The Conversation Has Been Flipped
Decades ago, the message was total prohibition — no nuance, no information, no informed choice. Now the pendulum has swung to the opposite extreme. Ayahuasca retreats are marketed as trauma therapy. Psilocybin microdosing is sold as productivity enhancement. Ibogaine is presented as the cure for addiction. Kambo is framed as a full-body reset. And if you ask a question, you risk being told you're "not ready" or "your ego is afraid."
Neither prohibition nor uncritical enthusiasm is informed consent. Both deny you the information you need to make a real decision.
After twenty years in clinical practice, I have witnessed what happens before, during, and long after people engage with these substances in ceremonial, clinical, or recreational contexts. This page is not about whether psychedelics can produce meaningful experiences — they can. It is about what mainstream wellness culture is systematically failing to disclose.
The Dependency Pattern No One Talks About
Psychedelics are routinely described as "non-addictive" because they do not produce the same biochemical dependency as opioids or alcohol. This framing is incomplete. What psychedelics can create is a different kind of dependency — a psychological and spiritual one — that can be just as binding.
People return to ceremony again and again, chasing the breakthrough, the vision, the feeling of having cracked something open. The integration window — the period after a session where real change can be anchored — gets bypassed in favor of the next experience. The medicine becomes the process, rather than a catalyst for a process that happens in ordinary life.
Some develop a relationship with these substances that mimics every other pattern of avoidance: when life gets hard, go back in. When trauma surfaces, dose again. The ceremony becomes a refuge from the integration work that ceremony is supposed to initiate.
Psychedelic dependency does not look like opioid dependency. It often looks like someone who has done fifteen ceremonies in three years and still has not changed the relationship, the job, or the behavior pattern they went in to address. The medicine stopped working — not because it does not work, but because it was being used as a substitute for embodied change.
The Dark Shaman Problem
Traditional plant medicine traditions had protocols precisely because these substances open the psyche to states and dimensions that the ordinary waking mind does not navigate. A trained curandero spent years — sometimes decades — in apprenticeship, learning not just how to administer medicine but how to hold and protect the energetic container of a ceremony.
The global psychedelic tourism boom has produced a flood of facilitators with weekend certifications, no lineage, no training in what to do when someone dissociates, no ability to recognize a participant in a spiritual emergency, and in some cases active intent to exploit. Sexual assault in ceremony is documented and underreported. Energetic predation — taking advantage of an individual whose psychological defenses are entirely dissolved — is real. People emerge from ceremonies having been used, manipulated, or spiritually destabilized by someone operating as a healer.
Even within traditional lineages, not all practitioners are benevolent. The concept of the "dark shaman" — one who uses knowledge of the plant and the ceremonial space to harm rather than heal — is not a metaphor in the communities where these traditions originate. It is a documented reality.
When a substance removes your ordinary cognitive gatekeeping, you are entirely dependent on the integrity of the person holding the space. You cannot vet someone properly while you are under the influence. This is not a solvable problem with better screening — it is an inherent vulnerability of the state.
Doors You May Not Be Able to Close
Strong psychedelic experiences can permanently alter perception — not always in the direction of healing. HPPD (Hallucinogen Persisting Perception Disorder) is classified and documented, but it represents only the most measurable end of a larger spectrum. Some people emerge from psychedelic experiences with persistent altered states, an inability to return to ordinary baseline reality, new fear responses, or what is sometimes called "ontological shock" — a fundamental disruption in how reality is experienced that does not resolve with time.
These outcomes are not rare enough to be treated as edge cases in genuine informed consent conversations. And yet they are routinely omitted from promotional materials, retreat websites, and facilitator intake processes.
Certain individuals are significantly more vulnerable: those with personal or family history of psychosis, schizophrenia, or bipolar disorder; those with active trauma responses without a stable integration container; those on medications that interact; those in states of physical depletion, adrenal exhaustion, or low redox charge. For these individuals, the risk is not theoretical.
The Violation of Mind, Body, and Spirit
The psyche, like the body, has a protective boundary. Ordinary waking consciousness maintains that boundary. Psychedelics dissolve it — sometimes partially, sometimes entirely. In that dissolved state, experiences can enter that leave permanent marks: encounters with entities, reliving of trauma without containment, loss of self-boundaries that does not fully reconstitute. The person who returns is not always the person who went in.
When this happens without full informed consent, without adequate preparation, and without skilled support, it is a violation of the deepest kind — of mind, body, and spirit simultaneously. The fact that it was marketed as healing — or that the person wanted healing — does not change what it was.
This is not theoretical. It is the clinical reality I have encountered with people who came to me after ceremony. Rebuilding what was fractured in these experiences takes years, not weeks.
The Microdosing Push — and What It Leaves Out
Microdosing — taking a sub-perceptual fraction of a psychedelic dose (typically 1/10th to 1/20th of a full dose) — has been rebranded as a productivity tool, a creativity enhancer, and an antidepressant alternative. Tech culture adopted it. Media normalized it. Podcasts celebrate it. And the people promoting it are almost never disclosing what the research actually shows, what the risks are, or what "sub-perceptual" actually means when the source is an illegal supply chain with no standardization.
There is no standardized dose. The substance being sold as psilocybin may contain other compounds, may be a different species entirely, or may be significantly more or less potent than assumed. This is not a minor variable — the difference between a micro-dose and a dose that produces a full perceptual experience can be a fraction of a gram. People who believed they were microdosing have had full psychedelic experiences at work, while driving, and while parenting.
What the marketing says
Sub-perceptual doses improve mood, focus, and creativity with no psychedelic effect. Non-addictive. Neuroplasticity-enhancing. Depression alternative.
What is not disclosed
No long-term safety data. Illegal supply, no dose standardization. Serotonin receptor desensitization with chronic use. Anxiety amplification documented. HPPD risk at low doses. Tolerance forces escalation. Psychological dependency pattern identical to other avoidance cycles.
The serotonin receptor desensitization concern is not theoretical. Chronic activation of 5-HT2A receptors — even at low doses — triggers receptor downregulation over time. This is the mechanism behind SSRI tolerance. With microdosing, the result is often emotional blunting between doses, increasing difficulty feeling neutral or regulated without the substance, and a mood that cycles with the dosing schedule rather than improving independent of it. People report that stopping is harder than expected. That is dependency — it simply does not look like the cultural picture of addiction.
Ketamine Clinics — The Legal Psychedelic No One Is Questioning
Ketamine is a dissociative anesthetic — Schedule III, legally available, and since 2019, FDA-approved in nasal spray form (Spravato/esketamine) for treatment-resistant depression. IV ketamine infusion clinics have proliferated across the US. They are being marketed aggressively — directly to people who have failed antidepressants, who are in crisis, who are desperate. Celebrity culture has accelerated this: Elon Musk has openly discussed using ketamine for depression. Matthew Perry died of acute ketamine effects while reportedly receiving ketamine treatment. The demand has never been higher.
The clinical evidence for ketamine in treatment-resistant depression is real. So are the risks that clinics are not leading with. Ketamine is the same molecule whether it is administered in a clinical setting or used recreationally as Special K. The route and dose differ; the pharmacology does not. And what chronic use does to the bladder — ketamine cystitis — is one of the most devastating and underreported risks in medicine right now.
Ketamine is concentrated and excreted through the urinary tract. Chronic exposure causes progressive inflammation, scarring, and fibrosis of the bladder wall — a condition called ketamine-induced uropathy or ketamine cystitis. Symptoms include severe pelvic pain, frequency, urgency, and incontinence. In serious cases, bladder capacity shrinks to the point of requiring cystectomy — surgical removal of the bladder. This is documented in recreational users and is now emerging in clinical treatment populations receiving repeated infusions. Most ketamine clinics do not mention it.
The dissociative state itself is also not disclosed as clearly as it should be. During a ketamine infusion, you are in a K-hole — a profound dissociative state in which you may be incapable of signaling distress, expressing consent, or registering what is happening around you. You are entirely dependent on the integrity and vigilance of whoever is in the room. In a clinic where profit depends on throughput and sessions are stacked, that means a nurse or technician, checking in periodically. The person holding the space during the most psychologically open state you will be in is, in most clinics, not a trained trauma therapist. They are administering an anesthetic and monitoring vital signs.
Integration support — the follow-up work that research consistently identifies as determinative of outcomes — is often absent, minimal, or an expensive add-on. The business model sells infusions. The six-session starter package costs $3,000–$6,000 out of pocket in most markets. Insurance coverage is inconsistent and often denied. People in the most vulnerable psychiatric states, who have already failed standard treatment, are spending money they may not have on a treatment that requires ongoing infusions to maintain effect in many patients, with no clear exit protocol and risks that were never fully explained.
Who Should Not Engage With These Substances
Psychiatric History
Personal or first-degree family history of schizophrenia, bipolar I, schizoaffective disorder, or psychosis is a significant contraindication — particularly for high-dose or long-duration compounds.
Active Trauma Without Container
Unprocessed trauma without an established therapeutic relationship and integration plan significantly increases the risk of re-traumatization rather than resolution.
Medication Interactions
SSRIs, SNRIs, MAOIs, lithium, tramadol, and many other medications have documented — and sometimes life-threatening — interactions. See the Drug Interactions tab.
Cardiovascular Compromise
Ibogaine carries documented risk of fatal cardiac arrhythmia. Kambo triggers intense cardiovascular and autonomic stress. Any existing cardiac condition requires extreme caution.
Physical Depletion / Low Redox
A body that is chronically inflamed, minerally depleted, or operating on low cellular charge does not have the physiological reserves to process an intense psychedelic experience safely.
Pregnancy
No established safety data exists for any of these substances in pregnancy. Profound autonomic activation, purging, and cardiovascular stress are all contraindicated.
If You Choose to Engage Anyway
This is not a position of prohibition. It is a position of informed choice. If after understanding the full picture you choose to explore, here is what responsible engagement looks like:
- ✦ Vet the facilitator rigorously. Understand their lineage, training, years of experience, safety protocols, and what they do when something goes wrong. Ask for references from people who have worked with them over years — not weeks.
- ✦ Never go alone. Someone you trust — sober, grounded, not a participant — should be physically reachable throughout.
- ✦ Full medication disclosure. Provide your complete medication and supplement list. If the facilitator is not asking for this, that is already a red flag.
- ✦ Have a practitioner lined up for integration. The work happens in the weeks after, not during the session. Without this, you are leaving the most important part undone.
- ✦ Physical preparation matters. Clean nutrition, adequate sleep, mineral status, and low toxic load in the weeks prior are not optional. A depleted body is not equipped to process a strong experience.
- ✦ Start lower than you think you need. There is no emergency mechanism in the middle of a high-dose experience. You can always go deeper — you cannot go back.
- ✦ Long intervals between sessions. Six months to a year minimum between significant experiences. Real integration takes that long. Returning sooner is usually avoidance.
- ✦ Know the exit. Have a plan — in writing — for what happens if you experience persistent altered states or psychological destabilization after the session. Know who you call. Know where you go.
After twenty years of clinical practice I have worked with people before and after psychedelic experiences. I have helped rebuild people whose boundaries were violated in ceremony, supported those who could not return to baseline for months, and witnessed both genuine breakthrough and genuine harm. My position is not that these substances are never relevant — it is that the level of informed consent currently offered in the wellness space does not meet any reasonable ethical standard. You deserve the full picture. — Allie Johnson, DNM
Medicines
The Major Substances
Each substance has a distinct mechanism, duration, risk profile, and contraindication set. They are not interchangeable — and the promotional claim that "it's plant medicine" does not describe safety.
Ayahuasca
Amazonian brew · DMT + MAOI · 4–8 hours
- MAOI interaction — life-threatening
- Severe dietary restriction
- Cardiac stress
- Purging
Ayahuasca is a brew combining a DMT-containing plant (typically Psychotria viridis) with a vine containing beta-carboline MAOIs (Banisteriopsis caapi). The MAOIs prevent the breakdown of DMT in the gut, making it orally active. This MAOI activity persists for hours and creates life-threatening interactions with a wide range of foods and medications.
The purging (vomiting, diarrhea) is a central feature of the experience. The cardiovascular stimulation is significant — heart rate and blood pressure increase substantially. Duration is 4–8 hours with a full dose, during which the experience is not controllable or stoppable. Ayahuasca is the substance most associated with facilitator abuse in ceremony, due to the length of the experience and the complete dissolution of ordinary cognitive defenses.
Critical dietary restrictions while MAOI-active: Aged cheeses, cured meats, fermented foods, wine, beer, soy sauce, broad beans, overripe fruit — all contain tyramine. Combined with MAOI inhibition, this can trigger hypertensive crisis (severe, potentially fatal blood pressure spike). The restriction window extends before and after the ceremony.
Psilocybin / Psilocin
Magic mushrooms · 5-HT2A agonist · 4–6 hours
- SSRI interaction
- Psychosis risk
- Anxiety amplification
- HPPD
Psilocybin is converted to psilocin in the body, acting as a 5-HT2A serotonin receptor agonist. Duration is 4–6 hours. A "microdose" and a "heroic dose" are not on the same spectrum — they are different experiences with different risk profiles. Clinical trials cited in wellness media use highly controlled environments with trained monitors and careful screening. A retreat center is not that environment.
Serotonin syndrome risk when combined with SSRIs, SNRIs, tramadol, or other serotonergic agents. A common pattern: SSRIs blunt the psychedelic experience, so people taper or stop their antidepressants before a session without clinical supervision — creating a discontinuation syndrome risk during the same window.
Ibogaine
Tabernanthe iboga · multiple mechanisms · 24–36 hours
- Cardiac arrhythmia — potentially fatal
- Opioid interaction
- QT prolongation
Ibogaine has genuine, documented evidence in addiction interruption — particularly opioid dependency. This legitimate finding has been marketed into a broader "transformation" framework that strips out the critical safety context. Ibogaine prolongs the QT interval in a dose-dependent manner. This can trigger life-threatening ventricular arrhythmias. Deaths have been recorded in legal and retreat settings. A pre-session ECG/EKG with QTc interval assessment is not optional — it is the minimum requirement.
The experience lasts 24–36 hours. Medical supervision is not a recommendation — it is required. Ibogaine administered without a cardiologist-reviewed protocol, regardless of spiritual framing, is medical negligence.
Ibogaine given to someone who still has opioids (including methadone or buprenorphine) in their system can be fatal. Adequate clearance must be medically verified, not estimated. This is a known mechanism of death in underground settings.
Phyllomedusa bicolor secretion · peptide-based · 20–40 min acute
- Hyponatremia — fatal
- Cardiac stress
- Extreme purging
- Vasodilation/shock
Kambo is not a psychedelic — it does not produce visionary states. It is the secretion of an Amazonian tree frog applied to small burns on the skin. It contains peptides that trigger intense physiological responses: severe vomiting, vasodilation, blood pressure drop, and tachycardia.
The primary documented cause of death in kambo ceremonies is hyponatremia — dangerously low sodium from the combination of water loading (a common preparation protocol) and intense vomiting. Deaths have been recorded in Australia, the US, and the UK. Kambo is legal in most jurisdictions, completely unregulated, and administered outside any medical oversight — yet it is being marketed in wellness communities as an immune system reset, without disclosure of these documented fatalities.
Bufo / 5-MeO-DMT
Incilius alvarius toad secretion · inhaled vapor · 15–45 min acute
- Death documented
- Respiratory depression
- Seizure risk
- Cardiovascular stress
- Psychological trauma
Bufo is the dried secretion of the Sonoran Desert toad (Incilius alvarius), vaporized and inhaled. The active compound is 5-MeO-DMT — one of the most potent psychedelic substances known, producing near-instant and total ego dissolution within seconds of inhalation. Duration is short — 15 to 45 minutes — but the experience is frequently described as complete loss of self, body, and any reference point. It is not controllable, stoppable, or predictable in intensity once it begins.
The toad secretion also contains bufotenin, serotonin, epinephrine, and norepinephrine alongside 5-MeO-DMT — creating a compound cardiovascular and neurological load. The ceremony structure typically involves someone else administering the dose by blowing heated vapor into your lungs. You have no control over timing, dose, or stop. Several deaths have been recorded in Mexico, the UK, and the US — cardiac events, asphyxiation during loss of consciousness, and accidents during the acute phase when recipients are left unsupported. Deaths in ceremony settings have been linked to facilitators who left participants unattended or physically restrained them during the experience.
Unlike substances that produce overwhelming experiences over hours — where the person eventually metabolizes through and lands — 5-MeO-DMT hits the nervous system like a wall. The speed and totality of ego dissolution means there is no gradual threshold to ease across. People with trauma history, anxiety disorders, or undisclosed cardiovascular conditions face disproportionate risk. Documented outcomes include lasting PTSD from the experience itself, seizures, and cardiac arrest. The toad population in Mexico is being driven toward extinction by harvesting demand.
5-MeO-DMT combined with SSRIs, MAOIs, or lithium carries documented risk of serotonin syndrome. Anyone on psychiatric medication must disclose this — and most ceremony contexts provide no mechanism to safely verify or manage it. Synthetic 5-MeO-DMT is also being used in some retreat settings in place of or alongside toad secretion, with no standardization of dose.
3,4-methylenedioxymethamphetamine · entactogen · 3–6 hours
- Serotonin syndrome
- Hyperthermia
- Neurotoxicity (repeated use)
- Hyponatremia
MDMA is being studied for PTSD treatment with meaningful results in that specific, controlled context. The festival or retreat version — which may contain adulterants, variable potency, and no medical screening — is a different proposition. MDMA causes substantial simultaneous release of serotonin, dopamine, and norepinephrine, and dose-dependent serotonergic neurotoxicity with repeated use.
The clinical PTSD protocol uses MDMA twice across the full course of therapy, with extensive preparation and integration. The wellness retreat version uses it as a connection tool across multiple sessions. These are not the same thing.
Ketamine
Dissociative anesthetic · NMDA antagonist · 45–90 min IV · Schedule III · Legal
- Bladder destruction (cystitis)
- Addiction potential
- Dissociation — no consent capacity
- Psychosis risk
- Cardiovascular stimulation
Ketamine is a dissociative anesthetic — the same molecule used recreationally as Special K and clinically as an IV infusion for treatment-resistant depression. It blocks NMDA glutamate receptors, producing a dissociative state and a documented acute antidepressant effect, likely through rapid BDNF release. The FDA approved esketamine (Spravato) nasal spray in 2019. IV infusion clinics proliferated in the years following, aggressively marketing to people who have failed antidepressants. Effects are real — and so are the risks that most clinics do not lead with.
During administration, the patient is in a K-hole: a profound dissociative state in which they may be incapable of signaling distress or withdrawing consent. The effect lasts 45–90 minutes for IV, longer for intramuscular. In many clinic models, monitoring is minimal — a nurse checking vitals on a schedule, not a trained trauma therapist holding the space. Integration support — the determinative factor in outcomes — is often absent or a separate billable add-on. The typical starter course (6 infusions) costs $3,000–$6,000 out of pocket. Most insurance does not cover it.
Ketamine is concentrated and excreted through the bladder. Chronic exposure — recreational or clinical — causes progressive ulcerative cystitis: inflammation, scarring, and fibrosis of the bladder wall. Symptoms include severe pelvic pain, frequency, urgency, and incontinence. Advanced cases require cystectomy — surgical bladder removal. This is now appearing in clinical infusion patients, not only recreational users. Most ketamine clinics do not disclose this. Ask before your first session.
Microdosing — same molecule, same unanswered questions Ketamine microdosing (low-dose nasal, sublingual, or oral lozenges from compounding pharmacies) is now being marketed as a daily or weekly mood maintenance protocol. Sub-anesthetic doses do not produce the K-hole but retain NMDA antagonism. The bladder exposure concern does not disappear at lower doses with frequent use. Long-term safety data at sub-anesthetic frequencies does not exist. The business model incentivizes ongoing prescribing — not resolution.
Psilocybin Microdosing
1/10th–1/20th full dose · sub-perceptual (in theory) · Schedule I · Illegal in most jurisdictions
- No dose standardization — illegal supply
- Receptor desensitization
- Anxiety amplification
- Psychological dependency
- HPPD risk at low doses
Microdosing psilocybin is being widely promoted as a creativity enhancer, productivity tool, and antidepressant alternative — primarily by tech culture, podcasters, and wellness entrepreneurs. The premise is that doses too small to produce perceptual effects still confer neurological benefit without disrupting function. The research on this is genuinely mixed, with several placebo-controlled studies showing results indistinguishable from placebo. The enthusiast literature significantly outpaces the clinical evidence.
The sourcing problem is not minor. Psilocybin is Schedule I — illegal to possess in most of the US. What is sold or traded as psilocybin is unverified, unstandardized, and may vary in potency by an order of magnitude between batches. People who intended to microdose have had full psychedelic experiences while at work, driving, or caring for children. That is not a fringe outcome — it is what happens when a dose is measured by someone without equipment in an unregulated supply chain.
Chronic sub-threshold 5-HT2A activation drives receptor downregulation over time — the same mechanism that produces SSRI tolerance. The result is emotional blunting between doses, mood cycling that tracks the dosing schedule rather than genuine improvement, and increasing difficulty regulating without the substance. Stopping becomes harder than expected. HPPD has been documented at sub-full doses. Anxiety amplification — particularly in individuals with pre-existing anxiety — is consistent enough across reports to be a genuine contraindication, not an edge case.
Interactions
Drug Interactions
These interactions are not theoretical cautions — several have produced hospitalizations and deaths. Anyone on prescription or OTC medications must review these before any psychedelic engagement. This is not a complete list.
Stopping medications (especially SSRIs/SNRIs) to participate in ceremony is common, often unsupervised, and carries its own risks — including discontinuation syndrome, rebound symptoms, and destabilization of the condition being managed. This decision requires a prescribing clinician, not a retreat coordinator.
Ayahuasca / MAOI Interactions
| Drug / Class | Interaction | Severity |
|---|---|---|
| SSRIs / SNRIsfluoxetine, sertraline, venlafaxine, etc. | Serotonin syndrome — potentially fatal; tremor, hyperthermia, muscle rigidity, seizure, cardiac arrhythmia. SSRIs have long half-lives (fluoxetine: 1–4 weeks). Stopping days before is not adequate clearance. | Contraindicated |
| MAOIsphenelzine, tranylcypromine, selegiline | Additive MAOI activity — unpredictable potentiation, severe hypertensive crisis, serotonin syndrome. | Contraindicated |
| Tramadol | Serotonin syndrome. Tramadol has both opioid and serotonergic mechanisms. Often underestimated because it is considered mild. | Contraindicated |
| Dextromethorphan (DXM)NyQuil, DayQuil, Robitussin | Serotonin syndrome. DXM is a serotonin reuptake inhibitor at cough-suppressing doses. | Contraindicated |
| Meperidine (Demerol) | Serotonin syndrome, hyperpyrexia. Classic MAOI interaction — potentially fatal. | Contraindicated |
| Linezolid (antibiotic) | Linezolid has intrinsic MAOI activity — same interaction profile as MAOI antidepressants. | Contraindicated |
| Sympathomimeticspseudoephedrine, stimulant ADHD medications | Hypertensive crisis — dangerous blood pressure elevation with MAOI potentiation. | Contraindicated |
| Lithium | Unpredictable CNS effects, seizure risk. Cited in multiple emergency case reports. | Contraindicated |
| Antihypertensives | Additive hypotension — blood pressure drop during the MAOI-active window may be dangerously amplified. | High caution |
| St. John's Wort | Serotonergic — same risk as SSRIs. Often not disclosed because it is "just an herb." | Contraindicated |
Psilocybin Interactions
| Drug / Class | Interaction | Severity |
|---|---|---|
| SSRIs / SNRIs | Serotonin syndrome risk. SSRIs also blunt the experience — leading people to stop antidepressants unsupervised before ceremony, with discontinuation syndrome risk in that window. | High risk |
| Lithium | Seizure reports in published literature. Case reports of fatal outcomes. | Contraindicated |
| Tramadol | Serotonin syndrome potential. | Avoid |
| Cannabis | Significantly amplifies psilocybin intensity and dysphoria risk. Often used together — often regretted. | High caution |
| Antipsychotics | Block 5-HT2A receptors — reduce psychedelic effect, with unpredictable interaction. Discontinuing antipsychotics to allow a psychedelic experience carries severe psychiatric risk. | High caution |
Ibogaine Interactions
| Drug / Class | Interaction | Severity |
|---|---|---|
| Opioidsincluding methadone, buprenorphine | Fatal interaction possible — opioid presence during ibogaine administration is a documented cause of death. Adequate clearance must be medically verified, not estimated. | Potentially fatal |
| QT-prolonging drugsantiarrhythmics, some antibiotics, antipsychotics, antihistamines | Additive QT prolongation — risk of torsades de pointes and ventricular fibrillation. | Contraindicated |
| Stimulantscocaine, amphetamines, ADHD medications | Cardiovascular stress amplification. Not safe combinations. | Contraindicated |
| Antidepressants (most classes) | Complex and unpredictable interactions; some extend QT interval. Pre-ceremony discontinuation carries its own risks. | Requires clinical review |
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