Product image of Glucostop (Metformin Hydrochloride) supplied by GNH India

Glucostop

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Glucostop (Metformin Hydrochloride)

Glucostop is an oral medication that contains Metformin Hydrochloride, a biguanide used for managing blood glucose levels. It is marketed in the European Union as a prescription‑only product, with strength not specified. Glucostop belongs to the antidiabetic therapeutic class and works by reducing hepatic glucose production while improving peripheral insulin sensitivity. It is intended for adult patients with type 2 diabetes mellitus and should be taken under medical supervision.

Manufacturer / TM Owner

Ioulia And Irene Tseti Pharmaceutical Laboratories S.A.

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Indications & Clinical Uses

Glucostop is indicated for the treatment of type 2 diabetes mellitus as part of a comprehensive diabetes management plan.

  • As monotherapy in patients who do not achieve glycemic control with diet and exercise alone.
  • In combination with other oral antidiabetic agents such as sulfonylureas, DPP‑4 inhibitors, or SGLT2 inhibitors.
  • As an adjunct to insulin therapy when additional glucose lowering is needed.
  • For patients with overweight or obesity to aid modest weight stabilization.
  • To improve insulin sensitivity in peripheral tissues.

Side Effects

The safety profile of Glucostop reflects the typical adverse events associated with metformin therapy.

Common

  • Gastrointestinal upset such as nausea, abdominal discomfort, or diarrhea.
  • Metallic taste in the mouth.
  • Mild loss of appetite.
  • Headache.

Serious

  • Lactic acidosis, a rare but potentially life‑threatening condition.
  • Severe hypoglycemia when combined with insulin or insulin secretagogues.
  • Significant elevation of liver enzymes.
  • Persistent vomiting leading to dehydration.

Precautions & Warnings

Healthcare providers should evaluate several precautionary factors before prescribing Glucostop to ensure safe use.

  • Assess renal function; avoid use in patients with eGFR below 30 mL/min/1.73 m².
  • Review hepatic status, as liver disease may increase risk of lactic acidosis.
  • Monitor for signs of vitamin B12 deficiency with long‑term therapy.
  • Use caution in elderly patients due to higher incidence of gastrointestinal side effects.
  • Discontinue before any radiographic procedures that use iodinated contrast agents.
  • Consider dose adjustment during acute illness or dehydration.

Avoid Interactions

Glucostop can interact with other medicines, affecting its efficacy or safety.

Avoid

  • Iodinated contrast agents used for imaging studies; they may precipitate renal impairment.
  • Alcoholic beverages in excess, which can increase risk of lactic acidosis.

Use with caution

  • Other antidiabetic drugs that cause hypoglycemia, such as sulfonylureas or insulin.
  • Cimetidine, which may increase metformin plasma concentrations.
  • Certain diuretics that affect renal clearance.
  • Medications that may interfere with vitamin B12 absorption, like proton pump inhibitors.

Frequently Asked Questions

Glucostop is a prescription oral medication that contains the active ingredient Metformin Hydrochloride, a biguanide class drug used to lower blood glucose in type 2 diabetes.

Glucostop decreases hepatic glucose production and improves peripheral insulin sensitivity, helping the body use glucose more effectively.

Glucostop is intended for adult patients diagnosed with type 2 diabetes mellitus who need additional glucose control beyond diet and exercise.

Yes, Glucostop can be added to insulin therapy when further reduction of blood glucose is required, but dose adjustments and monitoring for hypoglycemia are recommended.

Common side effects include gastrointestinal symptoms such as nausea, abdominal discomfort, diarrhea, a metallic taste, mild loss of appetite, and occasional headache.

Glucostop should be stopped at least 48 hours before receiving iodinated contrast agents for imaging studies to reduce the risk of renal impairment.

Reduced renal function can increase metformin levels and the risk of lactic acidosis; Glucostop is contraindicated in patients with eGFR below 30 mL/min/1.73 m².

Lactic acidosis is a rare but serious adverse effect, more likely in patients with severe renal or hepatic impairment, dehydration, or excessive alcohol intake.

Long‑term metformin therapy may reduce vitamin B12 absorption; periodic monitoring of B12 status is advised, especially in patients with anemia or neuropathy.

Iodinated contrast agents and excessive alcohol should be avoided. Other drugs that may increase metformin concentrations, such as cimetidine, also require caution.

Glucostop can be prescribed to elderly patients, but they may experience more gastrointestinal side effects and should be monitored closely for renal function.

Regular monitoring of renal function, liver enzymes, blood glucose, and vitamin B12 levels is recommended, along with assessment for any signs of lactic acidosis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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