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IV Therapy in Orange County

IV Therapy in Orange County

Hydrate & Replenish

If your day-to-day is feeling like more of a struggle, your body may be missing something that’s contributing to that fatigue. If you’ve hit a wall with your workouts or your skin just feels tighter than usual, you may be lacking in some key nutrients, dehydrated, or in need of an immune system boost.

IV therapy from the Drip Lounge by Med Lounge is a safe, effective way to get you feeling your best, no matter what’s ailing you. Treatments deliver a menu of ingredients that target your specific needs. Those include IV fluids, vitamins, minerals, electrolytes, antioxidants, and more, strategically mixed together to return your body back to balance.

Get an energy boost, improve your mood, and brighten and replenish the skin you’re in. Shorten the duration of an illness, calm and destress, even beat that hangover with available blends. Give your body an overall boost of wellness before cold and flu season. The benefits are numerous. Your benefits are waiting. 

Our staff at the Med Lounge can match you with the right combination of ingredients to get your body back on track. Get hydrated, rejuvenated, and replenished from the inside out with IV therapy in Ladera Ranch.  

Benefits of IV Therapy

Strengthen immune system

Enhance workouts

Promote muscle recovery

Fight sickness

Detoxify your body

Improve focus and energy

Healthier skin, hair and nails

Recharge and replenish

Beat fatigue, including hangovers

Rehydrate your body

Frequently Asked Questions

IV therapy is a treatment where vitamins, minerals, and other depleted nutrients are delivered intravenously. The exact ingredients will depend on what you’re looking to target, even if that’s just an immune system boost.

The benefits of IV therapy depend on the cocktail of ingredients you’ve chosen for your treatment. If you’re seeking IV hydration therapy for dehydration or anti-aging effects, expect to leave your treatment feeling immediately rehydrated. IV therapy can also boost energy and target brain fog, replenish depleted nutrients in the body, even fight against illness or bad hangovers. Your provider will work with you to develop a drip that gets you feeling more like yourself.

Yes! IV vitamin therapy absolutely works. It’s particularly powerful for those who aren’t getting what they need from diet and lifestyle alone. IV therapy allows those nutrients to be rapidly absorbed into the bloodstream. It’s an efficient, effective way to give your body what it needs.

IV therapy can benefit a variety of individuals. It’s great for those lacking essential nutrients but also good for anyone seeking an energy or immune system boost, fighting back against illness, or looking for natural treatments for chronic fatigue. IV therapy can also improve your skin with its hydrating effects and make you feel better fast if you’re suffering from a bad case of jet lag or a hangover.

Your IV therapy provider will want a complete medical history before setting you up with treatments. That includes a complete allergy history. Some treatments may not be appropriate for women who are pregnant or nursing.

Our experts at Med Lounge can work within your budget to recommend a plan to help you reach your body goals.

Most sessions last about 45-60 minutes, but that can vary somewhat depending on your infusions and the concerns you’re bringing to your treatment. There is zero downtime after IV therapy treatments.

Our providers at the Med Lounge can help you decide on the right IV therapy treatment for you. There are numerous combinations available to target a variety of needs. Part of the process is identifying your areas of focus, even if it’s just an overall wellness boost.

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

Click the image to see an enlarged preview.

What to Expect With IV Therapy

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 IV therapy before and after your treatment.


  • Even if you’re scheduled for a boost of IV hydration therapy, make sure that you do your best to hydrate before your appointment. Hydrating will help your veins work more effectively and prep your body for your treatment. 
  • You don’t need a full meal before your treatment, but a light snack will prevent any lightheadedness and keep your blood sugar up. 
  • Dress comfortably. Wear something that will allow you to easily expose the inside of your elbow.
  • Avoid antihistamines and decongestants before your treatment. Both can have a constricting effect on your blood vessels and potentially reduce the effectiveness of your treatment. 
  • Make sure you share any medication information with your provider before your treatment. If you have anxiety over IV treatments, share that with your provider, too. They can help you manage those feelings during your treatment and give you tips on relaxation exercises.
  • At the Med Lounge, we pride ourselves on creating a warm and inviting atmosphere, especially when IVs are involved. Feel free to bring anything that will help you relax, though, including earbuds or the book you’re reading.


  • You should feel immediate results if you’re using IV therapy to combat things like fatigue, jet lag, or a bad hangover. Other wellness boosts may feel more gradual, but rest assured that you’re doing your body a big favor with your IV therapy.
  • You may experience some minor bruising or swelling at your injection sites. This is normal and should heal quickly. Cold packs can help with minor discomfort after your treatment. 
  • A cool feeling at the injection site or mineral taste in the mouth is normal during and after IV therapy treatments. Not all patients experience these side effects, but in those who do, both will go away shortly.
  • Drink plenty of water after your treatment, even if you’ve received hydration therapy. Water helps relieve nausea, headaches, cramping, and other mild symptoms sometimes associated with IV treatments. 
  • If you received a detoxifying IV therapy treatment, you may experience some fatigue to start. This is normal and part of your body’s natural process of sending out those toxins. What should happen next is a feeling of improved wellness. 
  • Your provider will monitor you to make sure you’re not experiencing any allergic reactions or adverse side effects during your treatment. If you experience any severe symptoms outside of minor swelling or bruising at the injection site, including significant pain at the injection site that has not gone away by the next day, call your doctor immediately.

CoolSculpting® and CoolSculpting® Elite are FDA-cleared for the treatment of visible fat bulges in the submental (under the chin) and submandibular (under the jawline) areas, thigh, abdomen, and flank, along with bra fat, back fat, underneath the buttocks (also known as banana roll), and upper arm. It is also FDA-cleared to affect the appearance of lax tissue with submental area treatments. CoolSculpting® and CoolSculpting® Elite are not treatments for weight loss.

Important Safety Information
These procedures are not for everyone. You should not be treated with CoolSculpting® or CoolSculpting® Elite if you suffer from cryoglobulinemia, cold agglutinin disease, or paroxysmal cold hemoglobinuria.

Tell your doctor if you have any medical conditions including recent surgery, pre-existing hernia, and any known sensitivities or allergies.

During the procedure you may experience sensations of pulling, tugging, mild pinching, intense cold, tingling, stinging, aching, and cramping at the treatment site. These sensations subside as the area becomes numb. Following the procedure, typical side effects include temporary redness, swelling, blanching, bruising, firmness, tingling, stinging, tenderness, cramping, aching, itching, or skin sensitivity, and sensation of fullness in the back of the throat after submental or submandibular area treatment.
Rare side effects may also occur. CoolSculpting® and CoolSculpting® Elite may cause a visible enlargement in the treated area, which may develop 2 to 5 months after treatment and requires surgical intervention for correction.

Please see CoolSculpting® full Important Safety Information and CoolSculpting® Elite full Important Safety Information for additional information.

Patient Results May Vary.

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BOTOX® Cosmetic (onabotulinumtoxinA) Important Information



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





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.


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.


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.


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%).


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.


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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