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How easy is it to get a script for Adderral?
- Thread starter Audio8
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Swoleyoley
New member
IMO TOO easy
See the thing is, I had a script for ritalin when i was a kid...and it didn't do shit for me..it actually made me depressed and edgy. so I'm thinking obtaining a script of ad's would be easier for me..but i really don't have A.D.D...maybe mild, but not extremely hindering. I just want some adderral so I can get my studying done 
Georgia Tech + slacker = get used to asking; "would you like fries with that?"
P.S. sorry for straying from anabolics here, but I know alot of you guys here and trust your opinions. It's like another family here
Georgia Tech + slacker = get used to asking; "would you like fries with that?"
P.S. sorry for straying from anabolics here, but I know alot of you guys here and trust your opinions. It's like another family here
Last edited:
You can get it, just find out which psychiatrist is the one who treats most of the add kids in town. Go to him with a story of a history of add - tell him you have a diagnosis, tell him you want to get back on your medication because school is kicking your ass. That should be sure way to get it.
C.
C.
techlifter_2
New member
It was easy as hell for me to get. the only problem is the long drawn out process to get the script. I started in Nov. with my college counseling center, then on to the psychologist, then to the psychiatrist. all together it took till feb. 28 to finally get it.
Is adderral a nootropic?You guys that are taking it,give me some feedback on what is does for you.
HUCKLEBERRY FINNaplex said:
Don't quote me on this, but as far as I know it's just a stronger form of ritalin, and ritalin is a mild amphetamine. Both are the most overly presribed drugs in the nation. Not meaning to step on anyone's toes, but I don't believe there is such a thing as ADD. I think it's just an excuse for 'stupidity'. I don't think anyone over the age of 14 should be taking either. If you want a good nootropic I'd recommend piracetam stacked with choline but the effects don't last for long and you should use an attack dosage to start out.
You're close worm....Ritalin is a methylphenidate. adderall is an amphetamine. the difference between the two is huge. I have talked to many people who have taken both ritalin and aderral and they say that aderral is MUCH better. It helps you concentrate AND makes you feel good at the same time. Higher doses peoduce a euphoric feeling, being an amphetamine. It is VERY addictive for these reasons and hence not prescribed as much as ritalin is.
Here's a little more info I found:
Adderall
Description:
A single entity amphetamine product combining the neutral salts of dextroamphetamine and amphetamine, with the dextro isomer of amphetamine saccharate and d, I-amphetamine aspartate. Each tablet contains:
TABLE 1 -
Each tablet contains 10 mg 20 mg
Dextroamphetamine Saccharate 2.5 mg 5 mg
Amphetamine Aspartate 2.5 mg 5 mg
Dextroamphetamine Sulfate USP 2.5 mg 5 mg
Amphetamine Sulfate USP 2.5 mg 5 mg
Total amphetamine base equivalence 6.3 mg 12.6 mg
Inactive ingredients: sucrose, lactose, corn starch, acacia and magnesium stearate.
Colors: Adderall 10 mg contains FD & C Blue #1
Adderall 20 mg contains FD & C Yellow #6 as a color additive.
Clinical Pharmacology:
Amphetamines are non-catecholamine sympathomimetic amines with CNS stimulant activity. Peripheral actions include elevation of systolic and diastolic blood pressures and weak bronchodilator and respiratory stimulant action. Drugs of this class used in obesity are commonly known as ``anorectics'' or ``anorexigenics''. It has not been established, however, that the action of such drugs in treating obesity is primarily one of appetite suppression. For example, other central nervous system actions or metabolic effects may be involved.
There is neither specific evidence which clearly establishes the mechanism whereby amphetamine produces mental and behavioral effects in children, nor conclusive evidence regarding how these effects relate to the condition of the central nervous system dysfunction may or may not be warranted.
Contraindications:
Advanced arteriosclerosis, symptomatic cardiovascular disease, moderate to severe hypertension, hyperthyroidism, known hypersensitivity or idiosyncrasy to the sympathomimetic amines, glaucoma.
Agitated states.
Patients with a history of drug abuse.
During or within 14 days following the administration of monoamine oxidase inhibitors (Hypertensive crises may result).
Warnings:
Clinical experience suggests that in psychotic children, administration of amphetamine may exacerbate symptoms of behavior disturbance and thought disorder.
Usage in Nursing Mothers: Amphetamines are excreted in human milk. Mothers taking amphetamines should be advised to refrain from nursing.
Precautions:
Caution is to be exercised in prescribing amphetamine for patients with mild hypertension.
Information for the Patient
Amphetamines may impair the ability of the patient to engage in potentially hazardous activities such as operating machinery or vehicles; the patient should therefore be cautioned accordingly.
Drug/Laboratory Test Interactions
Amphetamines can cause a significant elevation in plasma corticosteroid levels. This increase is greatest in the evening.
Amphetamines may interfere with urinary steroid determinations.
Carcinogenesis/Mutagenesis: Mutagenicity studies and long-term studies in animals to determine the carcinogenic potential of Amphetamine, have not been performed.
Pregnancy - Teratogenic Effects, Pregnancy Category C: Amphetamine has been shown to have embryotoxic and teratogenic effects when administered to A/Jax mice and C57BL mice in doses approximately 41 times the maximum human dose. Embryotoxic effects were not seen in New Zealand white rabbits given the drug in doses 7 times the human dose nor in rats given 12.5 times the maximum human dose. There are no adequate and well-controlled studies in pregnant women. Amphetamines should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
Nonteratogenic Effects: Infants born to mothers dependent on amphetamines have an increased risk of premature delivery and low birth weight. Also, these infants may experience symptoms of withdrawal as demonstrated by dysphoria, including agitation, and significant lassitude.
Pediatric Use: Long-term effects of amphetamines in children have not been well established. Amphetamines are not recommended for use as anorectic agents in children under 12 years of age.
Amphetamines have been reported to exacerbate motor and phonic tics and Tourette's syndrome. Therefore, clinical evaluation for tics and Tourette's syndrome in children and their families should precede use of stimulant medications.
Drug Interactions:
Acidifying agents: Gastrointestinal acidifying agents (guanethidine, reserpine, glutamic acid HCl, ascorbic acid, fruit juices, etc.) lower absorption of amphetamines.
Urinary acidifying agents: (ammonium chloride, sodium acid phosphate, etc.) increase the concentration of the ionized species of the amphetamine molecule, thereby increasing urinary excretion. Both groups of agents lower blood levels and efficacy of amphetamines.
Adrenergic blockers: Adrenergic blockers are inhibited by amphetamines.
Alkalinizing agents: Gastrointestinal alkalinizing agents (sodium bicarbonate, etc.) increase absorption of amphetamines. Urinary alkalinizing agents (acetazolamide, some thiazides) increase the concentration of the non-ionized species of the amphetamine molecule, thereby decreasing urinary excretion. Both groups of agents increase blood levels and therefore potentiate the actions of amphetamines.
Antidepressants, tricyclic: Amphetamines may enhance the activity of tricyclic or sympathomimetic agents; d-amphetamine with Desipramine or Protriptyline and possibly other tricyclics cause striking and sustained increases in the concentration of d=amphetamine in the brain; cardiovascular effects can be potentiated.
MAO inhibitors: MAOI antidepressants, as well as a metabolite of Furazolidone, slow amphetamine metabolism. This slowing potentiates amphetamines, increasing their effect on the release of norepinephrine and other monoamines from adrenergic nerve endings; this can cause headaches and other signs of hypertensive crisis. A variety of neurological toxic effects and malignant hyperpyrexia can occur, sometimes with fatal results.
Antihistamines: Amphetamines may counteract the sedative effect of antihistamines.
Antihypertensives: Amphetamines may antagonize the hypotensive effects of antihypertensives.
Chlorpromazine: Chlorpromazine blocks dopamine and norepinephrine reuptake, thus inhibiting the central stimulant effects of amphetamines, and can be used to treat amphetamine poisoning.
Ethosuximide: Amphetamines may delay intestinal absorption of Ethosuximide.
Haloperidol: Haloperidol blocks dopamine and norepinephrine reuptake, thus inhibiting the central stimulant effects of amphetamines.
Lithium carbonate: The antiobesity and stimulatory effects of amphetamines may be inhibited by lithium carbonate.
Meperidine: Amphetamines potentiate the analgesic effect of Meperidine.
Methenamine therapy: Urinary excretion of amphetamines is increased, and efficacy is reduced, by acidifying agents used in methenamine therapy.
Norepinephrine: Amphetamines enhance the adrenergic effect of norepinephrine.
Phenobarbital: Amphetamines may delay intestinal absorption of Phenobarbital; co-administration of Phenobarbital may product a synergistic anticonvulsant action.
Phenytoin: Amphetamines may delay intestinal absorption of phenytoin; co-administration of phenytoin may produce a synergistic anticonvulsant action.
Propoxyphene: In most cases of Propoxyphene overdosage, amphetamine CNS stimulation is potential and fatal convulsions can occur.
Veratrum alkaloids: Amphetamines inhibit the hypertensive effect of veratrum alkaloids.
Adverse Reactions:
Cardiovascular: Palpitation, tachycardia, elevation of blood pressure. There have been isolated reports of cardiomyopathy associated with chronic amphetamine use.
Central nervous system: Over stimulation, restlessness, dizziness, insomnia, euphoria, dysphoria, tremor, headache; rarely psychotic episodes at recommended doses.
Gastrointestinal: Dryness of the mouth, unpleasant taste, diarrhea, constipation, other gastrointestinal disturbances.
Allergic: Urticaria.
Endocrine: Impotence, changes in Libido.
Drug Abuse and Dependence:
Dextroamphetamine sulfate is a Schedule II controlled substance.
Amphetamines have been extensively abused. Tolerance, extreme psychological dependence, and severe social disability have occurred. There are reports of patients who have increased the dosage to many times that recommended. Abrupt cessation following prolonged high dosage administration results in extreme fatigue and mental depression; changes are also noted on the sleep EEG. Manifestations of chronic intoxication with amphetamines include severe dermatoses, marked insomnia, irritability, hyperactivity, and personality changes. The most severe manifestation of chronic intoxication is psychosis, often clinically indistinguishable from schizophrenia. This is rare with oral amphetamines.
Overdosage:
Individual patient response to amphetamines varies widely. While toxic symptoms occasionally occur as an idiosyncrasy at doses as low as 2 mg, they are rare with doses of less than 15 mg; 30 mg can produce severe reactions, yet doses of 400 to 500 mg are not necessarily fatal.
In rats, the oral LD50 of dextroamphetamine sulfate is 96.8 mg/kg.
Symptoms
Manifestations of acute overdosage with amphetamines include restlessness, tremor, hyperreflexia, rapid respiration, confusion, assaultiveness, hallucinations, panic states, hyperpyrexia and rhabdomolysis.
Fatigue and depression usually follow the central stimulation.
Cardiovascular effects include arrhythmias, hypertension or hypotension and circulatory collapse.
Gastrointestinal symptoms include nausea, vomiting, diarrhea, and abdominal cramps. Fatal poisoning is usually preceded by convulsions and coma.
Treatment
Consult with a Certified Poison Control Center for up to date guidance and advice. Management of acute amphetamine intoxication is largely symptomatic and includes gastric lavage, administration of activated charcoal, administration of a cathartic and sedation. Experience with hemodialysis or peritoneal dialysis is inadequate to permit recommendation in this regard. Acidification of the urine increases amphetamine excretion, but is believed to increase risk of acute renal failure if myoglobinuria is present. If acute, severe hypertension complicates amphetamine overdosage, administration of intravenous Phentolamine (Regitine, CIBA) has been suggested. However, a gradual drop in blood pressure will usually result when sufficient sedation has been achieved. Chlorpromazine antagonizes the central stimulant effects of amphetamines and can be used to treat amphetamine intoxication.
Dosage and Administration:
Regardless of indication, amphetamines should be administered at the lowest effective dosage and dosage should be individually adjusted. Late evening doses should be avoided because of the resulting insomnia.
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Here's a little more info I found:
Adderall
Description:
A single entity amphetamine product combining the neutral salts of dextroamphetamine and amphetamine, with the dextro isomer of amphetamine saccharate and d, I-amphetamine aspartate. Each tablet contains:
TABLE 1 -
Each tablet contains 10 mg 20 mg
Dextroamphetamine Saccharate 2.5 mg 5 mg
Amphetamine Aspartate 2.5 mg 5 mg
Dextroamphetamine Sulfate USP 2.5 mg 5 mg
Amphetamine Sulfate USP 2.5 mg 5 mg
Total amphetamine base equivalence 6.3 mg 12.6 mg
Inactive ingredients: sucrose, lactose, corn starch, acacia and magnesium stearate.
Colors: Adderall 10 mg contains FD & C Blue #1
Adderall 20 mg contains FD & C Yellow #6 as a color additive.
Clinical Pharmacology:
Amphetamines are non-catecholamine sympathomimetic amines with CNS stimulant activity. Peripheral actions include elevation of systolic and diastolic blood pressures and weak bronchodilator and respiratory stimulant action. Drugs of this class used in obesity are commonly known as ``anorectics'' or ``anorexigenics''. It has not been established, however, that the action of such drugs in treating obesity is primarily one of appetite suppression. For example, other central nervous system actions or metabolic effects may be involved.
There is neither specific evidence which clearly establishes the mechanism whereby amphetamine produces mental and behavioral effects in children, nor conclusive evidence regarding how these effects relate to the condition of the central nervous system dysfunction may or may not be warranted.
Contraindications:
Advanced arteriosclerosis, symptomatic cardiovascular disease, moderate to severe hypertension, hyperthyroidism, known hypersensitivity or idiosyncrasy to the sympathomimetic amines, glaucoma.
Agitated states.
Patients with a history of drug abuse.
During or within 14 days following the administration of monoamine oxidase inhibitors (Hypertensive crises may result).
Warnings:
Clinical experience suggests that in psychotic children, administration of amphetamine may exacerbate symptoms of behavior disturbance and thought disorder.
Usage in Nursing Mothers: Amphetamines are excreted in human milk. Mothers taking amphetamines should be advised to refrain from nursing.
Precautions:
Caution is to be exercised in prescribing amphetamine for patients with mild hypertension.
Information for the Patient
Amphetamines may impair the ability of the patient to engage in potentially hazardous activities such as operating machinery or vehicles; the patient should therefore be cautioned accordingly.
Drug/Laboratory Test Interactions
Amphetamines can cause a significant elevation in plasma corticosteroid levels. This increase is greatest in the evening.
Amphetamines may interfere with urinary steroid determinations.
Carcinogenesis/Mutagenesis: Mutagenicity studies and long-term studies in animals to determine the carcinogenic potential of Amphetamine, have not been performed.
Pregnancy - Teratogenic Effects, Pregnancy Category C: Amphetamine has been shown to have embryotoxic and teratogenic effects when administered to A/Jax mice and C57BL mice in doses approximately 41 times the maximum human dose. Embryotoxic effects were not seen in New Zealand white rabbits given the drug in doses 7 times the human dose nor in rats given 12.5 times the maximum human dose. There are no adequate and well-controlled studies in pregnant women. Amphetamines should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
Nonteratogenic Effects: Infants born to mothers dependent on amphetamines have an increased risk of premature delivery and low birth weight. Also, these infants may experience symptoms of withdrawal as demonstrated by dysphoria, including agitation, and significant lassitude.
Pediatric Use: Long-term effects of amphetamines in children have not been well established. Amphetamines are not recommended for use as anorectic agents in children under 12 years of age.
Amphetamines have been reported to exacerbate motor and phonic tics and Tourette's syndrome. Therefore, clinical evaluation for tics and Tourette's syndrome in children and their families should precede use of stimulant medications.
Drug Interactions:
Acidifying agents: Gastrointestinal acidifying agents (guanethidine, reserpine, glutamic acid HCl, ascorbic acid, fruit juices, etc.) lower absorption of amphetamines.
Urinary acidifying agents: (ammonium chloride, sodium acid phosphate, etc.) increase the concentration of the ionized species of the amphetamine molecule, thereby increasing urinary excretion. Both groups of agents lower blood levels and efficacy of amphetamines.
Adrenergic blockers: Adrenergic blockers are inhibited by amphetamines.
Alkalinizing agents: Gastrointestinal alkalinizing agents (sodium bicarbonate, etc.) increase absorption of amphetamines. Urinary alkalinizing agents (acetazolamide, some thiazides) increase the concentration of the non-ionized species of the amphetamine molecule, thereby decreasing urinary excretion. Both groups of agents increase blood levels and therefore potentiate the actions of amphetamines.
Antidepressants, tricyclic: Amphetamines may enhance the activity of tricyclic or sympathomimetic agents; d-amphetamine with Desipramine or Protriptyline and possibly other tricyclics cause striking and sustained increases in the concentration of d=amphetamine in the brain; cardiovascular effects can be potentiated.
MAO inhibitors: MAOI antidepressants, as well as a metabolite of Furazolidone, slow amphetamine metabolism. This slowing potentiates amphetamines, increasing their effect on the release of norepinephrine and other monoamines from adrenergic nerve endings; this can cause headaches and other signs of hypertensive crisis. A variety of neurological toxic effects and malignant hyperpyrexia can occur, sometimes with fatal results.
Antihistamines: Amphetamines may counteract the sedative effect of antihistamines.
Antihypertensives: Amphetamines may antagonize the hypotensive effects of antihypertensives.
Chlorpromazine: Chlorpromazine blocks dopamine and norepinephrine reuptake, thus inhibiting the central stimulant effects of amphetamines, and can be used to treat amphetamine poisoning.
Ethosuximide: Amphetamines may delay intestinal absorption of Ethosuximide.
Haloperidol: Haloperidol blocks dopamine and norepinephrine reuptake, thus inhibiting the central stimulant effects of amphetamines.
Lithium carbonate: The antiobesity and stimulatory effects of amphetamines may be inhibited by lithium carbonate.
Meperidine: Amphetamines potentiate the analgesic effect of Meperidine.
Methenamine therapy: Urinary excretion of amphetamines is increased, and efficacy is reduced, by acidifying agents used in methenamine therapy.
Norepinephrine: Amphetamines enhance the adrenergic effect of norepinephrine.
Phenobarbital: Amphetamines may delay intestinal absorption of Phenobarbital; co-administration of Phenobarbital may product a synergistic anticonvulsant action.
Phenytoin: Amphetamines may delay intestinal absorption of phenytoin; co-administration of phenytoin may produce a synergistic anticonvulsant action.
Propoxyphene: In most cases of Propoxyphene overdosage, amphetamine CNS stimulation is potential and fatal convulsions can occur.
Veratrum alkaloids: Amphetamines inhibit the hypertensive effect of veratrum alkaloids.
Adverse Reactions:
Cardiovascular: Palpitation, tachycardia, elevation of blood pressure. There have been isolated reports of cardiomyopathy associated with chronic amphetamine use.
Central nervous system: Over stimulation, restlessness, dizziness, insomnia, euphoria, dysphoria, tremor, headache; rarely psychotic episodes at recommended doses.
Gastrointestinal: Dryness of the mouth, unpleasant taste, diarrhea, constipation, other gastrointestinal disturbances.
Allergic: Urticaria.
Endocrine: Impotence, changes in Libido.
Drug Abuse and Dependence:
Dextroamphetamine sulfate is a Schedule II controlled substance.
Amphetamines have been extensively abused. Tolerance, extreme psychological dependence, and severe social disability have occurred. There are reports of patients who have increased the dosage to many times that recommended. Abrupt cessation following prolonged high dosage administration results in extreme fatigue and mental depression; changes are also noted on the sleep EEG. Manifestations of chronic intoxication with amphetamines include severe dermatoses, marked insomnia, irritability, hyperactivity, and personality changes. The most severe manifestation of chronic intoxication is psychosis, often clinically indistinguishable from schizophrenia. This is rare with oral amphetamines.
Overdosage:
Individual patient response to amphetamines varies widely. While toxic symptoms occasionally occur as an idiosyncrasy at doses as low as 2 mg, they are rare with doses of less than 15 mg; 30 mg can produce severe reactions, yet doses of 400 to 500 mg are not necessarily fatal.
In rats, the oral LD50 of dextroamphetamine sulfate is 96.8 mg/kg.
Symptoms
Manifestations of acute overdosage with amphetamines include restlessness, tremor, hyperreflexia, rapid respiration, confusion, assaultiveness, hallucinations, panic states, hyperpyrexia and rhabdomolysis.
Fatigue and depression usually follow the central stimulation.
Cardiovascular effects include arrhythmias, hypertension or hypotension and circulatory collapse.
Gastrointestinal symptoms include nausea, vomiting, diarrhea, and abdominal cramps. Fatal poisoning is usually preceded by convulsions and coma.
Treatment
Consult with a Certified Poison Control Center for up to date guidance and advice. Management of acute amphetamine intoxication is largely symptomatic and includes gastric lavage, administration of activated charcoal, administration of a cathartic and sedation. Experience with hemodialysis or peritoneal dialysis is inadequate to permit recommendation in this regard. Acidification of the urine increases amphetamine excretion, but is believed to increase risk of acute renal failure if myoglobinuria is present. If acute, severe hypertension complicates amphetamine overdosage, administration of intravenous Phentolamine (Regitine, CIBA) has been suggested. However, a gradual drop in blood pressure will usually result when sufficient sedation has been achieved. Chlorpromazine antagonizes the central stimulant effects of amphetamines and can be used to treat amphetamine intoxication.
Dosage and Administration:
Regardless of indication, amphetamines should be administered at the lowest effective dosage and dosage should be individually adjusted. Late evening doses should be avoided because of the resulting insomnia.
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Swoleyoley
New member
wonder why the didnt mention the 30mg or gel caps?
Best of luck getting adderall audio.I've been trying relentlessly to get it since I first heard about it on these boards about 3 wks ago.It's not available here from a doctor or anyone else for that matter,it's been a nightmare trying to find it.
I want to get it to help with studying myself aswell.
After a hell of a lot of searching I paid $10 per 30mg tab of the stuff this week........ that price is totally crazy,it hasn't arrived yet so I don't know if it was worth it.
It's 50/50 as to whether I've been scammed or not but I was desparate so I took the chance.
I want to get it to help with studying myself aswell.
After a hell of a lot of searching I paid $10 per 30mg tab of the stuff this week........ that price is totally crazy,it hasn't arrived yet so I don't know if it was worth it.
It's 50/50 as to whether I've been scammed or not but I was desparate so I took the chance.
techlifter_2
New member
I take adderall daily, and let me give you a simple description on how it makes me feel.
I take 20 mgs in the morning and 20 mgs in the afternoon. About an hour after I take it my body gets slight chills, feels good. Then I get the urge to be "productive." By this I mean, if I were to sit down and watch TV without adderall that would be that, but on adderall I'll clean up the coffee table while watching, or actually do homework during the commercials. Also I get extremely talkative. I can't talk fast enough to get all I want to say out. When doing anything I become somewhat of a perfectionist. If Im reading, instead of scanning I'll actually re-read until I really understand what Im reading. Basically this stuff is wonderful. You will never have a more productive day than when you take it. I dont know how good it is to take before lifting, but the days i have taken it I got the best workout ever. couldnt be intense enough.
I take 20 mgs in the morning and 20 mgs in the afternoon. About an hour after I take it my body gets slight chills, feels good. Then I get the urge to be "productive." By this I mean, if I were to sit down and watch TV without adderall that would be that, but on adderall I'll clean up the coffee table while watching, or actually do homework during the commercials. Also I get extremely talkative. I can't talk fast enough to get all I want to say out. When doing anything I become somewhat of a perfectionist. If Im reading, instead of scanning I'll actually re-read until I really understand what Im reading. Basically this stuff is wonderful. You will never have a more productive day than when you take it. I dont know how good it is to take before lifting, but the days i have taken it I got the best workout ever. couldnt be intense enough.
HUCKLEBERRY FINNaplex said:
I don't think you want to go through all that so I'll giv you the scoop.
Basically, I've been using it in low doses 10-15mg initially to study. Now I use it before the gym. Insane concentration. It takes about 2 hours to reach full plasma concentration.
It's an amphetamine and I found it to be VERY addictive. Unlike Ritalin, it makes you feel great and gives you great enegy. Once it wares off, you become irratible and paranoid. I was yelling at people and kept thinking that someone was talking about me.
adderall is much stronger then ritalin. Both used to be staples of my diet, since I am in college. I would never take it for pleasure though it works wonders for overnight cramming. If you got depressed off ritalin your going to get 10 times more depressed off adderal. And by the way you can cross eating of your calander for the next two days. That shit when takin daily really fucks you up. I would never take that shit again unless I had to cram. You become the tazmanian devil.
As to how you get it dont waste your time cause itll be expensive if you try it blackmarket, let your insurance take care of it. they dispense that shit like water by me. I go through a neurologist. I dont even have to see a psychologist or anything. I do have a history of ADHD my entire life, but the neurologist doesnt have record of it he just takes my word for it. If I want I can get 180 10mg pills a month!!! This doc is great he looks in the PDR scratches his head and gives you the maximum dose for everything. Three cheers for HIP HEALTH. I wonder if he will give me some Oxandrol
But beware I dont find it addictive at all, It just fucks you up you get rund down and crash really hard. I hate finals
As to how you get it dont waste your time cause itll be expensive if you try it blackmarket, let your insurance take care of it. they dispense that shit like water by me. I go through a neurologist. I dont even have to see a psychologist or anything. I do have a history of ADHD my entire life, but the neurologist doesnt have record of it he just takes my word for it. If I want I can get 180 10mg pills a month!!! This doc is great he looks in the PDR scratches his head and gives you the maximum dose for everything. Three cheers for HIP HEALTH. I wonder if he will give me some Oxandrol
But beware I dont find it addictive at all, It just fucks you up you get rund down and crash really hard. I hate finals
WormAAA77 said:
I will have to disagree with you on ADD being an excuse for stupidity. My G/F takes Adderall and if she does not she has a definate focus problem. She is highly inteligent as are most people diagnosed with ADD.
Peace, Quadsweep
I have friends who have had some real problems with long term ritalin and adderall usage. For some detailed stories about people with long term adderall usage there are some experiences on www.erowid.com click on plants & drugs and just do a search for adderall and go to the vault and scroll down to experiences. Some of them made me want to stay the hell away from it forever (I sometimes take it recreationally, maybe 3 times a year as I can NEVER get it).
Thanks for your feedback guys!
the_only_sepe
New member
heres a little help for those who dont like the feeling of coming down off adderall, take one 50mg. 5htp b4 taking your adderall and you will not crash afterwards(it keeps your serotonin balanced), it is a day and night diff without the 5htp, one 5 htp will do you for all day.
adderall helped me alot while I was in school, now I take a few prior to workingout, to amp things up a bit. I turned my girlfriend on to adderall, she loves them, she has adhd and it helps her to calm down and actually think, I am trying to get another script, shes sucking my adderall reserves down fast,lol I am going to try xr this time.
THE ONLY SEPE
adderall helped me alot while I was in school, now I take a few prior to workingout, to amp things up a bit. I turned my girlfriend on to adderall, she loves them, she has adhd and it helps her to calm down and actually think, I am trying to get another script, shes sucking my adderall reserves down fast,lol I am going to try xr this time.
THE ONLY SEPE
That's interesting sepe. I used to take 5-htp for coming off of ectacy, as I know it restores your seritonin levels back to normal...but i was not aware that Aderral depresses your seritonin. That's a huge negative right there..no wonder so many people get addicted to the stuff...
How effective do you guys find it for studying?Is it as good as people say it is?
I've been trying hard to make myself study for my exams but I just keep getting distracted,as I'm writing out theorems my mind inevitably wanders to some place a million miles away.I just can't sit still and study,my mental discipline is just gone cpmpletely to crap lately.I've 2 weeks left to exams and if I don't get my act together fast I'm fucked.I just can't focus on the task at hand no matter what was I approach it.
Do you think the adderall will help or am I as screwed as I think I am?
I've been trying hard to make myself study for my exams but I just keep getting distracted,as I'm writing out theorems my mind inevitably wanders to some place a million miles away.I just can't sit still and study,my mental discipline is just gone cpmpletely to crap lately.I've 2 weeks left to exams and if I don't get my act together fast I'm fucked.I just can't focus on the task at hand no matter what was I approach it.
Do you think the adderall will help or am I as screwed as I think I am?
techlifter_2
New member
I am a college student that knew nothing about ADHD or adderall until recently. My mom suggested I go to the university's testing center to measure my testing ability because I had been performing badly on timed tests. I went through the whole list of tests, then they sent me to a psychologist. A couple visits after seeing him I we referred to a psychiatrist and then I received an addderall prescription.
Important**Turns out I really do have ADD based upon all the tests and analyzing. From the very first day I walked into the university testing center till I got my script was from Oct. 20ish until Feb. 20ish. This whole process took forever.
Once I got my first script (10mg in morning, 10mg in afternoon), each visit after that he bumped me up; partly because I encouraged him to. After two or three visits I now get 60mg a day; which there is no way I could take that much every day. Then I started referring my friends straight to my psych. and they were getting hooked up without going through all the other bullshit I went through.
So I guess the answer is no, it isn't that hard to get adderall. It only depends on how long you are willing to wait for an appointment and what part of the country you live in. I have noticed smaller rural areas are less likely to prescribe it while urban regions are more likely.
Important**Turns out I really do have ADD based upon all the tests and analyzing. From the very first day I walked into the university testing center till I got my script was from Oct. 20ish until Feb. 20ish. This whole process took forever.
Once I got my first script (10mg in morning, 10mg in afternoon), each visit after that he bumped me up; partly because I encouraged him to. After two or three visits I now get 60mg a day; which there is no way I could take that much every day. Then I started referring my friends straight to my psych. and they were getting hooked up without going through all the other bullshit I went through.
So I guess the answer is no, it isn't that hard to get adderall. It only depends on how long you are willing to wait for an appointment and what part of the country you live in. I have noticed smaller rural areas are less likely to prescribe it while urban regions are more likely.
HUCKLEBERRY FINNaplex said:
I have moderate/severe ADHD. If you don't believe in it, that means I'm stupid. When I take 15mg Adderall, I'm a different person. I remember things... I am motivated to do things that aren't immediately rewarding. I can read them books without having to re-read every single paragraph, because my mind wanders when something in the paragraph reminds me of something, I can remember the first part of a math problem as I read the last part of a math problem.
In short, I'm just like a normal person... whose ability to selectively attenuate between stimuli is good. Without the ADDerall... and I'm ADHD boy.
Its not a nootropic... although "nootropics" like Piracetam also help. Its just a mixture of dextro-amphetamine and another amphetamine, to stimulate the brain and in doing so, stimluate the defunct areas of it that regulate selective attention.
Before getting Adderall, I used to be a bit of a speed freak. Stay up for a week kinda thing. It sucks that (at least in my area) in the states, the only street speed available is Methamphetamine, which is ENTIRELY too harsh, lasts too long, and is so fucking potent that the littlest bit has you up for days. Fuck meth. I hate that shit. Suppose I was self medicating.
Anyways, in regards to being addictive... in my experience, if you NEED Adderall, its not addictive. If you put a gram of amphetamine in front of me, its gonna be gone in as little time as my heart can handle. That's just how I am, so I avoid speed like the plague...
but Adderall? No. Doesn't do that for me. I don't get high on Adderall. If I take too much... (more than 15mg, but it gets bad after 30mg) I get sweating, racing pulse, anxiety, paranoia (after I don't sleep for a while), uncontrollable tics, and I just feel terrible. Now I still get all this shit on a gram of speed too... but I also get high.
Not on Adderall though, intranasal or eaten.Other people that I know that have ADHD, they don't abuse their Adderall. But everyone they know tries to.
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