Manufacturer: Novo Nordisk
Active Substance(s): SEMAGLUTIDE
Strength: 0.25mg
Pack Size: 1 Pen, 4 disposable NovoFine Plus needles
INFORMATION
WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – Key Features and Benefits
Wegovy® FlexTouch® is a once-weekly injectable treatment containing semaglutide, designed to support weight loss and maintenance. It mimics a natural hormone (GLP-1) that helps control appetite, making users feel fuller and less hungry. The 0.25mg dose is used as the initial step in the dosing escalation schedule.
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Active Ingredient: Semaglutide, a GLP-1 receptor agonist
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Indicated for: Obesity, overweight with comorbidities, and cardiovascular risk reduction
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Initial dose: 0.25 mg once weekly, part of a 16-week titration plan
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Administered via: Subcutaneous injection using a pre-filled FlexTouch® pen
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Helps with: Appetite suppression, weight loss, reduced food cravings
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Use in Adolescents: Approved for ages ≥12 years with body weight >60 kg
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Cardiovascular benefit: Reduces heart disease-related events in adults with BMI ≥27 kg/m² and heart history
WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – Indications
Wegovy® is indicated as an adjunct to a reduced-calorie diet and increased physical activity. It is used to manage chronic weight issues in both adults and adolescents, including reducing cardiovascular risk in specific patient groups.
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Adults:
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BMI ≥30 (obesity)
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BMI 27–29.9 with weight-related comorbidities
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With heart disease and BMI ≥27, even without diabetes
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Adolescents (≥12 years):
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With obesity and body weight >60 kg
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Continued use only if ≥5% BMI reduction is seen after 12 weeks on 2.4 mg
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Not recommended for:
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Type 1 diabetes
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Use with other weight-loss products
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Children under 12 years
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WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – Ingredients
The 0.25 mg dose of Wegovy® FlexTouch® contains both active and inactive components necessary for stability and effectiveness.
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Active ingredient:
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Semaglutide (0.68 mg/mL; 1.0 mg per 1.5 mL pen)
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Inactive ingredients:
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Dibasic sodium phosphate dihydrate
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Propylene glycol
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Phenol
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Water for injections
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Sodium hydroxide/hydrochloric acid (pH adjustment)
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Formulation:
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Clear, colorless solution
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Pre-filled pen contains 4 doses
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Sodium content:
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Less than 23 mg per dose (considered sodium-free)
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WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – How To Use
Wegovy® is administered once a week by subcutaneous injection. The 0.25 mg dose is used during the first 4 weeks of treatment to minimize gastrointestinal side effects before dose escalation.
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Administration site: Abdomen, thigh, or upper arm (under the skin only)
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Frequency: Once per week, same day if possible
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Dose escalation schedule:
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Week 1–4: 0.25 mg
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Week 5–8: 0.5 mg
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Week 9–12: 1.0 mg
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Week 13–16: 1.7 mg
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Week 17+: 2.4 mg maintenance
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Instructions:
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Do not inject into veins or muscles
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Can be taken any time of day, regardless of meals
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Missed dose:
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Take within 5 days, otherwise skip and resume regular schedule
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Storage:
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Refrigerate (2–8°C) or keep at room temp (below 30°C) for up to 6 weeks
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WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – Side Effects
Wegovy® can cause a range of side effects, mostly gastrointestinal. Most are mild and temporary, but some require urgent medical attention.
Common and less serious:
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Very common (≥1 in 10): Nausea, vomiting, diarrhea, constipation, headache, abdominal pain
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Common (≤1 in 10): Indigestion, dizziness, bloating, burping, fatigue, flatulence, dry mouth
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Uncommon (≤1 in 100): Fast heart rate, altered pancreas tests, stomach emptying delay
Serious (Seek immediate help):
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Acute pancreatitis: Severe abdominal pain radiating to the back
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Severe allergic reaction: Swelling of face, lips, throat, breathing difficulty, rash
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Bowel obstruction: Severe constipation with bloating, vomiting
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Diabetic retinopathy worsening: In patients with Type 2 diabetes
Risk of hypoglycemia:
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Especially if taken with insulin or sulfonylureas
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Warning signs: Cold sweats, shakiness, dizziness, blurred vision, confusion
WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – Clinical Studies
Wegovy®’s effectiveness and safety were established through long-term clinical trials involving adults and adolescents. These studies showed consistent, clinically meaningful weight loss and cardiovascular risk reduction.
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Primary mechanism: Mimics GLP-1 to reduce appetite and food intake
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Clinically proven outcomes:
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Significant weight loss when used with diet and exercise
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Improved cardiovascular outcomes in high-risk patients
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Adolescents:
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Must demonstrate ≥5% BMI reduction after 12 weeks on 2.4 mg to continue
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Safety monitoring:
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Ongoing due to recent approval and evolving data (additional monitoring status)
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WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – Manufacturer Information
Wegovy® is manufactured and distributed by Novo Nordisk, a leading global pharmaceutical company specializing in metabolic disorders.
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Manufacturer: Novo Nordisk A/S
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Distributor (Australia): Novo Nordisk Pharmaceuticals Pty. Ltd., North Sydney, NSW
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Distributor (New Zealand): Novo Nordisk Pharmaceuticals Ltd., Auckland
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Trademarks: Wegovy®, FlexTouch®, NovoFine®
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Support program: WegovyCare® (Australia) – https://wegovycare.com.au
WEGOVY® FLEXTOUCH 0.25mg (ITALIAN) – FAQ
Is Wegovy® 0.25 mg effective for weight loss?
Yes, but it’s intended as a starting dose. The 0.25 mg dose is used for the first 4 weeks to minimize nausea before escalating to the effective 2.4 mg dose.
How long should I stay on the 0.25 mg dose?
Only for the first 4 weeks. After that, the dose increases every 4 weeks up to 2.4 mg weekly.
Can I use Wegovy® 0.25 mg long-term?
No, it’s a starter dose. The long-term therapeutic dose is 2.4 mg weekly.
Does Wegovy® 0.25 mg have side effects?
Yes. Nausea, vomiting, diarrhea, and constipation are common, especially in the first weeks. These usually improve over time.
Can I skip a dose of Wegovy®?
Yes. If it’s been ≤5 days, inject it ASAP. If it’s been >5 days, skip and resume the regular schedule.
What is Wegovy® used for?
It is used for chronic weight management, cardiovascular risk reduction, and appetite regulation.
Can adolescents use Wegovy®?
Yes, if ≥12 years old and >60 kg, but they must show progress (≥5% BMI loss after 12 weeks at full dose) to continue.