Do you want to learn how to wean off Lexapro? The Royal College of Psychiatrists have warned that coming off antidepressant can cause symptoms lasting for months and that doses should be gradually lowered over months. That is why we have used a holistic approach for over 15 years, helping people in 78 countries to regain their lives. You can too. Help to Quit Lexapro is available so you can Get Off Lexapro properly, while gently stepping down and easing symptoms naturally as you Wean Off Lexapro. Our team has been through withdrawals so we know all too well how troubling the Lexapro Withdrawal Symptoms interfere with all aspects of life. We want you to continue working, living your life fully while we Help you to Get off Lexapro. Contact Us for a FREE consultation to see if you are a candidate for our Lexapro Withdrawal Program.
SUCCESSFUL CHOICES YOU CAN MAKE RIGHT NOW
"After almost 38 years on psychoactive drugs, I am now totally free of them with Point of Return's help!" - Holly (Lexapro Withdrawal Success Story)
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Our Lexapro weaning program is a slow taper that allows you to safely step down from Lexapro under the guidance of Our Team, Your Physician and Pharmacist. The Pre-Taper is for Symptom Relief. You will not wean Lexapro until you feel better. This is where our Advanced Nutraceuticals are critical. Point of Return provides healthy, Drug-Free Strategies to help ease Lexapro withdrawal and support well-being.*
Our areas of expertise are Antidepressants, Benzodiazepines, Sleeping Pills and Painkillers on a case-by-case basis. Our In-Home programs are individualized based on your situation. An assessment is done once you start the Lexapro Withdrawal Program which allows us to individualize your gameplan based on age; length of time on the medications; health challenges; lifestyle, stress levels; additional medications; and interactions. Don't Wean Lexapro alone, work with our Prescription Drug Experts.
Imagine being Free of Lexapro Dependency
- Proven Withdrawal Program completed In-Home with Expert Guidance
- Slowly Wean off Lexapro
- All-Natural Nutraceuticals to help Ease Lexapro Withdrawal
- Professional information on interactions
- Free Mentoring on our 24/7 private Discussion Board
- Free Assessment Upon Starting our Program (a $400 value)
LEXAPRO WITHDRAWAL SUCCESS STORIES
I hope that anyone who is seeking to change their life by stopping these medications finds Point of Return. Thank you! More...
Denise (Lexapro Withdrawal Success Story)
I just want to say thank you to all of you for helping me at the very worst time of my life. I can't tell you enough how much I appreciate Point of Return. I will refer anyone I know. More...
Bob (Lexapro Withdrawal Success Story)
I will forever be grateful for your help and will continue to tell others about your marvelous withdrawal program of prescription drug recover when the opportunity presents itself. More...
Tom (Lexapro Withdrawal Success Story)
Thank you from the bottom of my heart. Your team members, each one of you, are truly life-savers!!! More...
Dennis (Lexapro Withdrawal Success Story)
Karen (Lexapro Withdrawal Success Story)
N.L. (Lexapro Withdrawal Success Story)
EXPERIENCE and TEAMWORK
using a Natural Approach
Lexapro Info and History
The primary action of Lexapro is on Serotonin. Serotonin influences the cardiovascular, renal, immune and gastrointestinal systems, and is essential to regulate body temperature, heart rate, blood pressure and the sympathetic nervous system. During marketing of Lexapro there were spontaneous reports of withdrawal symptoms, particularly when stopping abruptly or rapidly tapering. Reports of serious discontinuation symptoms were also documented. Stopping Lexapro incorrectly can adversely affect many areas of the body.
Lexapro is the brand name for escitalopram, an antidepressant in a group of drugs called Selective Serotonin Reuptake Inhibitors (SSRIs). The mother compound of Lexapro is Celexa, which is a mixture of two different isomers (compounds): R-Celexa and S-Celexa, mirror images of each other. But the early studies by Forest Laboratories attributed the effectiveness of Celexa as an antidepressant was due largely to the S-isomer, while many of the side effects were linked to the R-isomer. Lexapro became the purified S-isomer of Celexa and required only 3.5 years to develop and was known as a 'cleaner and more potent SSRI."
Of all the SSRIs currently on the market, Lexapro has the highest affinity for the human Serotonin transporter, or the protein that transports Serotonin. This protein is also the target of stimulants drugs such as amphetamines and cocaine.
The FDA approved Lexapro in 2002 and according to a document released by the U.S. Senate's Special Committee in 2009, Forest Labs was accused of marketing Lexapro for unapproved uses; failing to disclose negative results from the clinical trials; and paying kickbacks to doctors who prescribed the drug. In 2010 Forest Pharmaceuticals agreed to pay $313 million to settle the charges over Lexapro and two other Forest drugs (Levothyroid and Celexa). In addition, Lexapro has been linked to birth defects and many lawsuits have been filed since the company marketed Lexapro as being safe for pregnant women and women of childbearing age.
In June 2015 twelve lawsuits were filed against Forest Pharmaceuticals after children were born with birth defects. The plaintiffs claim that Forest knew through pre and post market studies the drug was associated with a significant increased risk of birth defects in babies whose mothers ingested the antidepressants during pregnancy, and despite this knowledge continued to aggressively and actively promote the use by women in child-bearing years.
Stopping Lexapro incorrectly can adversely affect many areas of the body. his is why our nonprofit uses gradual dose reduction schedules combined with specific all-natural nutraceuticals to help ease withdrawal symptoms.
Lexapro Withdrawal Symptoms, Side Effects, Adverse Reactions
LEXAPRO WITHDRAWAL SYMPTOMS MAY INCLUDE:
aggression, anxiety, balance issues , blurred vision, brain zaps, concentration impairment, constipation, crying spells, depersonalization, diarrhea, dizziness. electric shock sensations, fatigue, flatulence, flu-like symptoms, hallucinations, hostility, highly emotional, indigestion, irritability, impaired speech, insomnia, jumpy nerves, lack of coordination, lethargy, migraine headaches / increased headaches, nausea, nervousness, over-reacting to situations, paranoia, repetitive thoughts or songs, sensory & sleep disturbances, severe internal restlessness (akathisia), stomach cramps, tremors, tinnitus (ear ringing or buzzing), tingling sensations, troubling thoughts, visual hallucinations / illusions, vivid dreams, speech or visual changes, worsened depression
LEXAPRO SIDE EFFECTS MAY INCLUDE:
constipation, decreased appetite, decreased sex drive, diarrhea, dizziness, dry mouth, ejaculation disorder, fatigue, flu-like symptoms, impotence, indigestion, insomnia, nausea, runny nose, sinusitis, sleepiness, sweating, abdominal pain, abnormal dreaming, allergic reactions, blurred vision, bronchitis, chest pain, coughing, earache, fever, gas, heartburn, high blood pressure, hot flushes, increased appetite, irritability, joint pain, lack of concentration, lack of energy, lack of orgasm, light-headedness, menstrual cramps, migraine, muscle pain, nasal congestion, neck and shoulder pain, pain in arms or legs, palpitations, rash, ringing in the ears, sinus congestion, sinus headache, stomachache, tingling, toothache, tremors, urinary problems, vertigo, vomiting, weight changes, yawning
LEXAPRO ADVERSE REACTIONS MAY INCLUDE: per PDR
Severe: pancreatitis, tardive dyskinesia, seizures, suicidal ideation, SIADH, hemolytic anemia, agranulocytosis, GI bleeding, aplastic anemia, heart failure, bradycardia, hypertensive crisis, torsade de pointes, thrombosis, atrial fibrillation, stroke, myocardial infarction, ventricular tachycardia, anaphylactoid reactions, Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS, erythema multiforme, angioedema, toxic epidermal necrolysis, Stevens-Johnson syndrome, pulmonary embolism , visual impairment, ocular hypertension, hepatic failure, hepatic necrosis, spontaneous fetal abortion, renal failure (unspecified), rhabdomyolysis, serotonin syndrome, bone fractures, persistent pulmonary hypertension of the newborn, neonatal abstinence syndrome
Moderate: ejaculation dysfunction, constipation, impotence (erectile dysfunction), dysphagia , akathisia, choreoathetosis, pseudoparkinsonism, dysarthria, ataxia, migraine, myoclonia, dystonic reaction, nystagmus, amnesia, confusion, delirium, nmania, psychosis, hostilit, impulse control symptoms, hallucinations, depression, hyponatremia, platelet dysfunction, hypoprothrombinemia , anemia, thrombocytopenia, bleeding, leukopenia, hematoma, hypertension, peripheral vasodilation, chest pain (unspecified), phlebitis, QT prolongation, hypotension, orthostatic hypotension, sinus tachycardia, palpitations, edema, dyspnea, blurred vision, hyperbilirubinemia, hepatitis, elevated hepatic enzymes, hyperprolactinemia, priapism, urinary retention, dysuria, myasthenia, hyperglycemia, diabetes mellitus, hypoglycemia, hypokalemia, hypercholesterolemia, osteopenia, withdrawal ,growth inhibition
Mild: headache, nausea, drowsiness, insomnia, xerostomia, diarrhea, fatigue, libido decrease, hyperhidrosis, dizziness, rhinitis, dyspepsia, vomiting, lethargy, sinusitis, orgasm dysfunction, dental pain, abdominal pain, paresthesias, yawning, menstrual irregularity, flatulence, weight loss, pyrosis (heartburn), gastroesophageal reflux, hypoesthesia, asthenia, nightmare, tremor, vertigo, restless legs syndrome (RLS), emotional lability, irritability, restlessness, agitation, paranoia, anxiety, purpura, epistaxis, ecchymosis, syncope, malaise, fever, rash, photosensitivity, flushing, urticaria, alopecia, cough, nasal congestion, diplopia, mydriasis, tinnitus, dysmenorrhea, menorrhagia, increased urinary frequency, muscle cramps, arthralgia, myalgia, back pain
LEXAPRO BOXED WARNINGS: per PDR
Safety and efficacy have not been established in pediatric populations for any indication except for the treatment of major depressive disorder in children and adolescents 12 years of age and older. There is a causal relationship between the use of antidepressants, such as escitalopram, and the risk of suicidal ideation and behavior in children, adolescents, and young adults (ages 18 to 24 years). The risk of suicidality for these drugs was identified in a pooled analysis of 24 placebo-controlled trials (n = 4,400) lasting up to 16 weeks in pediatric patients with major depressive disorder (MDD), obsessive compulsive disorder (OCD), or other psychiatric disorders. The analysis showed a greater risk of suicidality during the first few months of treatment in those receiving antidepressants (SSRIs and others). The average risk of such events on drug was 4% and 2% for placebo; however, no suicides occurred in these trials. Pooled analysis of short-term clinical trials during early phase treatment with SSRIs and other antidepressants in young adults (18 to 24 years) also showed an increased risk of suicidal thinking and behavior. The clinical need for an antidepressant in children or young adults for any use must be weighed against the risk of increased suicidality; patients who are started on therapy should be observed closely for clinical worsening, suicidality, or unusual changes in behavior, particularly within the first few months of starting therapy or at the time of dose increase or decrease. It is unknown if the suicidality risk in children and young adults extends to longer-term therapy (i.e., beyond several months). The possibility of a suicide attempt is inherent in patients with depressive symptoms, whether these occur in primary depression or in association with another primary disorder such as obsessive-compulsive disorder (OCD). All patients with a history of suicidal ideation or behaviors and those with a prominence of suicidal ideation prior to treatment are considered at an increased risk for suicidal ideation or attempts, and should be closely monitored during treatment with escitalopram. In patients who exhibit changes in symptoms, worsening of depression or emergent suicidality, a decision should be made to change or discontinue treatment. If discontinuing, medication should be tapered as rapidly as possible, but with recognition that abrupt discontinuation can also cause adverse symptoms. All antidepressants should be prescribed in the smallest quantity consistent with good patient management in order to reduce the risk of overdose. The potential for growth inhibition in pediatric patients should be monitored during SSRI therapy. Monitor height and weight periodically while the patient is receiving escitalopram. Data are inadequate to determine whether the chronic use of SSRIs causes long-term growth inhibition; however, decreased weight gain has been observed in children and adolescents receiving escitalopram.
Lexapro References and Information
According to the FDA regarding the discontinuation of Escitalopram, marketed as Lexapro and Cipralex: Discontinuing Lexapro: A gradual dose reduction is recommended (2.4). Discontinuation of Treatment with Lexapro: A gradual reduction in dose rather than abrupt cessation is recommended whenever possible (5.3). 2.4 Discontinuation of Treatment with Lexapro Symptoms associated with discontinuation of Lexapro and other SSRIs and SNRIs have been reported [see Warnings and Precautions (5.3)]. Patients should be monitored for these symptoms when discontinuing treatment. A gradual reduction in the dose rather than abrupt cessation is recommended whenever possible. If intolerable symptoms occur following a decrease in the dose or upon discontinuation of treatment, then resuming the previously prescribed dose may be considered. Subsequently, the physician may continue decreasing the dose but at a more gradual rate.
*While great care has been taken in organizing and presenting the material throughout this website, please note that it is provided for informational purposes only and should not be taken as Medical Advice.
*The statements/info on this website have not been evaluated by the Food and Drug Administration (FDA). The products and labels mentioned / sold are not intended to diagnose, treat, cure, or prevent any disease or illness.
* Testimonial results may vary person to person.
*The program outlined in Point of Return is not meant to substitute your doctor, instead it is to be utilized With Your physician to help you with your drug withdrawal process and with his or her consent and support throughout.
*This program is not meant to cure or prevent any disease or illness.
*Because prescription medications can cause severe withdrawal reactions, do not stop taking any medication without first consulting your physician. The decision to taper any medication should be discussed with your doctor and done with their consent and support throughout the process. More..