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Escitalopram: uses, dosing, side effects & brands

Escitalopram is a serotonin reuptake inhibitor sold in the U.S. under 2 brand and generic names, for major depressive disorder. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.

By the pharmaranks editorial teamReviewed against the FDA (openFDA label, NDC Directory & Enforcement) sourcesUpdated Jul 24, 2026How we research

Key facts

Drug class
Serotonin Reuptake Inhibitor
Treats
Major Depressive Disorder
Available as
Tablet
Sold as
2 products — Lexapro and Escitalopram Oxalate
Prescription?
Prescription only
Generic available?
Yes
Half-life
about 27 to 32 hours
What the pharmacy pays
about $0.16 per ml — not your price
Boxed warning
Boxed warning

How escitalopram is dosed

From the FDA label for Escitalopram Oxalate (application ANDA077412). Other escitalopram products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.

Indication and Population Recommended Dosage MDD in Adults (2.1) Initial: 10 mg once daily Recommended: 10 mg once daily Maximum: 20 mg once daily MDD in Pediatric Patients 12 years and older (2.1) Initial: 10 mg once daily Recommended: 10 mg once daily Maximum: 20 mg once daily GAD in Adults (2.2) Initial: 10 mg once daily Recommended: 10 mg once daily Maximum: 20 mg once daily No additional benefits were seen at 20 mg once daily (2.1) Administer once daily, morning or evening, with or without food (2.3) Elderly patients: recommended dosage is 10 mg once daily (2.4) Hepatic impairment: recommended dosage is 10 mg once daily (2.4, 8.6) When discontinuing escitalopram tablets, reduce dose gradually whenever possible (2.5) 2.1 Major Depressive Disorder Adults The recommended dosage of escitalopram tablets in adults is 10 mg once daily. A fixed-dose trial of escitalopram demonstrated the effectiveness of both 10 mg and 20 mg of escitalopram, but failed to demonstrate a greater benefit of 20 mg over 10 mg [see Clinical Studies (14.1)]. Depending on clinical response and tolerability, dosage may be increased to the maximum recommended dosage of 20 mg once daily at an interval of no less than 1 week. Pediatric Patients 12 years of age and older The recommended dosage of escitalopram tablets in pediatric patients 12 years of age and older is 10 mg once daily. Depending on clinical…

Escitalopram side effects

The following adverse reactions are discussed in greater detail in other sections of the labeling: Suicidal thoughts and behaviors in adolescents and young adults [see Warnings and Precautions (5.1)] Serotonin syndrome [see Warnings and Precautions (5.2)] Discontinuation syndrome [see Warnings and Precautions (5.3)] Seizures [see Warnings and Precautions (5.4)] Activation of mania or hypomania [see Warnings and Precautions (5.5)] Hyponatremia [see Warnings and Precautions (5.6)] Increased Risk of Bleeding [see Warnings and Precautions (5.7)] Interference with Cognitive and Motor Performance [see Warnings and Precautions (5.8)] Angle-closure glaucoma [see Warnings and Precautions (5.9)] Use in Patients with Concomitant Illness [see Warnings and Precautions (5.10)] Sexual Dysfunction [see Warnings and Precautions (5.11)] Most commonly observed adverse reactions (incidence ≥ 5% and at least twice the incidence of placebo patients) are: insomnia, ejaculation disorder (primarily ejaculatory delay), nausea, sweating increased, fatigue and somnolence, decreased libido, and anorgasmia (6.1). To report SUSPECTED ADVERSE REACTIONS, contact Ascent Pharmaceuticals, Inc., at 1-855-221-1622, or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical…

Who shouldn’t take escitalopram

Escitalopram tablets is contraindicated in patients: taking MAOIs with escitalopram tablets or within 14 days of stopping treatment with escitalopram tablets because of an increased risk of serotonin syndrome. The use of escitalopram tablets within 14 days of stopping an MAOI intended to treat psychiatric disorders is also contraindicated [see Dosage and Administration (2.7) and Warnings and Precautions (5.2)]. Starting escitalopram tablets in a patient who is being treated with MAOIs such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome [ see Dosage and Administration (2.6) and Warnings and Precautions (5.2)]. taking pimozide [see Drug Interactions (7)]. with a hypersensitivity to escitalopram or citalopram or any of the inactive ingredients in escitalopram tablets. Do not use MAOIs intended to treat psychiatric disorders with escitalopram tablets or within 14 days of stopping treatment with escitalopram tablets. Do not use escitalopram tablets within 14 days of stopping an MAOI intended to treat psychiatric disorders. In addition, do not start escitalopram tablets in a patient who is being treated with linezolid or intravenous methylene blue (4) Concomitant use of pimozide (4) Known hypersensitivity to escitalopram or citalopram or any of the inactive ingredients (4)

Escitalopram drug interactions

Table 6 presents clinically important drug interactions with escitalopram. TABLE 6 Clinically Important Drug Interactions with Escitalopram Concomitant use with SSRIs, SNRIs or Tryptophan is notrecommended (7) Use caution when concomitant use with drugs that affect Hemostasis (NSAIDs, Aspirin, Warfarin) (7) 7.1 7.2

Can you take escitalopram with…?

Source-cited answers for the combinations people actually ask about — each with a verdict and what to watch for.

Every escitalopram product we track (2)

Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.

Escitalopram products
#DrugRatingPharmacy pays
172/100$0View →
256/100$0View →

What escitalopram pills look like

Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.

Escitalopram pill imprints
ImprintStrengthColourShape
11;36;1010 mgwhiteround
7410 mgwhiteround
P;55 mgwhiteround
F;535 mgwhiteround
F;5;620 mgwhiteoval
P;55 mgwhiteround
P;1010 mgwhiteround
P;2020 mgwhiteround
11;37;2020 mgwhiteround
11;36;1010 mgwhiteround
7410 mgwhiteround
P;2020 mgwhiteround

How long does escitalopram take to work?

It may take several weeks before you feel the full benefit of escitalopram.” — MedlinePlus, U.S. National Library of Medicine.

What the NIH says about how quickly escitalopram works

How long escitalopram keeps

No escitalopram label we read sets a separate limit for after opening, but they do specify how it must be stored — and the stability behind any date assumes those conditions.

Does escitalopram expire? The in-use limits and storage rules from its labels

Escitalopram and breastfeeding

From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.

Escitalopram is the active S-isomer of the antidepressant, citalopram. Limited information indicates that maternal doses of escitalopram up to 20 mg daily produce low levels in milk and would not be expected to cause any adverse effects in breastfed infants, especially if the infant is older than 2 months. No adverse effects on development have been found in infants followed for up to 5 years of age. If the mother requires escitalopram, it is not a reason to discontinue breastfeeding. A safety scoring system finds escitalopram use to be possible during breastfeeding. Monitor the infant for excess drowsiness, restlessness, agitation, poor feeding and poor weight gain, especially in younger, exclusively breastfed infants and when using combinations of psychotropic drugs.

Full LactMed record for escitalopram: levels in milk, effects in breastfed infants, and the drugs it would consider instead

National Institute of Child Health and Human Development, record revised June 15, 2026. LactMed states its information is not a substitute for professional judgement.

What people report to the FDA about escitalopram

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 18,319 reports naming escitalopram, and the FDA flagged 74% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:

  • fatigue1,376 reports
  • headache1,322 reports
  • nausea1,322 reports
  • dyspnoea1,113 reports
  • diarrhoea1,105 reports
  • dizziness951 reports
  • fall821 reports
  • vomiting820 reports

Read these as a signal, not a rate. A report does not mean escitalopram caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.

Source: openFDA drug/event (FAERS), retrieved August 25, 2026.

How long escitalopram stays in your system

The elimination half-life of escitalopram is about 27 to 32 hours. This is the terminal (elimination) half-life of escitalopram itself; the drug's metabolites do not meaningfully add to its activity or duration. The half-life is longer in some people — about 50% longer in older adults and roughly doubled in those with reduced liver function.

LEXAPRO (escitalopram oxalate) tablet — DailyMed label, Clinical Pharmacology/Pharmacokinetics

Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.

Can you drink alcohol on escitalopram?

The label says avoid it

The label does address alcohol. It states that in a clinical trial escitalopram did not potentiate the cognitive and motor impairment caused by alcohol, so it does not describe a disulfiram-like reaction or additive CNS depression. Even so, the label says that, as with other psychotropic medications, the use of alcohol by patients taking escitalopram is not recommended, and it advises that concomitant use of escitalopram and alcohol in depressed patients is not advised.

Escitalopram Oral Solution — DailyMed label

Stopping escitalopram: withdrawal & how to come off

The label describes a Discontinuation Syndrome. Spontaneous reports of adverse reactions on stopping escitalopram and other SSRIs, especially when abrupt, include dysphoric mood, irritability, agitation, dizziness, sensory disturbances such as paresthesias (electric-shock sensations), anxiety, confusion, headache, lethargy, emotional lability, insomnia, and hypomania. These are usually self-limiting but serious discontinuation symptoms have been reported. The label directs that the prescriber reduce the dose gradually rather than stop abruptly whenever possible and monitor for these symptoms; if intolerable symptoms occur after a dose decrease or discontinuation, the prescriber may resume the prior dose and then decrease more gradually. This withdrawal guidance is not in the boxed warning (the boxed warning concerns suicidal thoughts and behaviors).

This describes what the label says about stopping — not a schedule to follow on your own. Any change to escitalopramis your prescriber’s decision; stopping some medicines abruptly is dangerous.

Escitalopram Oral Solution — DailyMed label

Is escitalopram safe during pregnancy?

The label states a known risk

The label does not establish an increased risk of major birth defects or miscarriage from published epidemiologic studies. However, it names specific risks: SSRI exposure (particularly the month before delivery) is associated with a less-than-2-fold increase in postpartum hemorrhage, and exposure during pregnancy carries risks of persistent pulmonary hypertension of the newborn (PPHN) and poor neonatal adaptation. Neonates exposed late in the third trimester have developed complications (respiratory distress, feeding difficulty, jitteriness, etc.) requiring prolonged hospitalization. Animal studies showed adverse embryo/fetal effects at doses above human therapeutic levels. The label also weighs the risk of untreated depression, noting women who discontinue antidepressants are more likely to relapse, and points to a National Pregnancy Registry for Antidepressants. It does not tell patients to start or stop the drug on their own -- decisions should be made with the prescriber.

This is what escitalopram’s FDA label says — not a recommendation to take or stop it. In pregnancy, that decision is your prescriber’s; do not start or stop a medicine on your own.

Escitalopram FDA Prescribing Information (DailyMed)

Does escitalopram cause weight gain?

The label reports no established weight effect

In controlled trials, patients treated with escitalopram did not differ from placebo-treated patients with regard to clinically important change in body weight. The label notes that decreased appetite and weight loss have been observed with SSRIs in children and adolescents, so weight and growth should be monitored in that group; and post-marketing reports list both increased and decreased weight. For adults, the label establishes no systematic weight effect.

Only what the FDA label reports — many drugs blamed for weight change online have no weight effect in their label, and we say so rather than repeat the folklore.

Escitalopram FDA Prescribing Information (DailyMed)

Related guides

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Frequently asked questions

What is escitalopram?

Escitalopram Oxalate is a serotonin reuptake inhibitor used to treat Major Depressive Disorder.

What kind of drug is escitalopram?

The FDA classifies escitalopram as a serotonin reuptake inhibitor. Selective serotonin reuptake inhibitors (SSRIs) block the transporter that pulls serotonin back into nerve cells, so more of this mood-related chemical stays in the gaps between neurons to keep signaling. They act mainly on serotonin, which tends to mean fewer side effects than older antidepressants. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.

Is escitalopram safe during pregnancy?

The label does not establish an increased risk of major birth defects or miscarriage from published epidemiologic studies. However, it names specific risks: SSRI exposure (particularly the month before delivery) is associated with a less-than-2-fold increase in postpartum hemorrhage, and exposure during pregnancy carries risks of persistent pulmonary hypertension of the newborn (PPHN) and poor neonatal adaptation. Neonates exposed late in the third trimester have developed complications (respiratory distress, feeding difficulty, jitteriness, etc.) requiring prolonged hospitalization. Animal studies showed adverse embryo/fetal effects at doses above human therapeutic levels. The label also weighs the risk of untreated depression, noting women who discontinue antidepressants are more likely to relapse, and points to a National Pregnancy Registry for Antidepressants. It does not tell patients to start or stop the drug on their own -- decisions should be made with the prescriber. This is what escitalopram's FDA label says; whether to use it in pregnancy is your prescriber's decision.

Does escitalopram cause weight gain?

In controlled trials, patients treated with escitalopram did not differ from placebo-treated patients with regard to clinically important change in body weight. The label notes that decreased appetite and weight loss have been observed with SSRIs in children and adolescents, so weight and growth should be monitored in that group; and post-marketing reports list both increased and decreased weight. For adults, the label establishes no systematic weight effect.

Can you drink alcohol while taking escitalopram?

The label does address alcohol. It states that in a clinical trial escitalopram did not potentiate the cognitive and motor impairment caused by alcohol, so it does not describe a disulfiram-like reaction or additive CNS depression. Even so, the label says that, as with other psychotropic medications, the use of alcohol by patients taking escitalopram is not recommended, and it advises that concomitant use of escitalopram and alcohol in depressed patients is not advised. This is what escitalopram's FDA label says; alcohol advice depends on your dose and health, so confirm with your pharmacist.

What happens if you stop taking escitalopram?

The label describes a Discontinuation Syndrome. Spontaneous reports of adverse reactions on stopping escitalopram and other SSRIs, especially when abrupt, include dysphoric mood, irritability, agitation, dizziness, sensory disturbances such as paresthesias (electric-shock sensations), anxiety, confusion, headache, lethargy, emotional lability, insomnia, and hypomania. These are usually self-limiting but serious discontinuation symptoms have been reported. The label directs that the prescriber reduce the dose gradually rather than stop abruptly whenever possible and monitor for these symptoms; if intolerable symptoms occur after a dose decrease or discontinuation, the prescriber may resume the prior dose and then decrease more gradually. This withdrawal guidance is not in the boxed warning (the boxed warning concerns suicidal thoughts and behaviors). Do not stop escitalopram on your own — any change is a prescriber-managed decision.

How long does escitalopram stay in your system?

The elimination half-life of escitalopram is about 27 to 32 hours — that is how long the body takes to clear half of a dose. This is the terminal (elimination) half-life of escitalopram itself; the drug's metabolites do not meaningfully add to its activity or duration. The half-life is longer in some people — about 50% longer in older adults and roughly doubled in those with reduced liver function. Half-life is not the same as how long a drug test can detect the drug, and it varies with age, kidney and liver function.

Can you take escitalopram with other medicines?

It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run escitalopram against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.

What brand names is escitalopram sold under?

We track 2 escitalopram-containing products in the U.S.: Lexapro and Escitalopram Oxalate. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.

What forms does escitalopram come in?

Across the brands we track, escitalopram is currently marketed as tablet, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.

Is there a generic escitalopram?

Yes. Our catalog lists 1 generic escitalopram product alongside the brand versions. A generic has the same active ingredient and must meet the FDA's bioequivalence standard; it usually costs less. Ask your pharmacist which one your plan covers.

How long does it take for escitalopram to work?

It works gradually, not overnight. You may notice some early changes — sleep, appetite or energy — within the first 1 to 2 weeks, but the full effect on mood or anxiety usually takes about 4 to 6 weeks (sometimes up to 8). That delay is normal and is why prescribers ask you not to judge it too soon or stop early; give it time and stay in touch about side effects, and never stop abruptly.

What should I avoid while taking escitalopram?

Alcohol: the FDA label says to avoid alcohol — see the alcohol section above for what it actually says. Other medicines: we hold source-cited interaction answers for Can you drink alcohol while taking Lexapro (escitalopram)?. This is what the FDA label and our cited sources say — it is not a complete list. Your pharmacist can check your own combination.

What are the common side effects of Lexapro (escitalopram)?

The most common, usually-mild side effects of Lexapro (escitalopram) are nausea, headache, trouble sleeping (insomnia) or drowsiness, dizziness, increased sweating, and sexual side effects such as lowered sex drive, delayed orgasm, or difficulty with ejaculation. Appetite and weight changes can also occur. The NHS notes that "most side effects should ease after a couple of weeks as your body gets used to the medicine, but some can last longer." If a common side effect is severe or does not go away, tell your prescriber rather than stopping on your own. This is not a complete list.

What are the serious side effects of Lexapro (escitalopram) — when should I call a doctor or go to the ER?

Get emergency help for a few specific red flags. Serotonin syndrome is a medical emergency — MedlinePlus lists "fever, sweating, confusion, fast or irregular heartbeat, severe muscle stiffness" (plus agitation, hallucinations, or twitching); it is more likely if Lexapro is combined with other serotonin drugs. Escitalopram can also affect heart rhythm: the NHS describes a rare but life-threatening problem causing "a fast, irregular heartbeat, light-headedness and fainting" (this QT-related risk is why the dose is capped, typically at 20 mg). Also call urgently for a serious allergic reaction (rash, hives, blisters, fever, joint pain, trouble breathing or swallowing), unusual bleeding or bruising, seizures, or hallucinations. This is not a complete list — when in doubt, seek care.

Does Lexapro (escitalopram) carry a boxed warning about suicidal thoughts?

Yes. Escitalopram carries the FDA boxed warning shared by all antidepressants. As MedlinePlus states, medications such as escitalopram "may increase the risk of suicidal thoughts and actions," and "this increase was found in children, teenagers, and young adults (less than 24 years of age)." The warning is most relevant when first starting the drug or after a dose change. Patients, families, and caregivers should watch for and immediately report "new or worsening depression" or "thinking about harming or killing yourself, or planning or trying to do so." This does not mean the drug causes suicide in most people — it means close monitoring is essential early on, especially in anyone under 24.

When do Lexapro (escitalopram) side effects start and how long do they last?

Physical side effects like nausea, headache, and sleep changes usually appear within the first days to weeks of starting Lexapro (escitalopram) or after a dose increase. Per the NHS, "most side effects should ease after a couple of weeks as your body gets used to the medicine, but some can last longer." Sexual side effects and weight changes are the ones most likely to persist for as long as you take the drug. Note that the mood benefit is on a different clock — antidepressant effect typically builds over several weeks, so early side effects often come before you feel better. If side effects are still troubling after a few weeks, talk to your prescriber about timing, dose, or alternatives.

Can I just stop taking Lexapro (escitalopram) if I feel side effects?

No — do not stop Lexapro (escitalopram) abruptly on your own. MedlinePlus warns that if you suddenly stop, "you may experience withdrawal symptoms such as mood changes, irritability, agitation, nausea, dizziness, burning, numbness, or tingling in the hands or feet, anxiety, confusion, headache, sweating, shaking." This is called antidepressant discontinuation syndrome. If you want to come off escitalopram, your prescriber will lower the dose gradually (a taper) to reduce these effects. Stopping or lowering the dose is a decision to make with your doctor, not alone — including when a side effect is bothering you.

Cite this page
APA
pharmaranks. (2026, July 24). Escitalopram: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/escitalopram
MLA
“Escitalopram: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/escitalopram.

We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.

Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.

Read the full FDA label for escitalopram on DailyMed (NIH) ↗ — including its boxed warning in full.