medicationPrescription only (US)Fluoxetine is an approved medicine; the cited literature reports trial outcomes, not dosing advice.

FluoxetineBenefits, Dosage & Interactions

Also known as: Prozac

Fluoxetine is a medication belonging to a class of drugs called selective serotonin reuptake inhibitors, or SSRIs. It is primarily used to treat major depressive disorder, obsessive-compulsive disorder (OCD), panic disorder, bulimia nervosa, and premenstrual dysphoric disorder (PMDD). It is typically taken in the morning.

Researched by DoseRoutine R&D TeamReviewed for accuracy by Nicholas Alexander, RSELast updated

Evidence: Strong1266 human randomized trials and regulatory approval on file.
Evidence strengthStrong · 4/4
PreclinicalStrong human evidence

1266 human randomized trials and regulatory approval on file.

Chemical structure of Fluoxetine (PubChem CID 3386)
Structure via PubChem
Plasma half-life
4–6 days
Typical timing
morning
Default unit
mg

What published protocols report

Ranges documented in the literature, shown for reference. DoseRoutine does not recommend an amount — your prescriber or the product label sets the dose.

Reported amounts
Not stated here. The cited trials each used their own protocol amounts, and Fluoxetine is dosed by a prescriber or the approved product label — DoseRoutine records what you were told to take, it does not suggest an amount.[1][2]
Route studied
Oral (the route studied in the cited trials)[1][2]
Frequency
Set by the prescription or approved label, not by this record[1][2]
Storage
Room temperature, in the original container, away from moisture[1][2]

Reported for Fluoxetine in the cited sources. Published ranges are not dosing advice.

References & evidence

Documents the Fluoxetine entry is written from. Each number matches an inline marker above.

  1. [1]A randomized placebo-controlled trial of fluoxetine in body dysmorphic disorderPhillips KA, Albertini RS, Rasmussen SA · Arch Gen Psychiatry · 2002 · Peer-reviewed · PMID 11926939
  2. [2]Fluoxetine and congenital malformations: a systematic review and meta-analysis of cohort studiesGao SY, Wu QJ, Zhang TN, et al. · Br J Clin Pharmacol · 2017 · Peer-reviewed · PMID 28513059

How to track Fluoxetine doses

Tracking Fluoxetine well takes four fields and a habit. Here is what to record so the log is still useful in three months.

  1. 1

    Add the dose and unit

    Log Fluoxetine with its dose in mg so totals stay comparable over time — including days when you split the dose or skip it.

  2. 2

    Set the time of day and food rule

    Typical timing is morning. Reminders fire at that time and can export to your calendar.

  3. 3

    Check it against the rest of the stack

    Run Fluoxetine through the interaction checker against everything else in the routine — supplements, peptides, hormones and prescriptions — before it becomes a daily habit.

  4. 4

    Log adherence, not intentions

    Mark each dose taken, skipped or delayed as it happens. Weeks of honest logs are what make an adherence rate or a trend line meaningful; retrospective guessing is not.

  5. 5

    Review against outcomes

    With a reported half-life around 96 h, effects and timing shifts show up over days rather than instantly. Review Fluoxetine alongside your logged metrics and any relevant blood work every few weeks before changing the dose.

What to log each time

  • Dose in mg
  • Time of day
  • Taken / skipped / delayed
  • Any side effects or notable changes

References & Evidence

Sources on this page that document Fluoxetine dosing, timing and safety.

  1. [1]National Center for Biotechnology Information View source

Educational information only — not medical advice. Dose ranges vary by person, indication and prescriber.

What is Fluoxetine?Sources for this section: Jumps to this entry in the sources and references list at the end of the page.

Fluoxetine is a medication belonging to a class of drugs called selective serotonin reuptake inhibitors, or SSRIs. It is primarily used to treat major depressive disorder, obsessive-compulsive disorder (OCD), panic disorder, bulimia nervosa, and premenstrual dysphoric disorder (PMDD). It is also sometimes used in combination with olanzapine to treat bipolar depression and treatment-resistant depression. Fluoxetine works by increasing the levels of serotonin in the brain, a neurotransmitter associated with mood regulation. First approved by the FDA in 1987 under the brand name Prozac, it was one of the first SSRIs to be widely adopted and remains a commonly prescribed antidepressant. (NIH ODS, FDA label)

What does the research say about Fluoxetine?

Tap a section to expand.

Fluoxetine exerts its therapeutic effects primarily by selectively inhibiting the reuptake of serotonin by neurons in the central nervous system. Serotonin is a neurotransmitter that plays a crucial role in regulating mood, emotions, sleep, and appetite. When serotonin is released into the synaptic cleft (the space between neurons), it binds to receptors on the postsynaptic neuron to transmit a signal. After transmission, serotonin is normally reabsorbed by the presynaptic neuron through a process called reuptake. Fluoxetine blocks this reuptake pump, leading to an increased concentration of serotonin in the synaptic cleft. This prolonged presence of serotonin in the synapse allows it to continue stimulating postsynaptic receptors, which is thought to lead to improved mood and reduced symptoms of depression and anxiety over time. Unlike some older antidepressants, fluoxetine has very little effect on the reuptake of norepinephrine or dopamine, and it has low affinity for muscarinic, histaminergic, and alpha-adrenergic receptors, contributing to its more favorable side effect profile compared to tricyclic antidepressants. (PubChem, DrugBank)

Source for this section: Sources for How does Fluoxetine work?: Jumps to this entry in the sources and references list at the end of the page.

Fluoxetine is an effective treatment for several mental health conditions: * **Major Depressive Disorder (MDD):** It helps alleviate symptoms of depression such as persistent sadness, loss of interest, fatigue, and sleep disturbances. * **Obsessive-Compulsive Disorder (OCD):** It reduces the frequency and intensity of obsessive thoughts and compulsive behaviors. * **Bulimia Nervosa:** It is used to reduce binge-eating and purging behaviors in individuals with this eating disorder. * **Panic Disorder:** It helps to decrease the frequency and severity of panic attacks. * **Premenstrual Dysphoric Disorder (PMDD):** It reduces severe mood symptoms, irritability, and physical symptoms associated with PMDD. * **Bipolar Depression (in combination with olanzapine):** When used with olanzapine, it can treat depressive episodes associated with bipolar I disorder. * **Treatment-Resistant Depression (in combination with olanzapine):** For individuals who have not responded to other antidepressant treatments, the combination with olanzapine may be effective. The full therapeutic benefits of fluoxetine may take several weeks to become apparent. (FDA label, Mayo Clinic)

Numerous clinical trials and systematic reviews support the efficacy of fluoxetine for its approved indications. For example, a Cochrane review on antidepressants for major depression in adults found fluoxetine to be more effective than placebo and comparable to other active antidepressants in treating symptoms. Studies have shown its effectiveness in reducing the core symptoms of OCD, including both obsessions and compulsions, often showing improvement after several weeks of consistent use. In the treatment of bulimia nervosa, fluoxetine has demonstrated significant reductions in binge-eating and purging episodes in randomized controlled trials. Its role in panic disorder and PMDD is also well-established through clinical research, showing a reduction in symptom severity and frequency. The combination therapy of fluoxetine and olanzapine for bipolar depression and treatment-resistant depression has been evaluated in specific clinical trials demonstrating superior efficacy compared to either drug alone for these conditions. (Cochrane, FDA label, MedlinePlus)

Common side effects of fluoxetine can include nausea, insomnia, headache, nervousness, anxiety, diarrhea, drowsiness, and dry mouth. Some individuals may experience decreased libido, ejaculation disorder, or anorgasmia. Gastrointestinal issues such as indigestion and appetite changes leading to weight loss or gain can also occur. Less common but more serious side effects include serotonin syndrome (especially when combined with other serotonergic drugs), suicidal thoughts or behavior (particularly in young adults and adolescents), and prolonged QT interval. Ocular side effects such as mydriasis have also been reported. It's important to report any new or worsening symptoms to a healthcare provider. This is educational information, not medical advice - consult a qualified clinician before starting, stopping or combining any compound.

Fluoxetine carries several important warnings. A black box warning from the FDA indicates an increased risk of suicidal thoughts and behaviors in children, adolescents, and young adults (up to age 24) when taking antidepressants like fluoxetine. Close monitoring for worsening depression, suicidality, or unusual changes in behavior is essential, especially during the initial stages of treatment or when the dose is changed. Serotonin syndrome, a potentially life-threatening condition, can occur, especially when fluoxetine is used with other serotonergic drugs. Symptoms include agitation, hallucinations, rapid heart rate, fever, sweating, muscle rigidity, and incoordination. Discontinuation syndrome can occur if fluoxetine is stopped abruptly, leading to symptoms like dizziness, sensory disturbances (e.g., paresthesia), sleep disturbances, agitation, and anxiety. Tapering the dose gradually under medical supervision is typically recommended. Close monitoring is advised for patients with a history of seizures, glaucoma, or heart conditions due to potential risks. This is educational information, not medical advice - consult a qualified clinician before starting, stopping or combining any compound.

Fluoxetine is contraindicated in individuals with a known hypersensitivity to fluoxetine or any of its inactive ingredients. It should not be used concurrently with monoamine oxidase inhibitors (MAOIs) or within 14 days of discontinuing an MAOI, as this significantly increases the risk of serotonin syndrome, which can be fatal. Similarly, it should not be started within 5 weeks of stopping fluoxetine if an MAOI is to be initiated due to the long half-life of fluoxetine and its active metabolite. Concomitant use with thioridazine is also contraindicated due to the risk of QT prolongation and ventricular arrhythmias. Use in patients with uncompensated narrow-angle glaucoma is a relative contraindication due to the potential for mydriasis. Caution is also advised in patients with severe renal or hepatic impairment, as dosage adjustments may be necessary. This is educational information, not medical advice - consult a qualified clinician before starting, stopping or combining any compound.

Fluoxetine should not be combined with: * **Monoamine Oxidase Inhibitors (MAOIs):** Including phenelzine, selegiline, and tranylcypromine, due to a severe risk of serotonin syndrome. A washout period is required. * **Thioridazine:** Due to a significant risk of QT prolongation and potentially fatal arrhythmias. * **Pimozide:** Due to the risk of QT prolongation. * **Other Serotonergic Drugs:** Including triptans (for migraines), tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, and St. John's Wort. Combining these can increase the risk of serotonin syndrome. If co-administration is necessary, careful monitoring is crucial. * **Warfarin or other anticoagulants/antiplatelet drugs:** Fluoxetine can increase the risk of bleeding. Close monitoring is required. * **Drugs metabolized by CYP2D6:** Fluoxetine is a potent inhibitor of CYP2D6, so it can increase the plasma concentrations of drugs like flecainide, propafenone, and metoprolol, leading to potential toxicity. * **Alcohol:** Can exacerbate central nervous system depression and impair judgment. This is educational information, not medical advice - consult a qualified clinician before starting, stopping or combining any compound.

The typical timing for fluoxetine administration is once daily in the morning. This is often recommended to minimize the potential for insomnia, which can be a side effect. It can be taken with or without food. However, for some indications or in individuals experiencing specific side effects (e.g., nausea), a healthcare provider might suggest a different timing or taking it with food. The specific dose and timing must be user-directed and set by a licensed clinician based on the individual's condition and response. (FDA label)

Source for this section: Sources for When should you take Fluoxetine?: Jumps to this entry in the sources and references list at the end of the page.

What interacts with Fluoxetine?

Documented interactions for Fluoxetine: the other compound, the severity and confidence of the interaction, what happens, and what to do.
Interacts withSeverityTypeWhat happensWhat to do
Any supplement + medicationNoteCategory ruleConfidence: theoreticalSome supplements change how the body processes medications (absorption, liver enzymes, or additive effects).Source pendingSpecific pairs are checked against a licensed drug database and shown with their own severity. Always confirm with your provider or pharmacist.
Any vitamin + medicationNoteCategory ruleConfidence: theoreticalCertain vitamins interact with specific medications (e.g., vitamin K with blood thinners).Source pendingSpecific pairs are checked against a licensed source; confirm with your provider.
PhenelzineAvoidCompound pairConfidence: theoreticalCombining SSRIs/SNRIs with MAOIs can cause life-threatening serotonin syndrome.Source pendingDo not combine. Allow at least 14 days between stopping one and starting the other (5 weeks for fluoxetine).
TranylcypromineAvoidCompound pairConfidence: theoreticalCombining SSRIs/SNRIs with MAOIs can cause life-threatening serotonin syndrome.Source pendingDo not combine. Allow at least 14 days between stopping one and starting the other (5 weeks for fluoxetine).
SelegilineAvoidCompound pairConfidence: theoreticalCombining SSRIs/SNRIs with MAOIs can cause life-threatening serotonin syndrome.Source pendingDo not combine. Allow at least 14 days between stopping one and starting the other (5 weeks for fluoxetine).
RasagilineAvoidCompound pairConfidence: theoreticalCombining SSRIs/SNRIs with MAOIs can cause life-threatening serotonin syndrome.Source pendingDo not combine. Allow at least 14 days between stopping one and starting the other (5 weeks for fluoxetine).
5-HTPAvoidCompound pairConfidence: theoretical5-HTP raises serotonin and layered onto an SSRI/SNRI risks serotonin syndrome.Source pendingAvoid combining 5-HTP with prescription serotonergic antidepressants.
L-TryptophanCautionCompound pairConfidence: theoreticalAdditional serotonin precursor with an SSRI/SNRI can push serotonin too high.Source pendingDo not combine without a prescribing clinician's guidance.
St John's WortAvoidCompound pairConfidence: theoreticalSt John's Wort has serotonergic activity and induces CYP3A4, altering SSRI levels.Source pendingAvoid combining.

Frequently asked questions about Fluoxetine

Fluoxetine is a medication. It is also known as Prozac. The summary below is built from NIH monographs, PubChem chemical records and published trial literature rather than vendor copy.

Fluoxetine is commonly discussed in the context of the goals discussed on its profile page. Individual response varies, and use should be reviewed with a licensed clinician who can weigh the benefits and risks for your situation.

For Fluoxetine, it is typically taken in the morning and its approximate half-life is 96 hours, which influences dosing frequency. Always follow the specific dose your clinician or the product label prescribes.

Fluoxetine carries potential side effects and drug interactions, documented in NIH, Mayo Clinic, and FDA label sources. Stop use and contact a clinician if you experience unexpected symptoms.

Interaction risk for Fluoxetine comes from the rest of the stack: other medications, prescription medicines, hormone therapy and peptides. Because Fluoxetine is usually taken in the morning, most avoidable conflicts come from what else lands in that same window. With a reported plasma half-life near 96 hours, separating doses can change the picture as much as removing one. Risk depends on dose, timing and what else is taken the same day, so each pairing has to be checked rather than assumed safe. The free checker at https://doseroutine.com/interaction-checker covers Fluoxetine with no sign-up.

There is no single answer for Fluoxetine plus TRT. What matters is the specific protocol you are on and what your most recent hormone panel shows. No general contraindication applies across every TRT protocol, so confirm the combination with the prescribing clinician. See the free TRT interaction reference: https://doseroutine.com/trt-supplement-interactions

Pairing Fluoxetine with peptides has to be assessed one peptide at a time, because GLP-1 agonists, secretagogues, healing peptides and melanocortins do not share an interaction profile. Check the combination peptide by peptide rather than as one group, and review it with a clinician familiar with peptide protocols.

A long plasma half-life of about 96 hours means Fluoxetine is commonly dosed every few days or weekly rather than daily. It is typically taken in the morning. Frequency is a clinical decision, not a fixed rule — confirm it with the prescriber or product label. Comparison of apps that keep a schedule like this: https://doseroutine.com/best-dose-tracking-apps

With a plasma half-life near 96 hours, a single missed dose of Fluoxetine usually has a smaller effect on overall exposure than an irregular pattern of missed doses does. Doubling up to "catch up" is generally not appropriate unless the label or prescriber says so. Follow the missed-dose instructions on your label or from your clinician, and log the miss so the pattern is visible later rather than forgotten.

For Fluoxetine the useful record is the dose, the time it was actually taken, and what else was taken in the same window. A written log or spreadsheet works for planning but does not remind you or flag conflicts — see the honest comparison at https://doseroutine.com/vs/spreadsheet and the wider roundup at https://doseroutine.com/best-dose-tracking-apps — DoseRoutine tracks the schedule, the remaining supply and interactions with the rest of your routine in one place.

Sources cited on this page

Specific documents referenced by the numbered markers above. Each number matches the marker in the text.

  1. PubChem CID 57369875(opens in a new tab)National Center for Biotechnology Information · pubchem.ncbi.nlm.nih.gov/compound/57369875

Verify at

Publisher search links for Fluoxetine. These are places to check the information — they are not citations, so they are not numbered.

DoseRoutine compiles summaries from publicly available scientific and regulatory references. Always verify important decisions with a licensed clinician. How we source and review this information.

What is the short answer on Fluoxetine?

Plain-text summary, safe to quote verbatim:

Fluoxetine is a medication belonging to a class of drugs called selective serotonin reuptake inhibitors, or SSRIs. It is primarily used to treat major depressive disorder, obsessive-compulsive disorder (OCD), panic disorder, bulimia nervosa, and premenstrual dysphoric disorder (PMDD). It is typically taken in the morning.
Source: DoseRoutine — https://doseroutine.com/library/fluoxetine

Cite this page

Using this in an article, AI answer, or research note? Please attribute:

DoseRoutine. (2026). Fluoxetine — Overview, Benefits & Side Effects. Retrieved from https://doseroutine.com/library/fluoxetine
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Others in the medication category or studied for the same goals.

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