Buy Farxiga
Farxiga

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Farxiga (Dapagliflozin) is an SGLT2 inhibitor used to treat type 2 diabetes by assisting the kidneys in removing glucose from the bloodstream through urine. This medication helps adults improve glycaemic control and may be used as part of a comprehensive management plan involving diet and exercise.


Ingredient
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)
Dapagliflozin
Reference Brand
Forxiga
Manufacturer
AstraZeneca
Product Form
Tablet
Regulatory Classification
Rx
Primary Category
Diabetes Management, Heart Failure, Kidney Protection
Product Category
Drugs Used in Diabetes, Blood Glucose Lowering Drugs, SGLT2 inhibitors
Pharmacological Class
SGLT2 Inhibitor
Manufacturer Description
A versatile medication that manages blood sugar in type 2 diabetes and reduces the risk of heart and kidney complications.
Mechanism of Action
Forxiga helps the kidneys remove excess sugar from the bloodstream through the urine. It also reduces the workload on the heart and helps protect the kidneys by lowering pressure and fluid buildup within them.
Route of Administration
Oral
Onset Time
Within 2-3 hours
Duration
24 hours
Contraindications
Severe kidney disease (dialysis), Hypersensitivity to dapagliflozin, Pregnancy (2nd/3rd trimester)
Severe Adverse Events
Diabetic ketoacidosis, Necrotising fasciitis of the perineum, Dehydration, Low blood sugar (when used with insulin)
Common Side Effects
Back pain, Increased urination, Dizziness
Uncommon Side Effects
Genital thrush, Urinary tract infections, Flu-like symptoms, Changes in urination frequency
Drug Interactions
Loop diuretics (Water tablets), Insulin, Sulfonylureas
Pregnancy Safety Warnings
Avoid during second and third trimesters of pregnancy.
Age Restrictions
Adults 18 years and older (some specific child use allowed in Type 2).
Storage Guidelines
Store at room temperature.
Related Products
Jardiance, Invokana, Steglatro

Farxiga FAQ

Can I take Farxiga if I have a urinary tract infection?

If you currently have an active urinary tract infection, discuss it with your clinician before starting Farxiga. The medication can increase glucose in urine, potentially worsening the infection, so treatment of the infection should be completed first.

Does Farxiga cause weight loss?

Many patients experience modest weight loss (typically 1-3 kg) because calories are lost through urinary glucose excretion. This effect is considered an added benefit but varies between individuals.

Will Farxiga affect my blood pressure?

Yes, the osmotic diuresis can lead to a modest reduction in systolic and diastolic blood pressure, especially in people who are volume-sensitive. Your clinician may monitor blood pressure after initiating therapy.

Can I take Farxiga while drinking alcohol?

Moderate alcohol consumption is permissible, but excessive intake can increase dehydration and the risk of low blood pressure. Combine alcohol with caution, especially if you are also on diuretics.

Is there a specific time of day I should take Farxiga?

Farxiga is usually taken in the morning to align with daily routines and to avoid nocturnal urination that might disrupt sleep. However, follow the timing advised by your prescriber.

What should I do if I develop a genital yeast infection while on Farxiga?

Promptly treat the infection with an appropriate antifungal medication as prescribed, and inform your healthcare provider. Good genital hygiene and keeping the area dry can help prevent recurrence.

How does Farxiga differ from other SGLT2 inhibitors like Jardiance?

All SGLT2 inhibitors share the same basic mechanism, but they differ in dosing schedules, approved indications, and specific clinical trial data. Choice of agent depends on individual health status, renal function, and clinician preference.

Can Farxiga be used in patients with mild kidney disease?

Yes, if eGFR is ≥ 60 mL/min/1.73 m², Farxiga can be initiated at 5 mg. For eGFR between 30-60, a reduced dose (5 mg) may be used, but regular renal monitoring is essential.

What should I know about travelling with Farxiga?

Carry the medication in its original packaging with a copy of the prescription. Keep it at room temperature and stay hydrated, especially on long flights where fluid loss can be higher.

Is Farxiga covered by NHS prescriptions?

In many regions of the UK, Farxiga is listed on the NHS Drug Tariff for approved indications, but coverage may depend on local formulary decisions and the specific condition being treated. Check with your GP or pharmacist for details.

What is Farxiga?

Farxiga is a prescription medicine used to help manage blood-sugar levels in adults with type 2 diabetes. The active ingredient in Farxiga is dapagliflozin, a member of the sodium-glucose co-transporter-2 (SGLT2) inhibitor class. It is supplied as an oral pill in two strengths: 5 mg and 10 mg. In the United Kingdom Farxiga is authorised by the Medicines and Healthcare products Regulatory Agency (MHRA) and is marketed by AstraZeneca. The medication is prescription-only (POM) and is typically prescribed when diet, exercise, and first-line oral agents such as metformin do not achieve target glucose control.

How Farxiga Works in the Body

Dapagliflozin blocks the SGLT2 protein located in the proximal tubules of the kidney. Under normal circumstances, SGLT2 re-absorbs about 90 % of the glucose filtered by the kidneys. By inhibiting this transporter, Farxiga reduces glucose re-absorption, allowing excess glucose to be expelled in the urine. This “urinary glucose loss” lowers circulating blood-sugar levels without directly stimulating insulin secretion.

Key pharmacologic points:

  • Onset of action: Within 24 hours of the first dose.
  • Peak effect: Approximately 1-2 weeks after continuous dosing.
  • Duration: Effects persist as long as the drug is taken daily.
  • Metabolism: Primarily glucuronidated in the liver; minimal involvement of cytochrome P450 enzymes, which limits drug-drug interaction potential.

Conditions Treated by Farxiga

Farxiga is approved by the European Medicines Agency (EMA) and the MHRA for the following indications in the UK:

  • Type 2 diabetes mellitus (as an adjunct to diet, exercise, and other antidiabetic agents).
  • Cardiovascular risk reduction in adults with type 2 diabetes who have established cardiovascular disease or multiple cardiovascular risk factors.
  • Chronic heart failure with reduced ejection fraction (HFrEF) in patients with or without diabetes.
  • Chronic kidney disease (CKD) to slow progression in adults with an eGFR ≥ 30 mL/min/1.73 m².

These uses align with NICE guidance (NG28, NG185) that recommends SGLT2 inhibitors for patients with type 2 diabetes who need additional glucose lowering and have a high cardiovascular or renal risk profile.

Evidence-Based Off-Label Uses

Some clinicians consider dapagliflozin for conditions that are not formally approved in the UK:

  • Type 1 diabetes - Small studies have explored dapagliflozin as an adjunctive therapy, but the risk of diabetic ketoacidosis (DKA) is higher. This use is not approved and requires specialist supervision.
  • Obesity management - Research shows modest weight loss with SGLT2 inhibition, but Farxiga is not licensed for weight reduction alone.

Disclaimer: Off-label use must be overseen by a qualified healthcare professional, with careful risk assessment and monitoring.

Evaluating Farxiga for Your Health Profile

Who May Benefit

  • Adults with type 2 diabetes whose HbA1c targets are not met with metformin alone or in combination with other agents.
  • Patients with established atherosclerotic cardiovascular disease, heart failure, or CKD who meet the renal function criteria.

Absolute Contraindications

  • Severe renal impairment (eGFR < 30 mL/min/1.73 m²), end-stage renal disease, or patients on dialysis.
  • Known hypersensitivity to dapagliflozin or any component of the tablet.
  • Pregnancy (farxiga is classified Category C in the UK) and breastfeeding, due to the potential for fetal exposure and unknown effects in infants.

Relative Contraindications / Cautions

  • Moderate renal impairment (eGFR 30-45 mL/min/1.73 m²): Use only if benefits outweigh risks, and dose may be limited to 5 mg.
  • Elderly patients: Increased risk of volume depletion and orthostatic hypotension.
  • History of recurrent genital mycotic infections or urinary tract infections.
  • Concomitant use of loop diuretics or high-dose thiazides, which may amplify dehydration.

Special Populations

  • Pregnancy & lactation: Discuss alternative glucose-lowering strategies with your clinician.
  • Renal impairment: Regular eGFR monitoring is essential; dosage may need adjustment.
  • Hepatic impairment: No specific dose change is required, but clinical judgment is advised.

Safety Profile and Interactions

Common Side Effects

  • Increased urinary frequency - usually transient.
  • Genital mycotic infections (e.g., yeast infections) - more common in women; good genital hygiene can reduce risk.
  • Urinary tract infections - may present with dysuria, urgency, or frequency.
  • Thirst and mild dehydration - stay well-hydrated, especially in hot weather or during exercise.

Serious Adverse Events

  • Diabetic ketoacidosis (DKA): May occur with normal or mildly elevated blood glucose; watch for nausea, abdominal pain, rapid breathing, or unusual fatigue.
  • Acute kidney injury: Prompt evaluation if serum creatinine rises sharply.
  • Severe genital infection (Fournier’s gangrene): Rare but life-threatening; seek immediate medical attention for severe pain, swelling, or foul-smelling discharge.
  • Hypotension: Particularly in patients on diuretics or with low fluid intake.

Drug Interactions

  • Insulin and sulfonylureas - Additive glucose-lowering effect; dose reduction may be needed to avoid hypoglycaemia.
  • Loop diuretics - Heightened risk of dehydration and electrolyte imbalance.
  • RAAS inhibitors (e.g., ramipril, losartan) - May increase the risk of renal function decline; monitor kidney tests.
  • Rifampicin, phenytoin - Inducers of glucuronidation can modestly reduce dapagliflozin exposure (clinical significance generally low).

Overall, dapagliflozin has a low potential for CYP-mediated interactions, but the above combinations require clinical awareness.

Food and Lifestyle Interactions

  • Food: Farxiga can be taken with or without meals; no specific dietary restrictions are required.
  • Alcohol: Excessive intake may exacerbate dehydration and raise the risk of hypoglycaemia when combined with insulin or sulfonylureas.
  • Driving / Machinery: No direct impairing effects, but severe dehydration or hypotension could affect concentration - be cautious until you know how the medication affects you.

How to Take Farxiga

  • Starting dose: 5 mg taken once daily in the morning.
  • Dose escalation: If renal function permits and additional glucose control is needed, your clinician may increase the dose to 10 mg once daily.
  • Renal-based dosing: For eGFR 30-45 mL/min/1.73 m², the maximum recommended dose is 5 mg daily. Farxiga should be stopped if eGFR falls below 30 mL/min/1.73 m².
  • Administration: Swallow the tablet whole with a glass of water. It may be taken with or without food.
  • Missed dose: Take the missed tablet as soon as you remember, unless it is near the time of the next scheduled dose. Do not double-dose.
  • Overdose: Symptoms may include excessive urination, dehydration, and low blood pressure. Seek urgent medical care; treatment is supportive (fluid replacement) as no specific antidote exists.
  • Discontinuation: If stopping Farxiga, tapering is not required, but monitor blood glucose closely to avoid rebound hyperglycaemia.

Monitoring and Follow-Up

Regular monitoring helps maximise benefit while minimising risk:

  • Renal function (eGFR, serum creatinine): Baseline, then at 2 weeks, 3 months, and periodically thereafter, especially if dose changes or other nephrotoxic drugs are added.
  • Electrolytes (sodium, potassium): Check if concomitant diuretics are used.
  • HbA1c: Every 3-6 months to assess long-term glucose control.
  • Blood pressure: Monitor for hypotensive episodes, particularly in the first weeks.
  • Signs of infection: Educate patients to report genital or urinary symptoms promptly.

Storage and Handling

  • Store Farxiga tablets below 30 °C (86 °F), away from direct sunlight and moisture.
  • Keep the container tightly closed and out of reach of children.
  • Do not use the medication after the expiry date printed on the pack.
  • If a tablet is damaged or broken, discard it and obtain a replacement.

Medication-Specific Glossary

SGLT2 inhibitor
A drug class that blocks the sodium-glucose co-transporter-2 in the kidney, promoting urinary glucose excretion.
eGFR (estimated glomerular filtration rate)
A calculation of kidney filtration capacity, expressed in mL/min/1.73 m², used to gauge renal function.
Diabetic ketoacidosis (DKA)
A serious complication where the body produces high levels of ketones, leading to metabolic acidosis despite normal or modest glucose levels.
Genital mycotic infection
A fungal infection (commonly Candida) affecting the genital area, more frequent with increased urinary glucose.
Osmotic diuresis
Increased urine production caused by the presence of glucose (or other osmotic agents) in the renal tubules, pulling water along with it.

Medical Disclaimer

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

Information for Farxiga 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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