Product image of Orlistat Stada (Orlistat) supplied by GNH India

Orlistat Stada

Active Ingredient:
Orlistat
Origin:
EU

Orlistat Stada (Orlistat)

Orlistat, the active ingredient in Orlistat Stada, is a lipase inhibitor presented as an oral tablet for oral use. It is prescribed to adults with obesity or overweight conditions to aid weight reduction when combined with a reduced‑calorie, low‑fat diet.

GNH India supplies Orlistat Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution. Our supply chain ensures timely delivery and product integrity across markets.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Orlistat is indicated for weight management in conditions related to excess body fat.

  • Obesity: helps reduce body weight when used with a reduced‑calorie, low‑fat diet.
  • Overweight adults with cardiovascular risk factors: supports modest weight loss to improve risk profile.
  • Weight management in adults: assists in achieving and maintaining weight loss goals as part of a comprehensive lifestyle program.

How It Works

  • Orlistat acts locally in the gastrointestinal tract by covalently binding to the active site of gastric and pancreatic lipases. This inhibition prevents the hydrolysis of dietary triglycerides into absorbable free fatty acids, thereby reducing the absorption of about 30% of ingested fat. The unabsorbed fat is eliminated in the feces, leading to a net caloric deficit that contributes to weight loss.

Side Effects

Orlistat may cause gastrointestinal and metabolic adverse reactions, most of which are related to reduced fat absorption.

Common Side Effects

  • Oily spotting: oily discharge on underwear after meals.
  • Flatulence with discharge: increased gas accompanied by oily stools.
  • Fecal urgency: sudden need to defecate after eating.
  • Abdominal discomfort: cramping or mild pain.

Serious or Rare Side Effects

  • Severe liver injury: rare cases of hepatitis or liver dysfunction.
  • Acute kidney injury: very uncommon renal impairment reported.

Precautions & Warnings

When prescribing Orlistat, clinicians should consider several safety measures to minimize risks.

  • Assess eligibility: confirm BMI ≥30 kg/m² or ≥27 kg/m² with obesity‑related comorbidities.
  • Advise low‑fat diet: recommend a diet containing ≤30% of total calories from fat to reduce gastrointestinal side effects.
  • Monitor vitamin levels: supplement vitamins A, D, E, K as fat‑soluble absorption may be reduced.
  • Contraindicated in pregnancy: avoid use during pregnancy and lactation.
  • Avoid in malabsorption syndromes: patients with chronic malabsorption or cholestasis should not use.
  • Store at ambient temperature below 25°C: keep in original packaging, protect from moisture.

Avoid Interactions

Orlistat can affect the absorption of several concomitant medications, requiring dose adjustments or monitoring.

Major Interactions (Avoid)

  • Cyclosporine: reduced absorption may lower immunosuppressive effect.
  • Warfarin: increased INR risk due to altered vitamin K absorption.
  • Levothyroxine: decreased absorption may reduce thyroid hormone efficacy.

Moderate Interactions (Monitor Closely)

  • Fat‑soluble vitamins (A, D, E, K): supplementation may be needed to prevent deficiency.
  • Oral contraceptives: efficacy may be reduced; consider alternative or additional contraception.
  • Antibiotics (e.g., amoxicillin): absorption may be decreased; monitor therapeutic response.

Frequently Asked Questions

Orlistat Stada is used as an adjunct to a reduced‑calorie, low‑fat diet for the management of obesity and overweight in adults. It helps to reduce body weight and improve associated health risk factors when combined with lifestyle modifications.

Orlistat works by inhibiting gastric and pancreatic lipases in the gastrointestinal tract. This prevents the breakdown of dietary triglycerides into absorbable fatty acids, reducing the amount of fat that is absorbed and increasing its excretion in the stool, which contributes to a caloric deficit.

The dosage of Orlistat Stada is determined by the prescribing healthcare professional based on the patient’s individual needs, body weight, and treatment plan. The prescriber will specify the appropriate dosing schedule and any necessary adjustments.

Orlistat is generally not recommended for use during pregnancy or while breastfeeding because its safety has not been established in these populations. Women who are pregnant, planning to become pregnant, or nursing should discuss alternative weight‑management options with their healthcare provider.

To order Orlistat Stada, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams across international markets, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Orlistat differs from systemic appetite‑suppressing agents because it acts locally in the gut to block fat absorption rather than affecting central nervous system pathways. This mechanism results in a distinct side‑effect profile, primarily gastrointestinal, and may be preferred for patients who cannot tolerate central stimulants.

Orlistat Stada should be stored at ambient temperature below 25 °C. Keep the tablets in their original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Orlistat Stada is taken orally, usually with each main meal that contains fat. The tablets are swallowed whole with water; they should not be crushed, chewed, or dissolved. If a meal is missed or contains no fat, the dose may be omitted.

The most serious risks, although rare, include severe liver injury and acute kidney injury. Patients should be monitored for signs of hepatic dysfunction or renal impairment, and any unusual symptoms should be reported to a healthcare professional promptly.

Orlistat Stada should not be used by individuals with chronic malabsorption syndromes, cholestasis, or those who are pregnant or breastfeeding. It is also contraindicated in patients with known hypersensitivity to orlistat or any of the tablet’s excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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