Nevolat - Liraglutide 6mg/ml Pack of 3 Pens (Starter Pack)
Nevolat - Liraglutide 6mg/ml Pack of 3 Pens (Starter Pack)
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Description
What is Nevolat
Nevolat is a prescription-only medicine used for weight management in adults, alongside a reduced-calorie diet and increased physical activity. It contains liraglutide, a glucagon-like peptide-1 (GLP-1) receptor agonist.
Liraglutide works by mimicking a naturally occurring hormone called GLP-1, which helps regulate appetite and food intake. It acts on areas of the brain that control hunger, helping you feel fuller and reducing the desire to eat.
It is administered as a once-daily injection, with dosing increased gradually to reach a maintenance dose. This stepwise approach helps the body adjust and may reduce the likelihood of gastrointestinal side effects.
Weight management outcomes vary between individuals, and ongoing lifestyle measures remain an important part of treatment.
Who Liraglutide is for
Liraglutide is indicated for weight management in adults aged 18 to 75 years when used alongside a reduced-calorie diet and increased physical activity.
It may be suitable for individuals who:
- have not achieved sufficient weight loss through dietary changes and increased physical activity alone, and
- meet one of the following criteria:
- Body Mass Index (BMI) of 30 kg/m² or higher, or
- BMI of 27 kg/m² or higher with at least one weight-related condition, such as:
- Hypertension
- Dyslipidaemia
- Obstructive sleep apnoea
- Type 2 diabetes
Dosage
Liraglutide is administered as a once-daily subcutaneous injection.
Treatment is started at a low dose and increased gradually each week until the recommended maintenance dose is reached. This gradual increase helps to improve tolerability.
The injection can be taken at any time of day, with or without food, but should be taken at approximately the same time each day.
If a dose is missed, it should be taken as soon as possible on the same day. A double dose should not be taken to make up for a missed dose.
For individuals with a BMI above 50 kg/m², additional medical supervision may be appropriate as part of overall weight management.
Liraglutide is the active ingredient in the branded medicine Saxenda. Nevolat contains the same active substance.
Consultation Process
Our service does not include a prescription. Instead, your treatment will be supplied under a legal framework called Patient Group Direction (PGD), and the process will follow these steps:
1. Complete a health questionnaire:
Provide detailed information about your health, medical history, and previous weight management attempts.
2. Pharmacist assessment:
Our pharmacist will review your responses and may reach out via phone or video call to confirm your suitability for Mounjaro.
3. Private consultation:
All consultations are private and confidential. This gives you the opportunity to ask questions and ensure Mounjaro is the right choice for your needs.
4. All-inclusive pricing:
The price you pay includes the consultation fee, with no hidden costs.
5. Identity verification:
You'll need to provide identification during the consultation to confirm that you are the intended user. This is required only during your first order.
6. Photographic evidence request:
You’ll be asked to submit photographic evidence of your weight, height, and relevant medical history to ensure safe and accurate consultation.
Purchasing this medication does not guarantee its supply. The decision if this medication is right for you will be made together with the pharmacist during your consultation, and ultimately the decision to supply the medication is with the pharmacist. Any orders found not suitable will be refunded.
Ingredients
Active ingredient: liraglutide. 1 ml solution for injection contains 6 mg liraglutide. One pre-filled pen contains 18 mg liraglutide.
Other ingredients: sodium citrate dihydrate, propylene glycol, phenol, water for injection, hydrochloric acid and/or sodium hydroxide solution.
Usage and Instructions
The starting dose is 0.6 mg once daily.
The dose should be increased to 3.0 mg once daily in increments of 0.6 mg with at least one-week intervals to improve gastrointestinal tolerability (see Table).
If escalation to the next dose step is not tolerated for two consecutive weeks, consider discontinuing treatment.
Daily doses higher than 3.0 mg are not recommended.
Dose Escalation Schedule (4 weeks)
| Dose | Weeks |
|---|---|
| 0.6 mg | 1 |
| 1.2 mg | 1 |
| 1.8 mg | 1 |
| 2.4 mg | 1 |
| Maintenance dose | |
| 3.0 mg |
Warnings
Liraglutide should not be used in people allergic to its ingredients or in those with severe heart failure (NYHA IV).
It is not recommended for:
- patients aged 75+,
- people with severe liver or kidney problems
- those using other weight-loss drugs.
Use cautiously in people with mild to moderate liver issues, thyroid disease, or gastrointestinal disorders such as gastroparesis. It may cause nausea, vomiting, diarrhoea, gallstones, or pancreatitis. Stop treatment if pancreatitis occurs.
Monitor for increased heart rate and dehydration. Liraglutide can interact with insulin, sulfonylureas, warfarin, digoxin, lisinopril, and oral contraceptives, though most effects are minor.
Avoid use during pregnancy and breastfeeding. It may slightly affect fertility in animals.
May cause dizziness during the first months of treatment; caution is advised when driving or operating machinery.
Side Effects
| Body system affected | Very common | Common | Uncommon | Rare | Not known |
|---|---|---|---|---|---|
| Immune system | Severe allergic reaction (anaphylaxis) | ||||
| Metabolism and nutrition | Low blood sugar (more likely if used with insulin or certain diabetes medicines) | Dehydration (loss of fluids) | |||
| Mental health | Difficulty sleeping (usually temporary) | ||||
| Nervous system | Headache | Dizziness, changes in taste | |||
| Heart | Fast heartbeat (tachycardia) | ||||
| Digestive system | Feeling sick (nausea), diarrhoea, being sick (vomiting), constipation | Dry mouth, indigestion, stomach inflammation, acid reflux, upper stomach pain, wind, burping, bloating | Inflammation of the pancreas (pancreatitis, reported in clinical studies), slowed stomach emptying (related to how the medicine works) | Blockage of the intestines (reported after the medicine was marketed) | |
| Liver and gallbladder | Gallstones, inflammation of the gallbladder (reported in clinical studies) | ||||
| Skin | Rash, hives (urticaria) | Build-up under the skin at injection site (cutaneous amyloidosis) | |||
| Kidneys and urinary system | Kidney problems, including kidney failure | ||||
| General and injection site | Reactions where the injection is given (e.g. redness, pain) | Feeling weak (asthenia), tiredness (fatigue) | Feeling unwell (malaise) | ||
| Tests | Increased levels of certain enzymes (lipase, amylase) |