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Prescription medication · Biguanide / Sulfonylurea Combination

metformin/glipizide

Also sold as Metaglip.

Data updated 2026-05-15

164,328
FDA reports
7
InteractionsFew interactions
Rx
Availability

What the data shows

metformin/glipizide (Metaglip) is a prescription Biguanide / Sulfonylurea Combination, with 164,328 FDA adverse-event reports on file, with 7 documented drug interactions.

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.

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What it does

Information not available.

Common side effects

Diarrhea, Upper respiratory tract infection (like a cold), Headache

Key warnings

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

Side Effects (from patient reports)

Based on 164,328 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for metformin/glipizide, 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)

Known Drug Interactions

moderate metformin

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 [OCT 2 ] / 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 )]. Alcohol Clinical Impact: Alcohol is known to potentiate the effect of metformin on lactate metabolism. ( 7 ) Drugs that reduce metformin clearance (such as ranolazine, vandetanib,...

Mechanism: Taking these two drugs together means you are taking the same medicine twice, which can cause metformin to build up to dangerous levels. This buildup increases the risk of a serious condition called lactic acidosis.

What to do: Do not take both of these medications at the same time. Your doctor should review your treatment plan to ensure you are not taking a double dose of metformin.

Examples: Topiramate, zonisamide, acetazolamide or dichlorphenamide.

Mechanism: Topiramate lowers the amount of bicarbonate in your blood, which can increase the risk of your blood becoming too acidic when combined with metformin.

What to do: Your healthcare provider should monitor your blood chemistry closely to ensure your acid-base balance stays within a safe range.

Examples: Ranolazine, vandetanib, dolutegravir, and cimetidine. ( 7 ) Drugs that reduce metformin clearance (such as ranolazine, vandetanib, dolutegravir, and cimetidine) may increase the accumulation of metformin.

Mechanism: Dolutegravir slows down the process of clearing metformin from your body, which can cause the medicine to build up to higher levels in your blood.

What to do: Your doctor may need to adjust your metformin dose or monitor you more frequently for side effects.

Examples: Ranolazine, vandetanib, dolutegravir, and cimetidine. ( 7 ) Drugs that reduce metformin clearance (such as ranolazine, vandetanib, dolutegravir, and cimetidine) may increase the accumulation of metformin.

Mechanism: Ranolazine slows down how quickly your body removes metformin, which can cause the drug to build up in your blood.

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

Examples: Ranolazine, vandetanib, dolutegravir, and cimetidine. ( 7 ) Drugs that reduce metformin clearance (such as ranolazine, vandetanib, dolutegravir, and cimetidine) may increase the accumulation of metformin.

Mechanism: Cimetidine blocks the path your body uses to get rid of metformin, which can lead to higher levels of the medicine in your system.

What to do: Watch your blood sugar levels carefully and report any new symptoms to your healthcare provider.

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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 metformin/glipizide?
The most commonly reported side effects of metformin/glipizide include Diarrhea, Upper respiratory tract infection (like a cold), Headache. Based on 164,328 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does metformin/glipizide interact with other medications?
Yes, metformin/glipizide has 7 known drug interactions. Notable interactions include metformin, topiramate, dolutegravir. Always inform your doctor about all medications you are taking.
What drug class is metformin/glipizide?
metformin/glipizide belongs to the Biguanide / Sulfonylurea Combination drug class. It requires a prescription (Rx).

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What the FDA Data Shows for metformin/glipizide

The FDA label for metformin/glipizide (sold under brand names such as Metaglip) classifies it as a prescription-only medication in the Biguanide / Sulfonylurea Combination class. Regulatory labeling describes its approved uses and the patient populations studied in pre-market trials. Official labeling lists 3 commonly reported side effects, including Diarrhea, Upper respiratory tract infection (like a cold), Headache.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 164,328 voluntary reports. The database also lists 7 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.

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).

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: June 9, 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