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Istamet

5.49
Istamet is a combination therapy for adults with type 2 diabetes. It contains sitagliptin, which increases insulin levels after meals, and metformin, which reduces the amount of sugar produced by the liver. Together, they provide a comprehensive approach to maintaining stable and healthy blood glucose levels.


Category
Availability
In Stock
Delivery Time
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Sitagliptin, Metformin
Reference Brand
Janumet
Manufacturer
MSD / Sun Pharmaceutical
Product Form
Tablet
Regulatory Classification
Rx
Primary Category
Diabetes Management
Product Category
Antidiabetics, DPP-4 Inhibitor Combinations
Pharmacological Class
DPP-4 Inhibitor, Biguanide
Clinical Indications
Manufacturer Description
A combination pill used alongside diet and exercise to lower blood sugar levels in adults with type 2 diabetes.
Mechanism of Action
Sitagliptin increases insulin release and reduces sugar production by the liver. Metformin improves the body's sensitivity to insulin and reduces the amount of sugar absorbed from food and made by the liver.
Route of Administration
Oral
Onset Time
1-2 hours
Duration
12-24 hours
Contraindications
Kidney failure, Diabetic ketoacidosis, Severe infection
Severe Adverse Events
Pancreatitis, Lactic acidosis, Severe joint pain
Common Side Effects
Nausea, Stomach upset, Gas
Uncommon Side Effects
Diarrhoea, Headache, Upper respiratory tract infection
Drug Interactions
Cimetidine, Glucocorticoids, Diuretics
Pregnancy Safety Warnings
Consult a doctor; insulin is often preferred during pregnancy.
Age Restrictions
Adults over 18
Storage Guidelines
Store at room temperature.
Related Products
Janumet, Sitagliptin/Metformin

Istamet FAQ

Can I take Istamet if I have mild renal impairment?

Yes, patients with an eGFR ≥ 45 mL/min/1.73 m² may continue the standard dose, but those with eGFR 30-44 mL/min/1.73 m² require dose adjustment or close monitoring. The prescribing clinician will decide the appropriate regimen based on renal function tests.

Will Istamet cause weight gain?

Sitagliptin is weight-neutral, while metformin is often associated with modest weight loss. Clinical experience shows that the combination does not typically cause weight gain; some patients even experience slight reductions in body weight.

Is it safe to travel internationally with Istamet?

Yes, but keep the medication in its original packaging with a copy of the prescription. Carry a pharmacist-verified letter if you are traveling to countries with strict drug-import regulations. Store the tablets at room temperature and avoid exposure to extreme heat or humidity.

Can I take Istamet with a sulfonylurea?

Co-administration is possible, but it increases the risk of hypoglycaemia. If a sulfonylurea is added, the clinician may lower its dose and advise regular blood-glucose monitoring, especially after meals.

What should I do if I miss a dose while fasting for Ramadan?

If you miss the evening dose, take it with the next main meal (i.e., the evening if you break your fast). Do not double the dose. Discuss any needed adjustments with your diabetes specialist before Ramadan begins.

Are there any differences between Istamet and taking sitagliptin and metformin separately?

Pharmacologically, the active ingredients are identical. The fixed-dose combination reduces pill burden, which can improve adherence. However, dose flexibility is limited; if a clinician wishes to adjust one component without changing the other, separate tablets may be preferred.

How long does it take for Istamet to lower my HbA1c?

Significant reductions in HbA1c are usually observed after 8-12 weeks of consistent therapy, provided diet and lifestyle measures are maintained.

Can I use Istamet if I am a competitive athlete subject to drug testing?

Both sitagliptin and metformin are not prohibited substances under UK Anti-Doping regulations. However, athletes should disclose all medications to their medical support team and retain documentation of the prescription.

What are the inactive ingredients in Istamet tablets?

The specific excipients are listed in the product’s Summary of Product Characteristics (SPC). Common tablet fillers include lactose, magnesium stearate, and microcrystalline cellulose, but the exact composition should be verified from the official label.

Is there a generic version of Istamet available in the UK?

Yes, generic formulations containing sitagliptin and metformin in the same strengths (50 mg/1000 mg) are available once the original product’s patent expires. They are therapeutically equivalent when prescribed by a prescriber.

What is Istamet?

Istamet is a prescription-only pill that combines two active ingredients-sitagliptin (50 mg) and metformin (1000 mg)-into a single tablet. It belongs to the therapeutic class of diabetes medicines and is used to improve blood-glucose control in adults with type 2 diabetes mellitus (T2DM). In the United Kingdom the product is regulated by the Medicines and Healthcare products Regulatory Agency (MHRA) and is available only with a medical prescription.

How Istamet Works in the Body

Istamet lowers blood glucose through two complementary mechanisms:

  • Sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor. By blocking the DPP-4 enzyme, it prolongs the activity of the incretin hormones glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP). These hormones increase insulin secretion from the pancreas and suppress glucagon release when blood glucose is elevated, helping to bring glucose levels down after meals.

  • Metformin belongs to the biguanide class. It primarily reduces hepatic glucose production (gluconeogenesis) and improves peripheral insulin sensitivity, allowing muscles and fat tissue to take up glucose more efficiently. Metformin also modestly reduces intestinal absorption of glucose.

Together, the drugs provide both an insulin-dependent (sitagliptin) and an insulin-independent (metformin) reduction in blood-sugar levels, which can lead to better overall glycaemic control than either agent alone.

Conditions Treated by Istamet

Istamet is approved in the UK for the treatment of adults with type 2 diabetes mellitus when diet, exercise, and monotherapy with either sitagliptin or metformin alone do not achieve adequate glycaemic control. It is intended for patients who require combined therapy but wish to reduce pill burden by using a fixed-dose combination.

Typical candidates include:

  • Adults (≥ 18 years) with a documented diagnosis of T2DM.
  • Individuals whose HbA1c remains above target despite lifestyle measures and single-agent therapy.
  • Patients without contraindications to either sitagliptin or metformin.

Patient Suitability and Contraindications

Who Should Use Istamet?

  • Adults with T2DM who need dual therapy.
  • Patients whose renal function is sufficient for metformin (estimated glomerular filtration rate, eGFR ≥ 45 mL/min/1.73 m²).
  • Individuals without a history of severe hypersensitivity to either ingredient.

Absolute Contraindications

  • Known hypersensitivity to sitagliptin, metformin, or any excipients in the tablet.
  • Severe renal impairment (eGFR < 30 mL/min/1.73 m²) or patients on chronic dialysis.
  • Acute or chronic metabolic acidosis, including diabetic ketoacidosis, with or without coma.
  • Use in pregnancy is contraindicated because metformin is classified as Category B3 in the UK and safety data for the combination are insufficient.
  • Breast-feeding mothers should not use Istamet unless the benefits outweigh the risks, as metformin passes into breast milk.

Relative Contraindications

  • Moderate renal impairment (eGFR 30-44 mL/min/1.73 m²): dose adjustment or careful monitoring required.
  • Hepatic impairment: consider reduced metformin dosing.
  • Elderly patients (≥ 75 years): increased risk of renal function decline; monitor closely.
  • Concomitant use of drugs that may increase the risk of lactic acidosis (e.g., iodinated contrast agents) - hold metformin temporarily as per MHRA guidance.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Gastro-intestinal upset (nausea, diarrhoea, abdominal discomfort) - frequently reported with metformin, usually transient.
  • Upper respiratory tract infection symptoms (runny nose, sore throat).
  • Headache or mild dizziness.

These events are generally mild and resolve without medical intervention. Taking the tablet with food can reduce gastrointestinal discomfort.

Serious Adverse Events

  • Lactic acidosis (rare but life-threatening): present with rapid breathing, muscle pain, abdominal pain, somnolence, or feeling cold. Immediate medical attention is required.
  • Severe hypersensitivity reactions (e.g., Stevens-Johnson syndrome, anaphylaxis) - discontinue drug and seek emergency care.
  • Pancreatitis (rare): persistent upper-abdominal pain radiating to the back, possibly with vomiting.

Major Drug Interactions

  • Cimetidine, trimethoprim, or other drugs that reduce renal clearance of metformin - may increase metformin plasma levels and lactic acidosis risk.
  • CYP3A4 inhibitors or inducers (e.g., ketoconazole, rifampicin) have minimal effect on sitagliptin but monitoring is advisable.
  • Contrast media for imaging (iodinated agents) - pause metformin dose for 48 hours after the procedure and verify renal function before restarting.

Food and Lifestyle Interactions

  • Alcohol: excessive intake raises lactic acidosis risk when combined with metformin; limit consumption.
  • High-fat meals: may slightly delay metformin absorption but not clinically significant.
  • Driving: neither component is known to impair cognition or reaction time; however, patients who experience dizziness should exercise caution.

If patients are taking over-the-counter supplements or herbal products, they should discuss them with a healthcare professional to avoid unforeseen interactions.

How to Take Istamet

  • Standard dosing: One tablet (50 mg sitagliptin / 1000 mg metformin) taken once daily with the evening meal. This aligns with metformin’s recommendation to reduce gastrointestinal upset.
  • Renal adjustment: For eGFR 30-44 mL/min/1.73 m², the MHRA advises a reduced dose of metformin; clinicians may consider a lower-strength combination or separate components.
  • Special populations: No dose change is required solely for age, but elderly patients should have renal function monitored every 3-6 months.
  • Administration: Swallow the tablet whole; do not crush, chew, or split it.
  • Missed dose: Take the missed tablet with the next main meal; do not double up.
  • Overdose: Symptoms may include severe nausea, vomiting, abdominal pain, and lactic acidosis. Seek emergency medical care; dialysis may be required to remove metformin.
  • Discontinuation: Gradual tapering is not required for sitagliptin, but metformin should be stopped if the patient develops lactic acidosis or severe renal impairment.

Monitoring and Follow-Up

  • HbA1c: Check every 3 months after therapy initiation or dose change, aiming for the target set by the treating clinician (often ≤ 48 mmol/mol or 6.5 %).
  • Renal function: Serum creatinine and eGFR at baseline, then at least annually; more frequently if eGFR < 60 mL/min/1.73 m².
  • Liver enzymes: Baseline test recommended; repeat if clinical suspicion arises.
  • Weight and blood pressure: Record at each visit as part of comprehensive diabetes management.

Storage and Handling

  • Store Istamet tablets at room temperature (15-30 °C), protected from moisture and light.
  • Keep the container tightly closed and out of reach of children.
  • Do not use any tablet that is discoloured, broken, or past the expiry date printed on the pack.
  • Dispose of unused tablets via a pharmacy take-back program or according to local NHS waste-disposal guidelines.

Medication-Specific Glossary

DPP-4 inhibitor
A class of oral anti-diabetic agents that block the dipeptidyl peptidase-4 enzyme, prolonging the action of incretin hormones and enhancing glucose-dependent insulin secretion.
Biguanide
The drug class to which metformin belongs; it lowers hepatic glucose production and improves peripheral insulin sensitivity.
Lactic acidosis
A rare but serious metabolic disturbance marked by accumulation of lactate in the blood, potentially fatal if not treated promptly. Metformin-associated lactic acidosis is more likely in patients with renal impairment.
eGFR (estimated Glomerular Filtration Rate)
A calculated measure of kidney function used to Adjust metformin dosing; values are expressed in mL/min/1.73 m².
HbA1c (glycated haemoglobin)
A laboratory test that reflects average blood glucose over the previous 2-3 months; used to assess the effectiveness of diabetes therapy.
GLP-1 (Glucagon-like peptide-1)
An incretin hormone that stimulates insulin release and suppresses glucagon; its activity is enhanced by DPP-4 inhibitors like sitagliptin.

Medical Disclaimer

This article provides educational information about Istamet and is not a substitute for professional medical advice. Treatment decisions, including the use of any medication for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes only and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Information for Istamet is sourced from established medical standards and updated frequently. It is provided for general guidance and should be confirmed with a healthcare professional before use.
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