Interactions on record — worth a quick check against your medications. Based on 4 of 17 ingredients. Check your meds →
Dietary supplement

Monster Plexx Ingredients & Drug Interactions

by Innovative Laboratories

Tablet Or Pill Category: Other Combinations
Most serious interaction: Moderate
The interaction bottom line Most serious interaction: Moderate

Monster Plexx is a dietary supplement by Innovative Laboratories with 17 active ingredients. Its ingredients are commonly taken for anti-aging and low dhea levels, mood and depression, vaginal dryness and sexual health.Based on those ingredients, 779 medications have a known interaction with it, the most serious rated moderate. The ingredients most likely to interact are 3beta-3-Hydroxyandrost-5-en-17-one Undecanoate, Serenoa serrulata Fruit Extract. Use the checker below to test your specific medication, or read the full HelloPharmacist Interaction Report.

HelloPharmacist Scorecard of Monster Plexx by Innovative Laboratories

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 17 active ingredients.
  • “Quintuple ProHormone & Anabolic Blend” is a proprietary blend — the label gives one combined amount (250 mg) without saying how much of each component you get.
  • “Plant Androgenic & Anabolic Blend” is a proprietary blend — the label gives one combined amount (200 mg) without saying how much of each component you get.
  • “Blend with Cyclosome Technology” is a proprietary blend — the label gives one combined amount (200 mg) without saying how much of each component you get.

Monster Plexx contains 17 active and inactive ingredients centered on hormone-like compounds. The active ingredients include multiple DHEA-related compounds—5a hydroxy laxogenin acetate, 3beta-3-hydroxyandrost-5-en-17-one undecanoate, 4-androsten-3beta-ol-17-one undecanoate, 1-androstan-3beta-ol-17-one decanoate, 3beta-hydroxy-5alpha-androst-1-en-17-one acetate, and a complex steroid glycoside—along with epiandrosterone, saw palmetto fruit extract, plant-derived compounds like dioscorea (diosgenin and progenin III), pine pollen extract, and ajuga root extract.

Inactive ingredients include microcrystalline cellulose, phosphatidylcholine, hydroxypropyl methylcellulose, phytosterols, stearic acid, starch, magnesium stearate, silica, and FD&C Red #3.

Does it work?

Leans against
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
Leans against

The strongest graded evidence we hold for the stated purpose leans against a benefit.

Why this rating?
  • The label markets this product for: muscle strength and size gains for athletes.
  • We looked for evidence on: Athletic performance, Physical performance, Muscle strength, Exercise-induced muscle damage, Lean body mass, Anabolic response — and 1 related terms.
  • The closest evidence on file: Dhea is rated "Possibly Ineffective" for Muscle strength (Natural Medicines).
  • Also on file: Dhea is rated "Possibly Ineffective" for Physical performance.
  • Also on file: Dhea is rated "Insufficient Reliable Evidence To Rate" for Athletic performance, Exercise-induced muscle damage.

The evidence for Monster Plexx's ingredients is mixed. The DHEA-related compounds have been rated possibly effective for depression and aging skin, and likely effective for vaginal atrophy, though data on other claimed uses is insufficient.

Epiandrosterone has insufficient evidence for athletic performance, muscle strength, erectile dysfunction, or obesity. Saw palmetto shows possibly effective evidence only for transurethral resection of the prostate (a surgical outcome); it was rated possibly ineffective for benign prostatic hyperplasia despite common use for that condition.

Ajuga and the plant-derived compounds in this product lack established evidence in our data.

The evidence, ingredient by ingredient Dhea Epiandrosterone Ajuga Nipponensis Saw Palmetto

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 3 of the 4 matched ingredients.
  • Pregnancy & breastfeeding safety ratings cover 4 of 4.
  • General safety write-ups exist for 4 of 4.
  • Remember: this measures how much safety information exists. Thin data is not the same as being safe.

The DHEA compounds are generally well tolerated in the short term at typical doses, but long-term use raises theoretical concerns about cancer risk. The most common side effects are acne (especially in women), headache, insomnia, mood changes, and nausea.

In women, DHEA can cause masculinization—voice deepening, increased body hair, irregular periods, and oily skin. Men may experience aggression and breast issues.

DHEA-related mood effects include mania, anxiety, irritability, and depression in clinical trials. Saw palmetto is generally well tolerated; mild side effects include abdominal pain, diarrhea, nausea, headache, and decreased libido.

Rare reports link saw palmetto to heart rhythm changes and a fixed drug rash. Ajuga root can cause diarrhea, nausea, and vomiting at typical doses, and one case reported acute kidney failure in an adult with liver cirrhosis who ingested about 45 grams.

Because these are hormonal compounds, medical guidance is important.

Side effects, ingredient by ingredient Dhea Epiandrosterone Ajuga Nipponensis Saw Palmetto

Meds to double-check

Moderate interaction found
Known Interaction Concern · database check
Moderate identified

The most serious documented interaction for these ingredients is Moderate. Check your medications for a personalized result.

Why this rating?
  • 2 of the 4 matched ingredients can interact with medications — Dhea, Saw Palmetto.
  • The most serious interaction on file is rated Moderate.
  • Some involve high-stakes drug classes: anticoagulant / antiplatelet drugs.
  • For scale: 780 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 Monster Plexx, check with your doctor or pharmacist if you take antidepressants (especially SSRIs), blood thinners or antiplatelet drugs, birth control pills or estrogens, aromatase inhibitors or tamoxifen for hormone-sensitive cancer, triazolam for sleep, liver enzyme substrates, or if you are due for a tuberculosis vaccine. These are Moderate-severity interactions documented in our data.

Check your own medication Run your meds through the checker above

The bottom line

Scorecard at a glanceFormula with limited ingredient disclosure with graded evidence leaning against its stated purpose. Moderate medication interactions have been identified, and safety information is well characterized.

Monster Plexx is a hormone-based supplement aimed at muscle and anabolic support, but it's not for everyone. If you take antidepressants, blood thinners, birth control, hormone cancer therapies, or CYP3A4-metabolized medications, you need to check with your doctor or pharmacist first—interactions here are real.

Women who may become pregnant and anyone concerned about long-term hormonal effects should discuss this product with their healthcare provider before starting.

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

Assessment coverage: 9 of 17 active ingredients matched to our full ingredient reviews (monographs). Based on the product label dated Feb 23, 2022.

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 Monster Plexx, straight from the product label.

Brand Innovative Laboratories
Barcode (UPC) 626570609148
Net contents 60 Tablet(s)
Market status On market
Date entered into DSLD Feb 23, 2022
DSLD ID 260958
Product type Other Combinations
Supplement form Tablet Or Pill
Dietary claims / uses All Other, Structure/Function
Intended target group(s) Adult Male (18-50 Years)
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 Monster Plexx by Innovative Laboratories, 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:
1 Tablet(s)
Maximum serving Sizes:
1 Tablet(s)
Servings per container
60
UPC/BARCODE
626570609148
IngredientAmount% DV
5a Hydroxy Laxogenin Acetate0 NP--
Iridoid Glycosides0 NP--
Ajuga turkestanica root extract0 NP--
Quintuple ProHormone & Anabolic Blend250 mg--
3beta-3-Hydroxyandrost-5-en-17-one Undecanoate0 NP--
5alpha-Androstan-3beta-ol-17-one Decanoate0 NP--
4-Androsten-3Beta-ol-17- one Undecanoate0 NP--
1-Androsten-3Beta-ol-17-one Decanoate0 NP--
Plant Androgenic & Anabolic Blend200 mg--
Diosterol brand Dioscorea nipponica makino 50-67:1 extract0 NP--
Progenin III0 NP--
Diosgenin0 NP--
Blend with Cyclosome Technology200 mg--
Pine Pollen 100:1 extract0 NP--
Serenoa serrulata Fruit Extract0 NP--
3Beta-Hydroxy-5Alpha-Androst-1-en-17 -one Acetate0 NP--
26-[(Beta-D-Glucopyranosyl)oxy] -22a-Hydroxyfurosta-5, 25(27)-Dien-1b, 3b, 11a-Triol0 NP--
Similax sieboldii Extract0 NP--
26-O-Beta-D-Glycopyranosyl-22-Hydroxyfurost-5-ene-3beta, 26-Diol-3-O-Beta-Diglucorhamnoside0 NP--
5-Methyl-7-Methoxisoflavone0 NP--

Other ingredients: Microcrystalline Cellulose, Phosphatidylcholine, Hydroxypropyl Methylcellulose, Phytosterols, Stearic Acid, Starch, Magnesium Stearate, Silica, FD&C Red #3

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.
General Statements

Mass & strength series

Formulation

Monster Plexx by Innovative Labs is one of the few legal pro hormone complexes that can actually give you intense gains in strength and size that you are looking for.

Made in USA

The ultimate anabolic powerhouse Monster strength Monster size Monster gains

Formula

Monster Plexx consists of 5 pro-hormones combined at high level milligrams making it the first ever "quintuple stack". Innovative Labs also added Dioscorea Nipponica Makino 50-67:1 (as Diosterol Brand), Ajuga Turkestanica Extract, 5-Methyl-7-Methoxyisoflavone and Pine Pollen 100:1 Extract to assist in protein synthesis to unleash the full effects of this powerful anabolic & androgenic testosterone boosting supplement.

Monster Plexx is the most anabolic complex available and is designed for competitive athletes only.

Maximum pro-hypertropic muscle matrix Quadruple stack

Precautions

Do not take if you are subject to any sports drug testing as you may fail.

Warning: Anabolic compounds are for the serious athletes and not intended for anyone under the age of 18 or women of any age.

Warning: Anabolic compounds are for the serious athletes and not intended for anyone under the age of 18 or women of any age. Do not use if you have liver problems, kidney, thyroid, high blood pressure, diabetes, heart disease or if you are taking MAOI's. Do not use fore more than 4-6 weeks w/o a 8 week break between cycles. Tested athletes for performance enhancing substances should consult w/ their sanctioning body prior to use as this product may cause a false reactive result. This product consists of Methylated compounds and upon completion the use of a proper Post Cycle Therapy (PCT) protocol is required. No exceptions

If you are on medication or medical treatment consult a licensed physician prior to use.

Keep out of the reach of children.

FDA Disclaimer Statement

These statements have not been approved by the FDA. This product is not intended to diagnose, treat, cure or prevent any diseases.

Storage

Store in a cool dry place away from moisture and sunlight.

FDA Statement of Identity

Dietary Supplement

Suggested/Recommended/Usage/Directions

Suggested use: As a dietary supplement take 1 tablet in the morning and 1 tablet 6-8 hours later. Do not exceed more than 3 tablets in any 24 hour period.

See for yourself

Monster Plexx by Innovative Laboratories label

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

What’s inside

The Ingredients in Monster Plexx by Innovative Laboratories

These are the 17 active ingredients this product is made of. Select any to open its full monograph.

Serving size1 Tablet(s) Dosage formTablet Or Pill Servings per container60 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.

Plant Androgenic & Anabolic Blend

200 mg per serving

Blend with Cyclosome Technology

200 mg per serving

Other (inactive) ingredients: Microcrystalline Cellulose, Phosphatidylcholine, Hydroxypropyl Methylcellulose, Phytosterols, Stearic Acid, Starch, Magnesium Stearate, Silica, FD&C Red #3. These complete the product’s ingredient list but are not active constituents.

Interaction report

Monster Plexx by Innovative Laboratories Drug Interactions

Want to check YOUR meds against Monster Plexx?

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
779Drugs
776 Moderate 3 Minor

Ingredients driving the most interactions

Each ingredient & the kinds of drugs it affects

For each ingredient in Monster Plexx with known interactions, here are the types of medications they can affect. Open any type for the detail — or search your exact drug in the checker above.

3beta-3-Hydroxyandrost-5-en-17-one Undecanoate10 drug types · 776 drugs

Anticoagulant/Antiplatelet Drugs

Theoretically, DHEA might increase the risk of bleeding if used with anticoagulant or antiplatelet drugs.
Human and laboratory research show that DHEA and DHEA-S can inhibit platelet aggregation.

Likelihood Possible Evidence D
Antidepressant Drugs

Theoretically, DHEA might increase the risk of psychiatric adverse events when used with antidepressants.
In a human case report, the use of a selective serotonin reuptake inhibitor (SSRI) with DHEA caused a manic episode. Concern for this interaction may be greater in younger individuals with higher baseline DHEA levels.

Likelihood Possible Evidence D
Aromatase Inhibitors

Theoretically, DHEA might interfere with the clinical effects of aromatase inhibitors.
DHEA is a potent estrogen agonist, which may antagonize the anti-estrogen activity of aromatase inhibitors.

Likelihood Possible Evidence D
Cytochrome P450 3A4 (Cyp3A4) Substrates

Theoretically, DHEA might increase the levels of drugs metabolized by CYP3A4.
Some preliminary evidence shows that DHEA may inhibit CYP3A4; however, the clinical significance of this potential interaction is not known.

Likelihood Possible Evidence D
Fulvestrant (Faslodex)

Theoretically, DHEA might interfere with the anti-estrogen effects of fulvestrant.
DHEA is a potent estrogen agonist. Some research shows that it can overcome the estrogen receptor antagonist action of fulvestrant in estrogen-receptor positive cancer cells.

Likelihood Possible Evidence D
Tamoxifen (Nolvadex)

Theoretically, DHEA might interfere with the anti-estrogen effects of tamoxifen.
DHEA is a potent estrogen agonist. Some research shows that it can overcome the estrogen receptor antagonist activity of tamoxifen in estrogen-receptor positive cancer cells.

Likelihood Possible Evidence D
Triazolam (Halcion)

DHEA can increase blood levels of triazolam.
Administration of DHEA 200 mg daily for two weeks was shown to inhibit the cytochrome P450 3A4 (CYP3A4) metabolism of triazolam. This inhibition appears to be due to DHEA-S, rather than DHEA.

Likelihood Probable Evidence D
Tuberculosis Vaccine

DHEA might reduce the effectiveness of the tuberculosis vaccine.
Animal research shows that high doses of DHEA can reduce the efficacy of the Bacillus Calmette-Guérin (BCG) tuberculosis vaccine.

Likelihood Possible Evidence D
Estrogens

Theoretically, DHEA might increase the effects and adverse effects of estrogen therapy.
DHEA is a precursor to estrogen and androgen and is metabolized into those substances. In clinical research, DHEA supplements increase the levels of these hormones. Also, in clinical research, estrogen-progestin oral contraceptives and conjugated estrogens reduce blood levels of DHEA and DHEA-S. The clinical significance of these findings is unclear.

Likelihood Possible Evidence D
Testosterone

Theoretically, DHEA might increase the effects and side effects of testosterone therapy.
DHEA is a precursor to estrogen and androgen and is metabolized into those substances. In clinical research, DHEA supplements increase the levels of these hormones. The clinical significance of these findings is unclear.

Likelihood Possible Evidence D

Serenoa serrulata Fruit Extract3 drug types · 174 drugs

Anticoagulant/Antiplatelet Drugs

Saw palmetto might increase the risk of bleeding with anticoagulant or antiplatelet drugs.
Saw palmetto is reported to prolong bleeding time. Theoretically, it might increase the risk of bleeding when used concomitantly with anticoagulant or antiplatelet drugs.

Likelihood Possible Evidence D
Contraceptive Drugs

Saw palmetto might reduce the effectiveness of contraceptive drugs.
Saw palmetto might have antiestrogenic effects. Theoretically, it might interfere with contraceptive drugs taken concomitantly.

Likelihood Possible Evidence B
Estrogens

Saw palmetto might reduce the effectiveness of estrogens.
Saw palmetto might have antiestrogenic effects. Theoretically, it might interfere with estrogens taken concomitantly.

Likelihood Possible Evidence B
The maker

Brand information

Manufacturer and brand details for Monster Plexx, from the product label.

Innovative Laboratories

See all Innovative Laboratories products
Name
Innovative Laboratories
Street Address
6015-B Unity Drive
City
Norcross
State
GA
ZipCode
30071
Web Address
www.innovativelaboratories.net
Pharmacist Counseling Corner

Monster Plexx by Innovative Laboratories: Common Questions

Does Monster Plexx by Innovative Laboratories interact with any medications?
Yes. Based on its ingredients, Monster Plexx has a known interaction with 779 medications. Use the checker to see how it interacts with a specific drug.
How can one product interact with so many drugs?
Monster Plexx contains 17 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 Monster Plexx while I'm pregnant or breastfeeding?
No. The DHEA-related compounds and saw palmetto all carry warnings against pregnancy because they affect hormone levels and lack adequate safety data. The safety data advises against use while breastfeeding for the same reasons. Talk with your doctor or pharmacist before taking this product if you're planning pregnancy or breastfeeding.
What are the most common side effects I might notice?
Acne is the most reported side effect, especially in women and often mild. Headache, insomnia, mood changes, and nausea are also common. Women may experience increased body hair, voice changes, or irregular periods. If acne develops, lowering the dose may help.
Does this product actually work for muscle and strength?
The DHEA compounds show possibly effective evidence for depression and aging skin, and likely effective for vaginal atrophy, but the evidence for athletic performance and muscle strength is insufficient in our data. Epiandrosterone and the plant-derived ingredients lack established evidence for those claims either.
Is there concern about cancer risk with long-term use?
Yes. The DHEA compounds are well tolerated short-term, but there's a theoretical concern that long-term oral use may be linked to greater cancer risk. This is why medical guidance is important if you're considering extended use.
What is ajuga root extract supposed to do in this product?
Ajuga root extract is included in the formula, but the evidence for it is insufficient to establish its effectiveness for any condition in our data. The main concern is that it can cause diarrhea, nausea, vomiting, and in rare cases of very high doses, kidney problems.

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

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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.

Monster Plexx label
Sources

Sources & How We Checked

Monster Plexx'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 122 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.

Ajuga Nipponensis 1 reference
  1. Liao SC, Chiu TF, Chen JC, Lin CC. Ajuga nipponensis Makino poisoning. Clin Toxicol (Phila) 2005;43:583-5.

See these in context on the Ajuga Nipponensis monograph →

Dhea 98 references
  1. Frye RF, Kroboth PD, Folan MM, et al. Effect of DHEA on CYP3A-mediated metabolism of triazolam. Clin Pharmacol Ther 2000;67:109 (abstract PI-82).
  2. Kuritzky L. DHEA: Science or wishful thinking? Hosp Pract 1998;33:85-6. PubMed
  3. Van Vollenhoven RF, Morabito LM, Engleman EG, et al. Treatment of systemic lupus erythematosus with dehydroepiandrosterone: 50 patients treated up to 12 months. J Rheumatol 1998;25:285-9.
  4. Van Vollenhoven RF, Engleman EG, McGurie JL. Dehydroepiandrosterone in Systemic Lupus Erythematosus. Arth Rheum 1995;38:1826-31. DOI
  5. Ebeling P, Koivisto VA. Physiological importance of dehydroepiandrosterone. Lancet 1994;343:1479-81. PubMed
  6. Yen SS, Morales AJ, Khorram O. Replacement of DHEA in aging men and women. Potential remedial effects. Ann N Y Acad Sci 1995;774:128-42. PubMed
  7. Labrie F, Diamond P, Cusan L, et al. Effect of 12 month dehydroepiandrosterone replacement therapy on bone, vagina, and endometrium in postmenopausal women. J Clin Endocrinol Metab 1997;82:3498-505. PubMed
  8. Casson PR, Faquin LC, Stentz FB. Replacement of dehydroepiandrosterone enhances T-lymphocyte insulin binding in postmenopausal women. (abstract) Fertil Steril 1995;63:1027-31. DOI
  9. Morales AJ, Haubrich RH, Hwang JY, et al. The effect of six months treatment with a 100 mg daily dose of dehydroepiandrosterone (DHEA) on circulating sex steroids, body composition and muscle strength in age-advanced men and women. Clin Endocrinol (Oxf)1 PubMed
  10. Arlt W, Justl H, Callies F, et al. Oral dehydroepiandrosterone for adrenal androgen replacement: pharmacokinetics and peripheral conversion to androgens and estrogens in young healthy females after dexamethasone suppression. [Abstract] J Clin Endocrinol PubMed
  11. Kline MD, Jaggers ED. Mania onset while using dehydroepiandrosterone (letter). Am J Psychiatry 1999;156:971. PubMed
  12. Callies F, Arlt W, Siekmann L, et al. Influence of oral dehydroepiandrosterone (DHEA) on urinary steroid metabolites in males and females. Steroids 2000;65:98-102. PubMed
  13. Markowitz JS, Carson WH, Jackson CW. Possible dihydroepiandrosterone-induced mania. Biol Psychiatry 1999;45:241-2. PubMed
  14. Stoll BA. Dietary supplements of dehydroepiandrosterone in relation to breast cancer risk. Eur J Clin Nutr 1999;53:771-5. PubMed
  15. Dean CE. Prasterone (DHEA) and mania. Ann Pharmacother 2000;34:1419-22. PubMed
  16. Himmel PB, Seligman TM. A Pilot Study Employing Dehydroepiandrosterone (DHEA) in the Treatment of Chronic Fatigue Syndrome. [Abstract]. J Clin Rheumatol 1999:5:56-9. PubMed
  17. Hunt PJ, Gurnell EM, Huppert FA, et al. Improvement in mood and fatigue after dehydroepiandrosterone replacement in Addison's disease in a randomized, double blind trial. J Clin Endocrinol Metab 2000;85:4650-6.. PubMed
  18. Johannsson G, Burman P, Wiren L, et al. Low dose dehydroepiandrosterone affects behavior in hypopituitary androgen-deficient women: a placebo-controlled trial. J Clin Endocrinol Metab 2002;87:2046-52. PubMed
  19. Calhoun KE, Pommier RF, Muller P, et al. Dehydroepiandrosterone sulfate causes proliferation of estrogen receptor-positive breast cancer cells despite treatment with fulvestrant. Arch Surg 2003;138:879-83.. PubMed
  20. Morris KT, Toth-Fejel S, Schmidt J, et al. High dehydroepiandrosterone-sulfate predicts breast cancer progression during new aromatase inhibitor therapy and stimulates breast cancer cell growth in tissue culture: a renewed role for adrenalectomy. Surgery PubMed
  21. Calhoun K, Pommier R, Cheek J, et al. The effect of high dehydroepiandrosterone sulfate levels on tamoxifen blockade and breast cancer progression. Am J Surg 2003;185:411-5.. PubMed
  22. Stomati M, Monteleone P, Casarosa E, et al. Six-month oral dehydroepiandrosterone supplementation in early and late postmenopause. Gynecol Endocrinol 2000;14:342-63.. PubMed
  23. Petri MA, Mease PJ, Merrill JT, et al. Effects of prasterone on disease activity and symptoms in women with active systemic lupus erythematosus. Arthritis Rheum 2004;50:2858-68. PubMed
  24. Villareal DT, Holloszy JO, Kohrt WM. Effects of DHEA replacement on bone mineral density and body composition in elderly women and men. Clin Endocrinol (Oxf) 2000;53:561-8. PubMed
  25. Acacio BD, Stanczyk FZ, Mullin P, et al. Pharmacokinetics of dehydroepiandrosterone and its metabolites after long-term daily oral administration to healthy young men. Fertil Steril 2004;81:595-604. PubMed
  26. Petri MA, Lahita RG, Van Vollenhoven RF, et al. Effects of prasterone on corticosteroid requirements of women with systemic lupus erythematosus: a double-blind, randomized, placebo-controlled trial. Arthritis Rheum 2002;46:1820-9. PubMed
  27. Pino JA, Marbot R. Volatile flavor constituents of acerola (Malpighia emarginata DC.) fruit. J Agric Food Chem 2001;49:5880-2.
  28. Nair KS, Rizza RA, O'Brien P, et al. DHEA in elderly women and DHEA or testosterone in elderly men. N Engl J Med 2006;355:1647-59. PubMed
  29. Alkatib AA, Cosma M, Elamin MB, et al. A systematic review and meta-analysis of randomized placebo-controlled trials of DHEA treatment effects on quality of life in women with adrenal insufficiency. J Clin Endocrinol Metab 2009;94:3676-81. PubMed
  30. Jesse, R. L., Loesser, K., Eich, D. M., Qian, Y. Z., Hess, M. L., Nestler, J. E. Dehydroepiandrosterone inhibits human platelet aggregation in vitro and in vivo. Ann N.Y.Acad Sci 1995;774:281-90.
  31. Bertoni, A., Rastoldo, A., Sarasso, C., Di Vito C., Sampietro, S., Nalin, M., Bagarotti, A., Sinigaglia, F. Dehydroepiandrosterone-sulfate inhibits thrombin-induced platelet aggregation. Steroids 2012;77(3):260-8. PubMed
  32. Cui, Y., Choi, I. S., Koh, Y. A., Lin, X. H., Cho, Y. B., Won, Y. H. Effects of combined BCG and DHEA treatment in preventing the development of asthma. Immunol Invest 2008;37(3):191-202. PubMed
  33. Aisaka, K., Mori, H., Ogawa, T., Kigawa, T. Effects of dehydroepiandrosterone-sulphate (DHEA-S) administration on puerperal lactation and maternal prolactin and estradiol levels. Nippon Sanka Fujinka Gakkai Zasshi 1984;36(10):1935-42.
  34. Lauritzen, C. [Therapeutic attempts with dehydroepiandrosterone sulfate in threatened pregnancies]. Arch Gynakol 1971;211(1):247-9.
  35. Mortola, J. F. Yen, S. S. The effects of oral dehydroepiandrosterone on endocrine-metabolic parameters in postmenopausal women. J Clin Endocrinol Metab 1990;71(3):696-704. PubMed
  36. Rabijewski, M., Zgliczynski, W. [Positive effects of DHEA therapy on insulin resistance and lipids in men with angiographically verified coronary heart disease--preliminary study]. Endokrynol Pol 2005;56(6):904-10.
  37. Weiss, E. P., Shah, K., Fontana, L., Lambert, C. P., Holloszy, J. O., Villareal, D. T. Dehydroepiandrosterone replacement therapy in older adults: 1- and 2-y effects on bone. Am J Clin Nutr 2009;89(5):1459-67. PubMed
  38. Jankowski, C. M., Gozansky, W. S., Kittelson, J. M., Van Pelt, R. E., Schwartz, R. S., Kohrt, W. M. Increases in bone mineral density in response to oral dehydroepiandrosterone replacement in older adults appear to be mediated by serum estrogens. J Clin E PubMed
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  40. Libe, R., Barbetta, L., Dall'Asta, C., Salvaggio, F., Gala, C., Beck-Peccoz, P., Ambrosi, B. Effects of dehydroepiandrosterone (DHEA) supplementation on hormonal, metabolic and behavioral status in patients with hypoadrenalism. J Endocrinol Invest 2004;27 PubMed
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