Modiodal 60 tablets

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SKU: MOD-60-00001 Category:

Description

Modafinil
Modafinil.svg
Chemical Nomenclature
Common names Modafinil, Alertec, Modavigil, Modiodal, Provigil, Modalert
Substitutive name Modafinil
Systematic name 2-[(Diphenylmethyl)sulfinyl]acetamide
Routes of Administration
WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.
[Collapse]Oral
Dosage
Threshold Common Heavy
25 50 100 200 300 mg
Light Strong
Threshold 25 – 50 mg
Light 50 – 100 mg
Common 100 – 200 mg
Strong 200 – 300 mg
Heavy 300 mg +
Duration
Total 5 – 10 hours
Onset 20 – 60 minutes
Come up 20 – 60 minutes
Peak 3.5 – 5 hours
Offset 1 – 3 hours
After effects 2 – 6 hours
DISCLAIMER: PW’s dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Modafinil (also known by the brand names ProvigilAlertecModavigil, among others) is a eugeroic substance of the benzhydryl class that produces wakefulness-promoting and stimulant effects when administered. It is commonly used to enhance cognition, reduce fatigue, and increase alertness in both medical and non-medical contexts.

Dose

Oral
Common 100-300mg

Dosage chart for Oral Modafinil Experience Level Dose (mg)

Duration
All ROAs
Onset 30-45 minutes
Duration 12-16 hours
After-effects 1-16 hours

Interactions

Dangerous

  • αMT
  • Tramadol
    • Tramadol and stimulants both increase the risk of seizures.
  • MAOIs
    • MAO-B inhibitors can increase the potency and duration of phenethylamines unpredictably. MAO-A inhibitors with amphetamine can lead to hypertensive crises.

Unsafe

  • DOx
    • The combined stimulating effects of the two can lead to an uncomfortable body-load, while the focusing effects of amphetamine can quickly lead to thought loops. Coming down from amphetamines while the DOx is still active can be quite anxiogenic.
  • NBOMes
    • Amphetamines and NBOMes both provide much stimulation. When combined they can result in tachycardia, hypertension, vasoconstriction and extreme cases heart failure. The anxiogenic and focusing effects of stimulants are also not sound in combination with psychedelics as they can lead to unpleasant thought loops. NBOMes are known to cause seizures and stimulants can increase this risk.
  • 2C-T-x
    • Stimulants increase anxiety levels and the risk of thought loops which can lead to negative experiences. In extreme cases, they can result in severe vasoconstriction, tachycardia, hypertension, and in extreme cases heart failure.
  • 5-MeO-xx
    • The anxiogenic and focusing effects of stimulants increase the chance of unpleasant thought loops. The combination is generally unnecessary because of the stimulating effects of psychedelics.
  • DXM
    • Both substances raise heart rate, in extreme cases, panic attacks caused by these drugs have led to more severe heart issues.
  • PCP
    • This combination can quickly lead to hypomanic states

Caution

  • Mushrooms
    • Stimulants increase anxiety levels and the risk of thought loops which can lead to negative experiences
  • LSD
    • Stimulants increase anxiety levels and the risk of thought loops which can lead to negative experiences
  • DMT
    • Stimulants increase anxiety levels and the risk of thought loops which can lead to negative experiences
  • Mescaline
    • The focus and anxiety caused by stimulants is magnified by psychedelics and results in an increased risk of thought loops
  • 2C-x
    • The anxiogenic and focusing effects of stimulants increase the chance of unpleasant thought loops. The combination is generally unnecessary because of the stimulating effects of psychedelics. Combination of the exciting effects may be uncomfortable.
  • Cannabis
    • Stimulants increase anxiety levels and the risk of thought loops which can lead to negative experiences
  • Ketamine
    • No unexpected interactions, though likely to increase blood pressure but not an issue with sensible doses. Moving around on high doses of this combination may be ill-advised due to the risk of physical injury.
  • MXE
    • Risk of tachycardia, hypertension, and manic states
  • Cocaine
    • This combination of stimulants will increase strain on the heart. It is not generally worth it as cocaine has a mild blocking effect on dopamine releasers like amphetamine
  • Caffeine
    • This combination of stimulants is not usually necessary and may increase strain on the heart, as well as potentially causing anxiety and greater physical discomfort.
  • Alcohol
    • Drinking on stimulants is risky because the sedative effects of the alcohol are reduced, and these are what the body uses to gauge drunkenness. This typically leads to excessive drinking with significantly decreasing inhibitions, high risk of liver damage and increased dehydration. They will also allow you to drink past a point where you might usually pass out, increasing the risk. If you do decide to do this, then you should set a limit of how much you will drink each hour and stick to it, bearing in mind that you will feel the alcohol and the stimulant less. Extended-release formulations may severely impede sleep, further worsening the hangover.
  • GHB/GBL
    • Stimulants increase respiration rate allowing a higher dose of sedatives. If the stimulant wears off first, then the opiate may overcome the patient and cause respiratory arrest.
  • Opioids
    • Stimulants increase respiration rate allowing a higher dose of opiates. If the stimulant wears off first, then the opiate may overcome the patient and cause respiratory arrest.

Low risk & Increased Effects

  • N2O
  • MDMA
    • Amphetamines increase the neurotoxic effects of MDMA

Low risk & Decreased Effects

  • Benzodiazepines
    • Both can dull each other’s results, so if one wears off before the other it’s possible to overdose due to the lack of counteraction

Low risk & No Synergy

References & Notes

General