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Glycofren

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Glycofren (Metformin Hydrochloride)

Glycofren is a prescription oral medication that contains the active ingredient metformin hydrochloride, a biguanide class antidiabetic drug. It is marketed in the European Union and is supplied as tablets, although the specific strength is not disclosed. Glycofren is used under medical supervision to help manage blood glucose levels in certain endocrine disorders.

Manufacturer / TM Owner

Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A.

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Indications & Clinical Uses

Glycofren is indicated for several metabolic conditions where glucose regulation is required.

  • Management of type 2 diabetes mellitus in adults.
  • Treatment of insulin resistance associated with polycystic ovary syndrome (PCOS).
  • Adjunct therapy for weight management in diabetic patients when diet and exercise are insufficient.
  • Off‑label consideration for pre‑diabetes under physician guidance.
  • May be used in combination with other antidiabetic agents to achieve target glycemic control.

Side Effects

Metformin hydrochloride can cause a range of side effects, most of which are mild and transient.

Common

  • Gastrointestinal upset such as nausea, abdominal discomfort, or diarrhea.
  • Metallic taste in the mouth.
  • Decreased appetite.
  • Mild headache.
  • Vitamin B12 deficiency with long‑term use.

Serious

  • Lactic acidosis, a rare but potentially life‑threatening condition.
  • Severe skin reactions like Stevens‑Johnson syndrome.
  • Hepatic dysfunction in patients with pre‑existing liver disease.
  • Persistent or worsening gastrointestinal symptoms.
  • Hypoglycemia when combined with other glucose‑lowering drugs.

Precautions & Warnings

Before starting Glycofren, certain health considerations should be reviewed with a healthcare professional.

  • Assess renal function; metformin is contraindicated in severe renal impairment.
  • Evaluate liver function, as hepatic disease can increase risk of lactic acidosis.
  • Use with caution in patients with heart failure or chronic hypoxia.
  • Monitor vitamin B12 levels during prolonged therapy.
  • Discontinue before any radiographic studies involving iodinated contrast agents.
  • Pregnancy category B: generally considered safe, but use only if clearly needed.
  • Breastfeeding mothers should consult their physician before use.

Avoid Interactions

Metformin may interact with several medications, affecting its efficacy or safety.

Avoid

  • Iodinated contrast agents used in imaging studies.
  • Cimetidine, which can increase metformin plasma concentrations.
  • Certain diuretics that may impair renal function.

Use with caution

  • Alcohol, as it can increase the risk of lactic acidosis.
  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Other antidiabetic agents (e.g., sulfonylureas, insulin) that can potentiate hypoglycemia.
  • ACE inhibitors or ARBs, requiring monitoring of renal function.

Frequently Asked Questions

Glycofren contains metformin hydrochloride, which belongs to the biguanide class of antidiabetic medications.

No, Glycofren is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Glycofren is primarily prescribed for type 2 diabetes mellitus and for insulin resistance associated with polycystic ovary syndrome (PCOS).

Metformin decreases hepatic glucose production and improves peripheral insulin sensitivity, helping to lower circulating blood glucose levels.

Glycofren is classified as pregnancy category B, indicating it is generally considered safe, but it should only be used if the potential benefit justifies any potential risk to the fetus.

Common side effects include gastrointestinal upset such as nausea, diarrhea, abdominal discomfort, a metallic taste, mild headache, and decreased appetite.

Lactic acidosis is a rare but serious adverse reaction that can occur, especially in patients with significant renal or hepatic impairment.

Yes, metformin should be discontinued at least 48 hours before receiving iodinated contrast agents and resumed only after confirming normal renal function.

Alcohol can increase the risk of lactic acidosis when taken with metformin, so excessive alcohol consumption should be avoided.

Renal function should be assessed before initiating therapy and periodically thereafter, especially in patients with risk factors for renal impairment.

Long‑term use of metformin may reduce vitamin B12 absorption, so periodic monitoring of B12 levels is recommended.

Glycofren can be combined with other antidiabetic agents, but dose adjustments and close monitoring for hypoglycemia are necessary.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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