduces joint and tissue stiffness, enabling better engagement in physical rehabilitation.\n\nStreamlined Regimen: Combines two therapeutic agents into a single convenient dosage form.\n\nUsage Guidelines\nThis medication must be taken strictly in accordance with a medical prescription.\n\nAdministration: Swallow the tablet whole with water. Do not crush, chew, or split the film-coated tablet.\n\nTiming: Take immediately after a meal to reduce potential gastrointestinal upset, unless directed otherwise by a doctor.\n\nCompliance: Complete the full course prescribed by your physician, and do not alter the recommended dosage.\n\nPotential Side Effects\nWhile generally well-tolerated, some individuals may experience mild side effects, including:\n\nGastrointestinal distress or mild nausea\n\nTransient dizziness or lightheadedness\n\nHeadaches\n\nGeneral fatigue or muscular weakness\n\nRare: Hypersensitivity reactions or cutaneous skin rashes (discontinue use and consult a physician immediately if severe symptoms appear).\n\nSafety Precautions and Considerations\nConsult a medical practitioner prior to initiating treatment if any of the following apply:\n\nPre-existing hepatic (liver) or renal (kidney) impairment\n\nKnown hypersensitivity to Tolperisone, Paracetamol, or related compounds\n\nPregnancy, plans for pregnancy, or active breastfeeding\n\nHistory of chronic alcohol dependency (due to increased liver sensitivity with Paracetamol)\n\nConcurrent use of other medications, particularly other products containing Paracetamol or central nervous system depressants\n\nStorage and Handling\nStore in a cool, dry area below 25°C (77°F).\n\nProtect from direct light, heat, and moisture.\n\nKeep strictly out of reach of children and pets.\n\nCheck the packaging expiration date before administration.\n\nFrequently Asked Questions\nWhat primary conditions does TOPERITIME P 150/325 treat?\n\nIt is indicated for short-term relief from acute musculoskeletal pain, muscle spasms, neck strains, backaches, and related orthopedic disorders.\n\nWhy is Tolperisone combined with Paracetamol?\n\nTolperisone eases muscle tightness at the neurological level, while Paracetamol lowers overall pain perception, creating a synergistic effect that addresses both spasm and pain together.\n\nWill this medication cause severe drowsiness?\n\nTolperisone is specifically designed to exert less sedating activity compared to older muscle relaxants. However, individual sensitivity varies, so caution is advised when driving or operating machinery until individual tolerance is established.\n\nIs TOPERITIME P 150/325 available over the counter?\n\nNo. It requires a valid medical prescription and direct supervision by a registered healthcare professional.", "price": 95.0, "discountamount": 29.0, "currencycode": "INR", "priority": 1000000, "isfreeshipmentavailable": false, "shipmentduration": 1, "_keywords": null, "isarchived": false, "isavailable": true, "applicationid": null, "productindex": 2493, "imageuri": "https://productimages.withfloats.com/actual/6a7722b0ed25653efa18364e.png", "tileimageuri": "https://productimages.withfloats.com/tile/6a7722b0ed25653efa18364e.png", "images": null, "totalqueries": 0, "gpid": null, "groupproductid": null, "createdon": "2026-08-08T12:35:59.075Z", "updatedon": "2026-08-08T12:35:59.075Z", "buyonlinelink": null, "producturl": "http://WWW.STERISINDIA.COM//tolperisone-hydrochloride-paracetamol-tablets/2493", "availableunits": -1.0, "iscodavailable": false, "isprepaidonlineavailable": false, "maxcodorders": 0, "maxprepaidonlineorders": 0, "uniquepaymenturl": null, "brandname": "TOPERITIME P 150/325", "category": "ORTHOLOGYRANGE", "tags": [], "variants": false, "keyspecification": null, "otherspecifications": null, "pickupaddressreferenceid": null, "paymenttype": "UniquePaymentUrl", "producttype": "products", "hsncode": null, "gstslab": 0.0, "isnotforsale": false } ], "hasmoreitems": false, "isapirequest": false, "totalresults": 27, "query": null, "floatingpoint": null }