BTL Vanquish ME

BTL Vanquish ME

Target & Reduce

BTL Vanquish ME is the upgraded version of BTL Vanquish, body contouring technology that uses radiofrequency energy to heat fat cells to the point of destruction. Heatwaves sent using a harness around targeted areas eliminate fat cells permanently, leading to long-term fat layer reduction in places you haven’t been successful with otherwise. 

Treatments are efficient and safe, with none of the downtime you’d require for surgical procedures like liposuction. BTL Vanquish ME is ideal for those who already lead a healthy lifestyle, but despite those efforts, stubborn fat remains in hard-to-target areas. Have you been struggling with how to lose belly fat fast? This is targeted fat loss rather than overall weight loss. Eliminate belly fat, get rid of love handles and slim down your tights with BTL Vanquish ME in Orange County. The experts at the Med Lounge will help come up with a treatment plan that’s customized to your needs and body goals. Say goodbye to unwanted fat with BTL Vanquish ME.

Benefits of BTL Vanquish ME

Lose inches

Reduce body fat

Zero downtime

Fast-acting

Targeted fat reduction

Fat cells are permanently gone

Improvement over time

Extremely safe

Painless procedure

No discomfort

Frequently Asked Questions

BTL Vanquish and Vanquish ME use radiofrequency (RF) energy to heat up cells to the point of apoptosis or cell death. Vanquish ME is the advanced version of the technology, with a higher rate of fat reduction than its predecessor.

Vanquish ME treatments work by heating targeted fat cells to temperatures extreme enough that those cells break apart and are permanently destroyed. The cells are then excreted as waste using your body’s natural processes for dead cells. The heat itself is delivered at a maximum of 120 degrees Fahrenheit using a harness. Temperatures are safe but highly effective, never putting the surrounding muscles and tissue at risk for any scarring.

The cost of your Vanquish ME treatments will vary and are based on how many sessions you’ll need to get your desired results. Our staff at the Med Lounge can meet with you at a complimentary consultation to go over your options and recommend a treatment plan based on your unique goals and areas of the body you’d like to target for fat reduction. We can work with your budget on a program that will get you to where you’d like to be.

As heat is the primary driver of fat cell loss in Vanquish ME treatments, all you’ll likely feel is a warm sensation at the treatment sites during and after your therapy. Most compare the feeling to a heating pad, with no pain or discomfort. Some sweating is normal. 

The heat you’ll experience never exceeds 120 degrees Fahrenheit, so you’re never in danger of any burning or scarring. The heat on muscles and tissue around your treatment sites never exceeds 101 degrees Fahrenheit. Sessions last between 30-45 minutes.

The loss of fat cells you’ll experience after a Vanquish ME treatment is permanent. It’s important to note that while the old fat cells in those treated areas won’t return, new fat cells can form in other areas if you don’t follow a healthy lifestyle post-treatment. Good diet and exercise will help your results go a long way.

Regular exercise after your Vanquish ME treatments will help extend your results. It’s also important to stay hydrated before and after your treatment to kick your metabolism into gear and help it work more efficiently. Finally, weight maintenance with a healthy diet free of too many processed foods and sugars is highly recommended. Some patient experiences report extended results by going on a detox post-treatment focused on a plant-based diet.

See the amazing difference in our clients, before and after treatment.

Click the image to see an enlarged preview.

What to Expect With Vanquish

For the best results and to reduce the chance of any side effects after your treatment, our experts at the Med Lounge have a few tips around what to expect with Vanquish ME before and after your procedure.

PRE-TREATMENT

  • Follow a regular exercise and healthy diet routine before your treatments. 
  • Drink plenty of water before your appointment so that you aren’t dehydrated. This will make your treatments more efficient and kick your metabolism into gear. Providers recommend at least eight glasses of water per day in the days leading up to your treatments. 
  • Women should schedule treatment sessions around their menstrual cycles. The treatments can cause some cramping and a heavier flow otherwise. 
  • Wear loose, comfortable clothing to your VANQUISH ME appointment. Your provider will need easy access to areas being treated by the device.
  • Remove any jewelry and put away electronic devices before starting your treatment. 
  • Talk to your provider about any cardiovascular conditions, implants or injuries you’ve experienced in the areas you’d like to target. Your provider will be able to tell you whether Vanquish ME is safe for you or whether you’re a better candidate for a different kind of treatment. 

POST-TREATMENT

  • There is no expected recovery time after a Vanquish ME session. You’ll be able to resume normal activities after your treatment. Light physical activity after your sessions is recommended.
  • After a session, any tenderness or redness at the treatment site is normal and should go away within a few days. Your skin may feel warm to the touch after your treatments. This is also normal.
  • Maintain a high level of hydration post-treatment. Again, drink at least eight glasses of water per day in the days following your Vanquish ME treatments. 
  • The recommended number of sessions for optimal results is four sessions. Schedule your sessions as advised by your provider at the end of your Vanquish ME appointment, and follow treatment instructions to the letter. 
  • Regular exercise and a healthy eating plan will go a long way in extending your results. Work out those newly toned muscles regularly and maintain a healthy lifestyle to get the biggest bang for your buck with Vanquish ME.
  • Talk to your provider if you’re experiencing any severe symptoms after your session, such as intense pain, blistering or extreme fatigue.
BTL Vanquish ME™ is indicated for temporary reduction in the circumference of the abdomen and thighs.

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BOTOX® Cosmetic (onabotulinumtoxinA) Important Information

 

Indications

BOTOX® Cosmetic (onabotulinumtoxinA) is indicated in adult patients for the temporary improvement in the appearance of:

– Moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity

– Moderate to severe lateral canthal lines associated with orbicularis oculi activity

 

– Moderate to severe forehead lines associated with frontalis activity

 

IMPORTANT SAFETY INFORMATION, INCLUDING BOXED WARNING

 

WARNING: DISTANT SPREAD OF TOXIN EFFECT

Postmarketing reports indicate that the effects of BOTOX® Cosmetic and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These may include asthenia, generalized muscle weakness, diplopia, ptosis, dysphagia, dysphonia, dysarthria, urinary incontinence, and breathing difficulties. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficulties can be life threatening and there have been reports of death. The risk of symptoms is probably greatest in children treated for spasticity, but symptoms can also occur in adults treated for spasticity and other conditions, particularly in those patients who have an underlying condition that would predispose them to these symptoms. In unapproved uses and approved indications, cases of spread of effect have been reported at doses comparable to those used to treat cervical dystonia and spasticity and at lower doses.

CONTRAINDICATIONS

BOTOX® Cosmetic is contraindicated in the presence of infection at the proposed injection site(s) and in individuals with known hypersensitivity to any botulinum toxin preparation or to any of the components in the formulation.

WARNINGS AND PRECAUTIONS

Lack of Interchangeability Between Botulinum Toxin Products

The potency units of BOTOX® Cosmetic are specific to the preparation and assay method utilized. They are not interchangeable with other preparations of botulinum toxin products and, therefore, units of biological activity of BOTOX® Cosmetic cannot be compared to nor converted into units of any other botulinum toxin products assessed with any other specific assay method.

Spread of Toxin Effect

Please refer to Boxed Warning for Distant Spread of Toxin Effect.

No definitive serious adverse event reports of distant spread of toxin effect associated with dermatologic use of BOTOX® Cosmetic at the labeled dose of 20 Units (for glabellar lines), 24 Units (for lateral canthal lines), 40 Units (for forehead lines with glabellar lines), 44 Units (for simultaneous treatment of lateral canthal lines and glabellar lines), and 64 Units (for simultaneous treatment of lateral canthal lines, glabellar lines, and forehead lines) have been reported. Patients or caregivers should be advised to seek immediate medical care if swallowing, speech, or respiratory disorders occur.

Serious Adverse Reactions With Unapproved Use

Serious adverse reactions, including excessive weakness, dysphagia, and aspiration pneumonia, with some adverse reactions associated with fatal outcomes, have been reported in patients who received BOTOX® injections for unapproved uses. In these cases, the adverse reactions were not necessarily related to distant spread of toxin, but may have resulted from the administration of BOTOX® to the site of injection and/or adjacent structures. In several of the cases, patients had pre-existing dysphagia or other significant disabilities. There is insufficient information to identify factors associated with an increased risk for adverse reactions associated with the unapproved uses of BOTOX®. The safety and effectiveness of BOTOX® for unapproved uses have not been established.

Hypersensitivity Reactions

Serious and/or immediate hypersensitivity reactions have been reported. These reactions include anaphylaxis, serum sickness, urticaria, soft-tissue edema, and dyspnea. If such reactions occur, further injection of BOTOX® Cosmetic should be discontinued and appropriate medical therapy immediately instituted. One fatal case of anaphylaxis has been reported in which lidocaine was used as the diluent and, consequently, the causal agent cannot be reliably determined.

Cardiovascular System

There have been reports following administration of BOTOX® of adverse events involving the cardiovascular system, including arrhythmia and myocardial infarction, some with fatal outcomes. Some of these patients had risk factors including pre-existing cardiovascular disease. Use caution when administering to patients with pre-existing cardiovascular disease.

Increased Risk of Clinically Significant Effects With Pre-existing Neuromuscular Disorders

Individuals with peripheral motor neuropathic diseases, amyotrophic lateral sclerosis, or neuromuscular junction disorders (eg, myasthenia gravis or Lambert-Eaton syndrome) should be monitored when given botulinum toxin. Patients with neuromuscular disorders may be at increased risk of clinically significant effects including generalized muscle weakness, diplopia, ptosis, dysphonia, dysarthria, severe dysphagia, and respiratory compromise from onabotulinumtoxinA (see Warnings and Precautions).

Dysphagia and Breathing Difficulties

Treatment with BOTOX® and other botulinum toxin products can result in swallowing or breathing difficulties. Patients with pre-existing swallowing or breathing difficulties may be more susceptible to these complications. In most cases, this is a consequence of weakening of muscles in the area of injection that are involved in breathing or oropharyngeal muscles that control swallowing or breathing (see Boxed Warning).

Pre-existing Conditions at the Injection Site

Caution should be used when BOTOX® Cosmetic treatment is used in the presence of inflammation at the proposed injection site(s) or when excessive weakness or atrophy is present in the target muscle(s).

Dry Eye in Patients Treated With BOTOX® Cosmetic

There have been reports of dry eye associated with BOTOX® Cosmetic injection in or near the orbicularis oculi muscle. If symptoms of dry eye (eg, eye irritation, photophobia, or visual changes) persist, consider referring patients to an ophthalmologist.

Human Albumin and Transmission of Viral Diseases

This product contains albumin, a derivative of human blood. Based on effective donor screening and product manufacturing processes, it carries an extremely remote risk for transmission of viral diseases and variant Creutzfeldt-Jakob disease (vCJD). There is a theoretical risk for transmission of Creutzfeldt-Jakob disease (CJD), but if that risk actually exists, the risk of transmission would also be considered extremely remote. No cases of transmission of viral diseases, CJD or vCJD have ever been identified for licensed albumin or albumin contained in other licensed products.

ADVERSE REACTIONS

The most frequently reported adverse reactions following injection of BOTOX® Cosmetic for glabellar lines were eyelid ptosis (3%), facial pain (1%), facial paresis (1%), and muscular weakness (1%).

The most frequently reported adverse reaction following injection of BOTOX® Cosmetic for lateral canthal lines was eyelid edema (1%).

The most frequently reported adverse reactions following injection of BOTOX® Cosmetic for forehead lines with glabellar lines were headache (9%), brow ptosis (2%), and eyelid ptosis (2%).

DRUG INTERACTIONS

Co-administration of BOTOX® Cosmetic and aminoglycosides or other agents interfering with neuromuscular transmission (eg, curare-like compounds) should only be performed with caution as the effect of the toxin may be potentiated. Use of anticholinergic drugs after administration of BOTOX® Cosmetic may potentiate systemic anticholinergic effects.

The effect of administering different botulinum neurotoxin products at the same time or within several months of each other is unknown. Excessive neuromuscular weakness may be exacerbated by

administration of another botulinum toxin prior to the resolution of the effects of a previously administered botulinum toxin.

Excessive weakness may also be exaggerated by administration of a muscle relaxant before or after administration of BOTOX® Cosmetic.

USE IN SPECIFIC POPULATIONS

There are no studies or adequate data from postmarketing surveillance on the developmental risk associated with use of BOTOX® Cosmetic in pregnant women. There are no data on the presence of BOTOX® Cosmetic in human or animal milk, the effects on the breastfed child, or the effects on milk production.

 

Please see BOTOX® Cosmetic full Prescribing Information including Boxed Warning and Medication Guide.

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