Bitter Candytuft (Iberis amara)

Iberis amara
Evidence Level
Preliminary
6 Clinical Trials
6 Documented Benefits
1/5 Evidence Score

Bitter candytuft (Iberis amara) is a small European plant of the mustard family. The whole fresh flowering plant is the lead herb in STW 5, sold in Germany as the licensed liquid medicine Iberogast, an alcohol-based extract of nine herbs that also contains peppermint, chamomile, caraway, licorice, lemon balm, angelica, milk thistle and greater celandine. Nearly all human research tested that blend in people with functional dyspepsia or irritable bowel syndrome, so the results cannot be credited to bitter candytuft. In the one placebo-controlled trial that gave a bitter candytuft extract on its own, symptoms did not improve significantly more than with placebo. The plant contains cucurbitacins and glucosinolates. Iberogast has carried a German liver warning since 2018, linked mainly to its greater celandine.

Studied Dose No dose of bitter candytuft alone has shown an effect. A 315-person trial of the nine-herb liquid blend STW 5 used 20 drops three times daily for 8 weeks; the abstract of the one trial of a bitter candytuft extract alone does not give its dose.
Active Compound Extract of the whole fresh flowering plant (Iberis amara totalis); constituents include cucurbitacins, glucosinolates (mustard oil glycosides), flavonoid glycosides and amines.

Benefits

Bitter candytuft extract on its own versus placebo

In the one placebo-controlled trial that gave a bitter candytuft mono-extract by itself, 208 adults with IBS were split among four groups for 4 weeks. The extract alone did not differ significantly from placebo on abdominal pain or the overall symptom score, while two multi-herb blends that contain it did beat placebo.

Lead herb of the nine-herb blend STW 5

In an 8-week placebo-controlled trial in 315 adults with functional dyspepsia, 20 drops of the nine-herb blend STW 5 three times daily improved a symptom score by 6.9 points versus 5.9 with placebo, a small but significant difference. Tolerability matched placebo. This is the whole blend, and nothing here is credited to bitter candytuft alone.

Pooled trials of the nine-herb blend

A Cochrane review pooled 5 trials (814 participants with functional dyspepsia) and found the nine-herb blend STW 5 may improve overall symptoms more than placebo, but judged that evidence very uncertain. Side effects were about as common as with placebo. An earlier pooled analysis found its trials partly through the maker.

What removing bitter candytuft from the blend changed

In a 60-person trial in functional dyspepsia, the nine-herb blend and a version without bitter candytuft both beat placebo over 4 weeks, with no significant difference between them in the end. Relief came somewhat sooner with the full blend. This is a small German-language trial and does not isolate the herb's own effect.

Stomach muscle activity after a single blend dose

In healthy men, one 1.1 mL dose of the nine-herb blend relaxed the upper stomach and increased contractions in the lower stomach compared with control, without changing how fast solid food emptied. In a 103-person dyspepsia trial the blend did not speed stomach emptying either. Neither study tested bitter candytuft alone.

Gut muscle tone in laboratory tissue

Lab work: in guinea pig gut tissue, the bitter candytuft extract did not relax the muscle as peppermint and chamomile extracts did; it raised the resting tone and contraction of slack segments instead. In receptor tests it bound muscarinic M3 receptors, which help control gut contraction. None of this has been measured in people.

Mechanism of action

1

Raises tone in slack gut muscle (lab work)

In guinea pig intestine, the Iberis amara extract increased the resting tone of relaxed gut segments rather than relaxing them, and in receptor-binding tests it selectively bound muscarinic M3 receptors. The researchers proposed that this tonic action, alongside the relaxing herbs in the blend, gives it a dual action.

2

Cucurbitacins and glucosinolates

The plant contains cucurbitacins, highly oxygenated triterpenoids that deter insects from eating it, plus glucosinolates (mustard oil glycosides), flavonoid glycosides, kaempferol and sinapic acid. How much of each reaches the body from a liquid extract has not been reported in people.

3

Inflammation signals pointing both ways in lab studies

In rats, an Iberis amara extract reduced paw swelling and lowered TNF-alpha, interleukin 1-beta and prostaglandin E2. In human esophageal cells, however, the extract alone strongly raised the inflammation signal interleukin 8, which the full nine-herb blend did not. Both studies had co-authors from the blend's maker.

Clinical trials

1
Bitter Candytuft Extract Alone vs Two Herbal Blends vs Placebo: 4-Arm Trial
PubMed

Double-blind, randomized, placebo-controlled multicenter trial comparing the nine-herb blend STW 5, the six-herb research blend STW 5-II and a bitter candytuft mono-extract with placebo; main outcomes were changes in total abdominal pain and IBS symptom scores at 4 weeks. (Madisch et al. 2004, Aliment Pharmacol Ther)

208 adults with IBS (51 STW 5, 52 STW 5-II, 53 bitter candytuft extract, 52 placebo); 203 completed.

The bitter candytuft extract on its own did not differ significantly from placebo on abdominal pain (P = 0.1473) or the IBS symptom score (P = 0.1207). Both multi-herb blends were significantly better than placebo on both scores (P = 0.0003 to 0.001).

2
Nine-Herb Blend STW 5 vs Placebo: 8-Week Multicenter Trial
PubMed

Multicenter, placebo-controlled, double-blind trial of the nine-herb liquid blend STW 5 (Iberogast), 20 drops three times daily for 8 weeks, after endoscopy and a 7-day run-in; primary outcome was change in the Gastrointestinal Symptom Score. (von Arnim et al. 2007, Am J Gastroenterol)

315 adults with functional dyspepsia (158 STW 5, 157 placebo; 308 in the intention-to-treat analysis).

The symptom score improved by 6.9 points with STW 5 and 5.9 points with placebo (P < 0.05), a 1-point difference on top of a large placebo response. H. pylori status did not change the result, and tolerability was similar. The trial tested the whole blend; nothing can be credited to bitter candytuft alone.

3
Nine-Herb Blend With and Without Bitter Candytuft vs Placebo
PubMed

Randomized, double-blind, placebo-controlled multicenter trial (German language) comparing the nine-herb blend STW 5, a version without bitter candytuft (STW-5-S) and placebo for 4 weeks. (Madisch et al. 2001, Z Gastroenterol)

60 adults with functional dyspepsia; all completed.

Both blends improved the symptom score more than placebo at 2 and 4 weeks (P < 0.001). The blend without bitter candytuft did as well as the full blend overall (no significant difference), though relief came earlier with the full blend (P = 0.023). A small trial that compares blends rather than testing the herb alone.

4
Nine-Herb Blend STW 5 and Stomach Emptying: 28-Day Placebo Trial
PubMed

Multicenter, placebo-controlled, double-blind trial of the nine-herb blend STW 5 or liquid placebo for 28 days, with a 13C octanoic acid breath test for stomach emptying. (Braden et al. 2009, Neurogastroenterol Motil)

103 adults with functional dyspepsia, about half of them with slow stomach emptying.

The primary outcome, symptom score improvement, did not differ significantly from placebo (P = 0.08), though more people responded to STW 5 (P = 0.03). Stomach emptying did not speed up with STW 5. Bitter candytuft was not tested on its own.

5
Cochrane Review of Non-Chinese Herbal Medicines: Results for the STW 5 Blend
PubMed

Cochrane systematic review of randomized trials of non-Chinese herbal medicines for functional dyspepsia, with GRADE certainty ratings. (Báez et al. 2023, Cochrane Database Syst Rev)

41 trials with 4477 participants testing 27 herbal medicines; for STW 5 versus placebo, 5 trials with 814 participants for global symptoms.

STW 5 may improve global symptoms versus placebo at 28 to 56 days (mean difference -2.64), but the authors called the evidence very uncertain (very low certainty), with large differences between trials (I2 = 87%). Adverse events showed little to no difference from placebo (risk ratio 0.92). No result concerns bitter candytuft alone.

6
Lab Study: Bitter Candytuft Extract Raised Gut Muscle Tone (Guinea Pig Tissue)
PubMed

Laboratory study of the STW 5 blend and its single extracts on isolated guinea pig ileum, with and without acetylcholine or histamine stimulation. (Ammon et al. 2006, Phytomedicine)

Isolated guinea pig intestinal tissue; no human participants.

The blend and its peppermint, chamomile and licorice extracts relaxed induced contractions, but the Iberis amara extract showed no relaxing action and raised the resting tone and contraction of slack segments. Tissue results do not show effects in people.

Side effects and drug interactions

Common Potential side effects

In placebo-controlled trials of the nine-herb blend STW 5, side effects were about as common as with placebo. The only located trial of bitter candytuft alone lasted 4 weeks.
Liver injury: cases of hepatitis and liver failure, including a liver failure case that became known in July 2018 and ended in death after a liver transplant, have been linked to the nine-herb blend Iberogast and are mainly attributed to its greater celandine. Since 2018 the German label says to stop and see a doctor if yellow skin or eyes, dark urine, pale stools, upper belly pain, nausea, appetite loss or tiredness appear.
Pregnancy and breastfeeding: the German Iberogast label says it must not be taken while pregnant or breastfeeding, and the safety of bitter candytuft alone in pregnancy has not been established.
Iberogast-type liquid extracts are alcohol-based, which matters for children, people avoiding alcohol and people with liver disease.
Rodent and cell tests summarized in a review found no acute toxicity or genotoxicity from the fresh-plant extract, but these do not replace human safety data.

Important Drug interactions

Liver-damaging medicines: the German label for the nine-herb blend Iberogast says not to take it together with medicines that can harm the liver, or with past or current liver disease.
Bitter candytuft alone has not been tested for interactions with medicines in people. In receptor tests its extract bound muscarinic M3 receptors, so anyone taking drugs that act on these receptors, such as some bladder or gut-spasm medicines, may wish to check with a pharmacist.

Frequently asked questions about Bitter Candytuft (Iberis amara)

Does bitter candytuft work on its own, or only as part of a blend?

The only placebo-controlled trial of a bitter candytuft extract on its own, in 208 adults, found no significant difference from placebo after 4 weeks, while two blends containing it did better than placebo. In another small trial, removing bitter candytuft from the nine-herb blend did not change the final result. So far the human evidence supports the blends, not the herb alone.

Why did Iberogast get a liver warning in Germany in 2018?

Germany's drug regulator had ordered liver warnings for all lower-dose medicines containing greater celandine back in 2008. After new reports of liver injury, including a liver failure case that ended in death after a transplant, Bayer added them to the Iberogast label in 2018. The warnings concern greater celandine, which is one of the nine herbs; bitter candytuft has not been identified as the cause.

Which plant compounds does bitter candytuft contain?

The plant makes cucurbitacins, triterpenoid compounds that keep insects from eating it, and also contains glucosinolates (the mustard oil compounds typical of its plant family), flavonoids and sinapic acid. How much of these reaches the body from a liquid extract has not been measured in people.

Does the nine-herb blend speed up stomach emptying?

Apparently not. In a 103-person trial, stomach emptying did not speed up on the blend, and in healthy men a single dose did not change how fast solid food left the stomach. It did relax the upper stomach and increase contractions in the lower stomach, which researchers suggest may matter more for symptoms.

What is Bitter Candytuft?

Bitter candytuft (Iberis amara) is a small European plant of the mustard family. The whole fresh flowering plant is the lead herb in STW 5, sold in Germany as the licensed liquid medicine Iberogast, an alcohol-based extract of nine herbs that also contains peppermint, chamomile, caraway, licorice, lemon balm, angelica,…

What is Bitter Candytuft used for?

NutraSmarts does not list Bitter Candytuft under a health category. What the research covers: In the one placebo-controlled trial that gave a bitter candytuft mono-extract by itself, 208 adults with IBS were split among four groups for 4 weeks.

What is the recommended dosage of Bitter Candytuft?

No dose of bitter candytuft alone has shown an effect. A 315-person trial of the nine-herb liquid blend STW 5 used 20 drops three times daily for 8 weeks; the abstract of the one trial of a bitter candytuft extract alone does not give its dose. Always follow the product label and check with a healthcare provider for personal advice.

Is Bitter Candytuft safe, and does it have side effects?

Side effects and cautions reported for Bitter Candytuft include: In placebo-controlled trials of the nine-herb blend STW 5, side effects were about as common as with placebo. The only located trial of bitter candytuft alone lasted 4 weeks. It may also interact with some medications. Bitter Candytuft is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Bitter Candytuft interact with any medications?

Possible interactions include: Liver-damaging medicines: the German label for the nine-herb blend Iberogast says not to take it together with medicines that can harm the liver, or with past or current liver disease. Bitter candytuft alone has not been tested for interactions with medicines in people. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Bitter Candytuft?

NutraSmarts rates the evidence for Bitter Candytuft as Preliminary (1 out of 5). It is backed by 6 study summaries and 16 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(16 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Madisch A, Holtmann G, Plein K, Hotz J. Treatment of irritable bowel syndrome with herbal preparations: results of a double-blind, randomized, placebo-controlled, multi-centre trial. Aliment Pharmacol Ther. 2004;19(3):271-9. doi: 10.1111/j.1365-2036.2004.01859.x.PubMedUsed to support: Double-blind, placebo-controlled multicenter trial in 208 people with IBS randomized to the nine-herb blend STW 5, the six-herb research blend STW 5-II, a bitter candytuft mono-extract or placebo. At 4 weeks both blends beat placebo on abdominal pain and IBS symptom scores, while the bitter candytuft extract alone did not differ significantly from placebo (P = 0.1473 and P = 0.1207).
  2. von Arnim U, Peitz U, Vinson B, Gundermann KJ, Malfertheiner P. STW 5, a phytopharmacon for patients with functional dyspepsia: results of a multicenter, placebo-controlled double-blind study. Am J Gastroenterol. 2007;102(6):1268-75. doi: 10.1111/j.1572-0241.2006.01183.x.PubMedUsed to support: Multicenter, placebo-controlled, double-blind trial in 315 people with functional dyspepsia: 20 drops three times daily of the nine-herb blend STW 5 (mainly a fresh-plant extract of Iberis amara) for 8 weeks improved a gastrointestinal symptom score by 6.9 points versus 5.9 with placebo (P < 0.05), with similar tolerability. Tests the whole blend, not bitter candytuft alone.
  3. Madisch A, Melderis H, Mayr G, Sassin I, Hotz J. [A plant extract and its modified preparation in functional dyspepsia. Results of a double-blind placebo controlled comparative study]. Z Gastroenterol. 2001;39(7):511-7. doi: 10.1055/s-2001-16142.PubMedUsed to support: German-language randomized, double-blind multicenter trial in 60 people with functional dyspepsia: over 4 weeks both the nine-herb blend STW 5 and a version without bitter candytuft (STW-5-S) improved a symptom score more than placebo (P < 0.001), with no significant difference between the two blends; improvement came earlier with the full blend (P = 0.023).
  4. Braden B, Caspary W, Börner N, Vinson B, Schneider AR. Clinical effects of STW 5 (Iberogast) are not based on acceleration of gastric emptying in patients with functional dyspepsia and gastroparesis. Neurogastroenterol Motil. 2009;21(6):632-8, e25. doi: 10.1111/j.1365-2982.2008.01249.x.PubMedUsed to support: Multicenter, placebo-controlled, double-blind trial in 103 people with functional dyspepsia given the nine-herb blend STW 5 or a liquid placebo for 28 days. The primary symptom score improvement did not reach significance (P = 0.08); the share of responders was higher with STW 5 (P = 0.03). Gastric emptying time did not speed up with STW 5.
  5. Báez G, Vargas C, Arancibia M, Papuzinski C, Franco JV. Non-Chinese herbal medicines for functional dyspepsia. Cochrane Database Syst Rev. 2023;6(6):CD013323. doi: 10.1002/14651858.CD013323.pub2.PubMedUsed to support: Cochrane review of 41 trials (4477 participants, 27 herbal medicines). For the nine-herb blend STW 5 versus placebo at 28 to 56 days, global dyspepsia symptoms improved (mean difference -2.64, 5 studies, 814 participants) but the certainty of evidence was very low; adverse events showed little to no difference (risk ratio 0.92, 4 studies, 786 participants).
  6. Melzer J, Rösch W, Reichling J, Brignoli R, Saller R. Meta-analysis: phytotherapy of functional dyspepsia with the herbal drug preparation STW 5 (Iberogast). Aliment Pharmacol Ther. 2004;20(11-12):1279-87. doi: 10.1111/j.1365-2036.2004.02275.x.PubMedUsed to support: Meta-analysis of reanalysed raw data from three placebo-controlled trials of the nine-herb blend STW 5 (138 verum, 135 placebo), with trials identified partly through consultation of the producer: STW 5 reduced the severity of the most bothersome symptom more than placebo (odds ratio 0.22). A trial against cisapride showed no significant difference; adverse events were similar to placebo.
  7. Pilichiewicz AN, Horowitz M, Russo A, Maddox AF, Jones KL, Schemann M, Holtmann G, Feinle-Bisset C. Effects of Iberogast on proximal gastric volume, antropyloroduodenal motility and gastric emptying in healthy men. Am J Gastroenterol. 2007;102(6):1276-83. doi: 10.1111/j.1572-0241.2007.01142.x.PubMedUsed to support: Double-blind randomized studies in 8 to 12 healthy men given a single 1.1 mL oral dose of the nine-herb blend Iberogast or control: Iberogast increased upper stomach volume and antral contraction activity and slightly increased liquid retention in the stomach, with no effect on emptying of solids.
  8. Ammon HP, Kelber O, Okpanyi SN. Spasmolytic and tonic effect of Iberogast (STW 5) in intestinal smooth muscle. Phytomedicine. 2006;13 Suppl 5:67-74. doi: 10.1016/j.phymed.2006.08.004.PubMedUsed to support: Laboratory study in guinea pig gut tissue: the STW 5 blend and its peppermint, chamomile and licorice extracts relaxed induced contractions, whereas the Iberis amara extract showed no relaxing action and instead raised the resting tone and contraction of slack gut segments. Tissue work, not a human study.
  9. Simmen U, Kelber O, Okpanyi SN, Jaeggi R, Bueter B, Weiser D. Binding of STW 5 (Iberogast) and its components to intestinal 5-HT, muscarinic M3, and opioid receptors. Phytomedicine. 2006;13 Suppl 5:51-5. doi: 10.1016/j.phymed.2006.03.012.PubMedUsed to support: Receptor-binding study in gut tissue preparations: of the nine extracts in STW 5, the fresh-plant extract of bitter candytuft selectively inhibited binding to muscarinic M3 receptors, which help control gut muscle contraction. Test-tube work only.
  10. Ulrich-Merzenich G, Welslau L, Aziz-Kalbhenn H, Kelber O, Shcherbakova A. Synergy quantifications to identify individual contributions of combination partners to the overall activity - The example of STW 5. Phytomedicine. 2019;60:153013. doi: 10.1016/j.phymed.2019.153013.PubMedUsed to support: Cell-culture study (two co-authors from maker Steigerwald, Bayer Consumer Health): in human esophageal cells the full STW 5 blend left the inflammation signal interleukin 8 near control levels, while the Iberis amara extract alone raised it strongly (441 versus 46 pg/ml without an inflammatory trigger); milk thistle extract was the main partner that lowered it.
  11. Khayyal MT, Agha AM, Zaki HF, El-Sahar A, Abdel-Aziz H. Mechanisms Involved in the Anti-inflammatory and Vascular Effects of Iberis amara Extract. Planta Med. 2015;81(12-13):1097-102. doi: 10.1055/s-0035-1546244.PubMedUsed to support: Rat study with one co-author from maker Steigerwald: an Iberis amara extract dose-dependently reduced paw swelling in acute and chronic inflammation models and lowered TNF-alpha, interleukin 1-beta and prostaglandin E2 in the chronic model. Names cucurbitacins, kaempferol and sinapic acid as constituents. Animal work only.
  12. Reichling J, Saller R. [Iberis amara L. (bitter candytuft)--profile of a medicinal plant]. Forsch Komplementarmed Klass Naturheilkd. 2002;9 Suppl 1:21-33. doi: 10.1159/000068646.PubMedUsed to support: German-language review: the plant contains amines, cucurbitacins, flavonoid glycosides and mustard oil glycosides (glucosinolates); the whole flowering fresh plant is used in Iberogast. Reports a tonic effect on gut smooth muscle and an anti-ulcer effect in rats, and no acute toxicity or genotoxicity in cell and rodent tests.
  13. Dong L, Almeida A, Pollier J, Khakimov B, Bassard JE, Miettinen K, Stærk D, Mehran R, Olsen CE, Motawia MS, Goossens A, Bak S. An Independent Evolutionary Origin for Insect Deterrent Cucurbitacins in Iberis amara. Mol Biol Evol. 2021;38(11):4659-4673. doi: 10.1093/molbev/msab213.PubMedUsed to support: Plant-biology study: Iberis amara makes cucurbitacins, triterpenoids that deter insect feeding, through its own biosynthetic route, and the paper identifies the first enzymes in that pathway. Describes the plant's chemistry, not effects in people.
  14. Leroy A, Perrin H, Porret R, Sempoux C, Chtioui H, Fraga M, Bart PA. Iberogast®-Induced Acute Liver Injury-A Case Report. Gastro Hep Adv. 2022;1(4):601-603. doi: 10.1016/j.gastha.2022.02.020.PubMedUsed to support: Case report of acute severe hepatitis in a previously healthy 32-year-old woman 6 weeks after starting the nine-herb blend Iberogast, judged probable by a standard causality score and resolving after stopping. The authors note that liver injury with Iberogast has mostly been attributed to its greater celandine component, including one case that needed a liver transplant.
  15. Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM). Schöllkrauthaltige Arzneimittel zur innerlichen Anwendung (greater celandine-containing medicines for internal use): risk information with updates of 11.09.2018, 01.10.2018 and 05.10.2018 BfArM Pharmakovigilanz Risikoinformationen (accessed 2026). 2018;German Federal Institute for Drugs and Medical Devices web page..SourceUsed to support: Official German regulator page, not PubMed-indexed. In 2008, celandine medicines above 2.5 mg total alkaloids a day lost authorization and those from 2.5 micrograms to 2.5 mg were ordered to change their product information. In September 2018, after a liver failure case with transplant that became known in July 2018 and ended in death, Bayer agreed to add liver warnings to Iberogast within four weeks: no use with liver disease or liver-damaging drugs, stop at signs of liver injury, no use in pregnancy or breastfeeding.
  16. Rosien U. Iberogast® verursacht potenziell lebensbedrohliche Leberschäden: Endlich werden Warnhinweise in der Fach- und Gebrauchsinformation durch Bayer umgesetzt Arzneiverordnung in der Praxis (Drug Commission of the German Medical Association, AkdÄ). 2019;Issue 1/2019 (published online 17 October 2018)..SourceUsed to support: German drug-commission article, not PubMed-indexed. Describes Iberogast (STW 5) as an alcohol-based extract of nine herbs including greater celandine, marketed by Bayer since it took over maker Steigerwald in 2013, and says the 2008 liver warnings were added only in 2018 under BfArM pressure. The author concluded that a celandine-containing Iberogast could no longer be recommended.