LK-Plus
Generic Name
Losartan Potassium
Manufacturer
Popular Pharmaceutical Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
Variant | Unit Price | Strip Price |
---|---|---|
lk plus 50 mg tablet | ৳ 9.00 | ৳ 90.00 |
Description
Overview of the medicine
LK-Plus 50 mg Tablet contains Losartan Potassium, an angiotensin II receptor blocker (ARB), used to treat high blood pressure (hypertension) and to reduce the risk of stroke in patients with high blood pressure and an enlarged heart. It also protects the kidneys in patients with type 2 diabetes and hypertension.
Uses & Indications
Dosage
Adults
Initial dose 50 mg once daily. May be increased to 100 mg once daily if needed. For diabetic nephropathy, the usual dose is 50 mg once daily, increased to 100 mg once daily based on blood pressure response.
Elderly
No initial dosage adjustment is usually required for elderly patients, but careful monitoring is advised.
Renal_impairment
No initial dosage adjustment is required for patients with mild to moderate renal impairment. For severe renal impairment or dialysis, a lower starting dose (e.g., 25 mg) may be considered, but generally no adjustment needed.
How to Take
Administer orally, with or without food, usually once daily.
Mechanism of Action
Losartan selectively blocks the binding of angiotensin II to the AT1 receptor found in many tissues (e.g., vascular smooth muscle, adrenal gland). This blockade inhibits the vasoconstrictive and aldosterone-secreting effects of angiotensin II, leading to vasodilation and reduced blood pressure.
Pharmacokinetics
Onset
Onset of antihypertensive effect is within 1 hour; peak effect occurs at 3-6 hours. Full blood pressure reduction achieved in 3-6 weeks.
Excretion
Approximately 35% of the dose is excreted in the urine and 60% in the feces (both unchanged Losartan and its metabolites).
Half life
Losartan: 2 hours; Active metabolite (EXP3174): 6-9 hours.
Absorption
Rapidly absorbed from the gastrointestinal tract. Undergoes significant first-pass metabolism by cytochrome P450 enzymes. Bioavailability is approximately 33%.
Metabolism
Undergoes hepatic metabolism by cytochrome P450 enzymes (primarily CYP2C9 and CYP3A4) to an active carboxylic acid metabolite, EXP3174, which is more potent than Losartan.
Side Effects
Contraindications
- Hypersensitivity to Losartan or any component of the formulation
- Pregnancy (second and third trimesters)
- Concomitant use with Aliskiren in patients with diabetes mellitus
Drug Interactions
Lithium
Increased serum lithium concentrations and toxicity have been reported. Monitor lithium levels.
NSAIDs (e.g., ibuprofen, naproxen)
May reduce the antihypertensive effect of Losartan and increase the risk of renal impairment, especially in elderly or dehydrated patients.
Diuretics and other antihypertensive agents
May have an additive hypotensive effect.
Potassium-sparing diuretics (e.g., spironolactone), potassium supplements, salt substitutes containing potassium
May increase serum potassium levels, leading to hyperkalemia.
Storage
Store in a cool, dry place, below 30°C, away from direct sunlight and moisture. Keep out of reach of children.
Overdose
Symptoms of overdose include hypotension and tachycardia; bradycardia could occur from parasympathetic (vagal) stimulation. Treatment should be supportive and symptomatic. Hemodialysis is unlikely to remove Losartan or its active metabolite.
Pregnancy & Lactation
Contraindicated during the second and third trimesters of pregnancy due to fetal harm. Not recommended during breastfeeding as it is unknown if Losartan is excreted in human milk.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 24 to 36 months from the date of manufacture.
Availability
Available in pharmacies and hospitals
Approval Status
Approved by major regulatory bodies (e.g., FDA, DGDA)
Patent Status
Generic available (Patent expired)
WHO Essential Medicine
YesClinical Trials
Losartan has been extensively studied in numerous clinical trials, including the LIFE Losartan Intervention For Endpoint reduction in hypertension study, which demonstrated its efficacy in reducing cardiovascular morbidity and mortality, particularly stroke, in hypertensive patients with left ventricular hypertrophy. Other trials have supported its use in diabetic nephropathy and hypertension.
Lab Monitoring
- Serum creatinine and BUN especially in renal impairment
- Serum potassium especially with potassium-sparing diuretics or renal impairment
- Liver function tests if symptoms of hepatic dysfunction occur
Doctor Notes
- Regularly monitor patient's blood pressure, renal function, and serum potassium levels.
- Counsel patients on the importance of adherence to therapy and lifestyle modifications.
- Strictly avoid use in pregnancy, especially in the 2nd and 3rd trimesters.
- Caution with concomitant use of NSAIDs due to increased risk of renal impairment.
Patient Guidelines
- Take this medicine exactly as prescribed by your doctor.
- Do not stop taking this medicine suddenly without consulting your doctor, even if you feel well.
- Monitor your blood pressure regularly as instructed by your doctor.
- Avoid consuming potassium supplements or salt substitutes containing potassium without consulting your doctor.
Missed Dose Advice
If a dose is missed, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular dosing schedule. Do not double the dose to catch up.
Driving Precautions
This medicine may cause dizziness or lightheadedness, especially at the start of treatment or when the dose is increased. Avoid driving or operating machinery until you know how it affects you.
Lifestyle Advice
- Adopt a healthy diet low in sodium and rich in fruits and vegetables.
- Engage in regular physical activity as advised by your doctor.
- Maintain a healthy weight.
- Limit alcohol consumption and avoid smoking.
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