JUVÉDERM® ULTRA 3 Indications for Use
Order juvéderm ultra 3 .JUVÉDERM® ULTRA 3 is a hyaluronic acid-based injectable dermal filler designed for mid- and deep dermal injections to address moderate to deep face wrinkles and enhance lip volume and definition. The product’s formulation includes lidocaine to help patients feel less uncomfortable during treatment.
Crucial Indications:
- fixing facial hollows that range from minor to severe
- Lip augmentation and contouring
- Injections both deep and middermal to enhance facial attractiveness
Lidocaine is used to reduce pain during treatments.
JUVÉDERM® ULTRA 3 Dosage Information
JUVÉDERM® ULTRA 3 is packaged in a pre-filled, sterile, and disposable syringe containing 1 mL of product. Each box includes two syringes and 4 single-use 27G1/2” needles.
Composition:
- Hyaluronic Acid (HA): 24 mg/mL
- Lidocaine Hydrochloride: 3 mg/mL
- Phosphate Buffer (pH 7.2): q.s. 1 mL
- Volume per syringe: 1 mL
The cross-linked hyaluronic acid used is non-animal in origin, making it biocompatible and effective for long-lasting results.
JUVÉDERM® ULTRA 3 Side Effects and Precautions
As with other dermal fillers, patients should be made aware of the potential side effects of JUVÉDERM® ULTRA 3 prior to starting therapy. It is important to consider the individual history of each patient, even if most side effects are mild and temporary. Order juvéderm ultra 3
Common Side Effects:
- Inflammatory reactions: Up to a week-long redness, swelling, or pain at the injection site.
- Bruising: May result in the development of a hematoma, particularly in individuals using blood thinners.
- Nodules or induration: Tiny lumps could develop where the injection was made.
- Discoloration (Tyndall effect): If the product is injected too superficially, it may turn blue.
- Inadequate filling effect: The filler might not always give the desired increase in volume.
Serious Risks (though rare):
- Intravascular injection: May result in ischemia, infarction, embolism, or vascular blockage. Immediate medical assistance is necessary for symptoms such as skin blanching, unusual discomfort, or changes in vision during or after injection.
- Stroke and necrosis: There have been reports of tissue damage or more serious vascular problems, such as cerebral ischemia, cerebral hemorrhage, and temporary or permanent blindness.
Precautions:
- JUVÉDERM® ULTRA 3 should not be used to the glabellar (forehead) or periorbital (eyelids and crow’s feet) regions.
- A skin hypersensitivity test should be performed on patients who have a history of autoimmune illnesses, severe allergies, or hyaluronic acid or lidocaine hypersensitivity.
- Patients taking non-steroidal anti-inflammatory medicines (NSAIDs) or anticoagulants (such as aspirin or warfarin) should be informed of their increased risk of bleeding and bruises.
- Children and women who are pregnant or nursing shouldn’t get JUVÉDERM® ULTRA 3 injections.
It has shown great efficacy in both clinical trials and real-world applications. The full effects of the hyaluronic acid filler take a few days to show, but the results are immediately apparent. Most patients are quite pleased with the results of clinical exams, particularly when it comes to nasal fold treatment and lip augmentation.
Results Duration:
Depending on the patient’s metabolism, the injection technique, and the treatment location, the effects may last for nine to twelve months. Order juvéderm ultra 3
JUVÉDERM® ULTRA 3 Drug Interactions
Despite JUVÉDERM® ULTRA 3’s general safety, it is important to be aware of potential interactions, especially given the lidocaine component.
Crucial Points to Remember:
- Because they can affect the metabolism of lidocaine, avoid usage in individuals on drugs that lower hepatic metabolism, such as beta-blockers or cemetidine.
- Patients with cardiac conduction abnormalities should be treated carefully because lidocaine can make them worse.
- As this raises the risk of bruises and hematoma formation, make sure the patient is not using NSAIDs or other drugs that can extend bleeding time.
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