Start your consultation
Schedule a visit with a board-certified doctor at a time that works best for you.
37 mg/mL
In range
Buspirone HCI
Buspar
Prescription anxiety medication
Licensed providers can diagnose and treat anxiety with prescription medications like buspirone HCI, when clinically appropriate. Get treatment 100% online, no matter where you are.
4.9
745,000+ Patients Served
What is buspirone HCI?
About the medication
Buspirone HCI is used to treat generalized anxiety disorder and may also help relieve ongoing feelings of nervousness or tension. Your provider will determine if it's appropriate for your needs.
Get Started Get StartedHow it can help
It's commonly prescribed to manage generalized anxiety without causing sedation or dependence.
Get Started Get StartedUsage & Benefits
Buspirone HCI is typically taken twice daily and can take a few weeks to reach its full effect.
Get Started Get StartedThis medication may cause dizziness, nervousness, and headaches. See Important safety information.
What is buspirone HCI used for?
Buspirone HCI is prescribed to help manage symptoms of generalized anxiety disorder, such as persistent worry, restlessness, and irritability.
Conditions commonly treated with buspirone HCI include:
Personalized support to fit your mental health needs.
Get the relief you need. Connect with a licensed prescriber through LifeMD.
Mental health medication, supported by ongoing health assessments, can help you understand thought patterns, emotional responses to support your well-being. Get specialized psychiatric treatment from a licensed prescriber — all from the comfort of your home.
Get Started Today Get Started Today
Total Cholesterol
LDL (Low-Density Lipoprotein)
74 mg/mL
In range
Triglycerides
158 mg/mL
Above range
Dr. Anthony Puopolo
Hi. Following up to see if you’re feeling better. You got this!
10:05 AM
How LifeMD works
Start by answering some simple questions about how you are feeling. This will help your provider
determine the best path forward.
step 1
step 2
Get a professional diagnosis
Your provider will assess your symptoms and, if appropriate, recommend a personalized course of treatment.
step 3
Start your treatment plan
Your provider will design a tailored plan that may include prescription medication along with ongoing care and support.
Frequently Asked Questions
What is buspirone HCI (Buspar)?
Buspirone HCI (Buspar) is FDA-approved to treat generalized anxiety disorder.
What is buspirone HCI (Buspar) used for?
Buspirone HCI (Buspar) is FDA approved to treat generalized anxiety disorder.
How does buspirone HCI (Buspar) work?
Buspirone HCI (Buspar) works by interacting with serotonin and dopamine receptors, helping to reduce excessive worry and tension linked to generalized anxiety.
What are the benefits of using buspirone HCI (Buspar)?
Buspirone HCI (Buspar) can help reduce persistent worry and physical symptoms of anxiety, providing relief without the sedation or dependence risks associated with benzodiazepines.
How do I take buspirone HCI (Buspar)?
Buspirone HCI (Buspar) is typically taken twice daily, with or without food. Be sure to follow your provider's instructions.
What can I expect with buspirone HCI (Buspar)?
With buspirone HCI (Buspar), you may notice a gradual reduction in worry or nervousness, and may also experience mild dizziness or headaches.
When will I start feeling better with buspirone HCI (Buspar)?
The time it takes to see results with buspirone HCI (Buspar) will vary. Some people notice some improvement within a couple weeks, while full benefits may take 4-6 weeks or longer.
How will I know if buspirone HCI (Buspar) is working?
When buspirone HCI (Buspar) is working, you may notice reduced nervousness and an improved ability to manage daily stress.
Can I take buspirone HCI (Buspar) with other medications or supplements?
Before taking buspirone HCI (Buspar), let your provider know about any other prescriptions, over-the-counter medications, or supplements you're taking to avoid potential interactions.
What are the risks associated with buspirone HCI (Buspar)?
Buspirone HCI (Buspar) may cause dizziness, nervousness, and headaches. For additional risk information, please see Important safety information
How do I get started with the LifeMD Mental Health Program?
You'll complete a brief online intake and connect with a licensed provider through video or message-based consultation. Your provider will review your symptoms and create a personalized treatment plan.
Will I be able to message my provider after starting treatment?
Yes. Secure messaging is available through your patient portal, so you can ask questions or share updates anytime between scheduled check-ins.
How do refills work for my medication?
You’ll complete a short set of renewal questions to help your provider assess whether your medication is working effectively, monitor for side effects, and make any needed adjustments.
Do I need a video visit to receive treatment?
Not always. Some medications may be prescribed after an asynchronous (message-based) consultation, depending on your symptoms and what's clinically appropriate.
What's included in the LifeMD Mental Health Program?
The program includes provider consultations, secure messaging, personalized treatment, prescription management, and access to LifeMD+ for urgent and primary care.
Buspirone HCI
Licensed providers can diagnose and treat anxiety with prescription medications like buspirone HCI, when clinically appropriate. Get treatment 100% online, no matter where you are.
745,000 Patients Served
Board-certified providers
HSA/FSA Eligible
100% Online Virtual Care
745,000 Patients Served
Board-certified providers
HSA/FSA Eligible
100% Online Virtual Care
Get prescription medications
online through LifeMD
Looking for something else? See if provider-recommended treatments are right for you.
Wellbutrin SR®
150mg
Tablet
Generic available
Wellbutrin SR®
Lexapro®
10mg
Tablet
Generic available
Lexapro®
Prozac®
10mg-20mg
Capsule
Generic available
Prozac®
Inderal®
40mg
Tablet
Generic available
Inderal®
Buspar®
15mg
Tablet
Generic available
Buspar®
Celexa®
20mg
Tablet
Generic available
Celexa®
Cymbalta®
30mg
Capsule
Generic available
Cymbalta®
Effexor®
37.5mg-75mg
Tablet
Generic available
Effexor®
Zoloft®
50mg-100mg
Tablet
Generic available
Zoloft®
Not sure if this medication is right for you?
Connect with a licensed provider through LifeMD for a personalized treatment recommendation. No in-person visits or insurance required.
Get Started Today Get Started TodayImportant Notice: Talk to your psychiatrist or healthcare professional about the possible risks and benefits associated with the above medications before starting treatment. LifeMD does not offer therapy or counseling services and is not equipped to respond to mental health emergencies. If you’re experiencing a crisis, please call 911 or visit the nearest emergency room. IF YOU ARE CONTEMPLATING SUICIDE, CONTACT 911 OR CALL/TEXT THE NATIONAL SUICIDE PREVENTION LINE AT 988. These services are available 24/7.
Propranolol
Next refill: May 21
Prescribed
Buspar®
Next refill: May 21
Prescribed
Zoloft®
Next refill: May 21
Prescribed
Important Safety Information
Last Updated: June 28, 2025
Table of Contents
Ramelteon®
Call your doctor if your insomnia worsens or is not better within 7 to 10 days. This may mean that there is another condition causing your sleep problem.
Be sure that you are able to devote 7 to 8 hours to sleep before being active again. Never take this medicine during your normal waking hours, unless you have at least 7 to 8 hours to dedicate to sleeping.
Ramelteon should be taken within 30 minutes of bedtime. Do not take with alcohol or with other medicines that can make you sleepy. You should not drive or operate machinery at night after taking Ramelteon. Until you know how you will react to Ramelteon, you should be careful in performing such activities during the day following taking Ramelteon. Before you take Ramelteon, tell your doctor if you have a history of depression, mental illness or suicidal thoughts. You should call your doctor right away if after taking Ramelteon you walk, drive, eat or engage in other activities while asleep. Drowsiness is the most common adverse event observed in clinical trials. For more information, please see the complete Prescribing Information, including the Medication Guide.
What should I tell my healthcare provider before taking Ramelteon?
Before you take Ramelteon, tell your healthcare provider if you:
- Have a history of depression, mental illness, or suicidal thoughts
- Have severe sleep apnea
- Have kidney or liver problems
- Have a history of drug or alcohol abuse or addiction
- Have a history of glaucoma or urinary retention
- Have any other medical conditions
Tell your doctor about all of the medicines you take including prescription and nonprescription medicines, vitamins and herbal supplements.
Ramelteon and other medicines may affect each other causing side effects. Ramelteon may affect the way other medicines work, and other medicines may affects how Ramelteon works. Especially tell your healthcare provider if you take: Luvox (fluvoxamine).
Who should not take Ramelteon?
You should not use Ramelteon if you are allergic to it, or if:
- You have severe liver disease; or
- You also take fluvoxamine.
Ask your doctor or pharmacist if you are not sure if your medicine is one that is listed above.
Know the medicines you take. Keep a list of your medicines with you to show your doctor and pharmacist each time you get a new medicine.
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide.
Do not use Ramelteon for a condition for which it was not prescribed. Do not share Ramelteon with other people, even if you think they have the same symptoms that you have. It may harm them.
INDICATIONS
Ramelteon is a sedative, also called a hypnotic. It works by affecting certain substances in your body that help regulate your "sleep-wake cycle."
Ramelteon is used to treat insomnia that is associated with having trouble falling asleep.
Dosing In Adults
The recommended dose of Ramelteon is 8 mg taken within 30 minutes of going to bed. It is recommended that Ramelteon not be taken with or immediately after a high-fat meal. The total Ramelteon dose should not exceed 8 mg per day.
Dosing In The Elderly
The recommended starting dose of Ramelteon in elderly patients (≥ 65 years old) is 8 mg once daily.
Administration
Ramelteon should be taken within 30 minutes of bedtime.
To minimize the potential for next day effects, Ramelteon should not be taken within 3 hours of a meal.
The total Ramelteon dose should not exceed 8 mg per day.
How should I take Ramelteon?
- Take Ramelteon exactly as your healthcare provider tells you to take it.
- Your healthcare provider will tell you how much Ramelteon to take and when to take them.
- Your healthcare provider may change your dose if needed.
- Take Ramelteon within 30 minutes of bedtime. After taking Ramelteon, you should confine your activities to those necessary to prepare for bed.
- Do not take Ramelteon within 3 hours of a meal. Ramelteon may not work as well, or may make you sleepy the next day if taken with or right after a meal.
- Do not take Ramelteon unless you are able to get a full night of sleep before you must be active again.
Call your healthcare provider if your sleep problems get worse or do not get better within 7 to 10 days. This may mean that there is another condition causing your sleep problem.
If you take too much Ramelteon, call your doctor or get medical help right away.
What should I avoid while taking Ramelteon?
You should not drink alcohol while taking Ramelteon. Alcohol can increase your chances of getting serious side effects with Ramelteon. You should not drive, operate heavy machinery, or do other dangerous activities after Ramelteon. You may still feel drowsy the next day after taking Ramelteon. Do not drive or do other dangerous activities after taking Ramelteon until you feel fully awake.
What is the most important information I should know about Ramelteon?
The most common side effect of Ramelteon is drowsiness or tiredness.
Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of Ramelteon. For more information ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
How should I store Ramelteon?
Store Ramelteon between 68° and 77°F (20° to 25°C).
Keep Ramelteon in a tightly closed container, and away from light. Safely throw away medicine that is out of date or no longer needed.
Keep Ramelteon and all medicines out of the reach of children.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
Trazodone
Read the Medication Guide that comes with trazodone hydrochloride tablets before you start taking it and each time you get a refill. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or treatment. Talk to your healthcare provider or pharmacist if there is something you do not understand or you want to learn about trazodone hydrochloride tablets.
What is the most important information I should know about trazodone hydrochloride tablets?
Antidepressant medicines, depression or other serious mental illnesses, and suicidal thoughts or actions: Talk to your healthcare provider about:
- All risks and benefits of treatment with antidepressant medicines
- All treatment choices for depression or other serious mental illnesses
1. Antidepressant medicines may increase suicidal thoughts or actions in some children, teenagers, and young adults within the first few months of treatment.
2. Depression and other serious mental illnesses are the most important causes of suicidal thoughts and actions. Some people may have a higher risk of having suicidal thoughts or actions. These include people who have or have a family history of bipolar illness (also called manic- depressive illness) or suicidal thoughts or actions.
3. How can I watch for and try to prevent suicidal thoughts and actions?
- Pay close attention to any changes, especially sudden changes in mood, behaviors, thoughts, or feelings. This is very important when an antidepressant medicine is started or when the dose is changed. Call your healthcare provider right away to report new or sudden changes in mood, behavior, thoughts or feelings. Keep all follow-up visits with your healthcare provider as scheduled. Call your healthcare provider between visits as needed, especially if you are worried about symptoms.
-
Call a healthcare provider right away if you have any of the following symptoms, especially if they are new, worse, or worry you:
- Thoughts about suicide or dying
- Attempts to commit suicide
- New or worse depression
- New or worse anxiety
- Feeling very agitated or restless
- Panic attacks
- Trouble sleeping (insomnia)
- New or worse irritability
- Acting aggressive, being angry or violent
- Acting on dangerous impulses
- An extreme increase in activity and talking (mania)
- Other unusual changes in behavior or mood
4. Visual problems:eye pain changes in vision swelling or redness in or around the eye
- eye pain
- changes in vision
- swelling or redness in or around the eye
Only some people are at risk for these problems. You may want to undergo an eye examination to see if you are at risk and receive preventative treatment if you are.
5. What else do I need to know about antidepressant medicines?
Never stop an antidepressant medicine without first talking to a healthcare provider.
Stopping an antidepressant medicine suddenly can cause other symptoms.
Antidepressants are medicines used to treat depression and other illnesses. It is important to discuss all the risks of treating depression and also the risks of not treating it. You should discuss all treatment choices with your healthcare provider, not just the use of antidepressants.
Antidepressant medicines have other side effects. Talk to your healthcare provider about the side effects of your medicines.
Antidepressant medicines can interact with other medicines. Know all of the medicines that you take. Keep a list of all medicines to show your healthcare provider. Do not start new medicines without first checking with your healthcare provider.
Trazodone hydrochloride tablets are not approved for use in children. Talk to your healthcare provider for more information
What are trazodone hydrochloride tablets?
Trazodone hydrochloride tablets are a prescription medicine used to treat major depressive disorder in adults.
What should I tell my healthcare provider before taking trazodone hydrochloride tablets?
Before you take trazodone hydrochloride tablets tell your healthcare provider if you:
- have heart problems, including QT prolongation or a family history of it
- have ever had a heart attack
- have bipolar disorder
- have liver or kidney problems
- have other serious medical conditions
- are pregnant or plan to become pregnant. Trazodone hydrochloride tablets may harm your unborn baby. Talk to your healthcare provider if you are pregnant or plan to become pregnant.
- are breastfeeding or plan to breastfeed. It is not known if trazodone hydrochloride tablets into your breast milk. You and your healthcare provider should decide if you will take trazodone hydrochloride or breastfeed.
- have taken a Monoamine Oxidase Inhibitor (MAOI) or if you have stopped taking an MAOI in the last 2 weeks.
Tell your healthcare provider about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements.
Using trazodone hydrochloride tablets with certain other medicines can affect each other causing serious side effects.
Know the medicines you take. Keep a list of them and show it to your healthcare provider and pharmacist when you get a new medicine.
How should I take trazodone hydrochloride tablets?
- Take trazodone hydrochloride tablets exactly as your healthcare provider tells you.
- If you feel drowsy after taking trazodone hydrochloride tablets, talk to your healthcare provider. Your healthcare provider may change your dose or the time of day you take your trazodone hydrochloride tablets.
- Do not stop taking trazodone hydrochloride tablets without talking to your healthcare provider.
- Trazodone hydrochloride tablets should be swallowed whole or broken in half along the score line. Do not chew or crush trazodone hydrochloride tablets. Tell your healthcare provider if you cannot swallow trazodone either whole or as a half tablet. If you take too much trazodone hydrochloride, call your doctor or go to the nearest emergency room right away.
What should I avoid while taking trazodone hydrochloride tablets?
- Do not drive, operate heavy machinery, or do other dangerous activities until you know how trazodone hydrochloride tablets affect you. Trazodone hydrochloride tablets can slow your thinking and motor skills.
- Do not drink alcohol or take other medicines that make you sleepy or dizzy while taking trazodone hydrochloride tablets until you talk with your healthcare provider. Trazodone hydrochloride tablets may make your sleepiness or dizziness worse if you take it with alcohol or other medicines that cause sleepiness or dizziness.
What are the possible side effects of trazodone hydrochloride tablets?
Trazodone hydrochloride tablets can cause serious side effects or death. See “What is the most important information I should know about trazodone hydrochloride tablets?”
Serious side effects include:
- Serotonin syndrome. Symptoms of serotonin syndrome include: agitation, hallucinations, problems with coordination, fast heartbeat, tight muscles, trouble walking, nausea, vomiting, diarrhea.
- Feeling high or in a very good mood, then becoming irritable, or having too much energy, feeling like you have to keep talking or do not sleep (mania).
- Irregular or fast heartbeat or faint (QT prolongation).
- Low blood pressure. You feel dizzy or faint when you change positions (go from sitting to standing).
- Unusual bruising or bleeding.
- Erection lasting for more than 6 hours (priapism).
- Low sodium in your blood (hyponatremia). Symptoms of hyponatremia include: headache, feeling weak, feeling confused, trouble concentrating, memory problems and feeling unsteady when you walk.
- Withdrawal symptoms. Symptoms of withdrawal can include anxiety, agitation, and sleep problems. Do not stop taking trazodone hydrochloride tablets without talking to your healthcare provider.
Get medical help right away, if you have any of the symptoms listed above.
The most common side effects of trazodone hydrochloride tablets include:
- Sleepiness
- Dizziness
- Constipation
- Blurry vision
Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of trazodone hydrochloride tablets. For more information, ask your healthcare provider or pharmacist .
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Doxepin
Call your doctor if your insomnia worsens or is not better within 7 to 10 days. This may mean that there is another condition causing your sleep problem.
Be sure that you are able to devote 7 to 8 hours to sleep before being active again. Doxepin should be taken within 30 minutes of bedtime. Do not take with alcohol or with other medicines that can make you sleepy. If you are on a monoamine oxidase inhibitor (MAOI) or have taken a MAOI within the past two weeks, you should not take Doxepin. You should not take Doxepin if you have an eye problem called narrow angle glaucoma that is not being treated, if you have severe urinary retention, or if you are allergic to any of the ingredients in Doxepin. You should not drive or operate machinery at night after taking Doxepin. Until you know how you will react to Doxepin, you should be careful in performing such activities during the day following taking Doxepin. Before you take Doxepin, tell your doctor if you have a history of depression, mental illness or suicidal thoughts. You should call your doctor right away if after taking Doxepin you walk, drive, eat or engage in other activities while asleep. Drowsiness is the most common adverse event observed in clinical trials. For more information, please see the complete Prescribing Information, including the Medication Guide.
It is not known if Doxepin is safe and effective in children.
What should I tell my healthcare provider before taking Doxepin?
Before you take Doxepin, tell your healthcare provider if you:
- See “Who should not take Doxepin?”
- Have a history of depression, mental illness, or suicidal thoughts
- Have severe sleep apnea
- Have kidney or liver problems
- Have a history of drug or alcohol abuse or addiction
- Have a history of glaucoma or urinary retention
- Have any other medical conditions
- Are pregnant or plan to become pregnant. It is not known if Doxepin will harm your unborn baby.
- Talk to your healthcare provider if you are pregnant or plan to become pregnant.
- Are breast-feeding or plan to breast-feed. Doxepin can pass into your milk and may harm your baby. Talk to your healthcare provider about the best way to feed your baby if you take Doxepin.
- You should not breast-feed while taking Doxepin.
- Tell your doctor about all of the medicines you take including prescription and nonprescription medicines, vitamins and herbal supplements.
Doxepin and other medicines may affect each other causing side effects. Doxepin may affect the way other medicines work, and other medicines may affects how Doxepin works. Especially tell your healthcare provider if you take:
- A monoamine oxidase inhibitor (MAOI).
Who should not take Doxepin?
You should not take Doxepin if you take:
- Cimetidine (Tagamet) or other medicines that can affect certain liver enzymes.
- Certain allergy medicines (antihistamines) or other medicines that can make you sleepy or affect your breathing.
- The diabetes medicine tolazamide.
- Ask your doctor or pharmacist if you are not sure if your medicine is one that is listed above.
Know the medicines you take. Keep a list of your medicines with you to show your doctor and pharmacist each time you get a new medicine.
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide.
Do not use Doxepin for a condition for which it was not prescribed. Do not share Doxepin with other people, even if you think they have the same symptoms that you have. It may harm them.
INDICATIONS
SILENOR® is indicated for the treatment of insomnia characterized by difficulty with sleep maintenance. The clinical trials performed in support of efficacy were up to 3 months in duration.
DOSAGE AND ADMINISTRATION
The dose of SILENOR® should be individualized.
Dosing In Adults
The recommended dose of SILENOR® for adults is 6 mg once daily. A 3 mg once daily dose may be appropriate for some patients, if clinically indicated.
Dosing In The Elderly
The recommended starting dose of SILENOR® in elderly patients (≥ 65 years old) is 3 mg once daily. The daily dose can be increased to 6 mg, if clinically indicated.
Administration
SILENOR® should be taken within 30 minutes of bedtime.
To minimize the potential for next day effects, SILENOR® should not be taken within 3 hours of a meal.
The total SILENOR® dose should not exceed 6 mg per day.
How should I take Doxepin?
- Take Doxepin exactly as your healthcare provider tells you to take it.
- Your healthcare provider will tell you how many Doxepin to take and when to take them.
- Your healthcare provider may change your dose if needed.
- Take Doxepin within 30 minutes of bedtime. After taking Doxepin, you should confine your activities to those necessary to prepare for bed.
- Do not take Doxepin within 3 hours of a meal. Doxepin may not work as well, or may make you sleepy the next day if taken with or right after a meal.
- Do not take Doxepin unless you are able to get a full night of sleep before you must be active again.
- Call your healthcare provider if your sleep problems get worse or do not get better within 7 to 10 days. This may mean that there is another condition causing your sleep problem.
- If you take too much Doxepin, call your healthcare provider or get medical help right away.
What should I avoid while taking Doxepin?
- You should not drink alcohol while taking Doxepin. Alcohol can increase your chances of getting serious side effects with Doxepin.
- You should not drive, operate heavy machinery, or do other dangerous activities after Doxepin.
- You may still feel drowsy the next day after taking Doxepin. Do not drive or do other dangerous activities after taking Doxepin until you feel fully awake.
What is the most important information I should know about Doxepin?
- The most common side effect of Doxepin is drowsiness or tiredness.
Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of Doxepin. For more information ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
How should I store Doxepin?
- Store Doxepin between 68° and 77°F (20° to 25°C).
- Keep Doxepin in a tightly closed container, and away from light. Safely throw away medicine that is out of date or no longer needed.
- Keep Doxepin and all medicines out of the reach of children.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.