Lasgan

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

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 Lasgan

What is Lasgan?

Lasgan is a pharmaceutical medication classified as a prostaglandin analog. It is primarily utilized in ophthalmic care to manage conditions associated with increased intraocular pressure. The active ingredient works by mimicking the effects of naturally occurring prostaglandins in the body, which play a role in regulating the flow of fluids within the eye.

Mechanism of Action

The medication functions by increasing the outflow of aqueous humor, the clear fluid maintained within the front part of the eye. Under normal conditions, this fluid drains through specific pathways to maintain stable internal pressure. In conditions where drainage is insufficient or fluid production is excessive, internal pressure can rise. Lasgan enhances the uveoscleral drainage pathway, allowing the excess fluid to leave the eye more efficiently, thereby helping to lower and stabilize intraocular pressure.

Therapeutic Purpose

Lasgan is typically used for individuals diagnosed with open-angle glaucoma or ocular hypertension. Maintaining intraocular pressure within a healthy range is a key factor in ocular health management, as prolonged elevation in pressure can lead to progressive changes in the eye's internal structures. By facilitating fluid drainage, the medication helps support the long-term maintenance of ocular function in patients with these conditions.

Regulatory References

  1. Proton Pump Inhibitor (PPI)
  2. gastric fluid

What side effects are possible with Lasgan?

Possible side effects and safety information

Lansoprazole, the active substance in Lasgan, has a documented safety profile established through official regulatory documentation, which classifies adverse reactions by the frequency with which they appear. Safety information is organized across several System-Organ Classes (SOCs).


Classification of Adverse Reactions

  • Common Adverse Reactions (may affect up to 1 in 10 people) typically involve gastrointestinal disorders such as diarrhoea, constipation, abdominal pain, and nausea. Nervous system disorders like headache and dizziness are also commonly reported.
  • Uncommon Adverse Reactions (may affect up to 1 in 100 people) include changes in the skin, such as a skin rash and urticaria (hives), along with fatigue.
  • Rare Adverse Reactions (may affect up to 1 in 1,000 people) involve a wider array of SOCs, including blood and lymphatic system disorders (e.g., agranulocytosis) and hepatobiliary disorders (e.g., hepatitis).
  • Very Rare Adverse Reactions include severe cutaneous adverse reactions such as Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN).

Serious Safety Patterns and Constraints

Official labeling documents an increased risk of bone fracture of the hip, wrist, or spine associated with long-term and/or high-dose therapy. Prolonged use may also be associated with the development of Hypomagnesaemia (low serum magnesium levels) and Hyponatremia, categorized as Not Known frequency. The use of the medicine is subject to regulatory constraints in individuals with known severe hepatic impairment. A specific high-level safety note is also documented concerning the concomitant use with Clopidogrel.

Overdose and Emergency Response

Overdose and when to seek help

This section describes official overdose information strictly based on government regulatory documentation.

Feature Official Regulatory Statement
Documented overdose presentations No specific adverse effects or symptoms of overdose were reported in the single documented case involving acute ingestion of 600 mg of the active substance.
Dose-related or exposure-related factors The official labeling documents acute ingestion of doses up to 600 mg (significantly exceeding therapeutic doses).
Emergency-response statements The explicit instruction is to seek medical help or contact a Poison Control Center right away for any suspected overdose.

Overdose classifications (high-level)

Classification Feature Official Regulatory Statement
Regulatory basis Information is based on official documents, such as the U.S. FDA Prescribing Information.
Overdose-context constraints No specific antidote for the active substance is known.

Resulting overdose structure

Official overdose statements:

  • Emergency medical care is required for any suspected overdose, regardless of symptoms.
  • The clinical management for overdose is restricted to symptomatic and supportive treatment.
  • Regulatory documentation notes that the active substance is not expected to be significantly removed by hemodialysis.

Connection to the overall overdose profile (3 sentences): Regulatory documents define the overdose profile for Lasgan by noting the absence of reported adverse symptoms in a documented high-dose exposure, yet immediate medical care is required for any suspected overdose. Treatment is governed by the fact that the drug lacks a specific antidote, thereby mandating symptomatic and supportive management as the sole documented clinical procedure. No specific population-related acute overdose risks or severe outcomes are detailed in the official acute overdose section.

Therapeutic Uses of Lasgan

Main Uses of Lasgan

Lasgan is a medication primarily utilized in the management of specific conditions affecting the digestive system. Its active component works to address imbalances in gastric acid production and to support the healing of the mucosal lining in the upper gastrointestinal tract.

Primary Indications

  • Acid Reflux and GERD: Lasgan is used to manage symptoms associated with gastroesophageal reflux disease (GERD), such as heartburn and acid regurgitation. It helps reduce the irritation caused by stomach acid moving upward into the esophagus.
  • Gastric and Duodenal Ulcers: The medication is indicated for the treatment of ulcers located in the stomach or the first part of the small intestine. By lowering acid levels, it allows the ulcerated tissue to heal.
  • Erosive Esophagitis: Lasgan is employed to treat and prevent the recurrence of inflammation and damage to the esophagus resulting from chronic acid exposure.
  • Zollinger-Ellison Syndrome: It is used in the management of rare pathological hypersecretory conditions where the stomach produces excessive amounts of acid.

Therapeutic Benefits

Symptom Relief

The reduction of gastric acid production typically leads to a significant decrease in the frequency and severity of dyspeptic symptoms. This includes a reduction in the burning sensation in the chest and throat often experienced after meals.

Tissue Healing

By maintaining a less acidic environment in the stomach and esophagus, Lasgan facilitates the natural repair processes of the digestive tract's lining. This is particularly beneficial for patients with existing erosions or ulcerations.

Maintenance of Remission

Beyond acute treatment, Lasgan may be used to maintain the integrity of the gastrointestinal lining in patients with chronic conditions, helping to prevent the return of symptoms or the development of further complications associated with acid-related damage.

Eligibility and Restrictions for Use

Lasgan (lansoprazole) eligibility is determined by strict regulatory criteria defining who is permitted to use the medicine and who is prohibited.

Absolute Contraindications

Use is contraindicated for patients with a known hypersensitivity to lansoprazole or any of the product’s excipients. Co-administration is also contraindicated with certain HIV-protease inhibitors, including atazanavir and nelfinavir, as this can reduce the effectiveness of the antiretroviral medication. Furthermore, the possibility of a gastric malignancy must be excluded prior to therapy for gastric ulcer.

Age and Physiological Restrictions

Lasgan is approved for use in adults and older adults. Pediatric use is established only for children 1 year of age and older for specific short-term conditions; use in infants under 1 year of age is not recommended.

Use is not recommended for women who are pregnant or breastfeeding due to limited data or unknown excretion in human milk. Patients with severe hepatic impairment (liver disease) are subject to use restrictions or require supervision.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Official regulatory documents define the interaction profile of Lasgan (Lansoprazole) based on its powerful acid-suppressing effect and its role in modulating liver enzymes, primarily CYP2C19 and CYP3A4.

Formal Restrictions and Contraindications

Co-administration with Atazanavir and Rilpivirine-containing products is formally contraindicated. The primary reason is the risk of significant reduction in the bioavailability of these medicines. Concomitant use with antifungals like Ketoconazole or Itraconazole should be avoided, as their absorption is pH-dependent, potentially leading to sub-therapeutic concentrations.

Exposure-Modifying Interactions

Lasgan may increase the plasma levels of drugs such as Digoxin and the immunosuppressant Tacrolimus. Conversely, the co-administration of enzyme inducers like Rifampicin or the herbal product St John's wort can markedly reduce the plasma concentrations of Lansoprazole. When combined with Warfarin, monitoring of the International Normalized Ratio (INR) is required. Daily, long-term use is also documented to reduce the absorption of Cyanocobalamin (Vitamin B12).

Administration Timing Rules

Administration requires timing separation from certain non-systemic agents. Lasgan must be taken at least 1 hour after using antacids or Sucralfate to ensure proper Lasgan absorption. Additionally, official labeling notes that administration with food reduces the overall absorption of Lansoprazole.

Mechanism of Action

Lansoprazole (Lasgan) functions as an inactive prodrug that requires chemical activation within the highly acidic secretory canaliculi of the gastric parietal cell. The activated molecule then acts as an irreversible inhibitor of the H^+/ K^+- ATPase (Proton Pump), which is the final enzyme in the acid-secreting process. Inhibition is achieved by forming a stable, covalent bond with specific cysteine residues on the enzyme. This mechanism effectively blocks the final acid-secretion pathway regardless of the incoming physiological stimulus (e.g., gastrin or histamine). The irreversible nature of the bond leads to a sustained cessation of hydrogen ion ( H^+) transport and a persistent elevation of gastric pH. The duration of this physiological effect is maintained until the parietal cell synthesizes new, functional pump enzymes, as the process only targets the active proton pumps, confining the modulation to cells currently in a secretory state.

Dosage and Administration Information

How to Use Lasgan

Lasgan is administered via the oral route, primarily as delayed-release capsules or orally disintegrating tablets (ODTs). The administration of all forms is typically scheduled before eating (pre-prandially) to ensure proper systemic absorption and therapeutic action.

Dosing and Frequency

The standard dosage for most acute conditions, such as active ulcers or Erosive Esophagitis, is typically 15 mg or 30 mg once daily, with treatment duration varying from four to eight weeks. For pathological hypersecretory conditions, the initial dose is 60 mg once daily. Doses exceeding 120 mg daily for these conditions are administered in divided doses. The regimen for most indications is once daily, although specific anti-infective combination therapies may require twice or three times daily dosing.

Administration Requirements

The administration procedure requires that the delayed-release capsules and ODTs must not be crushed or chewed, as this compromises the integrity of the essential enteric coating. Capsules should be swallowed whole. For patients unable to swallow the capsule intact, the contents may be mixed with certain soft foods or specific fruit juices. The ODT is designed to disintegrate on the tongue before swallowing. If a once-daily dose is missed, it should be taken as soon as possible; however, if it is near the time of the next scheduled dose, the missed dose must be omitted.

Population-Specific Use

Dosage adjustments are utilized for certain patient populations: for individuals with severe hepatic impairment, the maximum daily dose generally should not exceed 15 mg. Pediatric dosing is determined based on the patient's weight.

Recent Clinical Evidence

Research evidence / Overview of Studies for Lasgan (Lansoprazole)

This section provides a structural overview of the clinical research conducted for Lasgan, detailing the types of studies performed and the high-level patient outcomes they investigated, as documented in regulatory and scientific literature.


Research for Healing and Managing Esophageal Damage

The evidence base for addressing damage in the esophagus largely comes from short-term, randomized controlled trials (RCTs). These studies were used in research exploring how symptoms change over time and how the damaged lining of the esophagus responds during the observation period. Studies examined whether patients experienced tissue healing during the observation period when Lasgan was included in the short-term study protocol, typically lasting four to twelve weeks.

Following the initial observation period, long-term maintenance trials were conducted, primarily in adult populations, to see if the tissue preservation could be maintained. Findings describe patterns observed in the studies where the continuous use of Lasgan was associated with the preservation of endoscopic remission in the observed population. However, long-term outcomes are not fully established regarding the absolute optimal duration of therapy needed for every patient.


Studies for Symptom Relief and Ulcer Healing

Research has also explored Lasgan in individuals experiencing frequent heartburn, which is a primary symptom of symptomatic Gastroesophageal Reflux Disease (GERD). These were typically short-term RCTs, often lasting only a few weeks, applied in studies examining patient-reported experiences. Research highlights changes measured during the study period, reporting that patient outcomes related to the absence of heartburn varied when compared to the placebo group.

Lasgan was studied for the healing of duodenal and benign gastric ulcers. Research describes patterns related to measured healing rates when Lasgan was studied against placebo. Evidence also suggests that Lasgan was evaluated in studies examining the formation of new ulcers in patients who continued to use Non-Steroidal Anti-Inflammatory Drugs (NSAIDs).


Evidence for Use in H. pylori Eradication Regimens

Lasgan is relevant in evidence describing how symptoms are measured within the context of multi-drug regimens for the eradication of Helicobacter pylori infection. These RCTs measured the rate of successful H. pylori eradication, confirmed using diagnostic tests several weeks after the treatment regimen was completed. Findings indicate that these multi-drug regimens, when studies monitored for defined time intervals, resulted in a measured rate of bacterial clearance.


Research in Special Populations and Rare Conditions

Research has explored Lasgan in specific demographic groups, including adolescents (age 12-17) with GERD symptoms or confirmed EE. Studies reported that patterns in measured symptom changes in adolescents showed similarities to those observed in adult study populations. However, evidence for certain groups, such as children under one year of age, provides limited insight into efficacy and dose responsiveness.

For rare pathological hypersecretory conditions, the evidence base relies more on long-term observational studies and case series rather than large-scale RCTs. Findings help contextualize how patients reported their experience over years of continuous management, but the evidence base is less extensive compared to more common indications.


Long-Term Evidence and Areas Still Under Research

Available data for Lasgan in the context of maintenance therapy for EE and long-term management of rare conditions provide insight into short-term changes and sustained acid control. However, long-term effects on other physiological systems are not the primary focus of the clinical efficacy trials, and research is ongoing in this area.

The research exploring Lasgan for functional dyspepsia shows that the findings were mixed. Some trials described patterns where patients reported an evolution in overall discomfort, while other similar studies showed little difference from placebo. This suggests that the evidence quality varies across studies for this particular use, and its role remains uncertain.

Key Studies & References

  1. Effective maintenance treatment of reflux esophagitis with low-dose lansoprazole. A randomized, double-blind, placebo-controlled trial.
  2. A systematic review of proton pump inhibitors for the treatment of adult patients with symptomatic gastroesophageal reflux disease or peptic ulcer disease (Systematic Review/Guideline)
  3. Comparative efficiency and safety of potassium competitive acid blockers versus Lansoprazole in peptic ulcer: a systematic review and meta-analysis

Frequently Asked Questions (FAQ)

Common questions about Lasgan (FAQ)


Q: How quickly should I expect Lasgan to start working?

Lasgan begins to work by inhibiting the proton pumps within a few hours of the first dose. However, official product labeling indicates that for some conditions, it may take between 1 and 4 days for a person to experience the full symptom relief.

Q: Does Lasgan require a special diet or lifestyle change?

The official instructions state that the medicine must be taken before eating (pre-prandially) for optimal absorption, which is a condition noted for administration. Regulatory information also contains a general warning that using alcohol or tobacco with certain medicines, including PPIs, may cause interactions to occur.

Q: Are there any common over-the-counter medicines that interact with Lasgan?

Regulatory documents mention that Lasgan is known to interact with certain prescription medicines and requires administration timing separation from non-systemic agents like antacids and Sucralfate. The full medicine information leaflet provides a comprehensive list of known and potential drug interactions for review by a healthcare professional.

Q: Are the side effects of Lasgan long-term or temporary?

Many commonly reported side effects, such as headache or mild gastrointestinal issues, are generally temporary. However, official warnings describe serious safety patterns, including the increased risk of bone fracture or low magnesium levels, associated with long-term use (typically a year or longer) and/or high doses.

Q: Is there a list of ingredients in Lasgan?

Yes, the official product labeling provides a complete list of all active and inactive ingredients (excipients). For example, the orally disintegrating tablet (ODT) form contains phenylalanine, and this detail is included in the official labeling.

Q: Does Lasgan interact with common supplements like multivitamins?

Regulatory warnings note that daily use, particularly when prolonged over several years, may lead to reduced absorption or deficiency of cyanocobalamin, which is also known as Vitamin B12. The official label specifies this as a possible concern with extended therapy.

Q: Is Lasgan commonly prescribed for something other than its main use?

The medicine is approved for specified gastrointestinal conditions. Studies have explored its use in other areas, such as managing symptoms of functional dyspepsia, but the evidence for these uses is sometimes reported as mixed or uncertain in official documents.

Q: Is the research evidence for Lasgan considered strong?

The evidence base for the primary approved uses is considered strong, often relying on multiple randomized controlled trials (RCTs). However, official clinical reviews indicate that evidence for certain specialized or long-term uses, such as rare hypersecretory conditions, may be less extensive, relying more on smaller observational studies.

Q: What is the success rate described in the Lasgan studies?

Official documents report measured outcomes rather than a single 'success rate' for the medicine overall. Examples of measured outcomes include the healing rate for ulcers, the rate of successful bacterial clearance in H. pylori regimens, and the percentage of observed patients with an absence of heartburn compared to placebo. Outcomes are specific to the condition being studied.

Q: Is it true that Lasgan can only be used short-term?

Official regulatory information indicates the medicine is approved for short-term treatment of acute conditions, such as 4 to 8 weeks for active ulcers. However, the medicine is also approved for long-term maintenance therapy in certain situations, such as preventing the return of healed erosive esophagitis.

Q: Are there any genetic factors that affect how Lasgan works?

Official pharmacokinetic information states that Lasgan is primarily processed by the liver enzymes CYP2 C19 and CYP3 A4. Variability in the activity of these enzymes, which can be influenced by genetic factors, may impact how the body metabolizes the medicine.

Q: Can Lasgan affect my ability to drive or operate machinery?

Official product information notes that some patients have reported adverse reactions such as dizziness and drowsiness. Official labeling notes that caution is warranted regarding driving or operating machinery if these effects are experienced.

Q: Does Lasgan affect birth control effectiveness?

Clinical studies published in regulatory dossiers have examined this potential interaction. Evidence indicates that Lasgan does not affect the bioavailability of a standard low-dose oral contraceptive containing ethinylestradiol and levonorgestrel.

Q: Does taking Lasgan affect routine blood tests?

Long-term use has been associated with imbalances in certain electrolytes, such as low serum magnesium (Hypomagnesaemia) and low sodium (Hyponatremia), which are detectable by blood tests. The medicine may also interfere with the results of certain specialized diagnostic tests for neuroendocrine tumors.

Q: What is the shelf life of Lasgan?

Regulatory approval documents confirm that the medicine is assigned a specific shelf life, such as 24 months, when stored under the conditions described in the product information. This duration is established based on stability testing.

Q: Is Lasgan classified as a controlled substance?

Based on government classifications, Lansoprazole (the active ingredient in Lasgan) is not classified as a controlled medication under the Controlled Substances Act in the United States.

Q: Does Lasgan have a black box warning?

The official U.S. Prescribing Information for Lansoprazole does not contain a Black Box Warning, which is the common term for a Boxed Warning—the FDA's most serious warning about potential adverse effects.

Q: Is Lasgan approved in other countries besides the US?

The active substance, lansoprazole, is widely accepted and approved by numerous regulatory authorities globally, including those in Europe, Canada, and Australia, for treating various acid-related conditions.

Q: What are the requirements for getting a prescription for Lasgan?

Lansoprazole is available in different regulatory statuses depending on its strength and formulation. Some lower-strength formulations are approved as over-the-counter (OTC) products, while higher strengths or specific indications require a prescription from a healthcare professional (Rx-only).

Q: What should I do if I feel like Lasgan is not working for me?

Official patient information advises consulting a healthcare professional if symptoms such as heartburn continue, worsen, or are not relieved after the recommended course of therapy. Symptomatic response to the medicine does not rule out the presence of a more serious underlying condition.

How should Lasgan be stored and disposed of?

How to Store and Dispose of Lansoprazole (Lasgan)

The storage and disposal of Lansoprazole must strictly adhere to regulatory requirements to maintain the product's stability and efficacy.

Storage Requirements

Condition Requirement
Temperature Store at controlled room temperature, typically 20 C to 25 C (68 F to 77 F).
Protection The product must be protected from moisture and kept out of high heat.
Container Store in the original container, which must be kept tightly closed to protect the integrity of the medicine.
Child Safety The medicine must be kept out of the sight and reach of children.

Disposal Instructions

Unused or expired Lansoprazole should be discarded following official guidelines. The preferred method is to utilize a drug take-back program. If no program is available, the product must be prepared for disposal in household trash by mixing it with an undesirable substance (e.g., used coffee grounds) and concealing it in a sealed container or bag. All personal information should be scratched out from the prescription label.

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

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