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Insulin Glulisine, Human

Published: July 26, 2026Updated: August 24, 2026

Insulin Glulisine is a rapid-acting insulin analog used to manage postprandial blood glucose levels in adults and children with diabetes mellitus, typically administered at mealtimes.

Quick summary

A rapid-acting insulin analog used to control blood sugar in diabetic patients, typically taken at mealtimes.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy

Key facts at a glance

ATC
A10AB06
RxNorm
400008
Generic
Insulin Glulisine, Human
Class
atc-a10
Brands
Apidra
Availability
rx
Lactation
unknown
Routes
—
Forms
solution
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)subcutaneous injection
Usual dose
0.2-0.5 units/kg per meal
Maximum
consult physician
Frequency
at mealtime (before or after meals)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)subcutaneous injection
Usual dose
0.2-0.5 units/kg per meal
Maximum
consult physician
Frequency
at mealtime (before or after meals)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)subcutaneous injection
Usual dose
0.2-0.3 units/kg per meal
Maximum
consult physician
Frequency
at mealtime (before or after meals)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Insulin has no defined toxic single dose as toxicity varies significantly based on individual factors including baseline insulin sensitivity, fasting status, and concurrent medications. Overdose can cause severe hypoglycemia leading to seizures, coma, and potentially death.
Chronic overdose: not_applicable
Immediate actions
administer oral glucose if conscious, glucagon injection, IV dextrose if available, call emergency services
Antidote
glucose (dextrose) and glucagon(highly effective when administered promptly)
Poison Control: 1-800-222-1222

Special Populations

8 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

individualize dose based on blood glucose monitoring

Key Recommendations

use when benefits outweigh risks; maintain tight glycemic control

Monitor

frequent blood glucose monitoring; regular fetal assessments

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

increased insulin requirements typically needed

Key Recommendations

continue therapy; insulin requirements increase during pregnancy

Monitor

regular blood glucose monitoring; fetal growth assessments

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

often requires increased doses; may need titration near delivery

Key Recommendations

maintain tight glycemic control; adjust insulin near term

Monitor

intensive glucose monitoring; fetal wellbeing assessments

Use with caution and monitor for adverse effects.

✓

pediatric_age

children 3 years and older
safe
FDA Category
N
Dose Adjustment

weight-based dosing starting at 0.2-0.5 units/kg

Key Recommendations

approved for use in pediatric patients age 3 years and older

Monitor

frequent blood glucose monitoring; adjust doses based on meals and activity

⚠

geriatric

elderly 65 years and older
caution
FDA Category
N
Dose Adjustment

start with lower doses; titrate slowly

Key Recommendations

use with caution due to increased hypoglycemia risk; consider cognitive status and renal function

Monitor

frequent glucose monitoring; monitor for hypoglycemia unawareness

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild to moderate renal impairment
caution
FDA Category
N
Dose Adjustment

dose reduction may be necessary; monitor closely

Key Recommendations

use with caution; insulin clearance may be reduced

Monitor

frequent glucose monitoring; adjust dose based on renal function

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

hepatic impairment
caution
FDA Category
N
Dose Adjustment

may require dose adjustment; monitor closely

Key Recommendations

use with caution; liver metabolism may be altered

Monitor

frequent blood glucose monitoring; watch for hypoglycemia

Use with caution and monitor for adverse effects.

✓

lactation

breastfeeding
safe
FDA Category
N
Dose Adjustment

no specific adjustment needed; monitor maternal glucose

Key Recommendations

compatible with breastfeeding; insulin does not pass into breast milk significantly

Monitor

monitor maternal blood glucose to maintain adequate milk production

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2005

FDA approval timeline for Insulin Glulisine (Apidra)

drug_classWHO
2023

Drug class

Value:Rapid-acting insulin analog

ATC classification for Insulin Glulisine

pharmacologyFDA
2023

Onset of action

Value:10-15 minutes

Pharmacokinetic properties

usageMedical guidelines
2023

Common uses

Value:Glycemic control in diabetes mellitus

Therapeutic indications for Insulin Glulisine

Treatment of diabetes mellitus in adults and children, primarily for controlling postprandial (after-meal) blood glucose levels. Used in both Type 1 and Type 2 diabetes when insulin therapy is needed.

Insulin Glulisine is a recombinant DNA-produced insulin analog with a rapid onset of action (approximately 15 minutes after subcutaneous injection). It binds to insulin receptors on cells throughout the body, promoting cellular glucose uptake and suppressing hepatic glucose production, thereby lowering elevated blood glucose levels.

Administered subcutaneously within 15 minutes before or immediately after a meal. Requires regular blood glucose monitoring to avoid hypoglycemia. Dosage must be individualized based on metabolic needs and response. May cause hypoglycemia, hypokalemia, and local injection site reactions. Patients should rotate injection sites and be educated on hypoglycemia recognition, treatment, and proper storage requirements.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 24, 2026. · Read our editorial policy