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"name": "buy Tadalafil 20mg softgel capsule Order",
"description": "Vikalis Vx Super Active is having the drug ingredient called Tadalafil that is used to treat Erectile Dysfunction in Men. This super active Vikalis Vx is softgel capsule so it can easily taken in mouth. it help to achieve Erection for 24 to 36 hours if you are sexually stimulated.\n\nVikalis Vx super active capsule has proven to improve erectile function in most men, even when men suffer with mild, moderate or severe erectile dysfunction. This medication is available in dose of tadalafil 20mg which has shown great promise with satisfactory results under clinical trials. Vikalis softgel capsule helps to enhance your self-confidence by improving your ability with power to maintain hard and strong erection.\n\nOther Information:\n\nPacking: Blister of 10 tabs\nDelivery lead Time: Immediate.\nPort of Dispatch: Mumbai.\nMode of Export: Air Cargo/Sea Cargo/Door Delivery Cargo Couriers.\nPayment terms: Bank wire terms",
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"name": "Buy omeprazole-20mg-domperidone-10mg-capsule-supplier-india",
"description": "Source Omeprazole 20mg + Domperidone 10mg capsules in bulk from Ernest Impex. B2B pharmaceutical supply for distributors, pharmacies, hospitals and licensed buyers across India.\n\nOmeprazole 20mg + Domperidone 10mg Capsule Supplier in India\n\nOmeprazole 20mg + Domperidone 10mg Capsule is a fixed-dose pharmaceutical combination containing omeprazole and domperidone. Omeprazole belongs to the proton-pump inhibitor class and reduces gastric-acid production, while domperidone affects gastrointestinal motility.\n\nIndia’s CDSCO approval list records the omeprazole 20 mg enteric-coated plus domperidone 10 mg capsule combination for GERD that does not respond to omeprazole alone. The medicine should be supplied and used strictly according to its approved label and a registered medical\n\nErnest Impex accepts B2B enquiries for Omeprazole 20mg + Domperidone 10mg capsules from pharmaceutical distributors, medicine wholesalers, hospitals, pharmacies and licensed institutional buyers. Customers can request information about available brands, packaging, minimum order quantity, batch documentation, pricing and delivery coverage.\n\nLooking for Omeprazole 20mg + Domperidone 10mg capsules in bulk? Contact Ernest Impex for current availability, packaging, documentation, MOQ and wholesale quotation.",
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"name": "Azilsartan Medoxomil 40mg & 80mg Tablet",
"description": "Azilsartan Medoxomil 40mg & 80mg Tablet \n\nAzilsmart contains Azilsartan Medoxomil, an angiotensin II receptor blocker (ARB) used for the management of hypertension. Azilsartan Medoxomil is a prodrug that is converted in the body to its active form, azilsartan.\n\nThe active drug selectively blocks angiotensin II AT1 receptors, reducing the vasoconstrictive and aldosterone-related effects of angiotensin II. This helps blood vessels relax, decreases peripheral vascular resistance and supports effective control of elevated blood pressure.\n\nAzilsmart 40 mg and Azilsmart 80 mg provide different strength options for individualized antihypertensive therapy. Treatment should be prescribed according to the patient's blood-pressure response and overall clinical condition. Blood pressure, renal function and serum potassium may require monitoring during therapy.\n\nProduct Variants:\n\nProduct\tActive Ingredient\tStrength\nAzilsmart 40 mg\tAzilsartan Medoxomil\t40 mg\nAzilsmart 80 mg\tAzilsartan Medoxomil\t80 mg\n\n\nUses of Azilsmart: \n\nAzilsartan Medoxomil is primarily used for:\n\nManagement of hypertension (high blood pressure)\nLong-term blood-pressure control in appropriate patients\nUse alone or with other antihypertensive medicines when clinically indicated\n\nMechanism of Action: \n\nAzilsartan Medoxomil is converted to active azilsartan, which selectively blocks angiotensin II from binding to AT1 receptors. This reduces vasoconstriction and aldosterone-mediated effects, resulting in reduced vascular resistance and lower blood pressure.\n\nPossible Side Effects: \n\nPotential adverse effects may include:\n\nDizziness\nLow blood pressure\nFatigue\nIncreased serum potassium\nChanges in kidney function\n\nPatients with renal impairment, volume depletion or those using other medicines that affect the renin-angiotensin system may require additional monitoring.\n",
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"name": "Dabigatran Etexilate Mesylate 110mg & 150mg Capsule",
"description": "Dabigatran Etexilate Mesylate\n\nDabita is an oral anticoagulant range containing Dabigatran Etexilate Mesylate, a prodrug that is converted in the body to active Dabigatran. Dabigatran is a direct thrombin inhibitor that reduces the formation and development of unwanted blood clots.\n\nDabita is available in 110 mg and 150 mg strengths, allowing clinicians to select an appropriate regimen according to the approved indication and individual patient factors.\n\nDabita Product Range\nProduct\tActive Ingredient\tStrength\nDabita 110\tDabigatran Etexilate Mesylate\t110 mg\nDabita 150\tDabigatran Etexilate Mesylate\t150 mg\n\nDosage Form: Capsule\nMedicine Group: Direct Oral Anticoagulant (DOAC)\nPharmacological Class: Direct Thrombin Inhibitor\nTherapeutic Area: Anticoagulation / Thromboembolism Management\n\nFrom Prodrug to Anticoagulant\n\nDabigatran Etexilate itself is a prodrug. After administration, it is converted to active Dabigatran.\n\nActive Dabigatran directly inhibits thrombin (Factor IIa).\n\nThrombin normally converts fibrinogen into fibrin, which is an important step in clot formation.\n\nDabigatran Etexilate\n→ converted to Dabigatran\n→ Thrombin inhibited\n→ Fibrin formation reduced\n→ Unwanted clot formation becomes less likely\n\nUnlike warfarin, Dabigatran does not produce its anticoagulant effect through vitamin K antagonism.\n\nKidney Function Has a Major Influence\n\nRenal function is particularly important with Dabigatran because a substantial proportion of active drug elimination occurs through the kidneys.\n\nReduced kidney function can increase Dabigatran exposure and consequently increase the risk of bleeding.\n\nRenal assessment may therefore be required before treatment and periodically during therapy, particularly when kidney function could decline.\n\nBleeding: The Main Risk to Recognize\n\nAnticoagulant therapy can make bleeding occur more easily or last longer.\n\nSigns That Need Attention\nUnexplained or extensive bruising\nPersistent nose or gum bleeding\nBlood in urine\nRed or black stools\nVomiting or coughing blood\nUnusually heavy menstrual bleeding\nPersistent weakness associated with suspected blood loss\n\nCapsule Handling Is Important\n\nDabigatran capsules have specific formulation characteristics.\n\nCapsules should generally be swallowed whole. Opening, crushing, breaking, or chewing them can significantly alter drug exposure.\n\nThey should also be stored according to the original product instructions and protected appropriately from moisture.\n\nFrequently Asked Questions\n\n1. What is the difference between Dabita 110 and Dabita 150?\nBoth contain Dabigatran Etexilate Mesylate but provide different strengths—110 mg and 150 mg. Selection depends on the prescribed indication and patient-specific factors.\n\n2. Is Dabigatran the same type of anticoagulant as warfarin?\nNo. Dabigatran is a direct thrombin inhibitor, whereas warfarin acts through the vitamin K pathway.\n\n3. Does Dabita require routine INR testing?\nRoutine INR monitoring used for warfarin is generally not used to guide Dabigatran therapy. Clinical assessment and renal-function monitoring remain important.\n\n4. Why is kidney function important?\nDabigatran is substantially eliminated through the kidneys. Impaired renal function can increase drug exposure and bleeding risk.\n\n5. Can Dabita capsules be opened?\nDabigatran capsules should generally be swallowed whole because opening or crushing them can alter drug exposure.\n\n6. What happens if Dabita is stopped suddenly?\nPremature interruption of anticoagulation can increase thromboembolic risk when anticoagulant protection is still required. Treatment changes should be clinician-directed.\n\n7. Should a dentist know about Dabita treatment?\nYes. Doctors, dentists, and other healthcare professionals should be informed before invasive procedures because Dabigatran affects blood clotting.\n\n8. What is the most important safety concern with Dabita?\nBleeding is the principal risk associated with Dabigatran and other anticoagulant medicines.\n",
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"name": "Neostigmine Methylsulfate Injection",
"description": "STIGVEX 0.5 & Stigvex 2.5 Injection\n\nGeneric Name: Neostigmine Methylsulfate\nDosage Form: Injection\nDrug Class: Acetylcholinesterase Inhibitor / Cholinergic Agent\n\nClinical Applications\n\nDepending on approved labeling, Neostigmine Injection may be used for:\n\nReversal of non-depolarizing neuromuscular blockade\nManagement of myasthenia gravis in selected situations\nOther medically supervised indications requiring increased cholinergic activity\nWhat Happens at the Neuromuscular Junction?\n\nNeostigmine inhibits the enzyme acetylcholinesterase, slowing the breakdown of acetylcholine. Increased acetylcholine helps improve communication between motor nerves and muscles.\n\nWhen used to reverse neuromuscular blockade, an antimuscarinic medicine such as glycopyrrolate or atropine is generally administered as appropriate to reduce unwanted muscarinic effects.\n\nEffects That Require Monitoring\n\nBecause Neostigmine increases cholinergic activity, patients should be monitored for:\n\nBradycardia\nIncreased salivation\nBronchial secretions\nBronchospasm\nAbdominal cramps\nNausea or vomiting\nMuscle weakness\n\nExcessive exposure can produce a cholinergic crisis, potentially causing severe weakness and respiratory complications.\n\nKey Precautions\n\nParticular care is required in patients with:\n\nBradycardia or cardiac conduction disorders\nAsthma or bronchospastic disease\nPeptic ulcer disease\nMechanical intestinal or urinary obstruction\nRecent gastrointestinal surgery\n\nFAQs\n\n1. What does Stigvex Injection contain?\nIt contains Neostigmine Methylsulfate, a reversible acetylcholinesterase inhibitor.\n\n2. What is Stigvex commonly used for?\nAn important use of injectable neostigmine is the reversal of certain non-depolarizing neuromuscular blocking medicines after surgery.\n\n3. How does Neostigmine work?\nIt inhibits acetylcholinesterase, resulting in increased acetylcholine at neuromuscular junctions.\n\n4. Why is an antimuscarinic medicine sometimes given with Neostigmine?\nIt helps counteract muscarinic effects such as bradycardia and excessive secretions.\n\n5. Can Neostigmine affect heart rate?\nYes. Bradycardia is an important potential adverse effect.\n\n6. Can Stigvex be self-administered?\nNo. Injectable Neostigmine should be administered by qualified healthcare professionals with appropriate monitoring.\n\n7. What happens if too much Neostigmine is administered?\nExcessive cholinergic activity can cause a cholinergic crisis, with symptoms including marked secretions, bradycardia, muscle weakness, and potentially respiratory compromise.\n\n8. What is the difference between STIGVEX 0.5 and Stigvex 2.5?\nThey appear to represent different strengths of Neostigmine Injection. The exact mg/mL concentration and container volume should be confirmed from each product label.\n",
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"name": "Sacubitril & Valsartan Tablets online",
"description": "Sacufox V Tablets contain a combination of Sacubitril and Valsartan, a cardiovascular medicine used in the management of certain patients with chronic heart failure. The combination helps reduce cardiovascular strain through complementary effects on the natriuretic peptide system and renin-angiotensin system.\n\n\nDual Mechanism\n\nSacubitril inhibits neprilysin, increasing levels of beneficial vasoactive peptides that can promote vasodilation and sodium excretion.\n\nValsartan blocks angiotensin II AT1 receptors, helping reduce vasoconstriction and aldosterone-related sodium and fluid retention.\n\nTogether, these actions can reduce cardiac workload and support heart-failure management.\n\nClinical Role\n\nDepending on approved labeling and patient characteristics, Sacubitril/Valsartan may be prescribed to:\n\nManage chronic heart failure\nReduce the risk of cardiovascular death and heart-failure hospitalization in appropriate patients\nSupport control of cardiovascular workload\nImprove heart-failure outcomes as part of a comprehensive treatment plan\nImportant Checks During Treatment\n\nHealthcare professionals may monitor:\n\nBlood pressure\nKidney function\nSerum potassium\nSymptoms of dizziness or hypotension\nSigns of angioedema\nOther medicines affecting the renin-angiotensin system\n\nPossible Side Effects\n\nPotential adverse effects include:\n\nLow blood pressure\nDizziness\nIncreased potassium levels\nReduced kidney function\nCough\n\nKey Safety Alert\n\nSacubitril/Valsartan must not be administered together with an ACE inhibitor. A 36-hour washout period is required when switching between an ACE inhibitor and Sacubitril/Valsartan because of the increased risk of angioedema.\n\nIt is also contraindicated during pregnancy because medicines acting on the renin-angiotensin system can cause serious fetal harm.\n\nAvailable Presentations\nProduct\tActive Ingredients\tLabeled Strength\nSacufox V 50 Tablets\tSacubitril + Valsartan\t50 mg total\nSacufox V 100 Tablets\tSacubitril + Valsartan\t100 mg total\n\nThe individual Sacubitril and Valsartan strengths should be confirmed from the actual product pack before publishing.\n\n\nFAQs\n\n1. What does Sacufox V contain?\nIt contains the cardiovascular combination Sacubitril and Valsartan.\n\n2. What is Sacufox V used for?\nSacubitril/Valsartan is used for the management of certain patients with chronic heart failure, according to approved labeling.\n\n3. What type of medicine is Sacubitril/Valsartan?\nIt belongs to a class called angiotensin receptor-neprilysin inhibitors (ARNIs).\n\n4. How does Sacufox V help in heart failure?\nIt combines neprilysin inhibition with angiotensin II receptor blockade, helping promote vasodilation, reduce fluid retention, and decrease cardiovascular workload.\n\n5. Can Sacufox V be taken with an ACE inhibitor?\nNo. Concurrent use is contraindicated, and a 36-hour interval is required when switching between an ACE inhibitor and Sacubitril/Valsartan.\n\n6. Does Sacufox V affect potassium levels?\nYes. It can cause hyperkalemia, so potassium monitoring may be required.\n\n7. Does kidney function need monitoring?\nYes. Kidney function should be assessed as clinically appropriate because Sacubitril/Valsartan can affect renal function, particularly in susceptible patients.\n\n8. Can Sacufox V be used during pregnancy?\nNo. Sacubitril/Valsartan can cause serious fetal harm and should not be used during pregnancy.\n\n",
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"description": "Pregafox 300 Capsules contain Pregabalin Capsules IP (300mg), a medicine widely used to manage neuropathic pain, epilepsy, fibromyalgia, and generalized anxiety disorder. Pregabalin works by calming overactive nerve signals in the brain, thereby reducing pain and preventing seizures. Buy Pregafox 300mg Capsules online or order Pregafox 300 Capsules in bulk from a reliable supplier. These 300mg Pregafix Pregabalin capsules are an effective solution for long-term nerve pain management.\n\nDosage\n\nPregafox 300 Capsules should be taken orally with water, exactly as prescribed by your doctor. The dosage may differ based on the condition being treated, patient’s age, weight, and overall health. For correct dosing and to buy Pregafox 300mg Capsules online, always consult your doctor.\n\nPrecautions\n\nDriving: Avoid driving or operating machinery if you feel dizzy or drowsy after taking the capsule.\nAlcohol: Do not consume alcohol, as it can intensify side effects like sleepiness and dizziness.\nKidney: Use cautiously in patients with kidney problems; dose adjustments may be necessary.\nPregnancy/Breastfeeding: Should only be taken under medical supervision during pregnancy or breastfeeding.\nLiver: Usually safe but should be used under guidance if you have liver issues.\nSide Effects\n\nSome common side effects of Pregafox 300 Capsules may include:\n\nDizziness\nDrowsiness\nBlurred vision\nWeight gain\nSwelling in hands or feet\nDry mouth\nSerious side effects such as mood changes, muscle pain, or vision disturbances should be reported to your doctor immediately.\n\nWarning\n\nDo not exceed the prescribed dose of Pregafox 300 Capsules. Overuse may lead to dependency, withdrawal symptoms, or worsening of side effects. Always follow your doctor’s advice when you buy Pregafox 300mg Capsules online or order Pregafox 300 Capsules in bulk.\n\nFAQ\n\n1.How long should I take Pregafox 300 Capsules?\nThe duration depends on your medical condition. Do not stop suddenly without consulting your doctor, as it may cause withdrawal symptoms.\n\n2. Are Pregafox 300 Capsules safe for daily use?\nYes, when taken as prescribed by your doctor. Long-term use requires medical supervision.\n\n3. How should I store Pregafox 300 Capsules?\nStore in a cool, dry place away from moisture and direct sunlight. Keep away from children and pets.\n\n4. Can I take Pregafox 300 Capsules with other medications?\nPregabalin may interact with other medicines, especially those for anxiety, sleep, or pain. Inform your doctor about all medications you are taking.\n \n\nBuy Pregafox 300mg Capsules online from us, as we are a bulk supplier of Pregafox 300mg Capsules. You can also order Pregafox 300 Capsules in bulk directly from our team. For more details on the third party manufacturer of Pregafox 300 Capsules and supply of 300mg Pregafix Pregabalin capsules, connect with us today!",
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"name": "Omeprazole Gastro-Resistant Capsules IP / Omeprazole for Injection",
"description": "Generic Name: Omeprazole\n\nOmeecan 20 mg Capsules: Omeprazole Gastro-Resistant Capsules IP – 20 mg\nOmeecan 40 Injection: Omeprazole for Injection – 40 mg, Lyophilized Powder\n\n\nOmeecan contains Omeprazole, a proton pump inhibitor (PPI) that reduces the production of gastric acid.\n\nOmeprazole works by irreversibly inhibiting the H+/K+-ATPase (proton pump) in gastric parietal cells. This suppresses both basal and stimulated gastric acid secretion.\n\nOmeecan 20 mg Gastro-Resistant Capsules are formulated to protect omeprazole from degradation by stomach acid and release the medicine appropriately after passing through the stomach.\n\nOmeecan 40 Injection is a lyophilized injectable formulation generally used when oral administration is unsuitable and intravenous acid-suppressive therapy is clinically required.\n\nAvailable Forms\nProduct\tComposition\tStrength/Form\nOmeecan 20 mg Capsules\tOmeprazole\t20 mg Gastro-Resistant Capsule IP\nOmeecan 40 Injection\tOmeprazole\t40 mg Lyophilized Powder for Injection\nTherapeutic Uses\n\nDepending on approved labeling and clinical circumstances, omeprazole may be used for:\n\nGastroesophageal reflux disease (GERD)\nPeptic ulcer disease\nAcid-related dyspepsia\nErosive esophagitis\nPathological hypersecretory conditions\nPart of combination therapy for H. pylori eradication\nPrevention or treatment of selected NSAID-associated gastrointestinal ulcers\n\nThe injectable formulation is generally reserved for situations where appropriate oral therapy cannot be used or where IV treatment is clinically indicated.\n\nDosage & Administration\n\nDosage depends on the indication, severity of disease, treatment duration, and patient's clinical condition.\n\nOmeecan 20 mg Capsules are administered orally. Gastro-resistant formulations should be taken according to the product instructions and generally should not be crushed or chewed in a way that damages their gastro-resistant properties.\n\nOmeecan 40 Injection requires appropriate reconstitution and intravenous administration by a trained healthcare professional. The specific diluent, concentration, infusion/injection method, and stability period should follow the manufacturer's instructions.\n\nPrecautions\nPersistent or recurrent gastrointestinal symptoms should be appropriately evaluated.\nInform the physician about significant liver impairment.\nLong-term PPI treatment may be associated with low magnesium levels.\nProlonged acid suppression can affect Vitamin B12 absorption in some patients.\nLong-term or high-dose PPI use has been associated with an increased risk of certain bone fractures.\nPPIs may increase susceptibility to some gastrointestinal infections.\nReview concurrent medicines because omeprazole can cause clinically relevant drug interactions.\nPregnancy and breastfeeding require appropriate medical assessment.\n\nSide Effects\n\nCommon side effects may include:\nHeadache\nAbdominal pain\nNausea\nVomiting\nDiarrhea\nConstipation\nFlatulence\n\nLess common but important effects associated particularly with prolonged treatment can include:\n\nHypomagnesemia\nVitamin B12 deficiency\nKidney inflammation\nSevere skin reactions\nIncreased risk of certain gastrointestinal infections\nWarning\n\nOmeecan should be used according to the prescribed indication and duration.\n\nLong-term proton pump inhibitor therapy should be periodically reviewed to ensure continued clinical need.\n\nSymptom improvement with omeprazole does not exclude serious gastrointestinal disease. Patients with concerning features such as unexplained weight loss, recurrent vomiting, difficulty swallowing, gastrointestinal bleeding, or anemia require appropriate medical evaluation.\n\nFAQ\n\n1. What does Omeecan contain?\nOmeecan contains Omeprazole, a proton pump inhibitor.\n\n2. What is Omeecan 20 mg Capsule?\nIt is an Omeprazole 20 mg gastro-resistant oral capsule used for appropriate acid-related gastrointestinal conditions.\n\n3. What is Omeecan 40 Injection?\nIt contains Omeprazole 40 mg as lyophilized powder for injection, requiring reconstitution before administration.\n\n4. How does Omeprazole work?\nIt blocks the proton pumps in gastric parietal cells, thereby reducing stomach acid production.\n\n5. Why is Omeecan 20 gastro-resistant?\nOmeprazole is sensitive to gastric acid. The gastro-resistant formulation helps protect the medicine from degradation in the stomach.\n\n6. When may injectable Omeprazole be used?\nIt may be used when oral administration is unsuitable or IV acid suppression is clinically required, according to approved indications.\n\n7. Can Omeprazole be used for a long time?\nSome patients require longer treatment, but prolonged PPI therapy should be periodically reviewed and appropriately monitored.\n\n8. Does Omeecan 40 Injection need reconstitution?\nYes. As a lyophilized powder, it must be properly reconstituted using the recommended diluent and administered according to the manufacturer's instructions.",
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"name": "Buy Lenalidomide Tablets online",
"description": "Mayoplast 10 Capsules & Mayoplast 25\n\nGeneric Name: Lenalidomide\nMayoplast 10 and Mayoplast 25 contain Lenalidomide, an oral immunomodulatory and antineoplastic medicine used in the treatment of certain hematological cancers and blood disorders.\n\nLenalidomide affects the immune system and the tumor microenvironment and can inhibit the growth of certain abnormal blood cells. Its actions include binding to cereblon, resulting in changes in the degradation of specific regulatory proteins involved in malignant cell survival.\n\nDepending on the approved indication and treatment regimen, lenalidomide may be used for conditions such as multiple myeloma, certain myelodysplastic syndromes (MDS), and selected lymphomas. It is often used as part of a combination treatment regimen.\n\nAvailable Strengths\nProduct\tActive Ingredient\tStrength\nMayoplast 10\tLenalidomide\t10 mg*\nMayoplast 25\tLenalidomide\t25 mg*\n\n*You mentioned “Lenalidomide Tablets,” while Mayoplast 10 is described as capsules. The exact dosage form should be confirmed from the individual product pack before publishing.\n\nDosage\n\nLenalidomide dosage must be determined by an oncologist or hematology specialist. The appropriate strength, treatment schedule, and duration depend on:\n\nDisease being treated\nTreatment regimen\nBlood-cell counts\nKidney function\nOther anticancer medicines being administered\nPrevious treatment\nClinical response and toxicity\n\nDose interruption or reduction may be necessary if significant neutropenia, thrombocytopenia, or other toxicity develops.\n\nPrecautions\nA complete blood count (CBC) should be monitored according to the prescribed treatment protocol.\nKidney function is important because lenalidomide is substantially eliminated through the kidneys.\nInform the specialist about previous or current blood clots.\nTell the healthcare professional about all other medicines being used.\nAppropriate thrombosis prevention may be considered when clinically indicated, especially with certain combination regimens.\nCapsules/tablets should be handled carefully and should not be unnecessarily opened, crushed, or broken.\nPregnancy must be strictly avoided during treatment because lenalidomide can cause severe fetal harm.\nAppropriate pregnancy testing and contraception requirements must be followed according to the applicable risk-management program and prescribing information.\nSide Effects\n\nPossible side effects include:\n\nFatigue\nWeakness\nNausea\nDiarrhea or constipation\nMuscle cramps\nSkin rash\nReduced appetite\nAnemia\nNeutropenia\nThrombocytopenia\n\nImportant serious risks include blood clots, severe blood-cell suppression, serious skin reactions, liver problems, and severe hypersensitivity reactions.\n\nWarning\n\nLenalidomide can cause severe, potentially life-threatening birth defects or fetal death and must not be used during pregnancy.\n\nStrict pregnancy-prevention requirements apply to patients who can become pregnant, and appropriate precautions also apply to male patients because lenalidomide can be present in semen.\n\nLenalidomide can cause significant neutropenia and thrombocytopenia, making regular blood monitoring essential.\n\nFAQ\n\n1. What does Mayoplast contain?\nMayoplast contains Lenalidomide, an immunomodulatory antineoplastic medicine.\n\n2. What strengths of Mayoplast are available?\nThe listed variants are Mayoplast 10 mg and Mayoplast 25 mg.\n\n3. What is Lenalidomide used for?\nDepending on the approved indication, lenalidomide is used for certain hematological conditions including multiple myeloma, selected myelodysplastic syndromes, and certain lymphomas.\n\n4. Why are regular blood tests required during treatment?\nLenalidomide can reduce white blood cells and platelets and may also cause anemia. Regular blood-cell monitoring helps identify these effects.\n\n5. Why is kidney function important with Lenalidomide?\nLenalidomide is substantially eliminated through the kidneys, so patients with renal impairment may require dose adjustment.\n\n6. Can Lenalidomide be used during pregnancy?\nNo. Lenalidomide can cause severe fetal harm and birth defects. Strict pregnancy-prevention measures are required.\n\n7. Can Mayoplast increase the risk of blood clots?\nYes. Lenalidomide can increase the risk of venous and arterial thromboembolism, particularly in certain combination treatment regimens.\n\n8. Is Mayoplast an anti-cancer medicine?\nYes. Lenalidomide is an antineoplastic/immunomodulatory medicine primarily used for selected hematological cancers and disorders.\n",
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