Incresina

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Incresina

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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 Incresina

What is Incresina?

Incresina is an oral medication used to help manage blood sugar levels in adults with type 2 diabetes mellitus. It belongs to a class of drugs known as dipeptidyl peptidase-4 (DPP-4) inhibitors, which are also referred to as gliptins.

Mechanism of Action

The medication works by affecting the action of incretin hormones in the body. Incretins are natural substances released by the intestines throughout the day, with levels increasing significantly after a meal. These hormones perform two primary functions to regulate glucose:

  • Insulin Stimulation: They signal the pancreas to produce more insulin when blood sugar levels are high.
  • Glucagon Reduction: They signal the liver to decrease the amount of sugar it produces by lowering glucagon levels.

Incresina functions by blocking the enzyme DPP-4, which normally breaks down these incretin hormones. By inhibiting this enzyme, the medication allows incretin hormones to remain active in the system for a longer period. This helps the body lower blood sugar only when it is elevated, reducing the likelihood of sugar levels dropping too low between meals.

Therapeutic Use

Incresina is used to improve glycemic control when diet and exercise alone do not provide sufficient blood sugar management. It may be used as a standalone treatment (monotherapy) or in combination with other glucose-lowering medications, such as metformin, sulfonylureas, or thiazolidinediones, depending on the individual's clinical needs.

What side effects are possible with Incresina?

Incresina: Possible Side Effects and Safety Information

This section outlines the officially documented adverse reactions and safety constraints for Incresina, strictly based on regulatory documents from government health authorities.

Adverse Reaction Classification

Adverse reactions are formally categorized by frequency of occurrence, as defined in regulatory labeling (e.g., EMA or FDA documents).

Frequency Classification Definition (Approximate Incidence)
Very Common Occurs in 1 in 10 patients or more ((ge 1/10))
Common Occurs in less than 1 in 10, but more than 1 in 100 patients ((ge 1/100 to < 1/10))
Uncommon Occurs in less than 1 in 100, but more than 1 in 1,000 patients ((ge 1/1,000 to < 1/100))
Rare / Very Rare Occurs in 1 in 1,000 to less than 1 in 10,000, or less than 1 in 10,000 patients

The most frequently reported adverse reactions often include effects classified under Gastrointestinal disorders (e.g., nausea) and Nervous system disorders (e.g., headache), which may be listed as Very Common or Common.

Serious Adverse Reactions and Safety Constraints

Regulatory documents also list rare but clinically significant events termed Serious Adverse Reactions, which require prompt medical attention. Examples of such reactions documented in the official profile may include anaphylactic reactions or specific types of organ-specific toxicity (e.g., severe liver or pancreatic events).

Population-Specific Safety: The official labeling includes specific statements regarding use in certain patient populations. For example, specific cautions or dose adjustments may be mandated for patients with severe renal or hepatic impairment. Furthermore, the safety and efficacy may be formally noted as not established in the pediatric population.

Safety Restrictions: Incresina is formally contraindicated (must not be used) in patients with a known hypersensitivity to the drug's components or in individuals with certain specific pre-existing medical conditions, as explicitly defined by the regulatory authority.

Overdose and Emergency Response

Overdose and When to Seek Help

This section explains the official overdose information for Incresina (Alogliptin) as documented in government regulatory sources, detailing required actions and management.

Documented Overdose Profile

Official regulatory documents indicate that in clinical trials, the administration of Incresina at doses significantly exceeding the maximum recommended therapeutic dose—such as a single dose of 800 mg—did not result in the reporting of specific adverse clinical manifestations or defined dose-limiting toxicities. Therefore, no specific signs or symptoms are currently documented as indicators of an Alogliptin-only overdose.

Management Fact Regulatory Statement
Antidote Availability No specific antidote for Incresina overdose is documented.
Dialysis Efficacy Hemodialysis is unlikely to be of clinical benefit as only minimal quantities of the drug are removed.

Required Emergency Actions

If an overdose of Incresina is suspected, the regulatory mandate is to seek emergency medical attention immediately or contact the Poison Help line. Management of a suspected overdose is focused on appropriate supportive measures based on the patient's clinical status, with the option for a healthcare professional to initiate the removal of unabsorbed material from the gastrointestinal tract using clinical judgment. Necessary clinical monitoring should be instituted in all cases.

Therapeutic Uses of Incresina

What Incresina Treats: Main Uses and Benefits


Incresina (Alogliptin) is considered relevant in the management of Type 2 Diabetes Mellitus (T2DM). Its use is aligned with domains involving significant symptom expression, and it is considered relevant when supportive symptom management is appropriate to manage the persistent systemic imbalance. It is commonly used in adults with T2DM when blood sugar levels remain suboptimally managed despite existing therapy with diet, exercise, or monotherapy.

Therapeutic Role and Symptom Management

The primary therapeutic use helps address symptom clusters that may create noticeable physiological strain, specifically those related to the persistent elevation of blood glucose. This supportive therapeutic benefit is applicable within clinical settings that involve acute or disruptive symptom patterns. Incresina is relevant for easing the symptoms of systemic imbalance in conditions where functional stability becomes affected.

Incresina is generally considered relevant when additional symptomatic support is needed and may be part of symptomatic management in dual or triple therapy regimens. This use in combination with other anti-diabetic agents supports general well-being during symptomatic phases for patients whose condition requires a more robust, multi-faceted approach to manage the symptoms related to systemic imbalance.


Quick Facts

Quick Fact Relevance
Support for Systemic Imbalance Management Helps address the underlying metabolic patterns of chronic blood sugar elevation.
Context of Use Applicable within clinical settings that involve acute or disruptive symptom patterns, often used as part of combination therapy.
Patient Group Relevant for adults needing assistance in achieving glycemic control.

Eligibility and Restrictions for Use

Incresina (alogliptin and pioglitazone) is a prescription combination medication used alongside diet and exercise to improve blood sugar control in adults with Type 2 diabetes mellitus. It is generally suitable for adults aged 18 and older.


Who Can Use Incresina?

Incresina may be prescribed for patients with Type 2 diabetes who are not achieving adequate blood sugar control with other specific treatments, such as pioglitazone alone, or a combination of pioglitazone and metformin. It can also be used to replace separate tablets of alogliptin and pioglitazone in patients already managed on this regimen.


Who Cannot Use Incresina?

This medication is not appropriate for all individuals. Patients should not use Incresina if they have:

  • Type 1 diabetes or diabetic ketoacidosis (a serious complication of diabetes).
  • Severe or uncontrolled heart failure (NYHA Class III or IV), as the pioglitazone component can worsen this condition.
  • Active bladder cancer.
  • A known allergic reaction to alogliptin, pioglitazone, or any other ingredients in the tablet.

Patients with moderate to severe kidney disease, liver disease, or a history of heart failure or pancreatitis should discuss these conditions thoroughly with their healthcare provider, as the use of Incresina may be contraindicated or require careful monitoring and dose adjustments.

What should I know about interactions with other medicines?

Interactions with other medicines and products

The official regulatory profile for Incresina (Alogliptin) is primarily defined by a low risk of pharmacokinetic interactions and specific constraints related to pharmacodynamic reinforcement in combination therapy.


Pharmacodynamic and Exposure Interactions

Co-administration with Insulin or an Insulin Secretagogue (such as a sulfonylurea) results in a documented increased risk of hypoglycemia. This pharmacodynamic effect requires that a lower dose of the co-administered agent may be considered. The combination profile for Alogliptin with Pioglitazone is subject to exposure modification by other agents. Specifically, strong CYP2C8 inhibitors (e.g., Gemfibrozil) significantly increase the exposure of Pioglitazone, which formally requires adherence to a maximum dose limitation for the combination product.


Metabolic Profile and Restrictions

Alogliptin exhibits negligible metabolism via the CYP P450 enzyme system. Consequently, no clinically relevant interactions are expected with commonly prescribed CYP inhibitors or inducers. Furthermore, regulatory information states that food intake has no clinically relevant effect on Alogliptin absorption. Restrictions apply to products containing Metformin, which are contraindicated in patients with acute or chronic metabolic acidosis and must be discontinued before and held after radiologic procedures that utilize iodinated contrast materials. Additionally, excessive alcohol consumption is a documented risk factor for lactic acidosis in Metformin-containing regimens.

Mechanism of Action

Targeted Enzyme Inhibition Preserves Incretin Hormones

Incresina acts by providing highly selective, competitive inhibition of the Dipeptidyl Peptidase-4 (DPP-4) enzyme. This molecular blockade prevents the rapid breakdown and inactivation of the body's natural signaling molecules, Glucagon-like peptide-1 (GLP-1) and Glucose-dependent insulinotropic polypeptide (GIP). This action results in the prolonged and amplified presence of these hormones within the circulation.


Glucose-Dependent Modulation of Pancreatic Function

The amplified levels of active incretin hormones modulate the Gut-Pancreas Axis, primarily by binding to receptors on the pancreatic islets. This signaling cascade results in a glucose-dependent enhancement of insulin secretion from the beta-cells, alongside a simultaneous suppression of glucagon release from the alpha-cells. This dual regulatory action reduces the liver's signal to produce endogenous glucose, enhancing peripheral glucose uptake and utilization, which contributes to systemic glucose homeostasis.

Dosage and Administration Information

How Incresina is Used (Alogliptin)

Incresina (Alogliptin) is a prescription antidiabetic agent administered as an oral tablet for the long-term management of type 2 diabetes mellitus. Its usage is standardized, with specific instructions governing dose, frequency, and administration conditions.


Standard Administration and Dosing

The standard recommended dose of Alogliptin is 25 mg taken once daily. The tablet can be taken at any time of day, with or without food, allowing for flexibility in the daily schedule. To maintain a consistent concentration, the medicine should be taken at approximately the same time each day.

Tablets must be swallowed whole with water and must not be split, crushed, or chewed. If a dose is missed, it should be taken as soon as the patient remembers; however, a double dose must not be taken to compensate for a forgotten one.


Population-Specific Adjustments

Dose adjustment is explicitly required for patients based on renal function, as determined by creatinine clearance (CrCl):

Renal Function Status Recommended Daily Dose
Mild impairment 25 mg
Moderate impairment (CrCl 30 to < 60 mL/min) 12.5 mg
Severe impairment (CrCl < 30 mL/min) or ESRD on dialysis 6.25 mg

For patients undergoing hemodialysis, the reduced dose (6.25 mg) may be administered without regard to the timing of dialysis. No specific dose adjustment is necessary for older adults based on age alone, or for those with mild to moderate hepatic impairment.

Recent Clinical Evidence

Evidence for Improving Blood Sugar Management in T2DM

Research has explored the presence of patterns related to blood sugar markers in adults with Type 2 Diabetes Mellitus (T2DM) through Randomized Controlled Trials (RCTs). These studies compared Incresina to a placebo or another active agent, both alone and when added to existing treatments like Metformin or Pioglitazone. The main outcomes research examined were shifts in markers like Glycosylated Hemoglobin (HbA1c) and Fasting Plasma Glucose (FPG). These studies reported measurements of blood sugar markers over short-term (up to 26 weeks) and intermediate periods (up to two years), with some studies monitoring durability over these defined time intervals. What remains less certain is the drug's long-term linkage to major disease complications, as the evidence primarily relies on these surrogate endpoints.


Research on Cardiovascular Outcomes and Uncertainty

Regulatory bodies required a large Cardiovascular Outcome Trial (CVOT), known as EXAMINE, to assess the drug's profile in high-risk T2DM patients who had recently experienced an acute coronary syndrome. This research focused on the composite endpoint Major Adverse Cardiovascular Events (MACE). The trial was designed to evaluate non-inferiority, which meant assessing whether the drug's association with these MACE events was similar to that of placebo. The findings indicated patterns related to the MACE rates were consistent with the placebo group. Research has also explored the drug in older adults and patients with renal impairment.

However, a post-trial analysis noted a signal regarding a potential numerical increase in hospitalization for heart failure in the specific subgroup of patients without a prior heart failure history, which contributes to ongoing uncertainty. Furthermore, the clinical evaluation of the drug for the pediatric population has not been completed.

Key Studies & References

  1. Alogliptin after acute coronary syndrome in patients with type 2 diabetes: a renal function stratified analysis of the EXAMINE trial

Frequently Asked Questions (FAQ)

Common questions about Incresina (FAQ)

Q: How quickly does Incresina start to have an effect?

The highest concentration of the active ingredient in the bloodstream is generally reached within one to two hours after the tablet is taken. However, the effects on long-term blood sugar markers are typically measured in clinical studies over periods of several weeks to months.

Q: Why is Incresina sometimes mentioned alongside other treatments?

Incresina is formally approved for use in combination with diet and exercise to improve blood sugar control. Official guidance describes its use alongside other treatments like Metformin or Pioglitazone for individuals whose blood sugar is not meeting goals with current specific therapies.

Q: Can Incresina be used long-term?

Incresina is indicated in regulatory documents for the long-term management of type 2 diabetes. Clinical studies have monitored its effects over intermediate periods, with some research tracking use for defined periods of up to two years.

Q: What is the expected timeline for seeing the full effects of Incresina?

Regulatory studies examining Incresina focus on improvements in blood sugar markers like HbA1c. The measurements in these studies are taken at specific intervals, such as 26 weeks and up to two years, to assess changes in blood sugar control.

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

Official information indicates that Incresina's active ingredient is generally associated with a low risk of metabolic interactions. No clinically relevant interactions are expected with commonly prescribed medications that affect liver enzymes. However, it is generally noted that any product, including over-the-counter medicines, has the potential to affect blood sugar and may need to be mentioned to a healthcare provider.

Q: Can Incresina be taken by women who are pregnant or planning to be?

There are limited data available to determine the specific drug-associated risk for women who are pregnant. Official documents state that the risk of poorly controlled diabetes during pregnancy should be considered, as this poses documented risks to both the mother and the fetus.

Q: What should I do if I notice a change in how I feel after starting Incresina?

Regulatory documents list certain rare but serious reactions, such as severe abdominal pain or symptoms of liver injury, that have been documented and are noted as conditions that require prompt evaluation by a healthcare provider.

Q: Is it normal to feel a certain symptom during the first week of taking Incresina?

Clinical trials have documented certain adverse reactions that were frequently reported, including common effects like headache or upper respiratory tract infection. Official information classifies these by overall frequency but does not specify the exact time frame in which they might occur, such as only during the first week.

Q: What happens if I miss a single dose of Incresina?

The prescribing information includes a safety statement that taking two doses at once is not recommended to make up for a missed dose.

Q: Can Incresina cause changes in mood or sleep patterns?

The official label lists nervous system effects like headache, and some patients have reported severe and disabling arthralgia (joint pain). However, specific changes in mood or sleep patterns are not listed among the commonly reported adverse reactions.

Q: Why does Incresina have specific storage instructions?

Official product information mandates specific storage requirements to ensure the medicine remains effective. Incresina must be protected from environmental factors like heat, moisture, and direct light and must be kept at a controlled room temperature.

Q: Why is Incresina not recommended for people with certain heart conditions?

Clinical trial results have indicated a possible increased risk of hospitalization for heart failure, particularly in patients with a prior history of heart failure or kidney impairment. Due to this evidence, the drug's official profile carries a warning related to its use in certain populations, particularly those with a prior history of heart failure or kidney impairment.

Q: Does Incresina affect my ability to drive or operate machinery?

Incresina alone is not typically expected to impair the ability to drive. However, when it is taken in combination with other anti-diabetes medicines that can cause hypoglycemia (very low blood sugar), the risk of low blood sugar may affect concentration and motor skills.

Q: Does Incresina have a black box warning in the US or similar caution in other regions?

The single-ingredient form of Incresina (Alogliptin) does not carry a Black Box Warning in the United States. However, combination products containing other medicines with Alogliptin, such as Pioglitazone or Metformin, do carry these specific warnings related to risks like heart failure or lactic acidosis.

Q: What happens to Incresina in the body (a high-level view)?

Incresina is classified as a DPP-4 inhibitor, meaning it is described as blocking the action of the DPP-4 enzyme. This action helps to prolong the life of natural hormones called incretins. This effect is associated with enhancing the body's ability to regulate blood sugar in a glucose-dependent manner.

Q: Is Incresina widely available, or is it a specialty drug?

The active ingredient, Alogliptin, is a commonly marketed drug for the treatment of type 2 diabetes. It is available as an oral tablet in multiple strengths, suggesting it is a widely distributed prescription drug.

Q: Is it true that Incresina can affect the function of the liver?

Official postmarketing reports have noted rare cases of liver injury, including liver failure, in patients using Incresina. The official labeling notes that patients should be observed for signs of potential liver abnormalities.

Q: What happens if Incresina is taken with alcohol?

Regulatory documents do not detail a specific interaction between alcohol and Alogliptin alone. However, alcohol consumption has the potential to affect blood sugar levels, which is a consideration for all individuals with diabetes. Additionally, combination products with Metformin carry a warning related to excessive alcohol intake.

Q: Is Incresina available generically?

Yes, the active ingredient in Incresina, Alogliptin, is available in authorized generic versions. This means that a version with the same active component is available.

Q: Can I take Incresina if I have an existing allergy to other medicines?

Incresina is formally contraindicated if a patient has a known history of a serious hypersensitivity reaction (severe allergy) to Alogliptin or any of its components. Official prescribing information notes that a history of angioedema with another DPP-4 inhibitor is a factor for consideration.

Q: What defines the appropriate population for Incresina use?

The appropriate population for Incresina is defined in official documents as adults with Type 2 Diabetes Mellitus. It is intended to be used as an addition to diet and exercise to help improve blood sugar control.

Q: What kind of evidence is still being collected about Incresina?

Regulatory bodies have required ongoing postmarketing studies for Incresina. This evidence collection is focused on key areas, including evaluation of its safety and efficacy for use in the pediatric population and enhanced surveillance for potential severe reactions like liver issues or pancreatitis.

How should Incresina be stored and disposed of?

Storage and Disposal Requirements

Incresina (alogliptin) tablets must be stored according to official regulatory specifications. The product must be kept at controlled room temperature, specifically between 20 C to 25 C (68 F to 77 F), with permitted excursions up to 30 C.

The medicine requires protection from environmental factors: it must be stored away from heat, moisture, and direct light, and should be kept from freezing. The tablets should be maintained in a closed container and remain in the blister pack until immediately before use.

Crucially, Incresina must be stored out of the sight and reach of children.

For disposal, unused or expired product must be discarded in accordance with local requirements. Do not dispose of the medicine by flushing it down a toilet or throwing it into household waste unless specifically advised by a healthcare professional or local authority.

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

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