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      • View All
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      • Laser Liposuction
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      • Vaginal Dryness
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      • Hair Thinning
      • Insufficient Eyelashes
      • Unwanted or Excessive Hair
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    • Blu-U (Light)
    • Cellulaze Cellulite Laser
    • CO2 Lumenis Laser
    • CoolSculpting®
    • DermaTyte 1319
    • Ellman (RF)
    • Erbium Laser
    • Fractional Laser
    • Fraxel Dual 1550 / 1927
    • Fraxel Re:pair Laser
    • Fraxel Restore Laser
    • GentleLASE
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    • Legend Pro
    • Lumenis IPL
    • Lumenis Nd:YAG
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    • Lumenis OPT
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    • MedLite C6-1064
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    • NuEra Tight
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    • Omnilux Revive Plus Combo
    • PrecisionTx Laser
    • Pro-V Sciton Joule
    • ProLipo Laser
    • SmartLipo™ Triplex
    • SmoothBeam Laser
    • Thermage® RF / ThermaCool™
    • ThermiRase®
    • ThermiSmooth®
    • ThermiTight®
    • ThermiVa®
    • Ultherapy®
    • UV Photography
    • Vasculight
    • VBeam
    • Venus Freeze
    • VersaPulse Alexandrite 755
    • VersaPulse Help-G 532 KTP
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    • VersaPulse Nd:YAG 532
    • VersaPulse Nd:YAG 1064
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      • Dark Circles & Pigmentation
      • View All
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      • CoolSculpting® Arm Treatments
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Kybella Neck Tightening Treatments – Case #36188

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Kybella® – Neck Tightening Treatment

« Previous

Before Kybella® Neck Tightening Treatment

Before

Before Kybella® Neck Tightening Treatment

Before

Before Kybella® Neck Tightening Treatment

Before

« Previous

After Kybella® Neck Tightening Treatment

After

After Kybella® Neck Tightening Treatment

After

After Kybella® Neck Tightening Treatment

After

« Back to Gallery

KYBELLA® (deoxycholic acid) injection 10 mg/mL Indication and Important Safety Information
KYBELLA® (deoxycholic acid) injection is indicated for improvement in the appearance of moderate to severe convexity or fullness associated with submental fat in adults.
The safe and effective use of KYBELLA® for the treatment of subcutaneous fat outside the submental region has not been established and is not recommended.

Contraindications
KYBELLA® is contraindicated in the presence of infection at the injection sites.

Warnings and Precautions
Marginal Mandibular Nerve Injury
Cases of marginal mandibular nerve injury, manifested as an asymmetric smile or facial muscle weakness, were reported in 4% of subjects in the clinical trials; all cases resolved spontaneously (range 1-298 days, median 44 days). KYBELLA® should not be injected into or in close proximity to the marginal mandibular branch of the facial nerve.

Dysphagia
Dysphagia occurred in 2% of subjects in the clinical trials in the setting of administration-site reactions, eg, pain, swelling, and induration of the submental area; all cases of dysphagia resolved spontaneously (range 1-81 days, median 3 days). Avoid use of KYBELLA® in patients with current or prior history of dysphagia as treatment may exacerbate the condition.

Injection-Site Hematoma/Bruising
In clinical trials, 72% of subjects treated with KYBELLA® experienced hematoma/bruising. KYBELLA® should be used with caution in patients with bleeding abnormalities or who are currently being treated with antiplatelet or anticoagulant therapy as excessive bleeding or bruising in the treatment area may occur.

Risk of Injecting Into or in Proximity to Vulnerable Anatomic Structures
To avoid the potential of tissue damage, KYBELLA® should not be injected into or in close proximity (1 cm-1.5 cm) to salivary glands, lymph nodes, and muscles.

Adverse Reactions
The most commonly reported adverse reactions in the pivotal clinical trials were: injection site edema/swelling, hematoma/bruising, pain, numbness, erythema, and induration.
Please see KYBELLA® full prescribing information.

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MilfordMD Cosmetic Dermatology Surgery & Laser Center
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