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Dietary supplement

Elimidrol Nighttime Tropical Fruit Punch Ingredients & Drug Interactions

by Sunrise Nutraceuticals

Powder Category: Other Combinations
Most serious interaction: Major
The interaction bottom line Most serious interaction: Major

Elimidrol Nighttime Tropical Fruit Punch is a dietary supplement by Sunrise Nutraceuticals with 2 active ingredients.Based on those ingredients, 1,670 medications have a known interaction with it, the most serious rated major. Use the checker below to test your specific medication, or read the full HelloPharmacist Interaction Report.

HelloPharmacist Scorecard of Elimidrol Nighttime Tropical Fruit Punch by Sunrise Nutraceuticals

Our pharmacy team’s full take, with four database checks built into the cards below — a summary of what is known, not a grade of the product itself.

From our pharmacy team — supplement deep dive

What’s inside

Low disclosure
Ingredient Transparency · database check
Low

Most active ingredients don't disclose an individual amount — you can't tell how much of each you're getting.

Why this rating?
  • The label discloses an exact amount for 0 of its 13 active ingredients.
  • “Elimidrol Nighttime Proprietary Blend” is a proprietary blend — the label gives one combined amount (5,751 mg) without saying how much of each component you get.
  • “[XKJ]-5 Formula” is a proprietary blend — the label doesn't break down how much of each component you get.
  • “Y90 Advanced Formula” is a proprietary blend — the label doesn't break down how much of each component you get.

Elimidrol Nighttime Tropical Fruit Punch is a powder supplement with 13 active ingredients. The main ones are herbal extracts and neurotransmitter precursors: hops, ginger, melatonin (a hormone that regulates sleep), 5-HTP (a precursor to serotonin), lemon balm, lavender, GABA (gamma-aminobutyric acid, a calming brain chemical), magnolia, N-acetyl-L-cysteine, German chamomile, kava kava, passionflower, and valerian powder.

Three additional components are proprietary blends whose exact ingredients aren't fully listed. The product also contains inactive ingredients (fillers and flavoring): citric acid, natural and artificial flavors, maltodextrin, sucralose, and FD&C Red #40.

Does it work?

Moderate evidence
Evidence for Intended Use · database check
By FDA rules, dietary supplements can’t claim to treat, cure, or prevent disease — so labels speak in careful marketing language. We discern each product’s intended use from its name, label claims, and label statements, then grade the clinical evidence for that use. How these ratings are computed
Moderate

Some clinical evidence supports this product's ingredients for its stated purpose, but it isn't conclusive.

Why this rating?
  • The label markets this product for: support mood, tranquility, comfort, and sleep.
  • We looked for evidence on: Anxiety, Adjustment disorders, Benzodiazepine withdrawal, Beta blocker-induced insomnia, insomnia, stress — and 2 related terms.
  • The strongest evidence on file: Lemon Balm is rated "Possibly Effective" for Stress (Natural Medicines).
  • Also on file: Valerian is rated "Possibly Effective" for Insomnia.
  • Also on file: Passion Flower is rated "Possibly Effective" for Pre-procedural anxiety, Insomnia.

The evidence for most of the active ingredients in this nighttime product is limited. For sleep and relaxation, melatonin is likely effective for delayed sleep phase syndrome and non-24-hour sleep-wake disorder (circadian rhythm disorders), and passionflower and valerian are possibly effective for insomnia.

Ginger is possibly effective for pregnancy-related nausea and vomiting and dysmenorrhea (menstrual pain), and osteoarthritis. Lemon balm and lavender are possibly effective for stress and cold sores, respectively.

For most other uses the ingredients are claimed for — anxiety, attention deficit disorder, depression, and various other conditions — the evidence we hold is either insufficient or possibly ineffective, meaning research is too thin or conflicting to confirm they work for those purposes.

How safe is it?

Well-documented data
Safety Information · database check
Well characterized

Adverse-effect, pregnancy, and general safety data are on file for most of these ingredients.

Why this rating?
  • We hold adverse-effect (side-effect) data for 13 of the 13 matched ingredients.
  • Pregnancy & breastfeeding safety ratings cover 13 of 13.
  • General safety write-ups exist for 13 of 13.
  • Remember: this measures how much safety information exists. Thin data is not the same as being safe.

Most ingredients are generally well tolerated short-term. However, kava carries the most serious safety concern: it has been linked to over 100 cases of liver injury, with some cases appearing after just 3–4 weeks of use.

Hops, ginger, melatonin, 5-HTP, lemon balm, lavender, GABA, magnolia, N-acetyl-L-cysteine, chamomile, and valerian may all cause drowsiness or sedation — a particular concern if you drive or operate machinery. Common mild side effects include gastrointestinal upset (nausea, diarrhea, heartburn), headache, and dizziness.

Kava may also cause tremor, memory problems, and dry mouth. Long-term safety data for most of these ingredients is limited or not well studied.

Meds to double-check

Major interaction found
Known Interaction Concern · database check
Major identified

At least one ingredient has a documented Major-severity interaction. Check your medications for a personalized result.

Why this rating?
  • 13 of the 13 matched ingredients can interact with medications — Magnolia, Lemon Balm, Gamma-aminobutyric Acid (gaba), 5-htp, Lavender, among others.
  • The most serious interaction on file is rated Major.
  • Some involve high-stakes drug classes: anticoagulant / antiplatelet drugs; seizure medications; immunosuppressants / transplant drugs; diabetes medications; Parkinson's medications.
  • For scale: 1,671 individual medications appear in the full list. A big number alone doesn't make a product dangerous — what matters is whether YOUR medication is on it, so run yours through the interaction checker on this page.

Before taking this product, double-check with your doctor or pharmacist if you take any of the following: blood thinners or clot-preventing drugs (anticoagulants/antiplatelet agents, including warfarin), nitroglycerin (Major interaction with N-acetyl-L-cysteine), blood pressure medications, blood sugar medications, heart or blood vessel drugs (including nifedipine and losartan), sedating medications (CNS depressants, including benzodiazepines and opioids), seizure medications, hormone therapies (birth control pills or hormone replacement), psychiatric medications (especially serotonin-boosting drugs and antipsychotics), and immunosuppressants. Kava has a Major interaction with all CNS depressants.

Check your own medication Run your meds through the checker above

The bottom line

Scorecard at a glanceFormula with limited ingredient disclosure with some supporting evidence for its stated purpose. Major medication interactions have been identified, and safety information is well characterized.

This product is intended for sleep and nighttime relaxation and contains ingredients with some evidence for insomnia (melatonin, passionflower, valerian) alongside herbs with weaker evidence. Because it combines many ingredients that lower blood pressure, thin blood, affect sedation, and interact with numerous medications — including a Major interaction with nitroglycerin and serious liver-injury risk from kava — you should check your exact medications with your doctor or pharmacist before starting.

Avoid driving or operating heavy machinery after taking it. If you take blood thinners, blood pressure drugs, diabetes medications, seizure medications, sedating drugs, or any psychiatric medication, confirm with your own healthcare provider first.

Educational only — not medical advice; always confirm with your pharmacist. Our editorial policy · How we use AI

Assessment coverage: 13 of 13 active ingredients matched to our full ingredient reviews (monographs). Based on the product label dated Jan 24, 2024.

This Scorecard evaluates available label information, ingredient evidence, and known medication-safety considerations. It does not independently verify product identity, purity, potency, contamination, or manufacturing quality. How these ratings are computed

At a glance

General information

Key facts about Elimidrol Nighttime Tropical Fruit Punch, straight from the product label.

Brand Sunrise Nutraceuticals
Barcode (UPC) 738435650995
Net contents 7.9 Ounce(s); 224 Gram(s)
Market status On market
Date entered into DSLD Jan 24, 2024
DSLD ID 304136
Product type Other Combinations
Supplement form Powder
Dietary claims / uses All Other, Structure/Function
Intended target group(s) Adult (18 - 50 Years), Women (not pregnant or lactating)
From the label
Everything in this section is reproduced from the manufacturer’s own product label — it’s the label speaking, not HelloPharmacist. We show it so you can see exactly what the maker states; we don’t verify or endorse those statements.

Supplement Facts

The label details for Elimidrol Nighttime Tropical Fruit Punch by Sunrise Nutraceuticals, sourced from the NIH Dietary Supplement Label Database.

Supplement Facts

Daily Value (DV) Target Group(s):
Adults and children 4 or more years of age
Minimum serving Sizes:
8 Gram(s)
Maximum serving Sizes:
8 Gram(s)
Servings per container
28
UPC/BARCODE
738435650995
IngredientAmount% DV
Hops0 NP--
Ginger0 NP--
Melatonin0 NP--
5-HTP0 NP--
Lemon Balm0 NP--
Lavender0 NP--
Gamma Aminobutyric Acid0 NP--
Magnolia0 NP--
N-Acetyl-L-Cysteine0 NP--
Chamomile0 NP--
Kava Kava root extract0 NP--
Passionflower0 NP--
Elimidrol Nighttime Proprietary Blend5751 mg--
[XKJ]-5 Formula0 NP--
Y90 Advanced Formula0 NP--
Valerian, Powder0 NP--

Other ingredients: Citric Acid, Natural & Artificial Flavors, Maltodextrin, Sucralose, FD&C Red #40

Tap any ingredient to jump to its full detail below.

Label statements
These statements are the manufacturer’s wording, reproduced from the product label — the label is saying it, not HelloPharmacist. We don’t verify or endorse them.
Formulation

Made with high quality ingredients Manufactured under strict GMP regulations

Elimidrol is scientifically formulated with ingredients to support your mood, tranquility, comfort, and sleep.

Mood - Tranquility - Comfort - Sleep Advanced formula for a feeling of mental and physical equilibrum Promotes restorative sleep for healthy mental and physical balance Relieves intermittent restlessness, irritability, and anxious feelings Promotes calmness, relaxation, and positive mood Maximum Strength

Suggested/Recommended/Usage/Directions

Directions: Mix 1 scoop with 10-12 ounces of water. Consume and wait approximately 30 minutes to assess your tolerance. After 30 minutes, consume an additional scoop mixed with 10-12 ounces of water if deemed necessary. Do not exceed 4 scoops of Elimidrol Nighttime in 24 hours. Recommended on an empty stomach for best results. Elimidrol Nighttime should be taken during nighttime hours and supplemented with Elimidrol Daytime.

Shake container prior to each use to redistribute ingredients.

Precautions

Do not exceed 4 scoops of Elimidrol Nighttime in 24 hours.

Warning: Please consult your physician prior to consuming this product especially if you have or have had liver problems, frequently use alcoholic beverages, are taking any medication, or if you have any pre-existing medical condition.

Stop use and see a doctor if you develop symptoms that may signal liver problems (e.g., unexplained fatigue, abdominal pain, loss of appetite, fever, vomiting, dark urine, pale stools, yellow eyes or skin).

Not for use by persons under 18 years of age or by pregnant or breastfeeding women.

Not for use by persons under 18 years of age or by pregnant or breastfeeding women.

Not for use with alcoholic beverages. Excessive use or use with products that cause drowsiness may impair your ability to operate a vehicle or heavy equipment. Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place, out of reach of children.

General Statements

See Elimidrol Daytime for daytime directions. Contents may settle after shipping.

Storage

Moisture and humidity can cause clumping and discoloration; however product is still safe for consumption. Store in a cool, dry place, out of reach of children.

Seals/Symbols

Made in U.S.A. Quality Assured

HQI High Quality Ingredients Scientifically Formulated

FDA Disclaimer Statement

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

FDA Statement of Identity

Dietary Supplement

See for yourself

Elimidrol Nighttime Tropical Fruit Punch by Sunrise Nutraceuticals label

The label scan from the NIH Dietary Supplement Label Database. Tap to enlarge.

What’s inside

The Ingredients in Elimidrol Nighttime Tropical Fruit Punch by Sunrise Nutraceuticals

These are the 2 active ingredients this product is made of. Select any to open its full monograph.

Serving size8 Gram(s) Dosage formPowder Servings per container28 Amounts shown are per serving.

Most supplement products combine several ingredients, and a medication can interact with the product through any one of them. Each ingredient below shows whether it has known drug interactions.

Elimidrol Nighttime Proprietary Blend

5751 mg per serving
  • › [XKJ]-5 Formula
  • › Y90 Advanced Formula

Other (inactive) ingredients: Citric Acid, Natural & Artificial Flavors, Maltodextrin, Sucralose, FD&C Red #40. These complete the product’s ingredient list but are not active constituents.

Interaction report

Elimidrol Nighttime Tropical Fruit Punch by Sunrise Nutraceuticals Drug Interactions

Want to check YOUR meds against Elimidrol Nighttime Tropical Fruit Punch?

Ask about interactions with your drugs in plain English — “Can I take it with lisinopril?” — and we find you the answer in seconds, ingredient by ingredient.

Go to the checker
1,670Drugs
249 Major 1,416 Moderate 5 Minor

Ingredients driving the most interactions

Each ingredient & the kinds of drugs it affects

For each ingredient in Elimidrol Nighttime Tropical Fruit Punch with known interactions, here are the types of medications it can affect. Open any type for the detail — or search your exact drug in the checker above.

The maker

Brand information

Manufacturer and brand details for Elimidrol Nighttime Tropical Fruit Punch, from the product label.

Sunrise Nutraceuticals

See all Sunrise Nutraceuticals products
Name
Sunrise Nutraceuticals, LLC
Street Address
2234 N. Federal Hwy Ste 479
City
Boca Raton
State
FL
ZipCode
33431
Web Address
www.sunrisenutraceuticals.com
Pharmacist Counseling Corner

Elimidrol Nighttime Tropical Fruit Punch by Sunrise Nutraceuticals: Common Questions

Does Elimidrol Nighttime Tropical Fruit Punch by Sunrise Nutraceuticals interact with any medications?
Yes. Based on its ingredients, Elimidrol Nighttime Tropical Fruit Punch has a known interaction with 1,670 medications, including 249 rated major. Use the checker to see how it interacts with a specific drug.
How can one product interact with so many drugs?
Elimidrol Nighttime Tropical Fruit Punch contains 2 active ingredients, and an interaction can come from any of them. We check every ingredient, combine the results into one list per medication, and show which ingredient and mechanism is responsible.
Where does this information come from?
The product label data comes from the NIH Dietary Supplement Label Database (DSLD); the interaction data is built on the Natural Medicines database and reviewed by HelloPharmacist pharmacists.
Can I take this if I'm pregnant or breastfeeding?
The safety data varies by ingredient, but most advise against it. Hops and magnolia are unsafe or best avoided in pregnancy; ginger is possibly safe if kept to food amounts; melatonin is possibly unsafe; 5-HTP, lemon balm, chamomile, passionflower, and valerian lack reliable safety information and should be avoided unless your doctor approves. For breastfeeding, hops, melatonin, 5-HTP, magnolia, GABA, and passionflower should be avoided; ginger and N-acetyl-L-cysteine are likely or possibly safe. Talk with your doctor or pharmacist before using this product during pregnancy or while nursing.
Will this make me drowsy?
Yes, very likely. Most ingredients — hops, melatonin, 5-HTP, lemon balm, lavender, magnolia, chamomile, kava, passionflower, and valerian — can cause drowsiness. That's the intention for a nighttime product, but it also means you should not drive or use heavy machinery after taking it. If drowsiness persists into the next day, talk to your doctor or pharmacist.
Does this actually work for sleep?
Melatonin is likely effective for certain sleep disorders (delayed sleep phase syndrome and non-24-hour sleep-wake disorder). Passionflower and valerian are possibly effective for insomnia. The other ingredients have insufficient evidence or lack established effectiveness for sleep in our data. Results vary by person.
What are the most common side effects?
Mild gastrointestinal upset (nausea, diarrhea, heartburn, abdominal discomfort), headache, dizziness, and drowsiness are the most frequently reported. Ginger at higher doses can increase these risks. If side effects are bothersome or don't fade, tell your pharmacist.
Is kava safe in this product?
Kava has been linked to over 100 cases of liver injury worldwide, some appearing after just 3–4 weeks of use. While many cases remain debated, the risk is real enough that kava is banned or restricted in some countries. If you have any liver disease or take other potentially liver-damaging drugs, avoid this product and talk to your doctor.
Can I take this with my blood pressure or blood thinner medications?
Multiple ingredients in this product — including ginger, melatonin, N-acetyl-L-cysteine, magnolia, and others — interact with blood pressure and blood-thinning drugs and may alter their effects or increase bleeding risk. Do not take this product without clearing it with your doctor or pharmacist first if you use any of these medications.

Written and reviewed by the HelloPharmacist editorial staff. Our editorial policy

Not sure if Elimidrol Nighttime Tropical Fruit Punch is safe with your meds?

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Ask a pharmacist

Label information is sourced from the NIH Dietary Supplement Label Database and reflects the product version on file; always read your actual product label. This page is for education only and is not a substitute for professional medical advice. Confirm with your pharmacist or doctor before combining supplements and medications.

Elimidrol Nighttime Tropical Fruit Punch label
Sources

Sources & How We Checked

Elimidrol Nighttime Tropical Fruit Punch's label data comes from the NIH Dietary Supplement Label Database; the ingredient interaction data is from the Natural Medicines database, reviewed by our pharmacists.

Content is written and reviewed by licensed HelloPharmacist pharmacists. See our data sources and editorial standards for how this information is built and checked.

The 510 references behind this product’s interaction data

Every citation that drives the interaction findings for this product’s ingredients, from the evidence-graded Natural Medicines (TRC Healthcare) database. Open an ingredient to browse its citations — links open the study on PubMed or the publisher’s site.

Hops 15 references
  1. Newall CA, Anderson LA, Philpson JD. Herbal Medicine: A Guide for Healthcare Professionals. London, UK: The Pharmaceutical Press, 1996.
  2. McGuffin M, Hobbs C, Upton R, Goldberg A, eds. American Herbal Products Association's Botanical Safety Handbook. Boca Raton, FL: CRC Press, LLC 1997.
  3. Zava DT, Dollbaum CM, Blen M. Estrogen and progestin bioactivity of foods, herbs, and spices. Proc Soc Exp Biol Med 1998;217:369-78. PubMed
  4. Milligan SR, Kalita JC, Heyerick A, et al. Identification of a potent phytoestrogen in hops (Humulus lupulus L.) and beer. J Clin Endocrinol Metab 1999;84:2249-52.. PubMed
  5. Milligan SR, Kalita JC, Pocock V, et al. The endocrine activities of 8-prenylnaringenin and related hop (Humulus lupulus L.) flavonoids. J Clin Endocrinol Metab 2000;85:4912-5.. DOI
  6. Henderson MC, Miranda CL, Stevens JF, et al. In vitro inhibition of human P450 enzymes by prenylated flavonoids from hops, Humulus lupulus. Xenobiotica 2000;30:235-51.. PubMed
  7. Mannering, G. J., Shoeman, J. A., and Deloria, L. B. Identification of the antibiotic hops component, colupulone, as an inducer of hepatic cytochrome P-4503A in the mouse. Drug Metab Dispos 1992;20(2):142-147. DOI
  8. Skorska, C., Mackiewicz, B., Gora, A., Golec, M., and Dutkiewicz, J. Health effects of inhalation exposure to organic dust in hops farmers. Ann.Univ Mariae.Curie Sklodowska [Med] 2003;58(1):459-465.
  9. Schiller, H., Forster, A., Vonhoff, C., Hegger, M., Biller, A., and Winterhoff, H. Sedating effects of Humulus lupulus L. extracts. Phytomedicine. 2006;13(8):535-541. PubMed
  10. van Hunsel, F. P. and Kampschoer, P. [Postmenopausal bleeding and dietary supplements: a possible causal relationship with hop- and soy-containing preparations]. Ned.Tijdschr.Geneeskd. 2012;156(41):A5095.
  11. Fenselau, C. and Talalay, P. Is oestrogenic activity present in hops? Food Cosmet.Toxicol. 1973;11(4):597-602. PubMed
  12. Godnic-Cvar, J., Zuskin, E., Mustajbegovic, J., Schachter, E. N., Kanceljak, B., Macan, J., Ilic, Z., and Ebling, Z. Respiratory and immunological findings in brewery workers. Am J Ind Med 1999;35(1):68-75. DOI
  13. Lee KM, Jung JS, Song DK, and et al. Effects of Humulus lupulus extract on the central nervous system in mice. Planta Med 1993;59(Suppl):A691.
  14. Assessment report on Humulus lupulus L., flos. European Medicines Agency, 2014. Available at: https://www.ema.europa.eu/en/documents/herbal-report/final-assessment-report-humulus-lupulus-l-flos_en.pdf. Accessed September 29, 2021.
  15. van Breemen RB, Chen L, Tonsing-Carter A, et al. Pharmacokinetic Interactions of a Hop Dietary Supplement with Drug Metabolism in Perimenopausal and Postmenopausal Women. J Agric Food Chem. 2020;68(18):5212-5220. PubMed

See these in context on the Hops monograph →

Ginger 64 references
  1. Fischer-Rasmussen W, Kjaer SK, Dahl C, Asping U. Ginger treatment of hyperemesis gravidarum. Eur J Obstet Gynecol Reprod Biol 1991;38:19-24. PubMed
  2. Jewell D, Young G. Interventions for nausea and vomiting in early pregnancy. Cochrane Database Syst Rev 2000;(2):CD000145. PubMed
  3. Vutyavanich T, Kraisarin T, Ruangsri R. Ginger for nausea and vomiting in pregnancy: randomized, double-masked, placebo-controlled trial. Obstet Gynecol 2001;97:577-82. DOI
  4. Backon J. Ginger in preventing nausea and vomiting of pregnancy; a caveat due to its thromboxane synthetase activity and effect on testosterone binding. Eur J Obstet Gynecol Reprod Biol 1991;42:163-4. PubMed
  5. Srivastava KC. Effect of onion and ginger consumption on platelet thromboxane production in humans. Prostaglandins Leukot Essent Fatty Acids 1989;35:183-5. PubMed
  6. Stewart JJ, Wood MJ, Wood CD, Mims ME. Effects of ginger on motion sickness susceptibility and gastric function. Pharmacology 1991;42:111-20. PubMed
  7. Smith C, Crowther C, Willson K, et al. A randomized controlled trial of ginger to treat nausea and vomiting in pregnancy. Obstet Gynecol 2004;103:639-45. PubMed
  8. Portnoi G, Chng LA, Karimi-Tabesh L, et al. Prospective comparative study of the safety and effectiveness of ginger for the treatment of nausea and vomiting in pregnancy. Am J Obstet Gynecol 2003;189:1374-7.. PubMed
  9. Wigler I, Grotto I, Caspi D, Yaron M. The effects of Zintona EC (a ginger extract) on symptomatic gonarthritis. Osteoarthritis Cartilage 2003;11:783-9. PubMed
  10. Ghayur MN, Gilani AH. Ginger lowers blood pressure through blockade of voltage-dependent calcium channels. J Cardiovasc Pharmacol 2005;45:74-80. PubMed
  11. Thomson M, Al-Qattan KK, Al-Sawan SM, et al. The use of ginger (Zingiber officinale Rosc.) as a potential anti-inflammatory and antithrombotic agent. Prostaglandins Leukot Essent Fatty Acids 2002;67:475-8. PubMed
  12. Kanerva L, Estlander T, Jolanki R. Occupational allergic contact dermatitis from spices. Contact Dermatitis 1996;35:157-62. PubMed
  13. Akhani SP, Vishwakarma SL, Goyal RK. Anti-diabetic activity of Zingiber officinale in streptozotocin-induced type I diabetic rats. J Pharm Pharmacol 2004;56:101-5.
  14. Kruth P, Brosi E, Fux R, et al. Ginger-associated overanticoagulation by phenprocoumon. Ann Pharmacother 2004;38:257-60. PubMed
  15. Jiang X, Williams KM, Liauw WS, et al. Effect of ginkgo and ginger on the pharmacokinetics and pharmacodynamics of warfarin in healthy subjects. Br J Clin Pharmacol 2005;59:425-32. PubMed
  16. Borrelli F, Capasso R, Aviello G, et al. Effectiveness and safety of ginger in the treatment of pregnancy-induced nausea and vomiting. Obstet Gynecol 2005;105:849-56. PubMed
  17. Smith C, Crowther C, Wilson K et al. A randomized controlled trial of ginger to treat nausea and vomiting in pregnancy. Obstet Gynecol 2004;103:639-45. PubMed
  18. Jiang X, Blair EY, McLachlan AJ. Investigation of the effects of herbal medicines on warfarin response in healthy subjects: a population pharmacokinetic-pharmacodynamic modeling approach. J Clin Pharmacol 2006;46:1370-8. PubMed
  19. Chittumma P, Kaewkiattikun K, Wiriyasiriwach B. Comparison of the effectiveness of ginger and vitamin B6 for treatment of nausea and vomiting in early pregnancy: a randomized double-blind controlled trial. J Med Assoc Thai 2007;90:15-20.
  20. Ozgoli G, Goli M, Moattar F. Comparison of effects of ginger, mefenamic acid, and ibuprofen on pain in women with primary dysmenorrhea. J Altern Complement Med 2009;15:129-32. PubMed
  21. Black CD, Herring MP, Hurley DJ, O'Connor PJ. Ginger (Zingiber officinale) reduces muscle pain caused by eccentric exercise. J Pain 2010;11:894-903. PubMed
  22. Heitmann K, Nordeng H, Holst L. Safety of ginger use in pregnancy: results from a large population-based cohort study. Eur J Clin Pharmacol 2012 Jun 17. PubMed
  23. Ryan JL, Heckler CE, Roscoe JA, et al. Ginger (Zingiber officinale) reduces acute chemotherapy-induced nausea: a URCC CCOP study of 576 patients. Support Care Cancer. 2012;20:1479-89. PubMed
  24. Backon J. Ginger as an antiemetic: possible side effects due to its thromboxane synthetase activity. Anaesthesia. 1991;46(8):705-6.. PubMed
  25. Abebe W. Herbal medication: potential for adverse interactions with analgesic drugs. J Clin Pharm Ther. 2002;27:391-401. PubMed
  26. Argento A, Tiraferri E, Marzaloni M. [Oral anticoagulants and medicinal plants. An emerging interaction]. Ann Ital Med Int. 2000;15:139-43.
  27. Young HY, Liao JC, Chang YS, et al. Synergistic effect of ginger and nifedipine on human platelet aggregation: a study in hypertensive patients and normal volunteers. Am J Chin Med. 2006;34:545-51. PubMed
  28. Greenway FL, Liu Z, Martin CK, et al. Safety and efficacy of NT, an herbal supplement, in treating human obesity. Int J Obes (Lond). 2006;30:1737-41. PubMed
  29. Shalansky S, Lynd L, Richardson K, et al. Risk of warfarin-related bleeding events and supratherapeutic international normalized ratios associated with complementary and alternative medicine: a longitudinal analysis. Pharmacotherapy. 2007;27:1237-47. PubMed
  30. Lesho EP, Saullo L, Udvari-Nagy S. A 76-year-old woman with erratic anticoagulation. Cleve Clin J Med. 2004;71:651-6. PubMed
  31. Okonta JM, Uboh M, Obonga WO. Herb-Drug Interaction: A Case Study of Effect of Ginger on the Pharmacokinetic of Metronidazole in Rabbit. Indian Journal of Pharmaceutical Sciences (India) 2008;70(230):232. PubMed
  32. Chiang HM, Chao PD, Hsiu SL, et al. Ginger significantly decreased the oral bioavailability of cyclosporine in rats. Am J Chin Med. 2006;34:845-55. PubMed
  33. Bhandari U, Kanojia R, Pillai KK. Effect of ethanolic extract of Zingiber officinale on dyslipidaemia in diabetic rats. J Ethnopharmacol. 2005;97:227-30. PubMed
  34. Ojewole JA. Analgesic, antiinflammatory and hypoglycaemic effects of ethanol extract of Zingiber officinale (Roscoe) rhizomes (Zingiberaceae) in mice and rats. Phytother Res. 2006;20:764-72.
  35. Al-Amin ZM, Thomson M, Al-Qattan KK, et al. Anti-diabetic and hypolipidaemic properties of ginger (Zingiber officinale) in streptozotocin-induced diabetic rats. Br J Nutr. 2006;96:660-6.
  36. Islam MS, Choi H. Comparative effects of dietary ginger (Zingiber officinale) and garlic (Allium sativum) investigated in a type 2 diabetes model of rats. J Med Food. 2008;11:152-9.
  37. Cady RK, Goldstein J, Nett R, et al. A double-blind placebo-controlled pilot study of sublingual feverfew and ginger (LipiGesic M) in the treatment of migraine. Headache 2011;51:1078-86.
  38. Futrell, J. M. and Rietschel, R. L. Spice allergy evaluated by results of patch tests. Cutis 1993;52(5):288-290.
  39. Sripramote, M. and Lekhyananda, N. A randomized comparison of ginger and vitamin B6 in the treatment of nausea and vomiting of pregnancy. J Med Assoc.Thai. 2003;86(9):846-853.
  40. Lohsiriwat, S., Rukkiat, M., Chaikomin, R., and Leelakusolvong, S. Effect of ginger on lower esophageal sphincter pressure. J.Med.Assoc.Thai. 2010;93(3):366-372.
  41. Liu, P. H. and Ho, H. L. Ginger and drug bezoar induced small bowel obstruction. J R.Coll.Surg.Edinb. 1983;28(6):397-398.
  42. Maghbooli M, Golipour F, Moghimi Esfandabadi A, Yousefi M. Comparison between the efficacy of ginger and sumatriptan in the ablative treatment of the common migraine. Phytother Res 2014;28(3):412-5. PubMed
  43. Mahluji S, Attari VE, Mobasseri M, Payahoo L, Ostadrahimi A, Golzari SE. Effects of ginger (Zingiber officinale) on plasma glucose level, HbA1c and insulin sensitivity in type 2 diabetic patients. Int J Food Sci Nutr 2013;64(6):682-6.
  44. Mozaffari-Khosravi H, Talaei B, Jalali BA, Najarzadeh A, Mozayan MR. The effect of ginger powder supplementation on insulin resistance and glycemic indices in patients with type 2 diabetes: a randomized, double-blind, placebo-controlled trial. Complement PubMed
  45. Paramdeep G. Efficacy and tolerability of ginger (Zingiber officinale) in patients of osteoarthritis of knee. Indian J Physiol Pharmacol 2013;57(2):177-83.
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  52. Martins LB, Rodrigues AMDS, Monteze NM, et al. Double-blind placebo-controlled randomized clinical trial of ginger (Zingiber officinale Rosc.) in the prophylactic treatment of migraine. Cephalalgia. 2020;40(1):88-95.
  53. Martins LB, Rodrigues AMDS, Rodrigues DF, Dos Santos LC, Teixeira AL, Ferreira AVM. Double-blind placebo-controlled randomized clinical trial of ginger (Zingiber officinale Rosc.) addition in migraine acute treatment. Cephalalgia. 2019;39(1):68-76.
  54. Ahad A, Raish M, Bin Jardan YA, Alam MA, Al-Mohizea AM, Al-Jenoobi FI. Effect of Hibiscus sabdariffa and Zingiber officinale on the antihypertensive activity and pharmacokinetic of losartan in hypertensive rats. Xenobiotica. 2020:1-11.
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  56. Yamprasert R, Chanvimalueng W, Mukkasombut N, Itharat A. Ginger extract versus Loratadine in the treatment of allergic rhinitis: a randomized controlled trial. BMC Complement Med Ther. 2020;20(1):116. PubMed
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  58. Alam MA, Bin Jardan YA, Alzenaidy B, et al. Effect of Hibiscus sabdariffa and Zingiber officinale on pharmacokinetics and pharmacodynamics of amlodipine. J Pharm Pharmacol 2021;73(9):1151-60.
  59. Akbarzadeh E, Heydari M, Atarzadeh F, Jaladat AM. Chronic dysuria following ginger (Zingiber officinale) use: a case report. Galen Med J 2018;7:e1086. DOI
  60. Haron MH, Dale O, Martin K, et al. Evaluation of the Herb-Drug Interaction Potential of Commonly Used Botanicals on the US Market with Regard to PXR- and AhR-Mediated Influences on CYP3A4 and CYP1A2. J Diet Suppl 2022. PubMed
  61. Rostamkhani H, Veisi P, Niknafs B, Jafarabadi MA, Ghoreishi Z. The effect of zingiber officinale on prooxidant-antioxidant balance and glycemic control in diabetic patients with ESRD undergoing hemodialysis: a double-blind randomized control trial. BMC Co PubMed
  62. Husain I, Dale OR, Idrisi M, et al. Evaluation of the Herb-Drug Interaction (HDI) Potential of Zingiber officinale and Its Major Phytoconstituents. J Agric Food Chem. 2023;71(19):7521-7534.
  63. Committee on Practice Bulletins-Obstetrics. ACOG Practice Bulletin No. 189: Nausea And Vomiting Of Pregnancy. Obstet Gynecol. 2018;131(1):e15-e30. PubMed
  64. Pochet S, Lechon AS, Lescrainier C, et al. Herb-anticancer drug interactions in real life based on VigiBase, the WHO global database. Sci Rep 2022;12(1):14178. PubMed

See these in context on the Ginger monograph →

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Parts of this content are provided by the Therapeutic Research Center, LLC.

DISCLAIMER: Currently this does not check for drug-drug interactions. This is not an all-inclusive comprehensive list of potential interactions and is for informational purposes only. Not all interactions are known or well-reported in the scientific literature, and new interactions are continually being reported. Input is needed from a qualified healthcare provider including a pharmacist before starting any therapy. Application of clinical judgment is necessary.

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