Major interaction on record — check this product against your medications before combining. Based on 3 of 7 ingredients. Check your meds →
Dietary supplement

Madness Blue Raspberry Ingredients & Drug Interactions

by Mutant

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

Madness Blue Raspberry is a dietary supplement by Mutant with 7 active ingredients. Its ingredients are commonly taken for high cholesterol, vitamin b3 deficiency (pellagra), heart health support.Based on those ingredients, 1,494 medications have a known interaction with it, the most serious rated major. The ingredients most likely to interact are Niacin, Magnesium, Vitamin B12. Use the checker below to test your specific medication, or read the full HelloPharmacist Interaction Report.

HelloPharmacist Scorecard of Madness Blue Raspberry by Mutant

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

Partial disclosure
Ingredient Transparency · database check
Partial

Most active ingredients list an amount, but at least one is hidden in a blend or missing.

Why this rating?
  • The label discloses an exact amount for 15 of its 19 active ingredients.
  • “MUTANT(TM) MADNESS FORMULA” is a proprietary blend — the label gives one combined amount (4,775 mg) without saying how much of each component you get.
  • “Performance Intensity Matrix” is a proprietary blend — the label gives one combined amount (4,250 mg) without saying how much of each component you get.
  • “L-Arginine/L-Citrulline 1:1 Blend” is a proprietary blend — the label gives one combined amount (1,000 mg) without saying how much of each component you get.

Mutant's Madness Blue Raspberry is a pre-workout powder with 19 ingredients. The active ingredients include niacin (a B vitamin), vitamin B12, malic acid, L-arginine, L-citrulline, beta-alanine, three forms of caffeine (anhydrous, citrate, and dicaffeine malate), cinnamon, magnesium, creatine monohydrate, hordenine HCl, olive leaf extract, citric acid, theobromine extract (from cocoa), green tea extract, and black pepper extract (BioPerine).

Folate is also listed but we could not check its interactions. The inactive ingredients include artificial and natural flavors, sucralose, potassium citrate, silicon dioxide, and Blue 1 colorant.

Does it work?

Strong 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
Strong

Clinical evidence supports at least one of this product's ingredients for its stated purpose.

Why this rating?
  • The label markets this product for: High intensity exercise performance and endurance.
  • We looked for evidence on: Athletic performance, Attention, Muscle strength, Workout recovery, Mental focus.
  • The strongest evidence on file: Caffeine is rated "Likely Effective" for Athletic performance (Natural Medicines).
  • Also on file: Creatine is rated "Possibly Effective" for Athletic performance, Muscle strength.
  • Also on file: Beta-alanine is rated "Possibly Effective" for Athletic performance.

The evidence for this product's individual ingredients varies widely. Niacin is likely effective for pellagra and possibly effective for HIV-related high cholesterol and metabolic syndrome.

Vitamin B12 is effective for B12 deficiency and possibly effective for canker sores and nerve pain. L-citrulline is possibly effective for athletic performance.

Beta-alanine is possibly effective for athletic performance and physical performance. Caffeine (across its three forms) is likely effective for mental alertness and athletic performance.

Creatine is possibly effective for muscle strength and athletic performance. L-arginine, malic acid, cinnamon, magnesium, hordenine, olive leaf, citric acid, theobromine, green tea, and black pepper either lack established effectiveness ratings in our data or show insufficient evidence for the claims this product might make.

As a pre-workout formula, the product's overall effectiveness depends on your specific goals and how these ingredients work together—something not addressed in the individual ingredient data we hold.

The evidence, ingredient by ingredient Niacin Vitamin B12 Magnesium

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 16 of the 16 matched ingredients.
  • Pregnancy & breastfeeding safety ratings cover 15 of 16.
  • General safety write-ups exist for 16 of 16.
  • Remember: this measures how much safety information exists. Thin data is not the same as being safe.

Caffeine is generally well tolerated in moderate amounts for healthy adults but can cause anxiety, sleep problems, jitteriness, and in rare cases, stroke. Niacin at high supplemental doses can cause flushing, liver problems, and in rare cases hepatotoxicity, especially with sustained-release forms; the safety notes advise against high-dose niacin unless prescribed.

Beta-alanine commonly causes harmless tingling and flushing of the skin starting on the scalp. Magnesium can cause diarrhea, nausea, and gastrointestinal upset, especially at higher doses.

Creatine may cause muscle cramps, water retention, and diarrhea. L-arginine and L-citrulline can lower blood pressure and cause gastrointestinal discomfort.

Green tea extract has been rarely linked to liver injury at high doses. Cinnamon in large amounts carries a concern for liver toxicity due to its coumarin content.

Hordenine has no clinical safety data in humans but is structurally similar to stimulants and theoretically may cause heart rate and blood pressure elevation. For pregnancy: niacin at high doses should be avoided; L-citrulline and beta-alanine should be avoided (insufficient data); creatine should be avoided (safety not established); caffeine has mixed data—limit intake; other ingredients either lack pregnancy data or are likely safe in normal dietary amounts.

For breastfeeding: caffeine passes into milk (keep intake moderate); beta-alanine, creatine, and L-citrulline should be avoided; other ingredients either lack data or are considered safe. Talk with your doctor or pharmacist before using this product if you are pregnant or nursing.

Side effects, ingredient by ingredient Niacin Vitamin B12 Magnesium

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?
  • 12 of the 16 matched ingredients can interact with medications — Black Pepper, Cocoa, L-arginine, Niacin, Vitamin B12, among others.
  • The most serious interaction on file is rated Major.
  • Some involve high-stakes drug classes: anticoagulant / antiplatelet drugs; immunosuppressants / transplant drugs; diabetes medications; heart-rhythm medications; lithium; Parkinson's medications.
  • For scale: 1,495 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.

Check with your doctor or pharmacist before taking this product if you use ephedrine (Major risk from caffeine), nadolol or atorvastatin (Major risk from green tea), levodopa (Major risk from magnesium), or any blood pressure medications, blood thinners, diabetes drugs, seizure medications, psychiatric drugs, gout medications, cholesterol medications, or acid reducers. Caffeine can also interfere with stress tests if dipyridamole is used, and some ingredients may affect how your body handles potassium or magnesium.

Check your own medication Run your meds through the checker above

The bottom line

Scorecard at a glancePartially disclosed formula with clinical evidence supporting its stated purpose. Major medication interactions have been identified, and safety information is well characterized.

Mutant's Madness Blue Raspberry is designed for athletic performance and workout support, with caffeine, creatine, and amino acids as its core actives. However, this product carries multiple medication interactions—most seriously, combining its caffeine with ephedrine is dangerous.

If you take any prescription or over-the-counter medications, especially blood pressure drugs, blood thinners, diabetes medications, seizure drugs, or psychiatric medications, check each of your drugs against this product's ingredients before starting. People with high blood pressure, heart disease, liver or kidney problems, or anxiety disorders should be cautious.

Pregnant or nursing women should avoid it without their doctor's approval. Talk with your doctor or pharmacist before adding this to your routine.

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

Assessment coverage: 18 of 19 active ingredients matched to our full ingredient reviews (monographs). Based on the product label dated Jul 24, 2015.

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 Madness Blue Raspberry, straight from the product label.

Brand Mutant
Barcode (UPC) 811662021094
Net contents 275 Gram(s); 9.69 oz.
Market status On market
Date entered into DSLD Jul 24, 2015
DSLD ID 47710
Product type Other Combinations
Supplement form Powder
Dietary claims / uses All Other, Structure/Function
Intended target group(s) Adult (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 Madness Blue Raspberry by Mutant, 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:
2.75 Gram(s)
Maximum serving Sizes:
5.5 Gram(s)
Servings per container
50
UPC/BARCODE
811662021094
IngredientAmount% DV
Niacin20 mg100%
Vitamin B126 mcg100%
Malic Acid0 NP--
L-Arginine0 NP--
L-Citrulline0 NP--
Beta-Alanine1250 mg--
Caffeine Anhydrous300 mg--
Folate400 mcg100%
Dicaffeine Malate80 mg--
Cinnamon10 mg--
Magnesium15 mg4%
Caffeine Citrate40 mg--
micronized Creatine Monohydrate1500 mg--
Hordenine HCl5 mg--
Olive leaf extract5 mg--
MUTANT(TM) MADNESS FORMULA4775 mg--
Performance Intensity Matrix4250 mg--
L-Arginine/L-Citrulline 1:1 Blend1000 mg--
Citric-Malic Acid Blend500 mg--
Citric {Acid}0 NP--
5-Caffeine Matrix500 mg--
Theobromine extract40 mg--
Green Tea extract40 mg--
Activation Matrix25 mg--
BioPerine(R) Black Pepper extract5 mg--

Other ingredients: Natural & Artificial flavors, Sucralose, Potassium Citrate, Silicon Dioxide, Blue 1

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

{mutant/'mju:tent/: an individual with freakish or absurdly exaggerated musculature, anatomy, abilities, etc.}

Engineered exclusively for high intensity workouts only, this extra premium formula will jolt your senses. We warn you – use responsibly!*

MUTANT(TM) RESEARCH NOTES: Niacin, Vitamin B12 and Folate contribute to the reduction of tiredness and fatigue. Caffeine contributes to an increase in endurance capacity & performance and helps improve concentration (eg: focus). Creatine helps increase strength, power and physical performance in successive bursts of short-term, high intensity exercise. (NNHPD, EFSA)*

Packed by weight, not by volume. Settling of product occurs after filling.

All New

Natural & Artificial Flavor

Vitals For high intensity workouts only* For increased power and performance* Helps improve focus and reduce fatigue* 50 Servings

MADE IN CANADA

Brand IP Statement(s)

MUTANT(TM) MADNESS seizes the pre-workout experience, and vaults it to a whole new extreme level!

All MUTANT names and MUTANT images are registered trademarks and/or property and/or licensed property of Fit Foods Distribution Ltd. BioPerine(R) is a registered trademark of Sabinsa Corporation, used under license by Fit Foods Distribution Ltd.

Suggested/Recommended/Usage/Directions

SUGGESTED USE: As a dietary supplement for healthy adults performing high intensity exercise, experienced and comfortable with high caffeine products, add 1/2 to 1 level scoop to 8 fl oz (240ml) of cold water, shake 5-10 seconds, and slam it back 30 minutes prior to workouts. First time users should try 1/2 scoop first to assess tolerance. Read, understand and follow the entire Warning before choosing to use. Do not consume within 4 hours prior to bedtime. Never exceed 2 servings per 24 hours.*

Precautions

WARNINGS: This product may not be appropriate for you. High caffeine content.

Not recommended for children or pregnant or breast-feeding women.

Not recommended for children or pregnant or breast-feeding women.

For use by healthy adults only, accustomed to and comfortable with high caffeine content products. Use at your sole risk. Never exceed suggested use. For occasional use only. Ensure to drink enough fluid before, during, and after exercise.

Consult a health care practitioner prior to use: if you are taking lithium; if you have or your family has a history of high blood pressure, cardiovascular disease, glaucoma, depression or any mental illness or issues, prostate/urinary diseases, renal/kidney diseases; if you are attempting to increase physical activity; if you are taking any medication at all and especially if for cardiovascular diseases, erectile dysfunction, and/or blood thinners. Do not use if you have had a heart attack/myocardial infarction. Consumption with other stimulant containing foods, drinks, dietary supplements (e.g. including but not limited to bitter orange extract, synephrine, octopamine, ephedra), other drugs (e.g. ephedrine) which increase blood pressure, or with other caffeine-containing products (e.g. medications, coffee, tea, colas, cocoa, guarana, mate) is not recommended.

Beta-alanine and niacin can cause a temporary flushing, tingling sensation of the skin. This product is not intended as a substitute for sleep. If hypersensitivity, chest pain or allergy occurs, discontinue use and consult a health care practitioner. This product is intended to be used to supplement the diet; not to be used as a substitute for a varied diet. A varied and balanced diet and healthy lifestyle are essential for good health. Do not use if packaging has been tampered with. Mutant Madness has not been clinically studied - statements are based on corresponding individual ingredient’s known and/or typical claims and warnings.

Do not consume silica packet. User assumes all liability & risk.

KEEP OUT OF REACH OF CHILDREN.

Produced on machinery that also handles ingredients from milk, egg, fish, crustacean shellfish (glucosamine source), tree nuts, soy, wheat, peanut, and sulfites – this product may inadvertently contain any of those ingredients.

For California Residents Only. Required Prop 65 Text: WARNING: This product contains chemicals known to the State of California to cause cancer and birth defects or other reproductive harm.

Formula

WARNINGS: This product may not be appropriate for you. High caffeine content.

-CONTAINS 4.5 TIMES AS MUCH CAFFEINE PER 8 FL OZ PREPARED (5.5 GRAM) SERVING AS THE LEADING 8 FL OZ ENERGY DRINK.

Produced on machinery that also handles ingredients from milk, egg, fish, crustacean shellfish (glucosamine source), tree nuts, soy, wheat, peanut, and sulfites – this product may inadvertently contain any of those ingredients. (Total net caffeine: 375mg/5.5g scoop)

Storage

STORE IN A COOL, DRY PLACE.*

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

Concentrated Pre-Workout supplement

Seals/Symbols

MUTANT(TM) Leave Humanity Behind!

General

PN 2614US 0.00

See for yourself

Madness Blue Raspberry by Mutant label

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

What’s inside

The Ingredients in Madness Blue Raspberry by Mutant

These are the 7 active ingredients this product is made of. Select any to open its full monograph.

Serving size2.75 Gram(s) Dosage formPowder Servings per container50 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.

Niacin

Interacts with
727 drugs
20 mg per serving

Niacin (vitamin B3) is an essential nutrient your body needs for energy and metabolism, and deficiency is uncommon in most developed countries. Prescr...

Niacin monograph & interactions

Vitamin B12

Interacts with
20 drugs
6 mcg per serving Form: Cyanocobalamin

Vitamin B12 (cobalamin) is an essential nutrient your body needs to make red blood cells, keep nerves healthy, and support DNA. Supplements are very h...

Vitamin B12 monograph & interactions

Folate

400 mcg per serving Form: Folic Acid

Magnesium

Interacts with
295 drugs
15 mg per serving Form: Magnesium Oxide

Magnesium is an essential mineral your body needs for muscles, nerves, blood pressure, and many other functions, and supplements are useful for preven...

Magnesium monograph & interactions

MUTANT(TM) MADNESS FORMULA

4775 mg per serving
  • › Performance Intensity Matrix
  • › 5-Caffeine Matrix
  • › Activation Matrix

Other (inactive) ingredients: Natural & Artificial flavors, Sucralose, Potassium Citrate, Silicon Dioxide, Blue 1. These complete the product’s ingredient list but are not active constituents.

Interaction report

Madness Blue Raspberry by Mutant Drug Interactions

Want to check YOUR meds against Madness Blue Raspberry?

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
1,494Drugs
19 Major 1,449 Moderate 26 Minor

Ingredients driving the most interactions

Niacin 727
Magnesium 295

Each ingredient & the kinds of drugs it affects

For each ingredient in Madness Blue Raspberry 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.

Niacin15 drug types · 727 drugs

Alcohol (Ethanol)

Concomitant use of alcohol and niacin might increase the risk of flushing and hepatotoxicity.
Alcohol can exacerbate the flushing and pruritus associated with niacin. Large doses of niacin might also exacerbate liver dysfunction associated with chronic alcohol use. A case report describes delirium and lactic acidosis in a patient taking niacin 3 grams daily who ingested 1 liter of wine. Advise patients to avoid large amounts of alcohol while taking niacin.

Likelihood Probable Evidence D
Allopurinol (Zyloprim)

Theoretically, niacin might antagonize the therapeutic effects of uricosurics such as allopurinol.
Large doses of niacin can reduce urinary excretion of uric acid, potentially resulting in hyperuricemia. Doses of uricosurics such as allopurinol might need to be increased to maintain control of gout in patients who start taking niacin. People who have frequent attacks of gout despite uricosuric therapy should avoid niacin.

Likelihood Probable Evidence C
Anticoagulant/Antiplatelet Drugs

Theoretically, niacin may have additive effects when used with anticoagulant or antiplatelet drugs.
Several cases of clotting factor synthesis deficiency and coagulopathy have been reported in patients taking sustained-release niacin. Also, thrombocytopenia has been reported in patients treated with niacin or niacin plus lovastatin.

Likelihood Possible Evidence D
Antidiabetes Drugs

Niacin can increase blood glucose levels and may diminish the effects of antidiabetes drugs.
Niacin impairs glucose tolerance in a dose-dependent manner, probably by causing or aggravating insulin resistance and increasing hepatic production of glucose. In diabetes patients, niacin 4.5 grams daily for 5 weeks can increase plasma glucose by an average of 16% and glycated hemoglobin (HbA1c) by 21%. However, lower doses of 1.5 grams daily or less appear to have minimal effects on blood glucose. In some patients, glucose levels increase when niacin is started, but then return to baseline when a stable dose is reached. Up to 35% of patients with diabetes may need adjustments in hypoglycemic therapy when niacin is added.

Likelihood Probable Evidence B
Antihypertensive Drugs

Theoretically, niacin may increase the risk of hypotension when used with antihypertensive drugs.
The vasodilating effects of niacin can cause hypotension. Furthermore, some clinical evidence suggests that a one-hour infusion of niacin can reduce systolic, diastolic, and mean blood pressure in hypertensive patients. This effect is not observed in normotensive patients.

Likelihood Possible Evidence B
Bile Acid Sequestrants

Bile acid sequestrants can bind niacin and decrease absorption. Separate administration by 4-6 hours to avoid an interaction.
In vitro studies show that colestipol (Colestid) binds about 98% of available niacin and cholestyramine (Questran) binds 10% to 30%.

Likelihood Possible Evidence D
Gemfibrozil (Lopid)

Theoretically, concomitant use of niacin and gemfibrozil might increase the risk of myopathy in some patients.
A case of myopathy from concomitant use of niacin and gemfibrozil has been reported. Niacin alone has also been associated with cases of myopathy. Using gemfibrozil with niacin might further increase the risk of developing myopathy.

Likelihood Possible Evidence D
Hepatotoxic Drugs

Theoretically, concomitant use of niacin and hepatotoxic drugs might increase the risk of hepatotoxicity.
Niacin has been associated with cases of liver toxicity, especially when used in pharmacologic doses. Sustained-release niacin preparations appear to be associated with a higher risk of hepatotoxicity than immediate-release niacin.

Likelihood Possible Evidence D
Hmg-Coa Reductase Inhibitors ("Statins")

Theoretically, concomitant use of niacin and statins might increase the risk of myopathy and rhabdomyolysis in some patients.
Some case reports have raised concerns that niacin might increase the risk of myopathy and rhabdomyolysis when combined with statins. However, a significantly increased risk of myopathy has not been demonstrated in clinical trials, including those using an FDA-approved combination of lovastatin and niacin (Advicor).

Likelihood Possible Evidence D
Probenecid (Benemid)

Theoretically, niacin might antagonize the therapeutic effects of uricosurics such as probenecid.
Large doses of niacin reduce urinary excretion of uric acid, potentially causing hyperuricemia. Doses of uricosurics such as probenecid might need to be increased to maintain control of gout in patients who start taking niacin. People who have frequent attacks of gout despite uricosuric therapy should avoid niacin.

Likelihood Probable Evidence C
Sulfinpyrazone (Anturane)

Theoretically, niacin might antagonize the therapeutic effects of uricosurics such as sulfinpyrazone.
Large doses of niacin reduce urinary excretion of uric acid, potentially causing hyperuricemia. Doses of uricosurics such as sulfinpyrazone might need to be increased to maintain control of gout in patients who start taking niacin. People who have frequent attacks of gout despite uricosuric therapy should avoid niacin.

Likelihood Probable Evidence C
Thyroid Hormone

Theoretically, niacin might antagonize the therapeutic effects of thyroid hormones.
Clinical research and case reports suggests that taking niacin can reduce serum levels of thyroxine-binding globulin by up to 25% and moderately reduce levels of thyroxine (T4). Patients taking thyroid hormone for hypothyroidism might need dose adjustments when using niacin.

Likelihood Probable Evidence D
Transdermal Nicotine (Nicoderm)

Theoretically, concomitant use of niacin and transdermal nicotine might increase the risk of flushing and dizziness.
Niacin and nicotine can both cause flushing and dizziness.

Likelihood Possible Evidence D
Warfarin (Coumadin)

There is limited evidence that niacin may increase the anticoagulant effects of warfarin.
In a case report, a patient on warfarin developed an elevated international normalized ratio (INR) of 3.9 after taking niacin for two weeks. The patient's INR was previously stable, ranging between 2 and 3 in recent months, and no other medication changes were identified. The elevated INR returned to therapeutic range within 4 days following the discontinuation of niacin.

Likelihood Possible Evidence D
Aspirin

Large doses of aspirin might alter the clearance of niacin.
Aspirin is often used with niacin to reduce niacin-induced flushing. Doses of 80-975 mg aspirin have been used, but 325 mg appears to be optimal. Aspirin also seems to reduce the clearance of niacin by competing for glycine conjugation. Taking aspirin 1 gram seems to reduce niacin clearance by 45%. This is probably a dose-related effect and not clinically significant with the more common aspirin dose of 325 mg.

Likelihood Likely Evidence B

Magnesium15 drug types · 295 drugs

Levodopa/Carbidopa (Sinemet)

Magnesium can reduce the bioavailability of levodopa/carbidopa.
Clinical research in healthy volunteers shows that taking magnesium oxide 1000 mg with levodopa 100 mg/carbidopa 10 mg reduces the area under the curve (AUC) of levodopa by 35% and of carbidopa by 81%. In vitro and animal research shows that magnesium produces an alkaline environment in the digestive tract, which might lead to degradation and reduced bioavailability of levodopa/carbidopa.

Likelihood Probable Evidence B
Aminoglycoside Antibiotics

Concomitant use of aminoglycoside antibiotics and magnesium can increase the risk for neuromuscular weakness.
Both aminoglycosides and magnesium reduce presynaptic acetylcholine release, which can lead to neuromuscular blockade and possible paralysis. This is most likely to occur with high doses of magnesium given intravenously.

Likelihood Possible Evidence D
Antacids

Use of acid reducers may reduce the laxative effect of magnesium oxide.
A retrospective analysis shows that, in the presence of H2 receptor antagonists (H2RAs) or proton pump inhibitors (PPIs), a higher dose of magnesium oxide is needed for a laxative effect. This may also occur with antacids. Under acidic conditions, magnesium oxide is converted to magnesium chloride and then to magnesium bicarbonate, which has an osmotic laxative effect. By reducing acidity, antacids may reduce the conversion of magnesium oxide to the active bicarbonate salt.

Likelihood Possible Evidence D
Bictegravir/Emtricitabine/Tenofovir Alafenamide (Biktarvy)

Magnesium might decrease levels of bictegravir/emtricitabine/tenofovir alafenamide by reducing its absorption.
Advise patients that bictegravir/emtricitabine/tenofovir alafenamide should be taken at least 2 hours before or 6 hours after magnesium containing products.

Likelihood Probable Evidence D
Bisphosphonates

Magnesium can decrease absorption of bisphosphonates.
Cations, including magnesium, can decrease bisphosphonate absorption. Advise patients to separate doses of magnesium and these drugs by at least 2 hours.

Likelihood Probable Evidence B
Calcium Channel Blockers

Magnesium can have additive effects with calcium channel blockers, although evidence is conflicting.
Magnesium inhibits calcium entry into smooth muscle cells and may therefore have additive effects with calcium channel blockers. Severe hypotension and neuromuscular blockades may occur when nifedipine is used with intravenous magnesium, although some contradictory evidence suggests that concurrent use of magnesium with nifedipine does not increase the risk of neuromuscular weakness. High doses of magnesium could theoretically have additive effects with other calcium channel blockers.

Likelihood Possible Evidence D
Digoxin

Magnesium salts may reduce absorption of digoxin.
Clinical evidence suggests that treatment with oral magnesium hydroxide or magnesium trisilicate reduces absorption of digoxin from the intestines. This may reduce the blood levels of digoxin and decrease its therapeutic effects.

Likelihood Possible Evidence B
Potassium-Sparing Diuretics

Potassium-sparing diuretics decrease excretion of magnesium, possibly increasing magnesium levels.
Potassium-sparing diuretics also have magnesium-sparing properties, which can counteract the magnesium losses associated with loop and thiazide diuretics. Theoretically, increased magnesium levels could result from concomitant use of potassium-sparing diuretics and magnesium supplements.

Likelihood Probable Evidence D
Quinolone Antibiotics

Magnesium decreases absorption of quinolones.
Magnesium can form insoluble complexes with quinolones and decrease their absorption. Advise patients to take these drugs at least 2 hours before, or 4 to 6 hours after, magnesium supplements.

Likelihood Probable Evidence D
Skeletal Muscle Relaxants

Parenteral magnesium alters the pharmacokinetics of skeletal muscle relaxants, increasing their effects and accelerating the onset of effect.
Parenteral magnesium shortens the time to onset of skeletal muscle relaxants by about 1 minute and prolongs the duration of action by about 2 minutes. Magnesium potentiates the effects of skeletal muscle relaxants by decreasing calcium-mediated release of acetylcholine from presynaptic nerve terminals, reducing postsynaptic sensitivity to acetylcholine, and having a direct effect on the membrane potential of myocytes. Magnesium also has vasodilatory actions and increases cardiac output, allowing a greater amount of muscle relaxant to reach the motor end plate. A clinical study found that low-dose rocuronium (0.45 mg/kg), when given after administration of magnesium 30 mg/kg over 10 minutes, has an accelerated onset of effect, which matches the onset of effect seen with a full-dose rocuronium regimen (0.6 mg/kg). In another clinical study, onset times for rocuronium doses of 0.3, 0.6, and 1.2 mg/kg were 86, 76, and 50 seconds, respectively, when given alone, but were reduced to 66, 44, and 38 seconds, respectively, when the doses were given after a 15-minute infusion of magnesium sulfate 60 mg/kg. Giving intraoperative intravenous magnesium sulfate, 50 mg/kg loading dose followed by 15 mg/kg/hour, reduces the onset time of rocuronium, enhances its clinical effects, reduces the dose of intraoperative opiates, and prolongs the spontaneous recovery time. It does not affect the activity of subsequently administered neostigmine.

Likelihood Probable Evidence A
Sulfonylureas

Magnesium increases the systemic absorption of sulfonylureas, increasing their effects and side effects.
Clinical research shows that administration of magnesium hydroxide with glyburide increases glyburide absorption, increases maximal insulin response by 35-fold, and increases the risk of hypoglycemia, when compared with glyburide alone. A similar interaction occurs between magnesium hydroxide and glipizide. The mechanism of this effect appears to be related to the elevation of gastrointestinal pH by magnesium-based antacids, increasing solubility and enhancing absorption of sulfonylureas.

Likelihood Probable Evidence B
Tetracycline Antibiotics

Magnesium decreases absorption of tetracyclines.
Magnesium can form insoluble complexes with tetracyclines in the gut and decrease their absorption and antibacterial activity. Advise patients to take these drugs 1 hour before or 2 hours after magnesium supplements.

Likelihood Probable Evidence D
Anticoagulant/Antiplatelet Drugs

Theoretically, magnesium may have antiplatelet effects, but the evidence is conflicting.
In vitro evidence shows that magnesium sulfate inhibits platelet aggregation, even at low concentrations. Some preliminary clinical evidence shows that infusion of magnesium sulfate increases bleeding time by 48% and reduces platelet activity. However, other clinical research shows that magnesium does not affect platelet aggregation, although inhibition of platelet-dependent thrombosis can occur.

Likelihood Unlikely Evidence B
Gabapentin (Neurontin)

Gabapentin absorption can be decreased by magnesium.
Clinical research shows that giving magnesium oxide orally along with gabapentin decreases the maximum plasma concentration of gabapentin by 33%, time to maximum concentration by 36%, and area under the curve by 43%. Advise patients to take gabapentin at least 2 hours before, or 4 to 6 hours after, magnesium supplements.

Likelihood Unlikely Evidence B
Sevelamer (Renagel, Renvela)

Sevelamer may increase serum magnesium levels.
In patients on hemodialysis, sevelamer use was associated with a 0.28 mg/dL increase in serum magnesium. The mechanism of this interaction remains unclear.

Likelihood Possible Evidence B

Vitamin B121 drug type · 20 drugs

Metformin (Glucophage)

Metformin, a common medication used to manage type 2 diabetes, has been associated with lower vitamin B12 levels in some individuals. Prolonged use of metformin can interfere with the absorption of B12 in the digestive system, potentially leading to a deficiency in this essential vitamin.

Likelihood Possible Evidence A
The maker

Brand information

Manufacturer and brand details for Madness Blue Raspberry, from the product label.

Mutant

See all Mutant products
Name
Fit Foods(TM) Distribution Inc.
Street Address
1124 Fir Ave.
City
Blaine
State
WA
ZipCode
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Pharmacist Counseling Corner

Madness Blue Raspberry by Mutant: Common Questions

Does Madness Blue Raspberry by Mutant interact with any medications?
Yes. Based on its ingredients, Madness Blue Raspberry has a known interaction with 1,494 medications, including 19 rated major. Use the checker to see how it interacts with a specific drug.
How can one product interact with so many drugs?
Madness Blue Raspberry contains 7 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.
Does this have caffeine, and how much?
Yes. This product contains caffeine in three forms: caffeine anhydrous, caffeine citrate, and dicaffeine malate. The product facts don't specify the total amount in each serving, so check the label or contact the manufacturer for the exact dose. If you're sensitive to caffeine or take medications affected by it, that's especially important to know.
Will this make me jittery or keep me awake?
Possibly. Caffeine commonly causes anxiety, restlessness, jitteriness, and insomnia, especially at higher doses. Beta-alanine also causes a tingling sensation on the skin, which some people find uncomfortable. If you're sensitive to stimulants or have sleep issues, this product may not be right for you.
Is this safe to use if I'm pregnant?
There isn't enough reliable information to know either way for most of its ingredients—L-citrulline, beta-alanine, creatine, and several others lack pregnancy safety data. Caffeine has mixed evidence; niacin at high supplement doses should be avoided. Talk with your doctor or pharmacist before using this product during pregnancy; they can weigh the risks and benefits for your situation.
Can I take this while breastfeeding?
Caffeine passes into breast milk in small amounts, so moderate intake is usually considered acceptable, though it can make your baby fussy. Beta-alanine, creatine, and L-citrulline lack safety data for breastfeeding and should be avoided. Check with your doctor or pharmacist before starting, especially if you're nursing a newborn or your baby is sensitive to caffeine.
What does creatine do, and is it safe?
Creatine is possibly effective for muscle strength and athletic performance. It's generally well tolerated in healthy adults, but common side effects include muscle cramps, water retention, and diarrhea. If you have kidney disease or liver problems, use only under medical supervision. Avoid it during pregnancy and breastfeeding—safety hasn't been established.
What's the tingling I might feel?
That's likely beta-alanine, which commonly causes a harmless dose-dependent tingling sensation (paresthesias) on the scalp and body that usually lasts about an hour. It starts about 20 minutes after you take the dose. This is a known side effect and not dangerous, but some people find it uncomfortable.

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.

Madness Blue Raspberry label
Sources

Sources & How We Checked

Madness Blue Raspberry'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 996 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.

Niacin 66 references
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  37. Dunn RT, Ford MA, Rindone JP, Kwiecinski FA. Low-Dose Aspirin and Ibuprofen Reduce the Cutaneous Reactions Following Niacin Administration. Am J Ther. 1995;2(7):478-480. PubMed
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  39. Drinka PJ. Alterations in thyroid and hepatic function tests associated with preparations of sustained-release niacin. Mayo Clin Proc. 1992;67(12):1206. PubMed
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  45. Goldberg A, Alagona P Jr, Capuzzi DM, et al. Multiple-dose efficacy and safety of an extended-release form of niacin in the management of hyperlipidemia. Am J Cardiol. 2000;85(9):1100-5. PubMed
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  47. Morgan JM, Capuzzi DM, Guyton JR, et al. Treatment Effect of Niaspan, a Controlled-release Niacin, in Patients With Hypercholesterolemia: A Placebo-controlled Trial. J Cardiovasc Pharmacol Ther. 1996;1(3):195-202. PubMed
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  53. Fraunfelder FW, Fraunfelder FT, Illingworth DR. Adverse ocular effects associated with niacin therapy. Br J Ophthalmol 1995;79:54-56. PubMed
  54. Ali EH, McJunkin B, Jubelirer S, Hood W. Niacin induced coagulopathy as a manifestation of occult liver injury. W V Med J. 2013 Jan-Feb;109(1):12-4
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  57. Davidson MH, Rooney M, Pollock E, Drucker J, Choy Y. Effect of colesevelam and niacin on low-density lipoprotein cholesterol and glycemic control in subjects with dyslipidemia and impaired fasting glucose. J Clin Lipidol. 2013 Sep-Oct;7(5):423-32. PubMed
  58. Guyton JR, Fazio S, Adewale AJ, Jensen E, Tomassini JE, Shah A, Tershakovec AM. Effect of extended-release niacin on new-onset diabetes among hyperlipidemic patients treated with ezetimibe/simvastatin in a randomized controlled trial. Diabetes Care. 2012 PubMed
  59. Loebl T, Raskin S. A novel case report: acute manic psychotic episode after treatment with niacin. J Neuropsychiatry Clin Neurosci. 2013 Fall;25(4):E14. PubMed
  60. Teo KK, Goldstein LB, Chaitman BR, Grant S, Weintraub WS, Anderson DC, Sila CA, Cruz-Flores S, Padley RJ, Kostuk WJ, Boden WE; AIM-HIGH Investigators. Extended-release niacin therapy and risk of ischemic stroke in patients with cardiovascular disease: the
  61. Goldie C, Taylor AJ, Nguyen P, McCoy C, Zhao XQ, Preiss D. Niacin therapy and the risk of new-onset diabetes: a meta-analysis of randomized controlled trials. Heart. 2016 Feb;102(3):198-203.
  62. Schandelmaier S, Briel M, Saccilotto R, Olu KK, Arpagaus A, Hemkens LG, Nordmann AJ. Niacin for primary and secondary prevention of cardiovascular events. Cochrane Database Syst Rev. 2017 Jun 14;6:CD009744. PubMed
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  64. Song S, Lee CJ, Oh J, Park S, Kang SM, Lee SH. Effect of Niacin on Carotid Atherosclerosis in Patients at Low-Density Lipoprotein-Cholesterol Goal but High Lipoprotein (a) Level: a 2-Year Follow-Up Study. J Lipid Atheroscler. 2019;8(1):58-66. PubMed
  65. Kimura H, Umemori Y, Yuki D. Anaphylactic shock-like symptoms due to niacin overdose: A case report. J Dermatol 2022;49(8):e287-e288. PubMed
  66. Nawaz N, Mistretta T, Karime C, Lewis J, Wolf E. Cholestatic Drug-Induced Liver Injury in a Patient Taking High-Dose Niacin for Hyperlipidemia. J Investig Med High Impact Case Rep 2024;12:23247096231224349. PubMed

See these in context on the Niacin monograph →

Vitamin B12 30 references
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  2. Hartman TJ, Woodson K, Stolzenberg-Solomon R, et al. Association of the B-vitamins pyridoxal 5'-phosphate (B6), B12, and folate with lung cancer risk in older men. Am J Epidemiol 2001;153:688-94.. DOI
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  9. Uhl, W., Nolting, A., Golor, G., Rost, K. L., and Kovar, A. Safety of hydroxocobalamin in healthy volunteers in a randomized, placebo-controlled study. Clin Toxicol (Phila) 2006;44 Suppl 1:17-28. PubMed
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  27. Khairan P, Sobue T, Eshak ES, et al. Association of dietary intakes of vitamin B12, vitamin B6, folate, and methionine with the risk of esophageal cancer: the Japan Public Health Center-based (JPHC) prospective study. BMC Cancer 2021;21(1):982. PubMed
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  30. Pegalajar-García MD, Cebolla-Verdugo M, Prados-Carmona Á, Llamas-Segura C, Navarro-Triviño FJ. Systemic allergic dermatitis to cobalt present in cyanocobalamin supplementation. Contact Dermatitis 2023;89(3):203-205. PubMed

See these in context on the Vitamin B12 monograph →

Malic Acid 7 references
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  7. Amended Safety Assessment of Malic Acid and Sodium Malate as Used in Cosmetics. Cosmetic Ingredient Review Expert Panel. Updated May 19, 2017. http://www.cir-safety.org/sites/default/files/malic%20acid.pdf. Accessed January 24, 2018.

See these in context on the Malic Acid monograph →

L-arginine 66 references
  1. Sapienza MA, Kharitonov SA, Horvath I, et al. Effect of inhaled L-arginine on exhaled nitric oxide in normal and asthmatic subjects. Thorax 1998;53:172-5.
  2. Clarkson P, Adams MR, Powe AJ, et al. Oral L-arginine improves endothelium-dependent dilation in hypercholesterolemic young adults. J Clin Invest 1996;97:1989-94. PubMed
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  5. Korting GE, Smith SD, Wheeler MA, et al. A randomized double-blind trial of oral L-arginine for treatment of interstitial cystitis. J Urol 1999;161:558-65. DOI
  6. Rector TS, Bank AJ, Mullen KA, et al. Randomized, double-blind, placebo-controlled study of supplemental oral L-arginine in patients with heart failure. Circulation 1996;93:2135-41.
  7. Siani A, Pagano E, Iacone R, et al. Blood pressure and metabolic changes during dietary L-arginine supplementation in humans. Am J Hypertens 2000;13:547-51. PubMed
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  10. Huynh NT, Tayek JA. Oral arginine reduces systemic blood pressure in type 2 diabetes: its potential role in nitric oxide generation. J Am Coll Nutr 2002;21:422-7.. PubMed
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  14. Higashi Y, Oshima T, Sasaki S, et. al. Angiotensin-converting enzyme inhibition, but not calcium antagonism, improves a response of the renal vasculature to L-arginine in patients with essential hypertension. Hypertension. 1998 Jul;32(1):16-24.
  15. Facchinetti, F., Longo, M., Piccinini, F., Neri, I., and Volpe, A. L-arginine infusion reduces blood pressure in preeclamptic women through nitric oxide release. J Soc Gynecol.Investig. 1999;6(4):202-207. DOI
  16. de Gouw, H. W., Verbruggen, M. B., Twiss, I. M., and Sterk, P. J. Effect of oral L-arginine on airway hyperresponsiveness to histamine in asthma. Thorax 1999;54(11):1033-1035. PubMed
  17. Komers, R., Komersova, K., Kazdova, L., Ruzickova, J., and Pelikanova, T. Effect of ACE inhibition and angiotensin AT1 receptor blockade on renal and blood pressure response to L-arginine in humans. J Hypertens. 2000;18(1):51-59. PubMed
  18. Cartledge, J. J., Davies, A. M., and Eardley, I. A randomized double-blind placebo-controlled crossover trial of the efficacy of L-arginine in the treatment of interstitial cystitis. BJU.Int. 2000;85(4):421-426.
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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.

© 2021 Therapeutic Research Center, LLC

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