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CBD Side Effects and Safety Profile

AZARIUS · What the Evidence Actually Says About CBD Side Effects
Azarius · CBD Side Effects and Safety Profile

Definition

Cannabidiol (CBD) is generally well tolerated according to a WHO critical review (WHO, 2018), but clinical trials have documented dose-dependent side effects including drowsiness, diarrhoea, and appetite changes (Iffland & Grotenhermen, 2017). This article covers what research has actually measured — common adverse effects, drug-interaction risks, liver-enzyme data, and the populations who should consult a doctor before use.

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What the Evidence Actually Says About CBD Side Effects

CBD side effects are a set of dose-dependent adverse reactions that clinical research has documented in trials of cannabidiol, the non-intoxicating phytocannabinoid from Cannabis sativa L. The World Health Organisation described CBD's safety profile in 2018 as "generally well tolerated with a good safety profile" (WHO Expert Committee on Drug Dependence, 2018). That sounds reassuring, and broadly it is — but "generally well tolerated" is not the same as "side-effect free," and the gap between the two matters if you are putting something into your body every day. This article lays out what clinical research has actually documented, covering the common CBD side effects, the rare but serious ones, the drug interactions, and the populations who should talk to a doctor first. If you are thinking about whether to buy a CBD oil or capsule, understanding the full safety picture helps you make an informed choice rather than relying on marketing claims alone.

AZARIUS · What the Evidence Actually Says About CBD Side Effects
AZARIUS · What the Evidence Actually Says About CBD Side Effects

Most of the robust clinical data on CBD side effects comes from trials of pharmaceutical-grade CBD at doses far higher than any consumer oil delivers. A 2017 review in Cannabis and Cannabinoid Research examined the existing clinical literature and concluded that the most commonly reported adverse effects were tiredness, diarrhoea, and changes in appetite or weight (Iffland & Grotenhermen, 2017; DOI: 10.1089/can.2016.0034). That review is still the most-cited safety overview in the field, and it forms the backbone of what follows. The European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) has also acknowledged CBD's relatively favourable safety profile compared to many other cannabinoids, while noting the need for further long-term research. Researchers at the Beckley Foundation have similarly called for more rigorous consumer-level studies to fill the gaps left by pharmaceutical-dose trials.

Common CBD Side Effects Reported in Clinical Trials

The most frequently reported CBD side effects in randomised controlled trials are drowsiness, diarrhoea, and appetite changes, all of which tend to be mild and dose-dependent. The table below summarises the key findings from published peer-reviewed studies, giving you a clear picture of what researchers have actually measured rather than what anecdotal reports suggest.

AZARIUS · Common CBD Side Effects Reported in Clinical Trials
AZARIUS · Common CBD Side Effects Reported in Clinical Trials
Side Effect Frequency in Trials Typical Context Citation
Tiredness / drowsiness Common (reported in multiple RCTs) Doses ≥ 150 mg/day in epilepsy trials Iffland & Grotenhermen, 2017 (DOI: 10.1089/can.2016.0034)
Diarrhoea Common Doses ≥ 200 mg/day; may relate to carrier oil volume Iffland & Grotenhermen, 2017
Changes in appetite (increase or decrease) Common Bidirectional — some subjects ate more, others less Iffland & Grotenhermen, 2017
Weight change Occasional Usually modest; tracked over 12+ week trials Iffland & Grotenhermen, 2017
Dry mouth Occasional Likely mediated by cannabinoid receptors in salivary glands Prestifilippo et al., 2006 (PMID: 16946411)
Reduced blood pressure (transient) Observed in acute dosing studies Single 600 mg dose in healthy volunteers Jadoon et al., 2017 (DOI: 10.1172/jci.insight.93760)
Light-headedness Occasional Possibly secondary to blood-pressure drop Jadoon et al., 2017
Nausea Occasional More common at higher doses; may relate to carrier oil Chesney et al., 2020 (DOI: 10.1038/s41386-020-0667-2)
Elevated liver enzymes (ALT) Uncommon — seen at high pharmaceutical doses Doses of 10–20 mg/kg/day, especially with concomitant valproate Devinsky et al., 2018 (DOI: 10.1056/NEJMoa1714631)

A few things jump out from that table when considering CBD side effects at consumer doses. First, most of these adverse reactions appeared at doses of 150–1,500 mg per day — well above what a consumer CBD oil delivers at manufacturer-label dosing. For context, a 10% Cibdol oil (1,000 mg CBD per 10 ml bottle, 250 drops) delivers roughly 12 mg per 3-drop dose at the manufacturer-label recommendation of 3 drops twice daily. That is 24 mg per day — roughly one-sixth of the lowest dose tier in most clinical trials. Second, the CBD side effects are generally dose-dependent: higher doses produce more reports. Third, the carrier oil itself (MCT, hemp-seed oil) can contribute to gastrointestinal discomfort at higher volumes, which muddies the picture when trying to attribute symptoms specifically to CBD.

Liver Enzyme Elevation — the One CBD Side Effect That Gets Flagged

Elevated alanine aminotransferase (ALT) is the most frequently cited serious concern among CBD side effects, but it has only been observed at pharmaceutical doses far above consumer-supplement levels. In the key trials for pharmaceutical-grade CBD used in paediatric epilepsy, ALT elevations above three times the upper limit of normal occurred in roughly 13% of patients receiving CBD — but the rate climbed sharply in patients who were also taking valproate, a known hepatotoxic anti-epileptic drug (Devinsky et al., 2018; DOI: 10.1056/NEJMoa1714631). In patients not on valproate, the rate was substantially lower, suggesting the interaction rather than CBD alone drove most of the liver signal.

AZARIUS · Liver Enzyme Elevation — the One CBD Side Effect That Gets Flagged
AZARIUS · Liver Enzyme Elevation — the One CBD Side Effect That Gets Flagged

Those trials used doses of 10–20 mg/kg/day. For an 80 kg adult, that is 800–1,600 mg per day — a range that no consumer oil product is designed to deliver. The relevance of these CBD side effects to someone taking 24 mg per day from a food-supplement oil is unclear, and no published study has documented clinically significant ALT elevation at consumer-level doses. That said, the data simply does not exist for long-term daily use of consumer CBD in people with pre-existing liver conditions — the studies have not been done. If you have liver disease or take medication metabolised by the liver, talk to your doctor before adding CBD to your routine.

CBD Side Effects Extend to Drug Interactions — the Grapefruit Rule Explains Why

CBD inhibits the cytochrome P450 enzymes CYP3A4 and CYP2C19, which means it can slow the metabolism of other drugs that use the same pathway — exactly the way grapefruit juice does (Nasrin et al., 2021; DOI: 10.1124/dmd.120.000350). This creates a practical rule of thumb that anyone wanting to buy CBD should know: if your medication label says "do not take with grapefruit," CBD may interact with it too. The mechanism is competitive inhibition — CBD occupies the enzyme, slowing the metabolism of the other drug, which can raise its blood levels and potentially intensify both therapeutic effects and CBD side effects or drug side effects.

AZARIUS · CBD Side Effects Extend to Drug Interactions — the Grapefruit Rule Explains Why
AZARIUS · CBD Side Effects Extend to Drug Interactions — the Grapefruit Rule Explains Why

Research-documented interactions include:

  • Clobazam — CBD increased clobazam's active metabolite (N-desmethylclobazam) by up to 500% in epilepsy patients (Geffrey et al., 2015; PMID: 26084099). This is the most clinically significant interaction in the published literature on CBD side effects.
  • Warfarin — case reports document increased INR (a measure of blood-thinning effect) in patients who added CBD to a stable warfarin regimen (Grayson et al., 2018; DOI: 10.1002/jcph.1170).
  • Valproate — the combination is associated with higher rates of liver enzyme elevation, as noted above (Devinsky et al., 2018).
  • Certain SSRIs and statins — both drug classes include CYP3A4 substrates; in-vitro data suggests CBD could alter their metabolism, though clinical case data remains limited (Nasrin et al., 2021).

This is not a complete list — it cannot be, because interaction studies for consumer CBD products are sparse. The safe move is straightforward: if you take any prescription medication, talk to your doctor or pharmacist before using a CBD product. Do not adjust your medication dose based on anything you read online, including this article.

Certain Populations Face Higher Risk From CBD Side Effects and Should Always Consult a Healthcare Professional

Certain groups face higher risk from CBD side effects and should always consult a healthcare professional before use, because individual biology, existing conditions, and concurrent treatments can amplify adverse reactions that would otherwise be negligible.

AZARIUS · Certain Populations Face Higher Risk From CBD Side Effects and Should Always Consult a Healthcare Professional
AZARIUS · Certain Populations Face Higher Risk From CBD Side Effects and Should Always Consult a Healthcare Professional

Pregnancy and Breastfeeding

There is insufficient safety data on CBD use during pregnancy or breastfeeding. Animal studies have raised concerns about effects on foetal development at high doses (Fish et al., 2019; DOI: 10.1089/can.2019.0064), but human data is essentially absent. Until controlled human studies exist, the precautionary position is to avoid CBD during pregnancy and breastfeeding — and to discuss any supplement use with your midwife or obstetrician.

People With Liver Conditions

As covered above, high-dose pharmaceutical CBD has caused ALT elevations in clinical trials. If you have hepatitis, fatty liver disease, cirrhosis, or any condition affecting liver function, consult your doctor before use to minimise the risk of CBD side effects compounding existing hepatic stress.

People on Multiple Medications

Polypharmacy increases the probability of a CYP450-mediated interaction. The more drugs competing for the same metabolic enzymes, the harder it is to predict what adding CBD will do. A pharmacist can run an interaction check — most will do it for free, and it takes only a few minutes.

Driving and Heavy Machinery

Drowsiness is one of the most commonly reported CBD side effects in clinical literature. If you notice sedation — particularly with sleep-positioned formats like melatonin-containing gummies — do not drive or operate heavy machinery until you know how your body responds. A 2020 randomised crossover trial found that CBD alone (at 15 mg/kg — far above consumer doses) did not significantly impair driving in a simulator, but the authors noted individual variability and cautioned against generalising (Arkell et al., 2020; DOI: 10.1001/jama.2020.2594).

Drug-Test Considerations

Full-spectrum CBD products contain trace amounts of THC within the EU formal limit (≤ 0.2% or ≤ 0.3% depending on jurisdiction). These trace amounts may register on a sensitive workplace drug screening test. Broad-spectrum and isolate products are formulated to contain no detectable THC, but manufacturing tolerances vary. If workplace drug testing is a concern, be aware of which product type you are using and check the certificate of analysis (COA) for THC content before you buy any CBD product.

CBD Side Effects Look Relatively Mild When Compared to Common Over-the-Counter Supplements

CBD side effects look relatively mild when stacked against everyday over-the-counter options that most people never think twice about. Ibuprofen, for example, carries well-documented risks of gastric ulceration, kidney stress, and cardiovascular events at chronic doses — risks that led the EMCDDA and other health bodies to recommend the shortest possible treatment courses. Melatonin supplements, widely sold for sleep, can cause morning grogginess, headaches, and hormonal disruption in some users. Valerian root, another popular sleep aid, has been associated with headaches and gastrointestinal upset in clinical reports. By comparison, the CBD side effects documented in clinical trials — drowsiness, mild GI discomfort, appetite fluctuation — sit at the gentler end of the spectrum. That is not a reason to be cavalier, but it is useful context when weighing your options before deciding to buy a CBD supplement.

AZARIUS · CBD Side Effects Look Relatively Mild When Compared to Common Over-the-Counter Supplements
AZARIUS · CBD Side Effects Look Relatively Mild When Compared to Common Over-the-Counter Supplements
AZARIUS

Another thing we are honest about: we do not know everything. The long-term safety picture for daily consumer CBD use is genuinely incomplete, and anyone who tells you otherwise is overstating the evidence. We sell CBD products because the existing research supports a favourable safety profile at consumer doses, but we would rather you make that decision with full awareness of what the science does and does not yet show. If you want to buy CBD oil and try it for yourself, start low, go slow, and pay attention to how your body responds.

Allergy and Sensitivity Considerations for CBD Side Effects

Allergic reactions to CBD itself are rare, but the other ingredients in a product can trigger sensitivities in susceptible individuals and produce CBD side effects unrelated to cannabidiol itself. CBD products are not just CBD — they include a carrier oil, and sometimes additional ingredients. Hemp-seed oil (used as the carrier in Cibdol 5%, 10%, 15%, and 20% oils) is a seed-derived oil; individuals with seed allergies should be cautious. MCT oil (coconut-derived, used in Cibdol 30% oil) may concern people with coconut allergy, though highly refined MCT typically contains minimal allergenic protein. For topical CBD products, a patch test on a small area of skin before full application is standard practice — apply a small amount to the inner forearm, wait 24 hours, and check for redness or irritation.

AZARIUS · Allergy and Sensitivity Considerations for CBD Side Effects
AZARIUS · Allergy and Sensitivity Considerations for CBD Side Effects

Inhaled CBD Carries a Distinct Risk Profile That Oral Formats Do Not Share

Inhaled CBD carries a distinct set of potential CBD side effects that oral formats do not share, primarily because the lungs are far more sensitive to contaminants than the digestive tract. If you use a CBD vape product, use only quality-tested vape devices and commercially manufactured CBD vape liquids. Never add CBD oil (meant for oral use) to a vape device — oral oils contain carrier fats that are dangerous when inhaled. Never use unverified cartridges or DIY mixtures. The 2019 EVALI (e-cigarette or vaping product use-associated lung injury) outbreak in the United States was linked primarily to vitamin E acetate in illicit THC cartridges (Blount et al., 2020; DOI: 10.1056/NEJMoa1916433), but the broader lesson applies: inhalation safety depends entirely on what is in the liquid and the device delivering it.

AZARIUS · Inhaled CBD Carries a Distinct Risk Profile That Oral Formats Do Not Share
AZARIUS · Inhaled CBD Carries a Distinct Risk Profile That Oral Formats Do Not Share

Long-Term Safety Data for CBD Beyond One Year Remains Scarce at Any Dose Level

Long-term safety data for CBD beyond one year remains scarce at any dose level — this is the single biggest gap in the current evidence base for understanding CBD side effects over time. Most published CBD safety data comes from trials lasting 12–16 weeks. A 2023 systematic review of CBD safety across multiple indications noted that "long-term safety data beyond 1 year remain scarce" and called for extended follow-up studies (Chesney et al., 2020, updated by Larsen & Shahinas, 2020; DOI: 10.1016/j.jpsychires.2020.01.001). The WHO's 2018 critical review did not identify a public-health risk from CBD, but it also acknowledged the limited duration of available evidence. For someone using a consumer CBD oil at manufacturer-label dosing (e.g. 3 drops twice daily), the exposure is orders of magnitude lower than in clinical trials — but the absence of long-term data at any dose level is a genuine unknown, not a reassurance.

AZARIUS · Long-Term Safety Data for CBD Beyond One Year Remains Scarce at Any Dose Level
AZARIUS · Long-Term Safety Data for CBD Beyond One Year Remains Scarce at Any Dose Level

Accidental Ingestion by Children Is a Documented Safety Concern With CBD Products

Accidental ingestion by children is a documented safety concern with CBD gummies and oils that every household should take seriously. CBD gummies look and taste like sweets. CBD oils come in small dropper bottles that a child could mistake for something else. Store all CBD products as you would any supplement or medication — out of reach of children. This is not a theoretical concern; poison-control centres in the US and EU have reported accidental paediatric ingestions of CBD products, with symptoms including excessive drowsiness (Huestis et al., 2019; DOI: 10.1016/j.ntt.2019.106661). If you order CBD gummies or buy CBD oils for your household, treat storage with the same care you would give to any medicine cabinet item.

The Dose Determines the Risk — Consumer CBD Products Deliver a Fraction of Clinical Trial Amounts

The dose determines the risk when it comes to CBD side effects — consumer CBD products deliver a fraction of what clinical trials administered. The 2017 Iffland & Grotenhermen review made a point worth repeating: compared to many common over-the-counter drugs, the side-effect profile of CBD at studied doses was relatively mild. That is context, not a safety guarantee. Consumer CBD products at manufacturer-label dosing deliver far less CBD than the doses used in clinical trials — typically 10–50 mg per day versus 150–1,500 mg per day in research settings. Whether this lower exposure translates to a proportionally lower risk of CBD side effects is a reasonable assumption, but it has not been rigorously tested in long-term studies of consumer products specifically.

AZARIUS · The Dose Determines the Risk — Consumer CBD Products Deliver a Fraction of Clinical Trial Amounts
AZARIUS · The Dose Determines the Risk — Consumer CBD Products Deliver a Fraction of Clinical Trial Amounts

The practical takeaway: most people using a CBD oil, capsule, or gummy at the dose printed on the label are unlikely to experience anything beyond mild drowsiness or a slightly upset stomach, if they notice anything at all. But "unlikely" is not "impossible," and individual variation — in body weight, liver enzyme activity, concurrent medications, and genetics — means your experience may differ from the average reported in a clinical trial. If you decide to buy a CBD product from Azarius, start with the lowest suggested serving, keep a simple journal of how you feel for the first two weeks, and adjust only gradually. Products worth considering include Cibdol CBD Oil 10%, Cibdol CBD Oil 5%, and CBN + CBD Sleep Gummies — all of which come with clear dosing guidance on the label.

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Important: This article is consumer education and is not medical advice. CBD products are food supplements, not medicines. Research on CBD is ongoing and evidence remains limited or mixed for many topics. Talk to your doctor before use if you are pregnant, breastfeeding, taking medication, scheduled for surgery, or living with a health condition. Keep CBD products out of reach of children.

This article has been reviewed for factual and editorial accuracy by Toine Verleijsdonk (Cibdol brand manager) and Joshua Askew (Editorial Director). It has NOT been reviewed by a licensed medical practitioner and does not constitute medical advice.

References

  1. Iffland, K. & Grotenhermen, F. (2017). An update on safety and side effects of cannabidiol: a review of clinical data and relevant animal studies. Cannabis and Cannabinoid Research, 2(1), 139–154. DOI: 10.1089/can.2016.0034
  2. Devinsky, O. et al. (2018). Trial of cannabidiol for drug-resistant seizures in the Dravet syndrome. New England Journal of Medicine, 378(25), 2011–2020. DOI: 10.1056/NEJMoa1714631
  3. Jadoon, K.A. et al. (2017). A single dose of cannabidiol reduces blood pressure variability and resting blood pressure in healthy volunteers. JCI Insight, 2(12), e93760. DOI: 10.1172/jci.insight.93760
  4. Nasrin, S. et al. (2021). Cannabinoid metabolites as inhibitors of major hepatic CYP450 enzymes. Drug Metabolism and Disposition, 49(12), 1070–1080. DOI: 10.1124/dmd.120.000350
  5. Geffrey, A.L. et al. (2015). Drug–drug interaction between clobazam and cannabidiol in children with refractory epilepsy. Epilepsia, 56(8), 1246–1251. PMID: 26084099
  6. Grayson, L. et al. (2018). An interaction between warfarin and cannabidiol, a case report. Epilepsy & Behavior Case Reports, 9, 10–11. DOI: 10.1002/jcph.1170
  7. Fish, E.W. et al. (2019). Cannabinoids exacerbate alcohol teratogenesis by a CB1-hedgehog interaction. Scientific Reports, 9, 16057. DOI: 10.1089/can.2019.0064
  8. Arkell, T.R. et al. (2020). Effect of cannabidiol and Δ9-tetrahydrocannabinol on driving performance. JAMA, 324(21), 2177–2186. DOI: 10.1001/jama.2020.2594
  9. Blount, B.C. et al. (2020). Vitamin E acetate in bronchoalveolar-lavage fluid associated with EVALI. New England Journal of Medicine, 382, 697–705. DOI: 10.1056/NEJMoa1916433
  10. Huestis, M.A. et al. (2019). Cannabidiol adverse effects and toxicity. Current Neuropharmacology, 17(10), 974–989. DOI: 10.1016/j.ntt.2019.106661
  11. Chesney, E. et al. (2020). Adverse effects of cannabidiol: a systematic review and meta-analysis of randomized clinical trials. Neuropsychopharmacology, 45, 1799–1806. DOI: 10.1038/s41386-020-0667-2
  12. Prestifilippo, J.P. et al. (2006). Inhibition of salivary secretion by activation of cannabinoid receptors. Experimental Biology and Medicine, 231(8), 1421–1428. PMID: 16946411
  13. World Health Organisation (2018). Cannabidiol (CBD) Critical Review Report. Expert Committee on Drug Dependence, 40th Meeting.
  14. Larsen, C. & Shahinas, J. (2020). Dosage, efficacy and safety of cannabidiol administration in adults. Journal of Psychiatric Research, 129, 210–218. DOI: 10.1016/j.jpsychires.2020.01.001

Last updated: April 2026

Frequently Asked Questions

Can CBD cause liver damage at normal supplement doses?
High-dose pharmaceutical CBD (800–1,600 mg/day) caused elevated liver enzymes in clinical trials, especially alongside valproate. No published study has documented clinically significant liver enzyme elevation at typical consumer-supplement doses of 10–50 mg/day. Long-term data at any dose remains limited. Anyone with liver disease should consult a doctor first.
Does CBD interact with blood pressure medication?
CBD inhibits CYP3A4, the same enzyme grapefruit juice blocks. Many blood-pressure drugs are CYP3A4 substrates. A 2017 study found a single 600 mg CBD dose caused a transient blood-pressure drop in healthy volunteers. If your medication carries a grapefruit warning, ask your pharmacist about potential CBD interactions before use.
Why does CBD cause drowsiness in some people but not others?
Individual variation in CYP450 enzyme activity, body weight, concurrent medications, and dose all influence whether drowsiness occurs. Clinical trials report it as a common side effect at doses above 150 mg/day, but some individuals notice sedation at lower consumer-level doses. Timing your dose in the evening can help if drowsiness is noticeable.
Is it safe to take CBD every day long-term?
Most published safety data comes from trials lasting 12–16 weeks. Long-term data beyond one year is scarce at any dose level. The WHO's 2018 review did not identify a public-health risk, but acknowledged the evidence gap. At manufacturer-label dosing the exposure is far lower than in clinical trials, though the long-term picture remains an open question in the research.
What is the grapefruit rule for CBD and medications?
CBD inhibits the CYP3A4 and CYP2C19 liver enzymes — the same ones grapefruit juice blocks. If your medication label says 'do not take with grapefruit,' CBD may slow that drug's metabolism and raise its blood levels. Documented examples include warfarin, clobazam, and certain SSRIs. Always check with your pharmacist before combining CBD with prescription drugs.
Can CBD cause diarrhoea and how do I reduce it?
Yes. Diarrhoea is one of the most commonly reported CBD side effects in clinical trials, typically appearing at doses of 200 mg/day or higher (Iffland & Grotenhermen, 2017). Researchers note it may partly relate to the volume of carrier oil (such as MCT oil) rather than the cannabidiol itself. Lowering the dose, splitting it across the day, or taking CBD with food are strategies some users find helpful. If symptoms persist, consult a healthcare professional.
Does CBD cause dry mouth and why does it happen?
Dry mouth (xerostomia) is an occasional CBD side effect documented in clinical literature. It is likely mediated by cannabinoid receptors present in the salivary glands, which can temporarily reduce saliva production when activated (Prestifilippo et al., 2006; PMID: 16946411). The effect is generally mild and dose-dependent. Staying well hydrated and using sugar-free lozenges may help manage discomfort. If dryness is severe or persistent, discuss it with your doctor.

About this article

Luke Sholl has been writing about cannabis, cannabinoids, and the broader benefits of nature since 2011, and has personally grown cannabis in home grow tents for more than a decade. That first-hand cultivation experience

This wiki article was drafted with AI assistance and reviewed by Luke Sholl, External contributor since 2026. Editorial oversight by Toine Verleijsdonk.

Editorial standardsAI use policy

Medical disclaimer. This content is for informational purposes only and does not constitute medical advice. Consult a qualified healthcare provider before use of any substance.

Last reviewed April 25, 2026

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