Javascript must be enabled to continue!
Losartan: A Pharmacotherapy in Cardiovascular Disease
View through CrossRef
Background:
A recently published article confirmed that in 2019, around 523 million people suffered from cardiovascular disease (including 18.6 million deaths) worldwide. Losartan, a drug, was patented 35 years ago and approved for medical use in the United States in 1995 (28 years ago). As an effective treatment for hypertension, losartan blocks the interaction of angiotensin II with its receptor by inhibiting the renin-angiotensin system.
Objective:
This article aims to review the available literature and recent studies demonstrating the efficacy, safety, mechanism of action and drug-drug interactions of losartan in cardiovascular disease.
Methods:
This is a focused literature review with the keywords relevant to the terms performed in PubMed, Scopus and Web of Science through May 28, 2023, according to the PRISMA guidelines. Based on the PICO standard format, fifty-two relevant in-depth consequent guide approaches and evidence-based choices were selected associated with a knowledgeable collection of current, high-quality manuscripts.
Results:
After oral administration, time to reach maximum concentration is about 1-2 hours. With a 78% binding to protein, it has a bioavailability of 25-35%. Losartan is not removed by hemodialysis. For the full effect to occur, it may take up to 6 weeks. The drug is mainly prescribed for patients with high blood pressure, diabetic nephropathy, hypertension and left ventricular hypertrophy. The publication reported higher drug exposures and adverse reactions in women than men with antihypertensive medications. Losartan could improve changes in gut microbiota that might be associated with hypertension. In the high-risk group of renal transplant recipients with arterial hypertension, research reported well-controlled blood pressure with losartan monotherapy.
Conclusion:
In addition to the major losartan interactions with captopril, enalapril, lisinopril, and lithium, there are moderate interactions with aspirin, pregabalin, alprazolam, amitriptyline, baclofen, betamethasone, buspirone. Muscle cramps, respiratory infection, cough, hyperkalemia, anemia and stuffy nose are the main reported side effects. As polypharmacy could hide pharmacokinetics interaction due to cytochrome P450, therefore, the combination of losartan with drugs such as phenobarbital, rifampin or fluconazole needs vigilant attention regarding therapeutic drug monitoring.
Title: Losartan: A Pharmacotherapy in Cardiovascular Disease
Description:
Background:
A recently published article confirmed that in 2019, around 523 million people suffered from cardiovascular disease (including 18.
6 million deaths) worldwide.
Losartan, a drug, was patented 35 years ago and approved for medical use in the United States in 1995 (28 years ago).
As an effective treatment for hypertension, losartan blocks the interaction of angiotensin II with its receptor by inhibiting the renin-angiotensin system.
Objective:
This article aims to review the available literature and recent studies demonstrating the efficacy, safety, mechanism of action and drug-drug interactions of losartan in cardiovascular disease.
Methods:
This is a focused literature review with the keywords relevant to the terms performed in PubMed, Scopus and Web of Science through May 28, 2023, according to the PRISMA guidelines.
Based on the PICO standard format, fifty-two relevant in-depth consequent guide approaches and evidence-based choices were selected associated with a knowledgeable collection of current, high-quality manuscripts.
Results:
After oral administration, time to reach maximum concentration is about 1-2 hours.
With a 78% binding to protein, it has a bioavailability of 25-35%.
Losartan is not removed by hemodialysis.
For the full effect to occur, it may take up to 6 weeks.
The drug is mainly prescribed for patients with high blood pressure, diabetic nephropathy, hypertension and left ventricular hypertrophy.
The publication reported higher drug exposures and adverse reactions in women than men with antihypertensive medications.
Losartan could improve changes in gut microbiota that might be associated with hypertension.
In the high-risk group of renal transplant recipients with arterial hypertension, research reported well-controlled blood pressure with losartan monotherapy.
Conclusion:
In addition to the major losartan interactions with captopril, enalapril, lisinopril, and lithium, there are moderate interactions with aspirin, pregabalin, alprazolam, amitriptyline, baclofen, betamethasone, buspirone.
Muscle cramps, respiratory infection, cough, hyperkalemia, anemia and stuffy nose are the main reported side effects.
As polypharmacy could hide pharmacokinetics interaction due to cytochrome P450, therefore, the combination of losartan with drugs such as phenobarbital, rifampin or fluconazole needs vigilant attention regarding therapeutic drug monitoring.
Related Results
Losartan Monotherapy vs Combination Regimens in IgA Nephropathy: A Systematic Review and Network Meta-analysis
Losartan Monotherapy vs Combination Regimens in IgA Nephropathy: A Systematic Review and Network Meta-analysis
Background: IgA nephropathy (IgAN) is a disorder in which Immunoglobulin A (IgA) antibodies build up, causing kidney damage. Losartan, an Angiotensin Receptor Blocker (ARB), has sh...
A systematic review and meta-analysis of candesartan and losartan in the management of essential hypertension
A systematic review and meta-analysis of candesartan and losartan in the management of essential hypertension
Background: Candesartan is a relatively novel antihypertensive agent of the angiotensin receptor blocker (ARB). Several clinical trials have compared candesartan with losartan in t...
Evaluation of Losartan Usage in a Regional Hospital in Hong Kong
Evaluation of Losartan Usage in a Regional Hospital in Hong Kong
Objective: To determine whether losartan usage follows the hospital's guidelines in terms of indications and reasons for use and to assess the accuracy of physicians in completing ...
Losartan and magnesium sulfate administration reduce gentamicin-induced nephrotoxicity in rat model
Losartan and magnesium sulfate administration reduce gentamicin-induced nephrotoxicity in rat model
Background: Nephrotoxicity is the most known side effect of gentamicin. In addition, renin angiotensin system (RAS) plays an important role in the pathogenesis of renal injury and ...
Losartan to reduce inflammation and fibrosis endpoints in HIV disease
Losartan to reduce inflammation and fibrosis endpoints in HIV disease
Background:
Persistent inflammation and incomplete immune recovery among persons with HIV (PHIV) are associated with increased disease risk. We hypothesized that the an...
Impact of Losartan on Portal hypertension and Liver Cirrhosis: A Systematic Review
Impact of Losartan on Portal hypertension and Liver Cirrhosis: A Systematic Review
Abstract
Background
Portal hypertension, a complication of chronic liver disease, results from elevated pressure between the po...
Losartan reduces collagen content and intimal thickening of iliac arteries after balloon injury in rabbits
Losartan reduces collagen content and intimal thickening of iliac arteries after balloon injury in rabbits
Intimal thickening and formation of extracellular matrix are parts of the repair process after vascular injury. Similar processes occur after coronary angioplasty. Prior studies ha...
Parental Attitudes Toward ADHD Pharmacotherapy: Associations with Parental Experience of the Child’s Treatment—A Cross-Sectional Study from Poland
Parental Attitudes Toward ADHD Pharmacotherapy: Associations with Parental Experience of the Child’s Treatment—A Cross-Sectional Study from Poland
Background: The efficacy of pharmacotherapy for attention-deficit/hyperactivity disorder (ADHD) has been confirmed in numerous controlled studies. However, in clinical practice, ph...

