Major interaction on record — check this product against your medications before combining. Based on 2 of 4 ingredients. Check your meds →
Dietary supplement

Ripped Freak RF Diuretic Ingredients & Drug Interactions

by PharmaFreak

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

Ripped Freak RF Diuretic is a dietary supplement by PharmaFreak with 4 active ingredients. Its ingredients are commonly taken for preventing or treating magnesium deficiency, constipation, muscle cramps.Based on those ingredients, 711 medications have a known interaction with it, the most serious rated major. The ingredients most likely to interact are Taraxacum Officinale Diuretic Complex, Magnesium. Use the checker below to test your specific medication, or read the full HelloPharmacist Interaction Report.

HelloPharmacist Scorecard of Ripped Freak RF Diuretic by PharmaFreak

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 4 of its 13 active ingredients.
  • “Magnesium Citrate” is listed as a grouped ingredient — the label doesn't break down how much of each component you get.
  • “Ripped Freak Diuretic Formula” is a proprietary blend — the label doesn't break down how much of each component you get.
  • “Taraxacum Officinale Diuretic Complex” is a proprietary blend — the label gives one combined amount (8,000 mg) without saying how much of each component you get.

Ripped Freak RF Diuretic contains 13 active and inactive ingredients. The main active components include magnesium (in two forms — plain magnesium and magnesium citrate), dandelion root 4:1 extract, juniper berry 4:1 extract, plus caffeic acid and several other botanical compounds designed to support fluid balance.

The product also holds inactive ingredients: gelatin (capsule) and magnesium stearate (a binder).

Does it work?

Couldn't assess
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
Not assessable

We hold no graded evidence for this product's ingredients for its stated purpose.

Why this rating?
  • The label markets this product for: water shedding and detoxification.
  • We looked for evidence on: water retention, edema, fluid balance.
  • Our graded evidence for these ingredients doesn't cover that particular purpose.

The evidence for most of the active ingredients in this product is not established in our data. Magnesium itself is rated Effective for constipation, indigestion (dyspepsia), and magnesium deficiency (hypomagnesemia), and also for preventing pre-eclampsia in pregnancy — though that use is specific and requires medical guidance.

Dandelion root, juniper berry, caffeic acid, and the other botanical compounds all carry Insufficient Reliable Evidence ratings for the conditions they're traditionally claimed to help (joint pain, swelling, wound healing, urinary tract infections, kidney stones, and others). This doesn't mean they don't work; it means the clinical evidence we have is not strong enough to make a claim either way.

The evidence, ingredient by ingredient Magnesium Dandelion

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.

Magnesium is generally well tolerated when taken at recommended doses. The most common side effects from oral magnesium are diarrhea, nausea, vomiting, and stomach irritation — which is notable in a diuretic product designed to reduce fluid.

In rare cases, taking very large doses of magnesium (1500 mg or more daily) has caused bezoars (indigestible blockages in the stomach). Dandelion is generally tolerated as food but supplement-strength doses are less studied; it can cause allergic reactions in sensitive individuals, including rare anaphylaxis in those allergic to the daisy family (ragweed, chrysanthemums, marigolds, daisies).

Juniper should not be used long-term as medicinal doses may irritate the kidneys. Caffeic acid at supplement doses is not well studied in humans.

Side effects, ingredient by ingredient Magnesium Dandelion

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?
  • 4 of the 4 matched ingredients can interact with medications — Dandelion, Juniper, Magnesium, Caffeic Acid.
  • The most serious interaction on file is rated Major.
  • Some involve high-stakes drug classes: anticoagulant / antiplatelet drugs; diabetes medications; heart-rhythm medications; lithium; Parkinson's medications.
  • For scale: 711 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 Ripped Freak RF Diuretic, check with your pharmacist if you take any of the following: levodopa/carbidopa (Sinemet) — Major risk; skeletal muscle relaxants, potassium-sparing diuretics, calcium channel blockers, acid-reducing drugs (PPIs or H2 blockers), blood sugar medications (sulfonylureas), quinolone antibiotics, or bisphosphonates — all Moderate risk from magnesium; dandelion contributes Moderate risk with blood thinners, blood sugar drugs, and lithium; and juniper adds Moderate risk with blood sugar drugs and Minor risk with other diuretics and lithium. We could not check several ingredients for interactions.

Check your own medication Run your meds through the checker above

The bottom line

Scorecard at a glanceFormula with limited ingredient disclosure with no assessable stated purpose. Major medication interactions have been identified, and safety information is well characterized.

This product is built mainly on magnesium and botanical diuretics. If you're on Parkinson's medication (levodopa/carbidopa), blood sugar drugs, lithium, potassium-sparing diuretics, blood thinners, or bone medications, you need to talk with your pharmacist or doctor before trying it.

Even if none of those apply, the long-term kidney safety of juniper and the common side effect of diarrhea from magnesium make it worth a quick check-in before you start.

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

Assessment coverage: 5 of 13 active ingredients matched to our full ingredient reviews (monographs). Based on the product label dated Mar 25, 2013.

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 Ripped Freak RF Diuretic, straight from the product label.

Brand PharmaFreak
Barcode (UPC) 855504001622
Net contents 48 Capsule(s)
Market status On market
Date entered into DSLD Mar 25, 2013
DSLD ID 19122
Product type Other Combinations
Supplement form Capsule
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 Ripped Freak RF Diuretic by PharmaFreak, 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:
4 Capsule(s)
Maximum serving Sizes:
4 Capsule(s)
Servings per container
12
UPC/BARCODE
855504001622
IngredientAmount% DV
Magnesium80 mg--
Phytosterols0 NP--
Magnesium Citrate0 NP--
Magnesium80 mg20%
Luteolin0 NP--
Chlorogenic Acid0 NP--
Dandelion root 4:1 extract2000 mg--
Isoquercetin0 NP--
Caffeic Acid0 NP--
Ripped Freak Diuretic Formula0 NP--
Taraxacum Officinale Diuretic Complex8000 mg--
Lactucopicrin0 NP--
Triterpenoids0 NP--
Juniperus Communis Diuretic Complex2000 mg--
500 mg Juniper berry 4:1 extract500 mg--
4-Terpineol0 NP--
Diuretic Flavonoids0 NP--
Muscle Function/Anti-Cramping Complex400 mg--

Other ingredients: Gelatin, Magnesium Stearate

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.
Brand IP Statement(s)

RIPPED FREAK(R) DIURETIC is the FIRST and ONLY diuretic product on the market that actually delivers a CLINICALLY-VALIDATED formula backed by human research studies!* This truly separates RIPPED FREAK DIURETIC from all other diuretic, detox and water pills currently available!

PHARMAFREAK(TM) is a trademark of PharmaFreak Holdings Inc. RIPPED FREAK(R) is a registered Trademark of PharmaFreak Holdings Inc.

RIPPED FREAK(R) DIURETIC works great on its own or it can be stacked with RIPPED FREAK Hybrid Fat Burner for even greater diuretic effects!

Suggested/Recommended/Usage/Directions

DIRECTIONS: Take 4 capsules in the morning and 4 capsules in the afternoon. Optional: take an additional 4 capsules in the evening. Drink at least 500 ml of water with each dose. Use for no more than 3 consecutive days.

Precautions

Do not use if you have liver or gall bladder disorders, and/or bowel obstruction. Discontinue use if you develop symptoms of liver trouble. Do not use if you have a kidney disorder. Consult a health care practitioner if symptoms persist or worsen. Use only as directed. Do not exceed recommended serving, as improper use of this product does not enhance results.

WARNING: NEVER EXCEED RECOMMENDED SERVING.

WARNING: KEEP OUT OF REACH OF CHILDREN.

Do not use if pregnant or nursing.

Not intended for use by persons under the age of 18.

Storage

Store in a cool, dry place.

General Statements

NEW

HYBRID DIURETIC/DETOX FORMULA*

100% Clinically-Validated Water-Shedding & Detoxifying Agents*

Increase Water Loss by up to 19.8%* Clinically Validated Formula*

Made in the USA.

World’s 1st Clinically Validated Natural Diuretic!*

FDA Statement of Identity

Dietary Supplement

General

USA-MAY-12

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.

Seals/Symbols

PHARMAFREAKpf(TM)

See for yourself

Ripped Freak RF Diuretic by PharmaFreak label

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

What’s inside

The Ingredients in Ripped Freak RF Diuretic by PharmaFreak

These are the 4 active ingredients this product is made of. Select any to open its full monograph.

Serving size4 Capsule(s) Dosage formCapsule Servings per container12 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.

Magnesium

Interacts with
295 drugs
80 mg per serving Form: Magnesium Citrate

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

Ripped Freak Diuretic Formula

0 NP per serving

Other (inactive) ingredients: Gelatin, Magnesium Stearate. These complete the product’s ingredient list but are not active constituents.

Interaction report

Ripped Freak RF Diuretic by PharmaFreak Drug Interactions

Want to check YOUR meds against Ripped Freak RF Diuretic?

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
711Drugs
6 Major 665 Moderate 40 Minor

Ingredients driving the most interactions

Magnesium 295

Each ingredient & the kinds of drugs it affects

For each ingredient in Ripped Freak RF Diuretic 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.

Taraxacum Officinale Diuretic Complex7 drug types · 457 drugs

Anticoagulant/Antiplatelet Drugs

Theoretically, taking dandelion root along with anticoagulant or antiplatelet drugs might increase the risk of bruising and bleeding.
In vitro research suggests that dandelion root inhibits platelet aggregation.

Likelihood Possible Evidence D
Antidiabetes Drugs

Theoretically, dandelion might increase the risk for hypoglycemia when used with antidiabetes drugs.
Laboratory research suggests that dandelion extract may have moderate alpha-glucosidase inhibitor activity and might also increase insulin secretion. Also, in a case report, a 58-year-old woman with type 2 diabetes who was being treated with insulin developed hypoglycemia 2 weeks after beginning to eat salads containing dandelion.

Likelihood Possible Evidence D
Cytochrome P450 1A2 (Cyp1A2) Substrates

Theoretically, dandelion might increase levels of drugs metabolized by CYP1A2.
Laboratory research suggests that dandelion might inhibit CYP1A2. So far, this interaction has not been reported in humans. However, until more is known, watch for an increase in the levels of drugs metabolized by CYP1A2 in patients taking dandelion.

Likelihood Possible Evidence D
Glucuronidated Drugs

Theoretically, dandelion might increase the clearance of drugs that are UDP-glucuronosyltransferase substrates.
There is some preliminary evidence that dandelion might induce UDP-glucuronosyltransferase, a phase II enzyme.

Likelihood Possible Evidence D
Lithium

Theoretically, through diuretic effects, dandelion might reduce excretion and increase levels of lithium.
Animal research suggests that dandelion has diuretic properties. As diuretics can increase serum lithium levels, the dose of lithium might need to be decreased when taken with dandelion.

Likelihood Probable Evidence D
Potassium-Sparing Diuretics

Theoretically, dandelion might increase the risk of hyperkalemia when taken with potassium-sparing diuretics.
Dandelion contains significant amounts of potassium.

Likelihood Possible Evidence D
Quinolone Antibiotics

Theoretically, dandelion might lower fluoroquinolone levels.
Animal research shows that dandelion reduces absorption of ciprofloxacin and can lower levels by 73%. However, this effect has not been reported in humans.

Likelihood Possible Evidence D

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
The maker

Brand information

Manufacturer and brand details for Ripped Freak RF Diuretic, from the product label.

PharmaFreak

See all PharmaFreak products
Name
PharmaFreak Sciences Inc.
Street Address
1801-1 Yonge St
City
Toronto
State
ON
ZipCode
M5E 1W7
Phone Number
1-888-674-0051
Pharmacist Counseling Corner

Ripped Freak RF Diuretic by PharmaFreak: Common Questions

Does Ripped Freak RF Diuretic by PharmaFreak interact with any medications?
Yes. Based on its ingredients, Ripped Freak RF Diuretic has a known interaction with 711 medications, including 6 rated major. Use the checker to see how it interacts with a specific drug.
How can one product interact with so many drugs?
Ripped Freak RF Diuretic contains 4 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.
Is it safe to take this while I'm pregnant or breastfeeding?
The magnesium in this product is rated Likely Safe, Possibly Safe, and Possibly Unsafe depending on context — magnesium is needed in pregnancy, but you should only use supplements under your doctor's guidance. Dandelion has limited safety data, so caution is advised. Juniper should be avoided in pregnancy (traditionally avoided because it may affect the uterus) and during breastfeeding due to insufficient safety information. Please talk with your doctor or pharmacist before use if you're pregnant or breastfeeding.
What side effects might I experience?
The most common side effect from magnesium is diarrhea, along with nausea, vomiting, or stomach upset. Dandelion may cause diarrhea, heartburn, or stomach discomfort; in sensitive individuals it can trigger allergic reactions including dermatitis (a rash). Juniper can cause skin irritation with topical exposure. In rare cases, very high doses of magnesium can cause serious effects like muscle weakness or bezoars (an indigestible mass in the stomach).
Will this product actually help me lose water weight or reduce bloating?
The evidence for most of the diuretic botanicals in this product — dandelion, juniper, and others — is rated Insufficient Reliable Evidence to say whether they work for that purpose. Magnesium has well-documented uses, but not for water loss or bloating. The product is not proven to deliver the effects its marketing suggests.
Can I take this long-term?
Juniper berry should not be used long-term because medicinal doses may irritate the kidneys. Magnesium at high doses long-term also carries theoretical concerns (case reports note bone loss in people taking very high cumulative amounts). There's no strong safety data supporting long-term use of this combination at supplement doses.
Why does the product have so many ingredients if most of them don't have proven effectiveness?
The product combines magnesium (which is proven for constipation and deficiency) with several botanical diuretics (dandelion, juniper, and flavonoids) that are traditionally used for fluid balance but lack strong clinical evidence. The manufacturers likely chose them based on traditional use and the theory that they work together — but the evidence doesn't back that up for most of them.
What are all these diuretic ingredients supposed to do?
Dandelion, juniper, and the diuretic flavonoids in this product are thought to increase urine output and reduce fluid retention — that's the 'diuretic' effect. However, the clinical evidence that they actually do this in humans is weak. Magnesium can also have a mild laxative effect and increase bowel water content, which may make you think you're losing water, but that's different from a true diuretic action.

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.

Ripped Freak RF Diuretic label
Sources

Sources & How We Checked

Ripped Freak RF Diuretic'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 118 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.

Magnesium 82 references
  1. Rodin SM, Johnson BF. Pharmacokinetic interactions with digoxin. Clin Pharmacokinet 1988;15:227-44.
  2. Covington TR, et al. Handbook of Nonprescription Drugs. 11th ed. Washington, DC: American Pharmaceutical Association, 1996.
  3. Dahle LO, Berg G, Hammar M, et al. The effect of oral magnesium substitution on pregnancy-induced leg cramps. Am J Obstet Gynecol 1995;173:175-80. PubMed
  4. Hansten PD, Horn JR. Drug Interactions Analysis and Management. Vancouver, WA: Applied Therapeutics Inc., 1997 and updates.
  5. Peikert A, Wilimzig C, Kohne-Volland R. Prophylaxis of migraine with oral magnesium: results from a prospective, multi-center, placebo-controlled and double-blind randomized study. Cephalalgia 1996;16:257-63. PubMed
  6. Food and Nutrition Board, Institute of Medicine. Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride. Washington, DC: National Academy Press, 1999. Available at: http://books.nap.edu/books/0309063507/html/index.html.
  7. Birrer RB, Shallash AJ, Totten V. Hypermagnesemia-induced fatality following epsom salt gargles. J Emerg Med 2002;22:185-8. PubMed
  8. Ryan MP. Diuretics and potassium/magnesium depletion. Directions for treatment. Am J Med 1987;82:38-47.. PubMed
  9. Hollifield JW. Magnesium depletion, diuretics, and arrhythmias. Am J Med 1987;82:30-7.. PubMed
  10. Heidenreich O. Mode of action of conventional and potassium-sparing diuretics--aspects with relevance to Mg-sparing effects. Magnesium 1984;3:248-56..
  11. Pfaffenrath V, Wessely P, Meyer C, et al. Magnesium in the prophylaxis of migraine--a double-blind placebo-controlled study. Cephalalgia 1996;16:436-40.. PubMed
  12. Wang F, Van Den Eeden SK, Ackerson LM, et al. Oral magnesium oxide prophylaxis of frequent migrainous headache in children: a randomized, double-blind, placebo-controlled trial. Headache 2003;43:601-10.. PubMed
  13. Sompolinsky D, Samra Z. Influence of magnesium and manganese on some biological and physical properties of tetracycline. J Bacteriol 1972;110:468-76.. PubMed
  14. Jeyabalan A, Caritis SN. Pharmacologic inhibition of preterm labor. Clin Obstet Gynecol 2002;45:99-113. PubMed
  15. Mittendorf R, Dambrosia J, Pryde PG, et al. Association between the use of antenatal magnesium sulfate in preterm labor and adverse health outcomes in infants. Am J Obstet Gynecol 2002;186:1111-8.. PubMed
  16. Witlin AG, Sibai BM. Magnesium sulfate therapy in preeclampsia and eclampsia. Obstet Gynecol 1998;92:883-9.. DOI
  17. Crowther CA, Hiller JE, Doyle LW. Magnesium sulphate for preventing preterm birth in threatened preterm labour. Cochrane Database Syst Rev 2002;4:CD001060. . PubMed
  18. Davey MJ, Teubner D. A randomized controlled trial of magnesium sulfate, in addition to usual care, for rate control in atrial fibrillation. Ann Emerg Med 2005;45:347-53.. PubMed
  19. L'Hommedieu CS, Nicholas D, Armes DA, et al. Potentiation of magnesium sulfate--induced neuromuscular weakness by gentamicin, tobramycin, and amikacin. J Pediatr 1983;102:629-31..
  20. Dunn CJ, Goa KL. Risedronate: a review of its pharmacological properties and clinical use in resorptive bone disease. Drugs 2001;61:685-712..
  21. Kass L, Weekes J, Carpenter L. Effect of magnesium supplementation on blood pressure: a meta-analysis. Eur J Clin Nutr 2012;66:411-8. PubMed
  22. Koontz SL, Friedman SA, Schwartz ML. Symptomatic hypocalcemia after tocolytic therapy with magnesium sulfate and nifedipine. Am J Obstet Gynecol. 2004;190(6):1773-6. PubMed
  23. Snyder SW, Cardwell MS. Neuromuscular blockade with magnesium sulfate and nifedipine. Am J Obstet Gynecol. 1989;161(1):35-6. PubMed
  24. Waisman GD, Mayorga LM, Cámera MI, et al. Magnesium plus nifedipine: potentiation of hypotensive effect in preeclampsia? Am J Obstet Gynecol. 1988;159(2):308-9. PubMed
  25. Brown DD, Juhl RP. Decreased bioavailability of digoxin due to antacids and kaolin-pectin. N Engl J Med. 1976;295(19):1034-7. PubMed
  26. Allen MD, Greenblatt DJ, Harmatz JS, et al. Effect of magnesium--aluminum hydroxide and kaolin--pectin on absorption of digoxin from tablets and capsules. J Clin Pharmacol. 1981;21(1):26-30. PubMed
  27. Ravn HB, Vissinger H, Kristensen SD, et al. Magnesium inhibits platelet activity--an in vitro study. Thromb Haemost. 1996;76(1):88-93. DOI
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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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