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Prescription medication · DPP-4 Inhibitor

alogliptin

Also sold as Nesina.

Data updated 2026-05-15

3,393
FDA reportsLightly reported
7
InteractionsFew interactions
62% less
Generic vs brandBig savings
$13.10
Brand price (NADAC)

What the data shows

alogliptin (Nesina) is a prescription DPP-4 Inhibitor, among the least-reported drugs the FDA tracks (3,393 FDA reports), whose generic runs roughly half the brand price or less (62% less).

Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.

Drug Pricing (NADAC)

Brand Price

$13.10/unit

Generic Price

$5.02/unit

Generic Savings

62%

Generic Available

Yes (0 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Information not available.

Common side effects

Upper respiratory tract infection, Common cold, Diarrhea

Key warnings

No specific warnings noted. Always follow your prescriber's instructions.

Side Effects (from patient reports)

Based on 3,393 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for alogliptin, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for alogliptin each year to the FDA Adverse Event Reporting System (FAERS).

-1000100200300400 20112013201520172019202120232025 129

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where alogliptin sits

alogliptin has more FDA adverse-event reports than 20% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is alogliptin; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 3,393 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2011–2025.

Total Reports

3,393

Reports Mentioning Death

356

10.5% of reports — not proof of cause

Hospitalization Reports

1,564

Top Indication

Type 2 Diabetes Mellitus

Gender Distribution

Female 1,323 (42%)
Male 1,828 (58%)

Age Distribution

0–17 73
18–44 140
45–64 803
65–74 849
75+ 885

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 DIARRHOEA 134
2 NAUSEA 124
3 VOMITING 110
4 ACUTE KIDNEY INJURY 101
5 PEMPHIGOID 101
6 MALAISE 93
7 RASH 92
8 BLOOD GLUCOSE INCREASED 86
9 DYSPNOEA 84
10 DECREASED APPETITE 82
11 PNEUMONIA 82
12 PYREXIA 78
13 DIZZINESS 77
14 PRURITUS 76
16 CEREBRAL INFARCTION 72

Reactions in Death Reports

DEATH 71
DIARRHOEA 19
PNEUMONIA 19
MALIGNANT NEOPLASM PROGRESSION 18
PYREXIA 16
INTERSTITIAL LUNG DISEASE 15
DECREASED APPETITE 14
CONDITION AGGRAVATED 13
SUDDEN DEATH 13
CARDIAC FAILURE 12

Reactions in Hospitalization Reports

ACUTE KIDNEY INJURY 75
PYREXIA 62
PNEUMONIA 60
VOMITING 58
DIARRHOEA 57
INTERSTITIAL LUNG DISEASE 53
DECREASED APPETITE 51
CEREBRAL INFARCTION 48
HYPOGLYCAEMIA 46
NAUSEA 44

Source: FDA FAERS (Adverse Event Reporting System) FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Known Drug Interactions

moderate topiramate

Examples: Topiramate, zonisamide, acetazolamide or dichlorphenamide Drugs that Reduce Metformin Clearance Clinical Impact: Concomitant use of drugs that interfere with common renal tubular transport systems involved in the renal elimination of metformin (e.g., organic cationic transporter-2 [OCT2]/multidrug and toxin extrusion [MATE] inhibitors) could increase systemic exposure to metformin and may increase the risk for lactic acidosis [see Clinical Pharmacology (12.3) ] .

Mechanism: Topiramate can stop your kidneys from clearing metformin properly, which may cause the drug to build up to dangerous levels.

What to do: Your doctor may need to monitor you more closely for side effects or adjust your dosage.

moderate zonisamide

Examples: Topiramate, zonisamide, acetazolamide or dichlorphenamide Drugs that Reduce Metformin Clearance Clinical Impact: Concomitant use of drugs that interfere with common renal tubular transport systems involved in the renal elimination of metformin (e.g., organic cationic transporter-2 [OCT2]/multidrug and toxin extrusion [MATE] inhibitors) could increase systemic exposure to metformin and may increase the risk for lactic acidosis [see Clinical Pharmacology (12.3) ] .

Mechanism: Zonisamide interferes with how your kidneys remove metformin from your body, which can increase the risk of a serious condition called lactic acidosis.

What to do: Use these drugs together with caution and follow your doctor's advice on monitoring your health.

( 7 ) Drugs that reduce metformin clearance (such as ranolazine, vandetanib, dolutegravir, and cimetidine), may increase the accumulation of metformin. ( 7 ) Alcohol can potentiate the effect of metformin on lactate metabolism. ( 7 ) Metformin HCl Carbonic Anhydrase Inhibitors Clinical Impact: Carbonic anhydrase inhibitors frequently cause a decrease in serum bicarbonate and induce non-anion gap, hyperchloremic metabolic acidosis.

Mechanism: These two drugs work in different ways to lower blood sugar. When taken together, they have an additive effect to help control blood sugar levels.

What to do: Monitor your blood sugar levels regularly and follow your doctor's advice on managing your condition.

( 7 ) Drugs that reduce metformin clearance (such as ranolazine, vandetanib, dolutegravir, and cimetidine), may increase the accumulation of metformin. Examples: Ranolazine, vandetanib, dolutegravir, and cimetidine Alcohol Clinical Impact: Alcohol is known to potentiate the effect of metformin on lactate metabolism.

Mechanism: Dolutegravir can slow down how quickly the body removes metformin. This can cause metformin to build up in the blood, increasing the risk of side effects.

What to do: Your doctor may need to monitor you more closely or adjust your medication doses.

( 7 ) Drugs that reduce metformin clearance (such as ranolazine, vandetanib, dolutegravir, and cimetidine), may increase the accumulation of metformin. Examples: Ranolazine, vandetanib, dolutegravir, and cimetidine Alcohol Clinical Impact: Alcohol is known to potentiate the effect of metformin on lactate metabolism.

Mechanism: Ranolazine can interfere with the body's ability to clear out metformin. This leads to higher levels of metformin in the body.

What to do: Your healthcare provider should monitor your response and may need to adjust your metformin dose.

Check all your medications →

This is a plain-language summary of interactions documented in FDA labeling, not individualized advice. Ask a pharmacist or prescriber before combining medications.

Common Questions

What are the common side effects of alogliptin?
The most commonly reported side effects of alogliptin include Upper respiratory tract infection, Common cold, Diarrhea, High blood pressure, Headache. Based on 3,393 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does alogliptin interact with other medications?
Yes, alogliptin has 7 known drug interactions. Notable interactions include topiramate, zonisamide, metformin. Always inform your doctor about all medications you are taking.
What drug class is alogliptin?
alogliptin belongs to the DPP-4 Inhibitor drug class. It requires a prescription (Rx).
Is there a generic version of alogliptin?
Yes, generic alogliptin is available. The generic costs $5.02 per unit compared to $13.10 for the brand version, saving approximately 62%. Pricing is based on NADAC (National Average Drug Acquisition Cost) data from CMS.

Related Medications in DPP-4 Inhibitor

Other drugs grouped near alogliptin - same-class peers and common alternatives.

Compare alogliptin vs acarbose side-by-side →

Medication Guides

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What the FDA Data Shows for alogliptin

The FDA label for alogliptin (sold under brand names such as Nesina) classifies it as a prescription-only medication in the DPP-4 Inhibitor class. Regulatory labeling describes its approved uses and the patient populations studied in pre-market trials. Official labeling lists 7 commonly reported side effects, including Upper respiratory tract infection, Common cold, Diarrhea.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 3,393 voluntary reports. The database also lists 7 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. NADAC pricing from CMS shows a generic unit cost of $5.02 versus $13.10 for the brand - a 62% generic savings.

Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: April 11, 2025

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.

All federal data sources used on this page