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(dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate) Tablets
AMPHETAMINES HAVE A HIGH POTENTIAL FOR ABUSE. ADMINISTRATION OF AMPHETAMINES FOR PROLONGED PERIODS OF TIME MAY LEAD TO DRUG DEPENDENCE AND MUST BE AVOIDED. PARTICULAR ATTENTION SHOULD BE PAID TO THE POSSIBILITY OF SUBJECTS OBTAINING AMPHETAMINES FOR NONTHERAPEUTIC USE OR DISTRIBUTION TO OTHERS, AND THE DRUGS SHOULD BE PRESCRIBED OR DISPENSED SPARINGLY.
MISUSE OF AMPHETAMINE MAY CAUSE SUDDEN DEATH AND SERIOUS CARDIOVASCULAR ADVERSE EVENTS.
A single-entity amphetamine product combining the neutral sulfate salts of dextroamphetamine and amphetamine, with the dextroisomer of amphetamine saccharate and d, l-amphetamine aspartate.
|EACH TABLET CONTAINS:||5 mg||7.5 mg||10 mg.||12.5 mg.||15 mg||20 mg.||30 mg.|
|Dextroamphetamine Saccharate||1.25 mg||1.875 mg||2.5 mg||3.125 mg||3.75 mg||5 mg||7.5 mg|
|Amphetamine Aspartate Monohydrate Equivalent||1.25* mg||1.875 mg†||2.5 mg‡||3.125 mg§||3.75 mg¶||5 mg#||7.5 mgÞ|
|Dextroamphetamine Sulfate, USP||1.25 mg||1.875 mg||2.5 mg||3.125 mg||3.75 mg||5 mg||7.5 mg|
|Amphetamine Sulfate, USP||1.25 mg||1.875 mg||2.5 mg||3.125 mg||3.75 mg||5 mg||7.5 mg|
|T otal Amphetamine Base Equivalence||3.13 mg||4.7 mg||6.3 mg||7.8 mg||9.4 mg||12.6 mg||18.8 mg|
|*1.25 mg of Amphetamine Aspartate Monohydrate equivalent
to 1.17 mg Amphetamine Aspartate (Anhydrous) as supplied
†1.875 mg of Amphetamine Aspartate Monohydrate equivalent to 1.755 mg Amphetamine Aspartate (Anhydrous) as supplied
‡2.5 mg of Amphetamine Aspartate Monohydrate equivalent to 2.34 mg Amphetamine Aspartate (Anhydrous) as supplied
§3.125 mg of Amphetamine Aspartate Monohydrate equivalent to 2.925 mg Amphetamine Aspartate (Anhydrous) as supplied
¶ 3.75 mg of Amphetamine Aspartate Monohydrate equivalent to 3.51 mg Amphetamine Aspartate (Anhydrous) as supplied
# 5 mg of Amphetamine Aspartate Monohydrate equivalent to 4.6 mg Amphetamine Aspartate (Anhydrous) as supplied
Þ7.5 mg of Amphetamine Aspartate Monohydrate equivalent to 7.03 mg
Colloidal silicon dioxide, compressible sugar, corn starch, magnesium stearate, microcrystalline cellulose and saccharin sodium.
Adderall® 5 mg is a white to off-white tablet, which contains no color additives.
Adderall® 7.5 mg and 10 mg contain FD&C Blue #1 Aluminum Lake as a color additive.
Adderall® 12.5 mg, 15 mg, 20 mg and 30 mg contain FD&C Yellow #6 Aluminum Lake as a color additive.
What are the possible side effects of amphetamine and dextroamphetamine (Adderall, Adderall XR)?
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Stop using this medication and call your doctor at once if you have a serious side effect such as:
- fast, pounding, or uneven heartbeats;
- pain or burning when you urinate;
- talking more than usual, feelings of extreme happiness or sadness;
- tremors, hallucinations, unusual behavior, or motor tics (muscle twitches); or
- dangerously high blood...
What are the precautions when taking amphetamine, dextroamphetamine mixed salts (Adderall)?
Before taking this medication, tell your doctor or pharmacist if you are allergic to it; or to sympathomimetic drugs (such as epinephrine, pseudoephedrine); or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.
Before using this medication, tell your doctor or pharmacist your medical history, especially of: blood circulation problems (such as Raynaud's disease), certain mental/mood conditions (such as severe agitation, psychosis), personal/family history of mental/mood disorders (such as bipolar disorder, depression, psychotic disorder, suicidal thoughts), heart problems (including irregular heartbeat/rhythm, coronary artery disease, heart failure,...
Last reviewed on RxList: 2/27/2015
This monograph has been modified to include the generic and brand name in many instances.
Additional Adderall Information
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Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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