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This page shows a quick schedule for this drug. For the guided path — pre-taper risk quiz, formulation-aware steps, and email delivery — start from the main calculator.
Cymbalta (Duloxetine) Tapering Guide
Cymbalta (duloxetine) is an SNRI antidepressant used for depression, anxiety, and some pain conditions. It is widely prescribed as a first- or second-line option when an SNRI is chosen. This guide and medication taper calculator help you plan how to taper off Cymbalta safely with your prescriber.
Dosage
Duloxetine is supplied as enteric-coated bead capsules — typically 20 mg, 30 mg, and 60 mg (availability varies by region). Capsules must not be split, crushed, or chewed, or the enteric coating is lost. The smallest routine capsule strength is often 20 mg/day.
Steps below the lowest capsule usually need careful bead counting or a compounded liquid. Duloxetine has a high withdrawal risk and a short half-life, so gradual hyperbolic tapering is standard when you want to get off antidepressants.
Duloxetine taper schedule
Choose a common starting dose to preview the full hyperbolic schedule — free, no email required. This schedule has 37 steps and takes about 144 weeks in total; your prescriber may adjust the pace based on how you feel.
Starting dose
- Selected start
- 60 mg/day · 1× daily
- Taper speed
- Slow
- Region (formulations)
- US
- Tablet/liquid products used for dosing tips — not your location. Example uses US formulary; change region in the custom builder.
- Modelled occupancy at start
- ~76.2%
Swipe sideways to see every column.
Rows highlighted: larger occupancy drop than target — consider smaller steps or longer holds. If symptoms are intolerable, return to the previous dose and talk to your prescriber.
Steps that cannot be made from whole or half licensed tablets point to the liquid / compounding note below — ask your prescriber before changing how you take your dose.
Want a copy to keep?
The full duloxetine schedule is already shown below. Enter your email to also receive a PDF and HTML copy you can save or share with your prescriber — optional, and we never gate the schedule behind it.
It's not a substitute for medical advice. This calculator can help you visualise a tapering schedule but before making any changes to your medication plan it's necessary to consult a medical professional. Ask a psychiatrist — available after you request your protocol.
Dose vs occupancy
This taper is spread across 37 gradual steps. The curve below shows why the last few milligrams matter most: at low doses, small dose changes produce large drops in serotonin-transporter occupancy.
What this shows: the non-linear relationship between dose and serotonin transporter (SERT) occupancy. The curve is flat at high doses — most transporters are already blocked, so a dose cut has little biological impact — and much steeper at low doses, where even a 1–2 mg reduction causes a disproportionately large drop in occupancy. Your taper steps are spaced along this curve so each step removes a similar amount of occupancy.
Hill curve of modelled receptor occupancy versus dose. Current dose near 60.0 milligrams per day.
Modelled Hill-curve occupancy — illustrative only. PET-derived parameters vary by study; your prescriber may use different clinical targets. Small mg changes near zero can still produce large occupancy shifts.
How to Taper Off Cymbalta (Duloxetine) Safely
How to taper off Cymbalta (duloxetine) safely means planning for a relatively short half-life (~12 hours) and capsules that cannot be split like scored tablets. Coming off duloxetine is often harder than the milligram numbers suggest — a hyperbolic taper schedule with bead counting or compounded liquid is the usual path, ideally supervised by your prescriber.
Duloxetine is an SNRI used for depression, anxiety, and some pain indications. Withdrawal can arrive quickly after a large cut. If you are looking up how to wean off Cymbalta or get off antidepressants after pain or mood treatment, start from occupancy-based reductions rather than alternating capsule strengths (Horowitz & Taylor, 2019; Maudsley Deprescribing Guidelines 2024; NICE NG222).
What coming off Cymbalta actually feels like, week by week
With a ~12-hour half-life, an oversized reduction often declares itself within 24–48 hours: dizziness, brain zaps, nausea, irritability, insomnia, and a flu-like malaise are common. Some people also notice a rebound of pain if duloxetine was helping neuropathic or musculoskeletal symptoms.
In a well-sized taper each step should produce only a short wobble that settles over one to two weeks. Missed doses feel punishing with this drug — timing matters as much as the size of the cut when you come off Cymbalta.
“By the morning after I skipped forward too fast, the zaps were constant and I felt sea-sick. This drug does not wait around.”
“Counting beads sounded ridiculous until I tried it. Taking maybe fifteen fewer beads at a time was the only way the side effects of coming off Cymbalta stayed manageable.”
Withdrawal or relapse — how to tell them apart
Duloxetine withdrawal tends to start within a day or two of a cut, is heavy on physical and sensory symptoms, and settles quickly if you reinstate. Relapse of depression, anxiety, or pain usually appears later, matches your original problem, and does not clear promptly with a short reinstatement (Cosci & Chouinard, 2020).
Cymbalta taper schedules by starting dose (60, 30, 20 mg)
Duloxetine capsules are commonly 20, 30, and 60 mg (higher strengths exist in some markets). Jumping 60 → 30 is a linear halving and a large occupancy drop on a hyperbolic curve. The calculator above generates finer steps; notes below run high → low.
From 60 mg: how to taper off Cymbalta 60 mg usually should not jump straight to 30. Aim for intermediate doses (for example ~50 → ~40 → 30) using bead counting between capsule strengths, then continue downward.
From 30 mg: steps shrink further. A Cymbalta taper schedule from 30 mg moves toward 20 mg and then into bead-counted fractions — this is where many people first need a method beyond whole capsules.
From 20 mg: how to taper off Cymbalta 20 mg is where listed strengths run out. Every further reduction needs bead counting or a compounded liquid (next section).
If it gets worse: pausing and reinstatement
If a reduction is too large, hold, partially reinstate the last stable dose, or seek urgent advice if symptoms are severe. Duloxetine's short half-life means both problems and relief after reinstatement can appear within a day.
After stabilising, resume with smaller occupancy steps and longer holds. Do not open, crush, or change capsules without a plan agreed with your prescriber and pharmacist.
Bead counting and small doses of duloxetine
Cymbalta capsules contain enteric-coated beads that should not be crushed or chewed. For doses between listed strengths, some people — with pharmacist guidance — open a capsule and count beads to approximate a target milligram amount, keeping unused beads dry and protected.
A compounded liquid or carefully prepared suspension can be easier for the final stretch. The aim is the same as other SNRIs: finish coming off duloxetine with small, even steps rather than a cliff from 20 mg to zero.
The bottom line
Cymbalta is stoppable when the plan accounts for fast withdrawal and non-splittable capsules. Use a hyperbolic taper schedule, bead count or compound below 20–30 mg, and reinstate promptly if a step is too aggressive.
Bead-counting estimator (Cymbalta / duloxetine)
Open a capsule and remove a measured portion of beads to approximate a fractional dose. Use this only with prescriber and pharmacist guidance — bead counts vary by lot.
Target next dose: 54 mg (≈ 468 beads from a 30 mg capsule; discard ≈ 0 beads).
The target dose exceeds the chosen capsule's content. Choose a larger capsule or a smaller reduction.
Beads per mg ≈ 8.67. Bead counts can vary 10–20% by lot — confirm with your pharmacist and only count once per dose.
Method described in the Maudsley Deprescribing Guidelines (2024). Compounded liquid is the more accurate option where available.
Milligram scale guidance (advanced — prescriber/pharmacist approval required)
When a dose is below what you can split from a licensed tablet, some people weigh crushed tablet powder. This is not exact chemistry — it is a last resort. Liquid or compounded formulations are safer when available.
- Resolution: at least 0.001 g (1 mg) — not a kitchen scale.
- Include a calibration weight and use a draft shield if possible.
- Weigh on a stable surface; tare your container first.
- Crushed tablet weight ≠ exact active ingredient — drug may not be evenly distributed; prefer liquid or compounded specials when available.
- Never split enteric-coated (EC) or extended-release (XR) products — discuss with your pharmacist.
Example searches (confirm specs before buying):
Key facts about hyperbolic antidepressant tapering
The calculator algorithm is based on peer-reviewed research and has been reviewed by our medical advisors to ensure the accuracy of the tapering model.
72%
discontinued their antidepressant using hyperbolic tapering strips in a real-world study
71% of the same people had previously tried to stop at least once and been unsuccessful; the study did not record which method those earlier attempts used. Figures come from tapering-strip research and may not generalise to every taper.
Source: Groot et al., Therapeutic Advances in Psychopharmacology 2021
56 days
median taper length in that tapering-strip study — not a target; many people taper over 6–12 months or longer
This median reflects tapering-strip use in one study. Your timeline depends on how long you have taken the medication, your withdrawal symptoms, and previous attempts — slower is often safer.
Source: Groot et al., Therapeutic Advances in Psychopharmacology 2021
10%
serotonin transporter occupancy per tapering step
This linear reduction prevents withdrawal. Slower, more gradual tapering over several months has shown greater success in reducing withdrawal symptoms than short tapers.
Claro — tapering companion
A protocol isn’t enough — you need support.
Tapering can take months, sometimes years. Claro helps you track each step, log symptoms, and spot when a reduction was too fast — with psychiatrist-reviewed guidance. Join early access while we launch the app.
Frequently asked questions about duloxetine
Common questions about how to taper off duloxetine, hyperbolic schedules, and withdrawal — written for people who want to come off antidepressants safely with their prescriber.
How do you taper off Cymbalta (duloxetine)?
How do bead-counting tapers work for Cymbalta?
How long does Cymbalta withdrawal last?
Can you stop Cymbalta cold turkey?
Do you have to taper off Cymbalta?
Why is Cymbalta withdrawal so hard?
What is an antidepressant tapering calculator?
Why use a tapering calculator?
How does an antidepressant taper calculator work?
What is hyperbolic tapering and why is it recommended?
What is the safest way to taper off antidepressants?
How slowly should antidepressants be reduced?
What are common antidepressant withdrawal symptoms?
What is the difference between antidepressant withdrawal and relapse?
Is it dangerous to stop antidepressants cold turkey?
Why are the last antidepressant dose reductions often the hardest?
Which antidepressants are hardest to taper off?
Need a different dose or speed?
Use the guided builder to enter your current dose, region, and taper preset — then email your personalised protocol.
Request custom protocol →Clinical references
- [1]Horowitz MA, Taylor D. Tapering of SSRI treatment to mitigate withdrawal symptoms. The Lancet Psychiatry 2019.doi:10.1016/S2215-0366(19)30032-XProposes hyperbolic dose reduction based on receptor-occupancy curves; the methodological basis of every modern taper calculator.
- [2]Horowitz MA, Taylor D. The Maudsley Deprescribing Guidelines. Wiley 2024.doi:10.1002/9781394291052Per-drug operational manual for hyperbolic tapering across SSRIs, SNRIs, benzodiazepines, gabapentinoids, and antipsychotics.
- [3]Davies J, Read J. A systematic review into the incidence, severity and duration of antidepressant withdrawal effects. Addictive Behaviors 2019.doi:10.1016/j.addbeh.2018.08.027Systematic review: 56% of people who discontinue antidepressants experience withdrawal effects; 46% rate them as severe.
- [4]Henssler J et al. Incidence of antidepressant discontinuation symptoms: a systematic review and meta-analysis. The Lancet Psychiatry 2024.doi:10.1016/S2215-0366(24)00133-0Meta-analysis of 79 studies (≈21,000 patients): pooled incidence of discontinuation symptoms ~31%; severe symptoms ~2.8%.
- [5]Groot PC, van Os J. Successful use of tapering strips for hyperbolic reduction of antidepressant dose: a cohort study. Therapeutic Advances in Psychopharmacology 2021.doi:10.1177/2045125321103932772% of patients successfully discontinued antidepressants after switching to the hyperbolic model; 71% had previously failed to come off without tapering strips.
- [6]Groot PC, van Os J. Antidepressant tapering strips to help people come off medication: real-world outcomes. Therapeutic Advances in Psychopharmacology 2023.doi:10.1177/20451253231171518Of 1,194 patients using hyperbolic taper strips after previous failed attempts, ~71% successfully discontinued their antidepressant.
- [7]Framer A. What I have learnt from helping thousands of people taper off antidepressants and other psychotropic medications. Therapeutic Advances in Psychopharmacology 2021.doi:10.1177/2045125321991274Describes the "windows and waves" pattern of withdrawal recovery and supports patient-led pacing.
- [8]Hengartner MP et al. Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives. Therapeutic Advances in Psychopharmacology 2020.doi:10.1177/2045125320967183Descriptive analysis of 69 protracted withdrawal cases: median duration 79 weeks; 47% report suicidality during withdrawal.
- [9]Cosci F, Chouinard G. Acute and persistent withdrawal syndromes following discontinuation of psychotropic medications. Psychotherapy and Psychosomatics 2020.doi:10.1159/000506868Taxonomy distinguishing new withdrawal symptoms, rebound, and persistent post-withdrawal disorder; the standard framework for withdrawal vs. relapse.
- [10]Kalfas M et al. Incidence and Nature of Antidepressant Discontinuation Symptoms. JAMA Psychiatry 2025.doi:10.1001/jamapsychiatry.2025.1362Recent meta-analysis: dizziness was the most common discontinuation symptom in the first 2 weeks after stopping antidepressants, followed by nausea, vertigo, and nervousness.
- [11]Gabriel M, Sharma V. Antidepressant discontinuation syndrome. Canadian Medical Association Journal 2017.doi:10.1503/cmaj.160991Clinical review of antidepressant discontinuation syndrome: onset within days of dose reduction, typical symptom course, and management.
- [12]Papp A, Onton J. Brain Zaps: An Underappreciated Symptom of Antidepressant Discontinuation. The Primary Care Companion for CNS Disorders 2018.doi:10.4088/pcc.18m02311Characterises "brain zaps" — brief electric-shock sensations — as a common antidepressant discontinuation symptom.
- [13]Wang J, Cosci F. Acute and persistent withdrawal syndromes following discontinuation of antidepressants in children and adolescents: a systematic review. Therapeutic Advances in Psychopharmacology 2025.doi:10.1177/20451253251404780Systematic review of acute and persistent antidepressant withdrawal syndromes; reinforces reducing only when stable and under supervision.
- [14]Horowitz M, Taylor D. Distinguishing relapse from antidepressant withdrawal: clinical practice and antidepressant discontinuation studies. BJPsych Advances 2022.doi:10.1192/bja.2021.62Frames how clinicians can distinguish antidepressant withdrawal from relapse of the underlying condition.
- [15]Sørensen A, Ruhé HG, Munkholm K. The relationship between dose and serotonin transporter occupancy of antidepressants — a systematic review. Molecular Psychiatry 2021.doi:10.1038/s41380-021-01285-wSystematic review of dose–SERT-occupancy relationships across antidepressants; confirms the hyperbolic curve underlying proportional tapering.
- [16]Reeve R, Turner JR. Pharmacodynamic models: parameterizing the Hill equation, Michaelis-Menten, the logistic curve, and relationships among these models. Journal of Biopharmaceutical Statistics 2013.doi:10.1080/10543406.2012.756496Explains how the Hill equation, Michaelis-Menten, and logistic models relate — the mathematical basis for the occupancy curve used here.
- [17]Preskorn SH. The use of biomarkers in psychiatric research: how serotonin transporter occupancy explains the dose-response curves of SSRIs. Journal of Psychiatric Practice 2012.LinkShows how SERT occupancy explains the non-linear dose–response curves of SSRIs.
- [18]Cohrs D, Shapiro B. The relationship between SERT occupancy and extracellular serotonin concentration is hyperbolic, not linear: implications for safely tapering SRI antidepressants. SSRN (preprint) 2026.doi:10.2139/ssrn.6176553Argues the SERT-occupancy to serotonin relationship is itself hyperbolic, reinforcing proportional (hyperbolic) tapering.
- [19]Moncrieff J et al. Evidence on antidepressant withdrawal: an appraisal and reanalysis of a recent systematic review. Psychological Medicine 2025.doi:10.1017/S0033291725100652Reappraisal of recent withdrawal-incidence evidence; relevant to how withdrawal rates are interpreted.
- [20]Wilson E, Lader M. A review of the management of antidepressant discontinuation symptoms. Therapeutic Advances in Psychopharmacology 2015.doi:10.1177/2045125315612334Practical review of how to manage antidepressant discontinuation symptoms, including tapering and reinstatement.
- [21]Groot PC, van Os J. Outcome of antidepressant drug discontinuation with tapering strips after 1–5 years. Therapeutic Advances in Psychopharmacology 2020.doi:10.1177/2045125320954609Long-term follow-up (1–5 years) of patients who discontinued antidepressants using hyperbolic taper strips.
- [22]Gury C, Cousin F. Pharmacokinetics of SSRI antidepressants: half-life and clinical applicability. L'Encéphale 1999.LinkHalf-life data for SSRIs — explains why short-half-life drugs (paroxetine, venlafaxine) provoke faster withdrawal.
- [23]Mayo Clinic. Antidepressant withdrawal: Is there such a thing?. Mayo Clinic — Expert Answers 2024.LinkPatient-facing explainer on antidepressant discontinuation symptoms and gradual tapering.
- [24]NHS Scotland — Right Decision Service. Antidepressants — quality prescribing: difficulty withdrawing from an SSRI/SNRI. NHS Scotland 2024.LinkNHS Scotland guidance on recognising and managing difficulty withdrawing from SSRIs/SNRIs.
- [25]The Carlat Psychiatry Report. Clinical pearls for hyperbolic tapering of psychiatric medications in older adults. The Carlat Report 2024.LinkPractical clinical pearls for applying hyperbolic tapering, including in older adults.
- [26]Royal College of Psychiatrists. Stopping antidepressants — information for patients and carers. Royal College of Psychiatrists 2024.LinkRCPsych patient-facing guidance on coming off antidepressants safely.
- [27]National Institute for Health and Care Excellence (NICE). Depression in adults: treatment and management. NICE guideline [NG222]. NICE 2022.LinkUK national guideline endorsing proportional (hyperbolic) tapering and the use of liquid formulations to enable small final doses.
- [28]Royal College of Psychiatrists. Stopping antidepressants — position statement (CR225). Royal College of Psychiatrists 2020.LinkRCPsych acknowledges withdrawal can be severe and long-lasting; recommends slow, individualised tapers.
- [29]NHG et al. Multidisciplinary document: Discontinuation of SSRIs and SNRIs (2018; revised 2023). Multidisciplinary Document (Netherlands) 2018.LinkFirst national guideline to explicitly endorse hyperbolic tapering and the use of taper strips (compounded by Regenboog Apotheek).
- [30]Medicines and Healthcare products Regulatory Agency (MHRA). Summary of Product Characteristics — SSRI and SNRI products (UK). electronic Medicines Compendium (emc) 2023.LinkAuthoritative UK formulary data (tablet strengths, oral solutions) used to validate the UK region in the calculator.
- [31]U.S. Food and Drug Administration. Prescribing information (Structured Product Labeling) for SSRI/SNRI products. FDA / DailyMed 2024.LinkAuthoritative US formulary data (tablet strengths, oral solutions/concentrates) used to validate the US region in the calculator.
- [32]Health Canada. Health Canada — Drug Product Database. Health Canada 2024.LinkAuthoritative Canadian formulary data used to validate the Canada region in the calculator.
- [33]Therapeutic Goods Administration (TGA). Therapeutic Goods Administration — Australian Register of Therapeutic Goods (ARTG). TGA / ARTG 2024.LinkAuthoritative Australian formulary data used to validate the Australia region in the calculator.
- [34]College ter Beoordeling van Geneesmiddelen (CBG-MEB). CBG-MEB — Medicines Information Bank (Netherlands). CBG-MEB 2024.LinkAuthoritative Dutch formulary data; cross-checked with Regenboog Apotheek taper-strip availability.
- [35]Regenboog Apotheek, Cinetto. Taperingstrip.com — Regenboog Apotheek. Patient resource (NL) 2024.LinkPioneer of standardised taper strips referenced in the Dutch national guideline.
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