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"name": "Triamcinolone Acetonide Injection 40mg/ml",
"description": "Tricanort 40 injection is a steroid used for various treatments and medical conditions given under a doctor’s supervision. Triamcinolone Acetonide injection is commonly given to patients suffering from immune-related conditions like asthma, osteoarthritis and rheumatic disorders. Triamcinolone Acetonide injection delivers considerable relief by inhibiting the release of elements that can lead to inflammation while suppressing the immune system.\n\nThe dosage of Triamcinolone Acetonide injection uses ideally suggested by the doctor after analyzing the treatment. Triamcinolone injection for asthma is not meant to be administered on your own. Tricort 40 INJ is suggested by experts to be taken at the same time of the day after equal intervals to repeat its benefits. Also, doctors highly recommend avoiding stopping or altering the dosage on your own.\n\n \n\nDosage\n\nTriamcinolone injection for asthma is generally injected into the muscles under medical supervision. Triam 40 mg injection helps block the production of certain chemical messengers in the body that lead to inflammation, such as swelling, redness and allergies. Avoid administering Tricort 40 INJ more often or for a longer duration than advised by the doctor.\n\n \n\nPrecautions\n\nDriving: Triam 40 mg injection must be administered strictly after consulting the medical expert to know if it would affect the ability to drive.\n\nAlcohol: It is not yet known if Triamcinolone Acetonide injection is safe to consume with alcohol. Ensure to consult your doctor to understand better.\n\nKidney: Triam 40 mg injection should be administered with caution who have kidney disease. Dose adjustment might be needed if there’s an existing kidney condition. Ensure to consult your doctor.\n\nPregnancy: Triamcinolone injection for asthma might not be safe to administer in pregnant women, as it could affect the fetus. Hence, it is highly recommended to consult the doctor before considering this treatment.\n\nLiver: Triamcinolone Acetonide for mouth ulcers should be used with caution in patients with liver disease. Dose adjustment might be needed if there’s an existing liver condition. Ensure to consult your doctor.\n\n \n\nSide Effects\n\nSome of the side effects of Triamcinolone Acetonide injection uses might not need any expert consultation, as they generally disappear on their own without treatment. In case it doesn’t go away on its own for long, ensure to consult your doctor. These common side effects of Tricort 40 INJ are pain at the injection site, fatigue, acne, bloating, rashes, joint pain, headache, insomnia, or abrupt sweating.\n\n Warning\n\nAvoid taking Triamcinolone Acetonide for mouth ulcers or other indications for a longer period without a doctor’s consultation. Some of the side effects could occur a week or months after taking this injection. Hence, if the problem persists, ensure to see the doctor.\n\n \n\nFAQ\n\n1.What is Tricanort 40 injection majorly used for?\nTricanort 40 injection is majorly used as an anti-inflammatory and immunosuppressant medicine to treat certain conditions such as osteoarthritis and rheumatoid arthritis. It also helps to treat other autoimmune diseases that involve the body’s immune system, like asthma and mouth ulcers.\n\n2. When can I see the effect of Tricanort 40mg injection after administering it?\nTricanort 40mg injection begins to work after some time in the body after administering. However, its effect might differ from one person to another, based on the condition of treatment, gender and body weight.\n\n3. Is Tricanort 40 injection safe?\nTricanort 40 injection is considered safe if it is administered in a specific dosage and duration as advised by the doctor. Ensure you follow all the guidelines as directed by the healthcare expert.\n\nBuy Triam 40 mg injection from us, as we are the reliable Tricanort 40 bulk exporters. You can contact our team to buy Tricanort 40 bulk exporters or get any further assistance regarding this medicine. To get more information on Tricanort 40 bulk exporters, connect with us today!",
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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": "Telmisartan 12.5mg/40mg & 80mg Tablets",
"description": "Telmaheal 80 mg contains Telmisartan, an angiotensin II receptor blocker (ARB) used primarily for the management of hypertension. It selectively blocks angiotensin II at the AT1 receptor, reducing vasoconstriction and helping blood vessels relax.\n\nBy reducing the effects of angiotensin II, Telmisartan helps lower peripheral vascular resistance and supports long-term blood-pressure control. Depending on locally approved indications and the patient's cardiovascular risk profile, it may also be prescribed for cardiovascular risk reduction in selected patients.\n\nTelmaheal 80 mg is a prescription medicine. Blood pressure, kidney function and serum potassium may require monitoring during treatment. Medicines acting on the renin-angiotensin system should not be used during pregnancy.\n\nTelmaheal 40H is a combination antihypertensive medicine containing Telmisartan and Hydrochlorothiazide. It combines two medicines with complementary actions to help manage high blood pressure when combination therapy is clinically appropriate.\n\nTelmisartan belongs to the angiotensin II receptor blocker (ARB) class. It selectively blocks AT1 receptors, reducing angiotensin II-mediated vasoconstriction and helping blood vessels relax. This action lowers peripheral vascular resistance and supports blood-pressure control.\n\nHydrochlorothiazide is a thiazide diuretic that acts on the kidneys to increase the excretion of sodium and water. This helps reduce excess fluid volume and contributes to lowering blood pressure. The combination can therefore provide additional blood-pressure reduction compared with either mechanism alone in appropriate patients.\n\nUses of Telmaheal 40H\n\nTelmaheal 40H is primarily used for the management of hypertension (high blood pressure). It may be prescribed when a single antihypertensive medicine does not provide sufficient blood-pressure control or when a clinician determines that combination therapy is appropriate.\n\nMaintaining controlled blood pressure is an important part of reducing the long-term cardiovascular and renal complications associated with persistent hypertension.\n\n\nFAQs\n\n1. What is Telmaheal 80 used for?\nIt contains Telmisartan 80 mg and is primarily used for hypertension management under medical supervision.\n\n2. What is the difference between Telmaheal 80 and Telmaheal 40H?\nTelmaheal 80 contains Telmisartan alone, whereas Telmaheal 40H combines Telmisartan with Hydrochlorothiazide.\n\n3. How does Telmisartan work?\nIt blocks angiotensin II at AT₁ receptors, helping blood vessels relax and reducing blood pressure.\n\n4. Why is Hydrochlorothiazide added to Telmaheal 40H?\nIt increases renal sodium and water excretion, providing an additional mechanism for lowering blood pressure.\n\n5. Can Telmaheal affect potassium?\nYes. Telmisartan may increase potassium, while Hydrochlorothiazide may reduce it. Monitoring may therefore be appropriate.\n\n6. Why is kidney function important?\nKidney function influences the safe use of renin-angiotensin-system medicines and diuretic therapy.\n\n7. Is Telmaheal suitable during pregnancy?\nNo. Telmisartan-containing medicines can cause serious fetal harm and should not be used during pregnancy.\n\n\nKey Properties\nProperty\tValue\n\nCombination Design: ARB + Thiazide Diuretic\nRAAS Component: Telmisartan – AT1 Receptor Blockade\nRenal Component: Hydrochlorothiazide – Promotes Sodium & Water Excretion\nTreatment Strategy: Dual-Mechanism Blood Pressure Control\n\nStorage & Handling Guide\n\nFor both Telmaheal products:\n\nKeep tablets in the original blister and carton.\nStore according to the temperature stated on the marketed pack.\nProtect from excessive heat and moisture.\nKeep packaging dry and intact.\nHandle tablets with clean, dry hands.\nDo not use medicine after its printed expiry date.\nAvoid tablets from significantly damaged packaging.\nKeep securely out of reach of children.\nDo not transfer tablets into unidentified containers for prolonged storage.",
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"name": "Propranolol Hydrochloride 10, 20 and 40mg Tablet",
"description": "P-Nolol 10, P-Nolol 20 & P-Nolol 40\nPropranolol Hydrochloride Tablets\n\nP-Nolol contains Propranolol Hydrochloride, a non-selective beta-adrenergic blocker used in several cardiovascular and other clinically selected conditions. By blocking both beta-1 and beta-2 receptors, propranolol can reduce heart rate, decrease cardiac workload, and limit the physical effects of excessive adrenergic stimulation.\n\nThe availability of 10 mg, 20 mg, and 40 mg strengths provides different strength options for clinician-directed therapy.\n\nThree Strengths Available\nBrand\tMedicine\tStrength\nP-Nolol 10\tPropranolol Hydrochloride\t10 mg\nP-Nolol 20\tPropranolol Hydrochloride\t20 mg\nP-Nolol 40\tPropranolol Hydrochloride\t40 mg\n\nDosage Form: Tablet\nDrug Family: Beta Blocker\nReceptor Activity: Non-selective β1 + β2 blockade\nRoute: Oral\nPrescription Category: Prescription medicine\n\nSide-Effect Spectrum\nEffects That May Occur\nTiredness or reduced energy\nDizziness\nSlow heartbeat\nCold hands or feet\nSleep disturbance\nNausea or gastrointestinal discomfort\nSymptoms Needing Prompt Assessment\nMarkedly slow heart rate\nFainting or severe dizziness\nNew or worsening breathing difficulty\nWheezing or bronchospasm\nWorsening heart-failure symptoms\nSignificant hypotension\nSerious allergic reaction\n\nRespiratory Precaution — An Important Difference\n\nP-Nolol is a non-selective beta blocker.\n\nBecause it blocks beta-2 receptors as well as beta-1 receptors, propranolol can cause bronchoconstriction and may interfere with beta-agonist bronchodilator activity.\n\nFor this reason, patients with asthma, bronchospastic disease, or a history of significant airway problems require particular medical assessment before propranolol is considered.\n\nStorage & Handling Guide\n\nTo preserve tablet quality:\n\nOriginal pack: Keep P-Nolol in its original blister/carton until use.\n\nMoisture protection: Avoid humid storage areas and unnecessary exposure to moisture.\n\nTemperature: Follow the storage temperature stated on the marketed product label.\n\nDirect heat/light: Keep away from excessive heat and inappropriate direct light exposure.\n\nDamaged tablets: Do not use tablets from severely damaged or compromised packaging.\n\nExpiry: Check the printed expiry date before use.\n\nChild safety: Keep all strengths out of the reach and sight of children\n",
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"name": "Sotalol Hydrochloride 40mg",
"description": "\nSotacheck 40 Tablets\nSotalol Hydrochloride 40 mg\n\nSotacheck 40 is a cardiovascular medicine containing Sotalol Hydrochloride 40 mg. Sotalol has a distinctive pharmacological profile because it combines non-selective beta-adrenergic blocking activity with Class III antiarrhythmic activity. It is used for the management of specific clinically significant cardiac rhythm disorders under specialist supervision.\n\nWhat Sets Sotalol Apart?\n\nSotalol is different from a conventional beta-blocker because it influences the heart through two electrophysiological actions.\n\nβ-Receptor Blockade\n\nSotalol blocks beta-1 and beta-2 receptors, reducing sympathetic stimulation of the heart. This can decrease heart rate and cardiac excitability.\n\nPotassium-Channel Effect\n\nIts Class III activity prolongs cardiac repolarization and the action-potential duration.\n\nThis dual activity explains both its antiarrhythmic benefit and its important QT-related safety considerations.\n\nRhythm Disorders Where Sotalol May Have a Role\n\nDepending on approved labeling and specialist assessment, Sotalol may be considered for certain:\n\nVentricular arrhythmias\nSymptomatic atrial fibrillation or atrial flutter\nSupraventricular rhythm disorders where Sotalol therapy is appropriate\n\nSotalol should not be used simply for occasional palpitations without appropriate cardiac evaluation.\n\nThe QT Interval Is Central to Safe Use\n\nOne of the most important characteristics of Sotalol is its ability to prolong the QT interval.\n\nExcessive QT prolongation can increase the risk of a potentially dangerous ventricular rhythm called torsades de pointes.\n\nFor this reason, treatment decisions may involve assessment of:\n\nECG / QT interval\nHeart rate\nKidney function\nSerum potassium\nSerum magnesium\n\nInitiation or dose adjustment may require a monitored clinical setting according to applicable prescribing guidance.\n\nKidney Function and Sotalol Are Closely Connected\n\nSotalol is eliminated substantially through the kidneys. Reduced renal function can increase drug exposure and therefore increase the likelihood of excessive QT prolongation and other adverse effects.\n\nRenal assessment is consequently an important part of determining whether Sotalol is appropriate and how it should be administered.\n\n\nSotacheck 40 FAQs\n\n1. Is Sotacheck 40 only a beta-blocker?\nNo. Sotalol combines non-selective beta-blocking activity with Class III antiarrhythmic properties.\n\n2. Why may an ECG be required during treatment?\nSotalol can prolong the QT interval, so ECG assessment helps identify excessive electrical changes that could increase arrhythmia risk.\n\n3. Why are potassium and magnesium important?\nLow levels of either electrolyte can increase the likelihood of serious ventricular arrhythmias during Sotalol therapy.\n\n4. Does kidney function affect Sotalol treatment?\nYes. Sotalol is substantially renally eliminated, making kidney function an important consideration in treatment selection and dosing.\n\n5. Can Sotacheck 40 be taken for ordinary palpitations?\nSotalol is a specialist antiarrhythmic medicine. Palpitations require appropriate diagnosis before deciding whether antiarrhythmic treatment is suitable.\n\n6. Can Sotalol affect breathing?\nYes. Its non-selective beta-blocking activity can contribute to bronchospasm, particularly in susceptible individuals with airway disease.\n\n7. Can other heart-rhythm medicines be taken with Sotacheck?\nSome combinations can increase QT prolongation, bradycardia, or other cardiac risks. Concomitant medicines should be reviewed by the treating clinician.\n\n8. Can Sotacheck be stopped when the heartbeat becomes normal?\nNot independently. Rhythm control may reflect successful treatment, and discontinuation should be planned by the prescribing clinician.",
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"description": "Teicocan 200 Injection & Teicocan 400 Injection\n\nGeneric Name: Teicoplanin for Injection IP\nAvailable Strengths: 200 mg & 400 mg\nDosage Form: Injection\nDrug Class: Glycopeptide Antibiotic\n\nTeicocan Injection contains Teicoplanin, an injectable glycopeptide antibacterial medicine primarily active against susceptible Gram-positive bacteria. It is generally reserved for serious infections where an injectable Gram-positive antibacterial agent is clinically appropriate.\n\nAvailable Variants\nProduct\tComposition\tStrength\nTeicocan 200 Injection\tTeicoplanin for Injection IP\t200 mg\nTeicocan 400 Injection\tTeicoplanin for Injection IP\t400 mg\nAntibacterial Spectrum\n\nTeicoplanin has activity against susceptible Gram-positive organisms, which may include:\n\nStaphylococcus aureus, including certain methicillin-resistant strains (MRSA)\nStreptococci\nEnterococci\nOther susceptible Gram-positive bacteria\n\nCulture and antimicrobial susceptibility testing should guide treatment whenever appropriate.\n\nHow Teicoplanin Fights Bacteria\n\nTeicoplanin interferes with bacterial cell-wall synthesis. By preventing susceptible bacteria from building a functional cell wall, it ultimately causes bacterial cell death.\n\nClinical Applications\n\nDepending on approved labeling and susceptibility results, Teicoplanin may be considered for serious infections involving:\n\nSkin and soft tissues\nBones and joints\nBloodstream\nHeart valves/endocardial infections\nOther severe Gram-positive bacterial infections\nMonitoring Focus\n\nFor patients receiving Teicoplanin, particularly during prolonged therapy, clinicians may consider monitoring:\n\nKidney Function → Blood Counts → Liver Function → Hearing → Clinical Response\n\nTherapeutic drug monitoring may also be appropriate in certain patients or treatment situations.\n\nImportant Safety Points\n\nExtra caution is required in patients with:\n\nKidney impairment\nPrevious glycopeptide hypersensitivity\nHearing impairment\nConcurrent nephrotoxic or ototoxic medicines\n\nRenal impairment can alter Teicoplanin elimination, so dose adjustment or interval modification may be required.\n\nPossible Adverse Effects\n\nPotential reactions include:\n\nInjection-site discomfort\nRash or itching\nFever\nNausea\nChanges in liver enzymes\nBlood-cell abnormalities",
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"name": "Actorise 40mg Injection",
"description": "Actorise 40 Injection is a prescription darbepoetin alfa injection used for the management of anemia associated with chronic kidney disease (CKD) and, in appropriate patients, cancer chemotherapy. Darbepoetin alfa belongs to a group of medicines known as erythropoiesis-stimulating agents (ESAs).\n\nThe medicine stimulates the bone marrow to increase red blood cell production. By supporting red blood cell formation, Actorise 40 may help improve hemoglobin levels and manage anemia-related symptoms such as weakness and tiredness.\n\nTreatment with Actorise 40 mcg Injection requires medical supervision. The dose and treatment schedule are determined by the physician according to the patient's condition, hemoglobin response and other clinical factors.\n\nBenefits of Actorise 40 Injection\n1. Management of Anemia in Chronic Kidney Disease\n\nPeople with chronic kidney disease may develop anemia when the kidneys are unable to produce sufficient natural erythropoietin, a hormone involved in red blood cell formation.\n\nDarbepoetin Alfa 40 mcg acts as a red blood cell stimulating medicine and helps the bone marrow produce more red blood cells. When prescribed appropriately, this can help manage CKD-related renal anemia and improve low hemoglobin associated with the condition.\n\n2. Management of Chemotherapy-Associated Anemia\n\nCertain chemotherapy treatments can suppress bone marrow function and decrease red blood cell production. This may lead to chemotherapy-induced anemia.\n\nActorise 40 works by stimulating erythropoiesis in the bone marrow. In selected cancer patients receiving chemotherapy, a healthcare professional may prescribe it to help manage anemia and support hemoglobin levels.\n\nHow Actorise 40 Injection Works\n\nThe active ingredient, darbepoetin alfa, is an erythropoiesis-stimulating agent that acts on erythropoietin receptors in the bone marrow. This promotes the development and production of red blood cells.\n\nBecause the response can vary between patients, hemoglobin and other blood parameters may need to be monitored regularly during treatment.\n\nHow to Use\n\nActorise 40 should be administered only as directed by a qualified healthcare professional. The route, dose and frequency are determined according to the patient's medical condition and response to therapy.\n\nDo not change the prescribed dose or treatment schedule without medical advice.\n\nMonitoring During Treatment\n\nRegular clinical monitoring may include:\n\nHemoglobin levels and complete blood count\nBlood pressure\nIron status when clinically indicated\nElectrolytes such as potassium when required\nResponse to darbepoetin alfa therapy\n\nAdequate iron status may also be evaluated because iron availability can affect red blood cell production.\n\nPossible Side Effects\n\nSide effects associated with darbepoetin alfa therapy may include increased blood pressure, headache, injection-site reactions or hypersensitivity reactions. Patients should promptly seek medical attention for concerning symptoms such as severe headache, vision problems, seizures, breathing difficulty or significant skin reactions.\n\nPrecautions\n\nActorise 40 requires careful use, particularly in patients with blood-pressure or cardiovascular concerns. Patients should inform their doctor about existing medical conditions and all medicines they are taking before starting therapy.\n\nActorise 40 is a prescription medicine and should be used only under professional medical supervision.",
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"name": "Pentoxifylline 400 mg Tablet",
"description": "Pentral 400 Tablets contain Pentoxyfyllin 400mg dose, a vasodilator used to improve blood flow in patients suffering from circulation disorders such as peripheral vascular disease, intermittent claudication, or cerebrovascular insufficiency. These tablets work by decreasing the thickness of blood, allowing it to flow more freely through narrowed blood vessels.\n\nPentral 400 Tablets are ideal for enhancing oxygen delivery in tissues, reducing pain while walking (claudication) and preventing further vascular complications. Order Pentral 400mg Tablets in bulk by connecting us.\n\nDosage\nEach Pentral 400 Tablet contains Pentoxyfyllin 400mg dose. The standard dosage is usually one tablet two to three times daily after meals, as directed by your healthcare expert. Always follow the medical advice specific to your condition. For specific instructions, especially when you buy Pentral 400 Tablets online or order Pentral 400mg Tablets in bulk, consult your doctor.\n\nPrecautions\n\nDriving: Pentral 400 Tablets may cause dizziness or drowsiness in some individuals. Avoid driving if affected.\nAlcohol: Consult your doctor before consuming alcohol during this medication, as it may enhance side effects.\nKidney: Dose adjustment may be needed for patients with kidney impairment. Always seek medical advice.\nPregnancy/Breastfeeding: Use with caution during pregnancy or breastfeeding. Always consult your healthcare expert.\nLiver: Monitor liver function regularly if prescribed for long-term use.\nSide Effects\nCommon side effects of Pentral 400 Tablets may include:\n\nNausea or upset stomach\nDizziness or headache\nFlushing or redness of skin\nChest discomfort (rare)\nIrregular heartbeat (rare)\nReport any unusual or serious reactions to your doctor immediately.\n\nWarning\n\nDo not exceed the recommended Pentoxyfyllin 400mg dose.\nDiscontinue use if allergic reactions such as rashes, swelling, or breathing issues occur.\nKeep out of reach of children.\nFAQ\n\nWhat are Pentral 400 Tablets used for?\nPentral 400 Tablets are used to treat circulation problems in the limbs and brain, especially in conditions like intermittent claudication.\nIs it safe to Order Pentral 400mg Tablets in bulk for regular hospital supply?\nYes, we are a reliable bulk supplier of Pentral 400 Tablets, offering consistent quality and timely supply for hospital and clinic needs.\nCan I Buy Pentral 400 Tablets online without a prescription?\nWhile you can buy Pentral 400 Tablets online, it's advised to use this medicine only under medical supervision.\nWhat is the storage instruction for Pentral 400 Tablets?\nStore in a cool, dry place away from direct sunlight and moisture. Keep in original packaging.\n \n\nBuy Pentral 400 Tablets online from the bulk supplier of Pentral 400 Tablets today. Contact us today to Order Pentral 400mg Tablets in bulk or get more details from the third party manufacturer of Pentral 400 Tablets.\n\n ",
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"name": "Propranolol Hydrochloride Tablets 10mg,20mg & 40mg",
"description": "P-Nolol Tablets contain Propranolol Hydrochloride, a non-selective beta-adrenergic receptor blocker (beta-blocker) used in the management of several cardiovascular and neurological conditions.\n\nPropranolol blocks both beta-1 and beta-2 adrenergic receptors, reducing the effects of adrenaline and related stress hormones. This can slow the heart rate, reduce cardiac workload and lower blood pressure.\n\nDepending on the approved indication, propranolol may be prescribed for conditions such as hypertension, angina, certain cardiac arrhythmias, migraine prevention, essential tremor, and selected other conditions.\n\nAvailable Strengths\nProduct\tActive Ingredient\tStrength\nP-Nolol 10 Tablets\tPropranolol Hydrochloride\t10 mg\nP-Nolol 20 Tablets\tPropranolol Hydrochloride\t20 mg\nP-Nolol 40 Tablets\tPropranolol Hydrochloride\t40 mg\nDosage\n\nThe dosage should be individualized by a healthcare professional according to:\n\nCondition being treated\nPatient's age\nBlood pressure and heart rate\nCardiovascular status\nLiver function\nResponse to treatment\nOther medicines being used\n\nP-Nolol Tablets are administered orally according to the prescribed schedule.\n\nSide Effects\n\nPossible side effects include:\n\nTiredness\nDizziness\nSlow heartbeat\nLow blood pressure\nCold hands and feet\nNausea\nSleep disturbances\n\nSerious adverse effects may include:\n\nSignificant bradycardia\nHeart block\nSevere hypotension\nWorsening heart failure\nBronchospasm, particularly in susceptible patients\n\nPrecautions\nInform the doctor about asthma, wheezing, or other bronchospastic disorders.\nUse cautiously in patients with bradycardia, heart block, low blood pressure, or heart failure.\nMonitor blood pressure and heart rate when clinically appropriate.\nPropranolol may mask some warning symptoms of hypoglycemia, particularly rapid heartbeat.\nInform the doctor if the patient has diabetes.\nTell the healthcare professional about liver disease.\nPropranolol can cause dizziness or fatigue.\nInform the physician about other heart-rate or blood-pressure-lowering medicines.\nPregnancy and breastfeeding require professional medical assessment.\n\nWarning\n\nP-Nolol Tablets should be used under appropriate medical supervision.\n\nBecause propranolol blocks beta-2 receptors in the airways, it can cause bronchoconstriction and may be unsuitable for patients with bronchial asthma or a history of bronchospasm.\n\nFAQ\n\n1. What does P-Nolol contain?\nP-Nolol contains Propranolol Hydrochloride, a non-selective beta-blocker.\n\n2. What strengths are available?\nP-Nolol is listed in 10 mg, 20 mg, and 40 mg Tablets.\n\n3. What is Propranolol used for?\nDepending on the approved indication, propranolol may be used for hypertension, angina, certain arrhythmias, migraine prevention, and essential tremor.\n\n4. How does Propranolol work?\nIt blocks beta-1 and beta-2 adrenergic receptors, reducing the cardiovascular effects of adrenaline and related catecholamines.\n\n5. Can P-Nolol slow the heart rate?\nYes. Propranolol can reduce heart rate, and excessive slowing (bradycardia) can occur in some patients.\n\n6. Can Propranolol be used in asthma?\nPropranolol can cause bronchospasm because it blocks beta-2 receptors and is generally unsuitable in patients with bronchial asthma or significant bronchospastic disease unless specifically assessed by a clinician.\n\n7. Can Propranolol affect blood sugar symptoms?\nYes. It can mask certain adrenergic warning symptoms of hypoglycemia, such as rapid heartbeat.\n\n8. Can P-Nolol be stopped suddenly?\nRegular propranolol treatment should generally not be stopped abruptly, particularly in patients with coronary heart disease. Dose changes should be made under medical guidance.\n",
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