Losarstad

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Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Losarstad

What is Losarstad?

Losarstad is a pharmaceutical medication containing the active substance losartan potassium. It belongs to a class of medicines known as angiotensin II receptor antagonists. These substances work by interacting with specific pathways in the body that regulate blood pressure and fluid balance.

Mechanism of Action

Angiotensin II is a naturally occurring substance in the body that binds to receptors on blood vessels, causing them to tighten and narrow. This process results in an increase in blood pressure. Losarstad works by blocking the binding of angiotensin II to these receptors. As a result, the blood vessels remain more relaxed and dilated, which helps to lower blood pressure and improves the efficiency of blood flow throughout the cardiovascular system.

Clinical Applications

Losarstad is primarily utilized in the management of long-term cardiovascular conditions. Its main applications include:

  • Hypertension: It is used to manage high blood pressure in adults as well as in children and adolescents within specific age ranges.
  • Renal Protection: It is used in certain patients with type 2 diabetes and a history of hypertension to help protect kidney function, particularly when there is clinical evidence of protein loss in the urine.
  • Chronic Heart Failure: It may be used in patients with chronic heart failure when specific other treatments, such as ACE inhibitors, are not considered suitable by a healthcare professional.
  • Stroke Risk Reduction: In patients with high blood pressure and a thickening of the left ventricle of the heart, the medication is used to help reduce the risk of stroke.

What side effects are possible with Losarstad?

Losarstad, containing Losartan potassium, has an established safety profile documented by regulatory authorities, with adverse reactions organized by frequency and affected body system. This information is derived strictly from official prescribing labels and does not constitute medical advice.

Frequency-Classified Adverse Reactions

Adverse effects are categorized based on their documented incidence in clinical studies:

  • Common: Reactions expected in 1 to 10 out of 100 users, including dizziness, headache, asthenia (fatigue), cough, and hyperkalemia (elevated potassium levels). These effects are grouped under System-Organ Classes (SOCs) such as Nervous System and Metabolism and Nutrition disorders.
  • Uncommon: Reactions expected in 1 to 10 out of 1,000 users, such as diarrhea, abdominal pain, rash, and somnolence (drowsiness).
  • Rare: Reactions expected in 1 to 10 out of 10,000 users, which include severe events like angioedema (severe swelling of the face or throat), anaphylaxis, and hepatic failure (severe liver impairment).

Official Safety Constraints and Considerations

The regulatory safety profile highlights specific limitations on use:

  • Serious Adverse Reactions: The label explicitly documents the potential for rare but serious reactions, including angioedema and symptomatic hypotension (severe low blood pressure), particularly in patients with volume depletion.
  • Population-Specific Restrictions: Losarstad is contraindicated during the second and third trimesters of pregnancy due to the risk of fetal harm. Specific warnings exist for patients with severe hepatic impairment.
  • Time-Related Patterns: Symptomatic hypotension is documented as an effect that may occur particularly at the initiation of therapy in certain susceptible individuals.

This framework formally defines the medicine's established safety characteristics and is based on regulatory standards for communicating risk.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdose involving Losarstad (Losartan potassium) is primarily defined by the exaggeration of its intended hemodynamic effect. The most common clinical sign documented in regulatory information is severe hypotension (low blood pressure), which may manifest as dizziness or fainting. Other manifestations include changes in the heart's rhythm, which may be either tachycardia (fast heartbeat) or bradycardia (slow heartbeat).

When to Seek Immediate Medical Attention

Official guidance mandates that immediate medical attention must be sought for any suspected overdose. Specific severe outcomes that require an urgent call to emergency services include collapse, experiencing a seizure, severe difficulty with breathing, or when the individual cannot be awakened. For situations assessed as less immediately life-threatening, official instructions direct the individual to call the poison control helpline.

Official Management Procedures

Regulatory authorities state that management is limited to symptomatic and supportive treatment, as no specific antidote is known. Hospital monitoring is required, particularly for managing persistent, symptomatic hypotension. Procedures such as gastric lavage may be considered for recent ingestion, but Losartan is documented as not likely to be removed by hemodialysis. Specific monitoring for neonates with in-utero exposure is required due to potential risks like hypotension, oliguria, and hyperkalemia.

Therapeutic Uses of Losarstad

What Losarstad Treats: Main Uses and Benefits

Losarstad (Losartan) is a prescription medicine used to assist in the management of specific cardiovascular and renal conditions. The core therapeutic domains involve managing symptoms related to heightened physiological activity and providing assistance in maintaining functional stability.


Easing High Blood Pressure (Hypertension)

Losarstad is commonly used to address symptoms related to heightened physiological activity caused by high blood pressure. This application is relevant in clinical settings marked by increased systemic burden. The medication supports the patient during difficult episodes by easing distress.


Addressing Functional Stress and Strain

Losarstad is also applied in contexts marked by increased discomfort or tension, such as when patients have high blood pressure paired with an enlarged heart, and in clinical settings involving chronic conditions where patients show signs of kidney functional stress. By assisting with the management of systemic strain, its use is considered relevant for easing symptoms linked to organ-specific functional stress. This supports general well-being during symptomatic phases.


Quick Fact: Support for Symptoms of Systemic Imbalance Losarstad is applicable in scenarios where the body experiences temporary physiological imbalance and associated heightened systemic burden.

Regulatory References

  1. NIH MedlinePlus overview on Losartan

Eligibility and Restrictions for Use

Losarstad's use is strictly defined by regulatory eligibility criteria, which establish groups that must avoid the medication and those for whom use is permitted or restricted.

Contraindications and Absolute Exclusions

The medicine is contraindicated in several groups due to potential harm:

  • Patients with known hypersensitivity to losartan or any of its components.
  • Women who are in the second or third trimesters of pregnancy. Losartan must be discontinued as soon as possible if pregnancy is detected.
  • Individuals with severe hepatic (liver) impairment.
  • Patients with diabetes mellitus or renal impairment (GFR < 60 mL/min/1.73 m^2) who are taking medication containing aliskiren (a contraindication known as dual RAS blockade).

Restricted and Non-Recommended Use

Use is not recommended for:

  • Children under 6 years of age and pediatric patients with a low estimated glomerular filtration rate ( GFR < 30 mL/min/1.73 m^2) due to limited data.
  • Breastfeeding women, as safety in infants is not established, making alternatives preferable.

Use is permitted but requires special consideration (conditional use) for patients with mild-to-moderate hepatic impairment or those who are volume/salt depleted, often requiring a lower starting dose.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Official regulatory documents describe specific interaction patterns for Losarstad (Losartan potassium), primarily categorized by pharmacodynamic effects and metabolic concentration changes. Co-administration of Losarstad with Aliskiren is contraindicated in patients with diabetes or impaired kidney function, reflecting an official restriction on dual blockade of the Renin-Angiotensin System (RAS). The simultaneous use of Losarstad with other RAS-acting agents like ACE Inhibitors is also generally avoided.

Pharmacodynamic and Concentration Effects

Interacting Substance Category Official Documented Outcome
Potassium-Sparing Diuretics/Potassium Supplements Increased risk of hyperkalemia (high serum potassium concentration).
NSAIDs (Non-Steroidal Anti-Inflammatory Drugs) May attenuate the antihypertensive effect; increased risk of renal impairment in the elderly or renally-impaired.
Lithium Increased serum lithium concentrations due to reduced clearance.
Fluconazole (CYP2C9 Inhibitor) Increases Losarstad exposure; decreases exposure of the active metabolite.
Rifampin (CYP Inducer) Decreases exposure of both Losarstad and its active metabolite.

These patterns dictate formal regulatory constraints. Losarstad can be administered with or without food, as meals cause only a minimal change in the active metabolite's overall exposure.

Mechanism of Action

Losartan, and its active metabolite EXP3174, function as selective and competitive antagonists at the Angiotensin II type 1 receptor ( AT1 receptor). The AT1 receptor is a G-protein coupled receptor expressed in high concentrations in tissues such as vascular smooth muscle, the heart, the kidneys, and the adrenal gland. By binding to this receptor, losartan and EXP3174 block the physiological actions of the endogenous ligand, Angiotensin II (Ang II).

Normally, Ang II binding to the AT1 receptor activates intracellular signaling cascades, including phospholipase C (PLC) and L-type calcium channels. These cascades result in an increase in intracellular calcium concentration, which drives the contraction of vascular smooth muscle cells (vasoconstriction) and stimulates the synthesis and secretion of aldosterone from the adrenal cortex. The binding of Ang II to AT1 receptors also promotes cellular proliferation and hypertrophy in the vasculature and myocardium.

Losartan's blockade of the AT1 receptor inhibits these molecular and intracellular pathways. This leads to the inhibition of vasoconstriction, resulting in a systemic decrease in total peripheral resistance. It also inhibits aldosterone secretion, promoting increased renal excretion of sodium and water. The ultimate system-level physiological consequence is the modulation of vascular tone, the reduction of circulating volume, and the attenuation of Ang II-mediated trophic effects on cardiovascular tissue.

Dosage and Administration Information

Administration Guidelines for Losartan (Losarstad)

The following instructions summarize the standard use of Losartan.

Feature Instruction
Route of Administration Oral use only (tablet or suspension form).
Standard Dosing Schedule 50 mg once daily is the usual adult starting dose, with a maximum dose of 100 mg once daily. Dosing may be adjusted to twice daily if needed.
Timing in Relation to Meals Losartan tablets may be administered with or without food.
Consistency in Dosing Take the medicine at approximately the same time each day to maintain consistency.
Preparation Requirements Tablets should be swallowed whole. An oral suspension may be prepared by a pharmacist for pediatric use; this suspension must be shaken for 20 seconds before use and used within 60 days of preparation.
Missed Dose Rule If a dose is missed, take it as soon as you remember. If it is almost time for the next scheduled dose, skip the missed dose and resume the regular schedule. Do not take two doses at the same time.

Population-Specific Use

Dose adjustments are utilized for certain patient populations:

  • Hepatic Impairment: Patients with mild-to-moderate liver dysfunction (hepatic impairment) should start with a lower dose of 25 mg once daily. Use has not been studied in severe hepatic impairment.
  • Volume Depletion: A starting dose of 25 mg once daily is recommended for patients with possible intravascular volume depletion (e.g., those on high-dose diuretic therapy). This condition should ideally be corrected prior to therapy.
  • Pediatric Patients (6 years): The starting dose is based on body weight (0.7 mg/kg once daily, up to 50 mg total). It is not recommended for children younger than 6 years or those with certain kidney problems.

These instructions define the standardized, procedural steps for Losartan intake.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Losarstad

Research Evidence for Managing High Blood Pressure

Losarstad (Losartan) was evaluated in research exploring how symptoms change over time related to elevated blood pressure, a condition linked to increased physiological strain and functional imbalance. The primary research base involves large-scale, controlled clinical trials (Randomized Controlled Trials or RCTs) and subsequent meta-analyses. These trials research examined how blood pressure measurements changed over defined time intervals when Losarstad was compared to an inactive substance (placebo) or to a comparator medicine.

These studies was observed in a wide range of adults with mild to moderate essential hypertension, including older adults. Researchers primarily monitored the change in systolic and diastolic blood pressure over 24 hours. The findings describe patterns observed in the studies where blood pressure measurements evolved in the observed populations. However, the research base does not include head-to-head comparisons against every established blood pressure medication class.


Research Evidence for Supporting Heart and Kidney Functional Stress

Losarstad was evaluated in research contexts involving fluctuating or unstable symptoms, specifically for conditions characterized by physiological strain or stress.

For patients with high blood pressure and an enlarged heart (LVH), research involved long-term RCTs. These studies explored whether Losarstad-based treatment influenced outcomes monitoring physiological strain or stress, such as stroke incidence, when compared to a treatment based on a comparator drug. Findings describe patterns observed in the studies related to outcomes monitoring physiological strain or stress, such as cardiovascular events. One key finding was observed in some studies that the reported measurements on stroke incidence varied in the subgroup of Black patients.

For patients with kidney functional stress related to Type 2 diabetes, research describes the results of dedicated long-term, placebo-controlled trials. These studies research examined outcomes related to changes in kidney function markers, such as the need for long-term kidney support. Findings describe patterns observed in the studies related to the time until these endpoints were reached. One trial reported no significant difference in all-cause mortality rates between the study groups.


What Remains Uncertain and Areas for Future Research

The research base is extensive, but certain research limitation frames are recognized in regulatory and scientific reviews:

  • Long-term effects are not fully established for pediatric patients.
  • Data are still emerging for Losarstad use in patients with the most advanced stages of heart failure or severe kidney impairment.
  • The research does not determine whether an individual will respond similarly to the group patterns observed in the studies, as study results reflect the specific conditions under which they were conducted.

Frequently Asked Questions (FAQ)

Common questions about Losarstad (FAQ)

Q: What is Losarstad and what is it used for?

Losarstad is the brand name for the medicine losartan. It belongs to a class of drugs called angiotensin II receptor blockers (ARBs). It works by blocking a substance in the body that causes blood vessels to tighten, which allows blood to flow more smoothly and the heart to pump more efficiently.

Losarstad is primarily used to treat:

  • High blood pressure (hypertension): It helps lower blood pressure, which reduces the risk of stroke and heart attack.
  • To reduce the risk of stroke in patients with high blood pressure and an enlarged heart (left ventricular hypertrophy).
  • Kidney problems (nephropathy) in patients with type 2 diabetes and a history of high blood pressure.

Q: How should I take Losarstad?

Take Losarstad exactly as your doctor has prescribed it. Do not change your dose or stop taking the medicine without consulting your healthcare provider.

  • Losarstad is usually taken once a day.
  • You can take it with or without food.
  • It is best to take it at the same time each day to help you remember.
  • Swallow the tablet whole with a glass of water.

If you miss a dose, take it as soon as you remember. If it is almost time for your next scheduled dose, skip the missed dose and resume your regular dosing schedule. Do not take two doses at the same time to make up for a missed dose.


Q: What are the common side effects of Losarstad?

Like all medicines, Losarstad can cause side effects, although not everyone gets them. Common side effects often tend to be mild and may go away as your body adjusts to the medicine. The most common side effects include:

  • Dizziness or lightheadedness, especially when first starting the medication.
  • Fatigue (feeling tired).
  • Headache.
  • Diarrhea.
  • Upper respiratory tract infection (like a cold or stuffy nose).

If any of these side effects persist or worsen, you should talk to your doctor.


Q: What are the serious side effects I should watch out for?

While serious side effects are rare, you should seek medical attention immediately if you experience any of the following:

  • Signs of an allergic reaction: Swelling of the face, lips, tongue, or throat (angioedema), difficulty breathing, or hives. This is an emergency.
  • Fainting or feeling like you might pass out.
  • Signs of high potassium levels (hyperkalemia): Muscle weakness, irregular heartbeat, or a slow heart rate.
  • Signs of kidney problems: Change in the amount of urine, or swelling in your hands or feet.

Q: Can Losarstad be taken during pregnancy or breastfeeding?

Pregnancy: Losarstad is not recommended for use during pregnancy, especially during the second and third trimesters, as it can harm the developing fetus. If you become pregnant while taking Losarstad, you must tell your doctor right away to discuss switching to an alternative treatment.

Breastfeeding: It is not known whether Losarstad passes into breast milk. Due to the potential risk to a nursing infant, a decision must be made with your healthcare provider whether to stop nursing or stop taking the medication, taking into account the importance of the drug to the mother.


Q: Does Losarstad interact with other medicines or supplements?

Losarstad can interact with other medications, which may affect how Losarstad works or increase the risk of side effects. It is crucial to inform your doctor about all prescription and non-prescription drugs, vitamins, and herbal supplements you are taking.

Key drug interactions to be aware of include:

  • Other blood pressure medicines: Taking Losarstad with other medications that lower blood pressure (like ACE inhibitors or diuretics) may cause an unsafe drop in blood pressure.
  • Potassium supplements or salt substitutes containing potassium: Using these with Losarstad can lead to dangerously high levels of potassium in the blood (hyperkalemia).
  • Non-Steroidal Anti-Inflammatory Drugs (NSAIDs): Medications like ibuprofen or naproxen may reduce the blood-pressure-lowering effect of Losarstad and can increase the risk of kidney problems, especially in elderly or dehydrated patients.

Always consult your healthcare provider or pharmacist before starting any new medication while taking Losarstad.


Q: Do I need to avoid any foods or drinks while taking Losarstad?

While there are no general dietary restrictions for Losarstad, there are a few important points regarding consumption:

  • Potassium-rich foods: Because Losarstad can increase potassium levels, your doctor may advise you to limit the amount of foods rich in potassium (such as bananas, oranges, and certain juices) or to avoid potassium supplements.
  • Alcohol: Drinking alcohol while taking Losarstad may increase the blood-pressure-lowering effect, leading to excessive dizziness or lightheadedness. It is best to limit or avoid alcohol consumption.
  • Grapefruit juice: While the interaction risk is considered low, some individuals may be sensitive. If you have concerns, speak with your doctor.

Your doctor may give you specific dietary instructions based on your health condition.

How should Losarstad be stored and disposed of?

Losarstad (Losartan potassium) must be stored at Controlled Room Temperature (CRT), typically defined as 20 C to 25 C (68 F to 77 F). The product must be protected from excess heat, direct light, and moisture, and must not be frozen. To maintain drug integrity, the tablets should be kept in the original container and the container must be tightly closed.

Child-Safety and Disposal

Losarstad must be stored out of the sight and reach of children to prevent accidental ingestion. For disposal, official regulations state that the unused medicine must not be thrown into wastewater or household trash. Instead, patients should consult a pharmacist or follow specific local regulations for the proper disposal of expired or unneeded tablets.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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