Key Takeaways
This overview explains repaglinide dosage in clear, practical terms for adults. It highlights meal timing, titration steps, and key safety considerations you should discuss with your clinician.
- Premeal dosing: Take shortly before eating; skip if skipping meals.
- Titrate thoughtfully: Adjust based on fasting and post-meal glucose patterns.
- Watch interactions: Some lipid and antiplatelet drugs raise exposure.
- Use in CKD: Start low and monitor glucose closely for hypoglycemia.
Repaglinide Dosage: Adult Ranges and Titration
Repaglinide is an insulin secretagogue used for prandial control in type 2 diabetes. Adults typically start at low doses and titrate based on self-monitoring results and A1C trends. The rapid onset and short duration allow flexible meal-based dosing, which helps target post-meal glucose spikes.
Initial dosing commonly begins at 0.5 mg before each main meal when switching from diet alone or from low-dose therapy. Individuals moving from another oral agent may start at 1 mg to 2 mg before meals. Dose increases are usually made at weekly intervals, guided by glucose logs, with careful attention to hypoglycemia risk. A commonly cited daily ceiling is 16 mg across all meals, but individual needs vary and should be clinician-directed.
| Clinical Context | Example Starting Dose | Adjustment Approach |
|---|---|---|
| Diet alone; lower A1C | 0.5 mg before meals | Increase weekly if post-meal values remain high |
| Switching from another oral agent | 1–2 mg before meals | Adjust using fasting and post-meal readings |
| High postprandial excursions | Meal-specific titration | Target the meal causing elevations |
These ranges reflect label-based practices and are not personalized advice. For detailed prescribing information, see the FDA label for repaglinide (Prandin), which outlines dosing limits and adjustments in official guidance. Use that source alongside local standards.
Timing With Meals and Missed Doses
Short-acting prandial agents work best when timed to carbohydrate intake. Patients often ask about exact timing windows and what to do when meals change. The goal is to match drug action with the rise in post-meal glucose while minimizing hypoglycemia.
Most clinicians advise dosing shortly before meals and skipping doses when a meal is skipped. If a meal is delayed, wait and take it closer to food intake. When dosing uncertainty arises, prioritize safety and document glucose results to aid future adjustments. For detailed symptom context on meal spikes, see Postprandial Hyperglycemia Signs for how post-meal highs are recognized and managed.
Only one phrase appears here for precision: repaglinide when to take. This helps clarify search intent for timing guidance without repeating similar questions.
Note: If you already started eating, taking a dose late may increase hypoglycemia risk at the next meal. Discuss a consistent plan with your care team.
Special Populations and Kidney or Liver Considerations
Renal function affects glycemic stability even when a drug is hepatically cleared. Lower appetite, variable meals, and reduced gluconeogenesis may amplify hypoglycemia risk. Start conservatively and titrate based on glucose patterns while watching for prolonged lows.
Repaglinide dose in ckd requires cautious initiation, typically at the lowest tablet strength with slow increases. Severe renal impairment warrants closer monitoring and smaller titration steps. Hepatic impairment can increase exposure because of reduced metabolism; starting at 0.5 mg and extending titration intervals is common practice. Labeling provides detailed guidance on organ impairment; consult the FDA prescribing information when tailoring therapy.
Chronic kidney disease often coexists with cardiovascular risk. For broader context on comprehensive care pathways beyond glucose control, review Diabetes Treatment Overview for how multi-morbidity can shape treatment choices.
Drug Class, Indications, and Mechanism
This medicine belongs to the meglitinides, a secretagogue drug class that stimulates insulin release. It is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes. It is not used for type 1 diabetes or diabetic ketoacidosis.
Mechanistically, repaglinide mechanism of action involves closing ATP-sensitive potassium channels on pancreatic beta cells. This depolarizes the membrane and triggers insulin exocytosis, with a quick onset and short action tailored to meals. For a therapy overview within current standards, see the ADA Standards of Care, which contextualize prandial agents among other options. You can also explore practical contexts in Repaglinide Uses to see where it fits clinically.
Names, Forms, and Tablets
The repaglinide brand name is Prandin in several markets, with widely available generics. Tablet strengths commonly include 0.5 mg, 1 mg, and 2 mg. All strengths are scored for flexible titration across meals. This flexibility supports tailored adjustments for variable eating patterns.
For dosage forms and dispensing details, see Repaglinide for a concise view of tablet strengths and labeling references. If you are reviewing options for combined oral therapy in type 2 diabetes, Janumet XR is a metformin-based combination discussed here only to illustrate combination strategies.
Safety Profile and Side Effects
Hypoglycemia is the most important adverse effect with meal-time secretagogues. Symptoms can include shakiness, sweating, hunger, and confusion. Other reactions may include headache, upper respiratory symptoms, joint aches, and mild gastrointestinal discomfort. Weight change can occur, especially when caloric intake increases without matching therapy adjustments.
A targeted phrase is used here: repaglinide side effects weight gain. In practice, weight effects vary with diet, activity level, and use of other agents. To explore symptom profiles and management discussions in depth, see Repaglinide Side Effects for a focused review and mitigation strategies. Labeling also flags rare but serious events; consult the official prescribing information for complete safety language.
Interaction Warnings and Contraindications
Some medications markedly increase exposure and hypoglycemia risk. Strong inhibitors such as gemfibrozil and certain macrolide antibiotics elevate plasma levels and necessitate avoidance or close supervision. Antiplatelet agents like clopidogrel may also raise concentrations, requiring careful glucose monitoring and dose adjustments.
Repaglinide contraindications include use with gemfibrozil and use in diabetic ketoacidosis. It is not indicated for type 1 diabetes. Caution is also appropriate when combining with basal insulin or other secretagogues, given additive hypoglycemia risk. For a broader view of where oral agents fit by class and interaction potential, consult Oral Diabetes Medications for side-by-side comparisons and mechanisms.
Practical Dosing Scenarios and Monitoring
Dose decisions work best when aligned to meals and glucose patterns. Many adults require dosing before two or three daily meals, with adjustments targeted to the meal causing the greatest postprandial rise. Keeping consistent logs helps identify the need for meal-specific increases or reductions.
Here we use the term repaglinide dose frequency once to clarify dosing cadence. Common practice includes three premeal doses with flexibility for snacks or smaller meals. Monitor capillary glucose during titration and reassess A1C every three months. For therapy comparisons across classes used alongside secretagogues, see Common Diabetes Medications for mechanisms and typical use cases. If exploring combination therapy frameworks that include metformin, review Janumet XR as an example of a metformin-based regimen rationale.
For structured reading paths by topic area, the Diabetes Articles hub can help you find related guidance on monitoring, nutrition, and medication classes.
Tip: When glucose logs are inconsistent, standardize premeal testing times for one week. A tighter sampling window can reveal patterns that guide safer adjustments.
Recap
This guide summarized adult dosing ranges, meal timing, and key safety issues. Short-acting action supports meal-by-meal control, but careful titration reduces lows. Interactions and organ impairment deserve specific attention, especially during changes in therapy or diet. Use label references and local standards to align dosing with individual risk and goals.
For a deeper overview combining indications, benefits, and practical dosing, see Repaglinide Prandin Dosage for an extended perspective and related references.
This content is for informational purposes only and is not a substitute for professional medical advice.


