Medical expert of the article
New publications
Preparations
Anti-anxiety pills
Last updated: 29.03.2026
All iLive content is medically reviewed or fact checked to ensure as much factual accuracy as possible.
We have strict sourcing guidelines and only link to reputable media sites, academic research institutions and, whenever possible, medically peer reviewed studies. Note that the numbers in parentheses ([1], [2], etc.) are clickable links to these studies.
If you feel that any of our content is inaccurate, out-of-date, or otherwise questionable, please select it and press Ctrl + Enter.
Anxiety disorders include generalized anxiety disorder, panic disorder, social anxiety, and specific phobias. Psychological therapy, particularly cognitive behavioral therapy, remains the primary strategy, while medications are used when symptoms are severe, interfere with daily life, relapse, comorbid depression, sleep disturbances, or access to psychotherapy is limited. Medications reduce the physical and emotional manifestations of anxiety, improve performance, and create a window for developing self-care skills. [1]
The choice of medication depends on the type of disorder, previous treatment experience, adverse reactions, comorbidities, pregnancy plans, risk of addiction, and interactions. Adults typically begin with medications that affect the serotonergic system. Treatment success is assessed after 4-6 weeks, and if there is a response, treatment is continued for another 6-12 months to reduce the risk of relapse. [2]
It's important to understand the role of benzodiazepines: they are not a primary therapy due to addiction, cognitive effects, and the risk of concomitant use with opioids and alcohol. They can be used briefly as a bridge for severe symptoms while simultaneously starting the main medication. The decision to prescribe and discontinue them is made by a physician. [3]
Main classes of drugs and their place
Selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs) are the first-line treatment for most anxiety disorders. They reduce baseline anxiety, panic attacks, and social avoidance. The clinical effect develops gradually, and initial side effects are usually reversible. [4]
Buspirone is a nonbenzodiazepine anxiolytic for generalized anxiety, without the risk of addiction, with onset of effect in 2-4 weeks. It is suitable when sedative effects are undesirable. [5]
Hydroxyzine is an antihistamine anxiolytic for short-term symptomatic relief, but with dose restrictions due to the risk of QT prolongation. It is suitable for temporary support when physiological anxiety is severe and a rapid sedative effect is needed. [6]
Pregabalin is indicated in Europe for generalized anxiety and may be an option in cases of antidepressant intolerance, but requires caution in the elderly and when combined with central nervous system depressants due to the risk of respiratory depression. [7]
Benzodiazepines rapidly reduce anxiety and panic symptoms and are used briefly during severe exacerbations. Long-term use is not recommended due to addiction, memory impairment, and the risk of combination with opioids. [8]
Beta-blockers relieve "somatic" anxiety during performances and exams, but do not treat the underlying anxious thoughts. They are used as an on-demand medication before a stressful situation. [9]
Table 1. Roles of classes in anxiety disorders
| Class | Role | Pros | Cons |
|---|---|---|---|
| Selective serotonin reuptake inhibitors | First line treatment for most anxiety disorders | Long-term remission, relapse prevention | It takes 4-6 weeks for the effect to take effect, gastrointestinal and sexual adverse reactions |
| Serotonin and norepinephrine reuptake inhibitors | First line for generalized anxiety, social anxiety, panic | Effective for anxiety and tension pain | Tachycardia, sweating, withdrawal syndrome |
| Buspirone | Option for generalized anxiety | No addiction, minimal sedation | The effect develops gradually |
| Hydroxyzine | Short-term symptomatic relief | Rapid sedative effect | Sedation, dose limitation due to QT |
| Pregabalin | Alternative for generalized anxiety | Rapid effect in some patients | Risk of respiratory depression in vulnerable groups |
| Benzodiazepines | Brief bridge for severe symptoms | Rapid anxiety relief | Addiction, cognitive effects, and risk with opioids |
| Beta blockers | Situational anxiety and performances | Reduces tremor and tachycardia | Does not affect "mental" anxiety |
Select by type of anxiety disorder
Generalized anxiety. First-line treatments include selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs). Pregabalin can be used if first-line treatment is intolerable or ineffective. Buspirone is added in cases of partial response or as monotherapy for mild to moderate severity. Benzodiazepines remain an option for short-term relief, but are not recommended for long-term use. [10]
Panic disorder. First-line treatment includes serotonin and serotonin-norepinephrine antidepressants. Initially, sensitive patients may experience a temporary increase in anxiety, so titrate slowly, sometimes briefly adding a benzodiazepine before discontinuing it. [11]
Social anxiety. First-line treatment: serotonin and serotonin-norepinephrine antidepressants. For occasional presentations, a beta-blocker may be appropriate. Antipsychotics are not routinely recommended. [12]
Specific phobias. Pharmacotherapy is limited to a supportive role in exposure therapy and is usually not needed on a permanent basis. [13]
Table 2. Recommended approaches by nosology
| Disorder | First line | Alternatives | What to avoid routinely |
|---|---|---|---|
| Generalized anxiety | Selective serotonin reuptake inhibitors, serotonin and norepinephrine reuptake inhibitors | Pregabalin, buspirone, hydroxyzine for short | Long-term courses of benzodiazepines |
| Panic disorder | Selective serotonin reuptake inhibitors, serotonin and norepinephrine reuptake inhibitors | Brief bridge with benzodiazepine | Long-term benzodiazepine monotherapy |
| Social anxiety | Selective serotonin reuptake inhibitors, serotonin and norepinephrine reuptake inhibitors | Beta blocker on demand for performance | Off-label antipsychotics |
| Specific phobias | Psychotherapy | Symptomatic remedies in brief | Constant patterns without psychotherapy |
Dosage and titration: how to start and what to aim for
The initial treatment is always "low and slow," with a reassessment after 2-4 weeks and a performance checkpoint at 4-6 weeks. Below are guidelines for adults. Final decisions depend on the diagnosis and tolerability.
Table 3. Antidepressants for anxiety disorders
| Preparation | Starting dose | Usual maintenance dose range | Notes on Titration |
|---|---|---|---|
| Sertraline | 25-50 mg per day | 100-200 mg per day | Increase by 25-50 mg weekly as tolerated |
| Escitalopram | 10 mg per day | 10-20 mg per day | For vulnerable patients, start with 5 mg per day. |
| Venlafaxine extended-release | 37.5-75 mg per day | 75-225 mg per day | Increase in increments of 37.5-75 mg every few days as tolerated. |
| Duloxetine | 30-60 mg per day | 60-120 mg per day | For the elderly, start with 30 mg per day for 2 weeks. |
Table 4. Non-benzodiazepine anxiolytics and pregabalin
| Preparation | Start | Range | Security comments |
|---|---|---|---|
| Buspirone | 10-15 mg per day in 2-3 doses | 20-60 mg per day | Effect in 2-4 weeks, no addiction |
| Hydroxyzine | 25-50 mg per dose, short-term | Maximum 100 mg per day in adults | Dose limitations and contraindications for risk of QT prolongation |
| Pregabalin | 75 mg twice daily | 150-600 mg per day in 2-3 doses | Risk of respiratory depression in the elderly and in combination with central nervous system depressants |
Table 5. Short-term funds on demand
| Situation | Preparation | Approximate diagram |
|---|---|---|
| Speech, exam, interview | Propranolol | 10-40 mg 30-60 minutes before the event, after assessing the pulse and blood pressure |
| Severe exacerbation before starting basic therapy | Benzodiazepine short course | Minimum effective dose for 3-14 days with a withdrawal plan |
Important Safety: What to Look Out For
Suicidal thoughts may occur when starting antidepressant therapy. The risk is slightly increased in children, adolescents, and people under 25 years of age during the first weeks and when the dose is changed. Frequent contact with a doctor, informing family members about warning signs, and developing an action plan if your condition worsens are essential. [14]
Benzodiazepines and opioids. Concomitant use increases the risk of severe drowsiness, respiratory depression, and death. The physician avoids these combinations and advises against the simultaneous use of alcohol and other sedatives. [15]
Hydroxyzine and the heart. Due to the risk of QT prolongation, restrictions have been established: no more than 100 mg per day for adults, avoid in those with an already prolonged QT interval, and do not prescribe to the elderly. Risk factors and interactions, such as with drugs that prolong the QT, should be assessed before use. [16]
Pregabalin and Respiration. Cases of severe respiratory depression have been reported, especially in the elderly, in patients with chronic lung disease, and when used concomitantly with sedatives. Careful titration and patient education on danger signs are necessary. [17]
Elderly. Anticholinergic drugs increase the risk of confusion and falls, so hydroxyzine is limited in this group, and the doses of almost all drugs are selected conservatively. [18]
Table 6. Common risks and monitoring
| Risk | What does a doctor do? | What is important to the patient |
|---|---|---|
| Increased anxiety in the first weeks on antidepressants | Slow titration, control at 2-4 weeks | Be patient, don't give up prematurely |
| Drowsiness and coordination | Appointment time selection, driving warning | Avoid alcohol and hazardous work |
| QT prolongation with hydroxyzine | Risk factor assessment, dose limitation | Report palpitations, fainting |
| Respiratory risks with pregabalin | Low start, taking into account pulmonary pathology | Report shortness of breath and apnea immediately. |
| Withdrawal syndrome | Planned phased cancellation | Do not stop abruptly without a doctor's advice. |
Drug interactions: what most often interferes
Serotonin-lowering antidepressants interact with monoamine oxidase inhibitors and certain antibiotics and antifungals, increasing the risk of serotonin syndrome and QT prolongation. Ibuprofen and anticoagulants increase the risk of bleeding. Benzodiazepines potentiate the sedative effects of alcohol, opioids, some antihistamines, and hypnotics. Pregabalin can cause additive central nervous system depression with other sedatives. Always inform your doctor about supplements and herbal remedies. [19]
Table 7. Clinically significant interactions
| Combination | Problem | Tactics |
|---|---|---|
| Sertraline plus nonsteroidal anti-inflammatory drugs | Bleeding | Minimize, add gastroprotection if necessary |
| Escitalopram plus QT-prolonging drugs | Arrhythmias | Avoid, monitor electrocardiogram |
| Benzodiazepines plus opioids | Respiratory depression, death | Avoid, consider alternatives |
| Pregabalin plus sedatives | Total sedation and respiratory depression | Dose reduction, observation, patient education |
How long to treat and how to stop correctly
If a sustained response is achieved, maintenance therapy is continued for at least 6-12 months, followed by a gradual dose reduction. Discontinuation too early increases the risk of relapse. Tapering is performed slowly, especially in sensitive patients and when taking venlafaxine and paroxetine, where withdrawal syndrome is more common. [20]
Benzodiazepines should not be discontinued abruptly. Withdrawal follows a coordinated plan, typically tapering in weekly increments with monitoring for insomnia, anxiety, irritability, and somatic symptoms. If difficulties persist, a slower withdrawal regimen is used. [21]
Table 8. Examples of dose reduction rates
| Class | The basic idea of cancellation | Example of tempo |
|---|---|---|
| Serotonin and serotonin-norepinephrine antidepressants | Minus 10-25% of the current dose every 2-4 weeks | Slower with long-term use and poor tolerance |
| Benzodiazepines | Minus 10% from week to week, then slower | In case of breakdowns, they return to the previous stage and stabilize |
| Pregabalin | Gradually over 1-2 weeks | In older people, it is slower and under control of symptoms. |
Special situations
Pregnancy and breastfeeding. Decisions are individualized. Some antidepressants have a better safety profile; for example, sertraline is often considered an option. Benzodiazepines are associated with a risk of neonatal sedation and withdrawal syndrome, and hydroxyzine is not recommended in early pregnancy. All decisions are made by the obstetrician and psychiatrist in consultation with the patient. [22]
Elderly. Minimize anticholinergic and sedative effects, use hydroxyzine cautiously, prefer low starting doses and slow titration with monitoring for risk of falls and cognitive effects. [23]
Associated addictions. Benzodiazepines are excluded whenever possible. Preference is given to antidepressants, psychotherapy, and, if necessary, specialized addiction treatment programs. [24]
Table 9. Selection of a drug for a clinical scenario
| Scenario | What to consider | What to avoid |
|---|---|---|
| Anxiety plus chronic pain | Serotonin-norepinephrine reuptake inhibitors, duloxetine | Long-acting benzodiazepines |
| Severe somatic anxiety during performances | Propranolol on demand | Constant schemes without need |
| Risk of substance abuse | Serotonin and serotonin-norepinephrine antidepressants, buspirone | Benzodiazepines |
| Old age | Sertraline, low-dose escitalopram | Hydroxyzine, polypharmacy |
Answers to frequently asked questions
When to expect a noticeable effect from the first line. Initial changes are possible by 2-4 weeks; a sustained effect is assessed by 4-6 weeks, after which the dosage is adjusted. Ineffectiveness at an appropriate dose and duration requires a change in strategy. [25]
Are tests and an electrocardiogram necessary? As indicated. For example, when planning hydroxyzine in patients with risk factors for arrhythmia, an electrocardiogram and interaction review are helpful. [26]
Are antidepressants dangerous because of the warning about suicidality? The risk is small and concentrated in the first few weeks in patients under 25, so monitoring and informing family members is key, rather than withholding treatment. For adults, the benefits generally outweigh the risks. [27]
Is there a place for antipsychotics? They are not routinely used for generalized anxiety in primary care due to the unfavorable risk profile, despite studies on quetiapine. Decisions at this level are made by a psychiatrist in cases of resistant disease. [28]
Table 10. Brief algorithms for starting therapy
| Initial situation | Step 1 | Step 2 after 4-6 weeks | Further |
|---|---|---|---|
| Newly diagnosed generalized anxiety disorder, moderate symptoms | Sertraline 25-50 mg per day or escitalopram 10 mg per day | Increase the dose if there is a partial response | Maintain for 6-12 months, then scheduled cancellation |
| First line intolerance | Duloxetine or extended-release venlafaxine | Rate the answer | Consider pregabalin when antidepressants are contraindicated. |
| Performance in 1 week, normal pulse and pressure | Propranolol on demand | Testing the dose at a trial performance | Return to the basic regimen without daily intake |
| Severe exacerbation at the start | Brief bridge with benzodiazepine | Reduction and Cancellation Plan | Just the basic outline below |
Quick safety reminder
- Do not combine benzodiazepines with opioids and alcohol. [29]
- For hydroxyzine, adhere to a maximum of 100 mg daily in adults and avoid if there is a risk of prolonging the QT interval. [30]
- When using pregabalin, beware of drowsiness and difficulty breathing, especially in the elderly and when combined with sedatives. [31]
- Do not stop antidepressants and pregabalin abruptly; discontinue only as planned. [32]

