Adderall
Adderall® CII is a pharmaceutical amphetamine used to treat
attention-deficit hyperactivity disorder and narcolepsy. It was
first prescribed in the 1970s as an anorectic (under the brand name
Obetrol®), but such usage is now rare.
ways to make money
Adderall is a central nervous system stimulant composed of four
amphetamine salts: amphetamine aspartate, amphetamine sulfate,
dextroamphetamine saccharate, and dextroamphetamine sulfate (the
last salt is also prescribed alone as Dexedrine®). The four
component salts are claimed to be metabolised at different rates.
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The average elimination half-life for dextroamphetamine is 10 hours
in adults, and for levoamphetamine, 13 hours. Its effects are
otherwise similar to other central nervous system stimulants (see
amphetamine for details.).
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The manufacturer claims that the mixture of salts makes Adderall's
effects smoother, with softer highs and lows, than those of other
treatments for the same disorders.
There is little evidence, however, to support this claim for
immediate-release Adderall. A recent patent application for Adderall
(USP #6,384,020 for details) was a pharmaceutical composition patent
listing a rapid immediate release oral dosage form. No claim of
increased or smooth drug delivery was made. A recent double-blind,
placebo-controlled crossover study, conducted among children,
indicated that Adderall behaved similarly to other immediate release
amphetamines. The authors found that sustained-release
dexamphetamine (the main isomeric-amphetamine component of Adderall)
had a longer duration of action, and cost less than Adderall, though
dexamphetamine was less effective in the first few hours of morning
dosing.
Adderall is now sold in either an immediate-release tablet or an
extended-release capsule, marketed as Adderall XR. Doses for both
immediate-release and extended-release form come in 5mg, 10mg, 15mg,
20mg, 25mg, and 30mg increments.
Adderall XR utilizes the Microtrol® delivery system to achieve the
extended-release mechanism. This delivery system incorporates two
beads: the first type of bead dissolves immediately and the second
type releases four hours later. Maximum plasma concentration is
achieved in seven hours, compared to regular Adderall IR
(immediate-release) which reaches maximum plasma concentration
within three hours. As a result of its high bioavailability,
Adderall XR's effectiveness is not altered by food absorption in the
GI tract. However, tmax (mean plasma concentration) is prolonged by
2.5 hours (using a standard high-fat meal as the control). Acidic
beverages should not be taken with Adderall XR as they alter the pH
balance of the stomach. However, parents may sprinkle Adderall XR on
applesauce if a child does not like swallowing pills.
Adderall works by blocking the reuptake of dopamine and
norepinephrine into the presynaptic neuron and increasing their
release from the presynaptic neuron into the extraneuronal space. In
other words, Adderall reverses the reuptake mechanism, turning it
into a pump instead of a vacuum.
The increased flow of dopamine and norepinephrine into the
extraneuronal space causes the brain, as one psychiatrist explains,
to experience a more intense level of concentration, causing an
increased ability to focus for extended periods of time, and a
heightened interest in performing mental tasks.
Though rare, it is possible for Adderall to cause psychotic episodes
at recommended doses.
Some people feel that they are less creative while taking Adderall,
while others report that the focusing effect can aid in creative
work. The famous Beat generation writer Jack Kerouac, for instance,
is said to have written much of his classic On The Road in a span of
three weeks, aided by dextroamphetamine (the active ingredient in
Adderall) from Benzedrine inhalers; country music star Johnny Cash
had a long period of amphetamine use in the 1960s; and mathematician
Paul Erdos was noted for habitual use of prescription amphetamine
throughout the final decades of his life; Smile was written by Brian
Wilson and Van Dyke Parks with heavy amphetamine use, among others.
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Arcus Senilis |
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| Arcus senilis (or Arcus
senilis corneae. Latin: senile bow) is a peripheral corneal opacity
caused by a deposition of phospholipid and cholesterol granules in the
corneal stroma (or substantia propria). It typically appears bilaterally
and symmetrically as a partial or complete whitish arc highly visible
over the iris. It is most often found in the elderly, hence the name. It
can be a sign of disturbance in lipid metabolism, an indicator of
conditions such as hypercholesterolemia, hyperlipoproteinemia or
hyperlipidemia. A unilateral arcus is a sign of carotid artery disease
or ocular hypotony. |
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