GNH USA

Europe — EMA

Jansitin Duo

GNH USA supplies Jansitin Duo (Metformin Hydrochloride, Sitagliptin), a biguanide and DPP‑4 inhibitor for type 2 diabetes mellitus.

Metformin Hydrochloride, Sitagliptin

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What is Metformin Hydrochloride, Sitagliptin?

Metformin Hydrochloride and Sitagliptin, the active ingredients in Jansitin Duo, are a biguanide and DPP‑4 inhibitor presented as an oral tablet for adult use. They treat type 2 diabetes mellitus in patients who need combined glucose‑lowering therapy.

GNH USA supplies Jansitin Duo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Metformin Hydrochloride, Sitagliptin used for?

Jansitin Duo is used in the management of type 2 diabetes mellitus, a chronic metabolic disorder requiring glycaemic control. - Type 2 diabetes mellitus: improves overall glycaemic control and reduces HbA1c. - In combination with diet and exercise: helps patients achieve target blood‑glucose levels. - When added to metformin monotherapy: provides additional reduction in fasting plasma glucose.

What are the side effects of Metformin Hydrochloride, Sitagliptin?

Common Side Effects: - Nausea: mild to moderate gastrointestinal upset. - Diarrhoea: frequent loose stools, usually transient. - Abdominal discomfort: cramps or bloating. - Headache: mild tension‑type headache. - Upper respiratory tract infection: nasopharyngitis symptoms. - Hypoglycaemia (when combined with insulin or sulfonylureas): dizziness or sweating.

Serious or Rare Side Effects: - Lactic acidosis: severe metabolic acidosis, potentially fatal. - Pancreatitis: acute abdominal pain with elevated enzymes. - Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Hepatic failure: jaundice, elevated liver enzymes. - Anaphylaxis: rapid onset of airway swelling and hypotension. - Renal impairment: worsening kidney function, especially in dehydration.

What precautions apply to Metformin Hydrochloride, Sitagliptin?

Before initiating Jansitin Duo, clinicians should evaluate patient-specific factors and monitor for adverse events. - Renal function: assess baseline eGFR and monitor periodically. - Lactic acidosis risk: avoid in patients with severe renal or hepatic impairment. - Hypoglycaemia: monitor closely if used with insulin or sulfonylureas. - Pregnancy and lactation: prescribe only if benefits outweigh potential risks. - Drug interactions: review concomitant medications for possible interactions. - Store at ambient temperature: keep below 25°C, retain original packaging, protect from moisture.

What does Metformin Hydrochloride, Sitagliptin interact with?

Jansitin Duo may interact with several medicines, requiring careful management. Major Interactions (Avoid): - Phenformin: co‑administration is contraindicated due to heightened lactic acidosis risk. - Severe renal impairment (eGFR <30 mL/min/1.73 m²): increased metformin accumulation. Moderate Interactions (Monitor Closely): - Sulfonylureas or insulin: heightened risk of hypoglycaemia. - Iodinated contrast agents: temporary renal function decline may necessitate drug interruption. - Cimetidine: may increase sitagliptin plasma concentrations. - Excess alcohol: can potentiate metformin‑related lactic acidosis.

Frequently asked questions

What is Jansitin Duo used for?+
Jansitin Duo is a prescription oral medication indicated for the treatment of type 2 diabetes mellitus. It combines metformin, a biguanide that improves insulin sensitivity, with sitagliptin, a DPP‑4 inhibitor that enhances insulin secretion, to provide complementary glucose‑lowering effects in adults who need additional control beyond diet, exercise, or monotherapy.
How does Metformin Hydrochloride work?+
Metformin Hydrochloride primarily reduces hepatic glucose production and increases peripheral glucose uptake, thereby lowering fasting plasma glucose and improving insulin sensitivity. It acts without directly stimulating insulin release, which helps minimize the risk of hypoglycaemia when used alone.
What is the usual dose of Jansitin Duo?+
The specific dose of Jansitin Duo is determined by the prescribing healthcare professional based on individual patient factors such as renal function, glycaemic targets, and concomitant therapies. Patients should follow the prescriber’s instructions and not adjust the dose without medical guidance.
Is Jansitin Duo safe during pregnancy or breastfeeding?+
Safety of Jansitin Duo in pregnancy or lactation has not been fully established. It should only be used if the potential benefits to the mother outweigh any possible risks to the fetus or infant, and this decision must be made by a qualified healthcare provider.
How do I order Jansitin Duo from GNH USA?+
To order Jansitin Duo, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.
How does Jansitin Duo compare with other antidiabetic options?+
Jansitin Duo combines two complementary mechanisms—biguanide action of metformin and DPP‑4 inhibition of sitagliptin—offering greater HbA1c reduction than metformin alone. Compared with sulfonylureas, it carries a lower intrinsic risk of hypoglycaemia, and unlike insulin, it is administered orally, making it convenient for many patients.
What are the storage requirements for Jansitin Duo?+
Jansitin Duo should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack or container, protect them from moisture and direct sunlight, and ensure they are out of reach of children.
How is Jansitin Duo administered?+
Jansitin Duo is taken orally, usually once daily with food to reduce gastrointestinal discomfort. The tablet should be swallowed whole with a full glass of water and not crushed or chewed, unless otherwise directed by a healthcare professional.
What are the most serious risks associated with Jansitin Duo?+
The most serious risks include lactic acidosis, particularly in patients with severe renal or hepatic impairment, and rare but severe hypersensitivity reactions such as Stevens‑Johnson syndrome. Patients should be educated to seek immediate medical attention for symptoms like unexplained muscle pain, rapid breathing, or severe skin rash.
Who should not use Jansitin Duo?+
Jansitin Duo is contraindicated in individuals with known hypersensitivity to metformin, sitagliptin, or any excipients, as well as patients with severe renal impairment (eGFR <30 mL/min/1.73 m²) or acute or chronic metabolic acidosis, including lactic acidosis. It should also be avoided in patients with a history of pancreatitis.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Metformin Hydrochloride, Sitagliptin
Route
Oral Use
Manufacturer
G.L. Pharma Gmbh
Origin
EU

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