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Loperamide / Simethicone Dosage

Applies to the following strengths: 2 mg-125 mg

Usual Adult Dose for:

Usual Pediatric Dose for:

Additional dosage information:

Usual Adult Dose for Diarrhea - Acute

Loperamide 4 mg-simethicone 250 mg orally once after the first loose stool, followed by loperamide 2 mg-simethicone 125 mg orally once after each subsequent loose stool


Comments:

Use: Relief of symptoms related to diarrhea and gas (bloating, cramps, pressure)

Usual Pediatric Dose for Diarrhea - Acute

Age-based dosing:
Under 2 years: Not recommended.

2 to 5 years: Patients should consult with their healthcare provider.

6 to 8 years: Loperamide 2 mg-simethicone 125 mg orally once after the first loose stool, followed by loperamide 1 mg-simethicone 62.5 mg orally once after each subsequent loose stool


9 to 11 years: Loperamide 2 mg-simethicone 125 mg orally once after the first loose stool, followed by loperamide 1 mg-simethicone 62.5 mg orally once after each subsequent loose stool

12 years and older: Loperamide 4 mg-simethicone 250 mg orally once after the first loose stool, followed by loperamide 2 mg-simethicone 125 mg orally once after each subsequent loose stool

Weight-based dosing:
Up to 15 kg: Not recommended.

15.5 to 21.4 kg: Patients should consult with their healthcare provider.

21.8 to 26.8 kg: Loperamide 2 mg-simethicone 125 mg orally once after the first loose stool, followed by loperamide 1 mg-simethicone 62.5 mg orally once after each subsequent loose stool

27.3 to 43.2 kg: Loperamide 2 mg-simethicone 125 mg orally once after the first loose stool, followed by loperamide 1 mg-simethicone 62.5 mg orally once after each subsequent loose stool

Comments:

Use: Relief of symptoms related to diarrhea and gas (bloating, cramps, pressure)

Renal Dose Adjustments

Data not available

Liver Dose Adjustments

Use with caution.

Dose Adjustments

Clinical improvement not observed or within 2 days OR worsening of symptoms during treatment: Discontinue administration. Patients should contact their healthcare provider.

Patients who develop abdominal swelling or bulging: Patients should promptly discontinue treatment and contact their healthcare provider.

Patients who have difficulty swallowing the caplet: Patients should stop treatment and consult with their healthcare provider.

Precautions

CONTRAINDICATIONS:


Safety and efficacy have not been established in patients younger than 2 years.

Consult WARNINGS section for additional precautions.

Dialysis

Data not available

Other Comments

Administration advice:


Storage requirements:

General:

Patient advice:

Frequently asked questions

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.