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PSYCHOPHARMACOLOGY
Psychopharmacology
 (from Greek, psȳkhē, "breath, life,
soul"; pharmakon, "drug"; and, -logia “study”)
 Psychopharmacology is the study of drug-
induced changes in mood, thinking, and
behavior.
 These drugs may originate from natural
sources such as plants and animals, or from
artificial sources such as chemical syntheses in
the laboratory.
Early Psychopharmacology
 Hunter-gatherer or surviving tribal cultures
used drugs depends on what the particular
ecosystem a given tribe lives in can support,
and are typically found growing wild.
 These societies generally attach spiritual
significance to such drug use, and often
incorporate it into their religious practices.
 With the dawn of the Neolithic and the
proliferation of agriculture, new drugs came
into use as a natural by-product of farming.
Among them were opium, cannabis,
and alcohol derived from the fermentation of
cereals and fruits.
Drugs
 Drug is “a chemical substance used in the
treatment, cure, prevention, or diagnosis of
disease or used to otherwise enhance physical
or mental well-being”.
 Pharmaceutical Drugs
 Recreational Drugs
Over-the-Counter Drug
 Medicines sold directly to a consumer without
a prescription from a healthcare professional,
as compared to prescription drugs, which may
be sold only to consumers possessing a valid
prescription.
 OTC drugs are selected by a regulatory
agency to ensure that they are ingredients that
are safe and effective when used without
a physician's care.
Drugs and its effects
 Depressants (Downers) - Chemicals that slow
down the central nervous system and suppress
brain activity causing relief from anxiety.
 CANNABIS- make users feel relaxed and
heighten their sensory awareness. Thus, users
may experience a more vivid sense of sight,
smell, taste and hearing.
 HALLUCINOGENS- drugs that alter users'
state of consciousness and produce different
kinds of hallucinations. Leads to strong
changes in thought, mood and senses in
addition to feelings of empathy and sociability.
 Stimulants (Upper) - act on the central nervous
system and are associated with feelings of
extreme well-being, increased mental and
motor activity.
 Cocaine can make users feel exhilarated and
euphoric. Furthermore, users often experience
a temporary increase in alertness and energy
levels, and a postponement of hunger and
fatigue.
 ECSTASY- can heighten users' empathy levels
and induce a feeling of closeness to people
around them. It is often used at "rave parties"
to increase participants' sociability and energy
levels.
 Opiates & Opioids- Drugs provide pain relief,
euphoria, sedation and in increasing doses
induce coma.
 HEROIN-Can make users feel an initial surge
of euphoria, along with a feeling of warmth and
relaxation. Users also often become detached
from emotional or physical distress, pain or
anxiety.
 METHAMPHETAMINE- stimulates a feeling of
physical and mental well being, as well as a
surge of euphoria and exhilaration. Users
experience a temporary rise in energy, often
perceived to improve their performance at
manual or intellectual tasks. Users also feel
postponement of hunger and fatigue.
 Methadone- is a synthetic opioid that is used
medically as a painkiller and as a substitute for
addiction to narcotics such as heroin.
 drowsiness, weakness, nausea, insomnia,
itching, lack of appetite, mood swings, skin
rashes, difficulty urinating, insomnia,
headaches. When taken in larger doses it can
cause slow breathing, irregular heartbeat and
death.
 Antipsychotics- class of psychiatric
medication primarily used to manage
psychosis (including delusions, hallucinations,
or disordered thought), in particular
in schizophrenia and bipolar disorder.
 Include nausea, emesis, anorexia , anxiety,
agitation, restlessness, and insomnia.
 Barbiturates- sedatives prescribed to patients
with sleep disorders and other mental illnesses
to calm them down and put them to sleep.
 Constant falling, bruised legs, excessive
nervousness, shaking, sensitivity to noise,
restlessness, sweating, hallucinations and
insomnia.
 Benzodiazepine- type of medication known as
tranquilizers or minor tranquilizers, as opposed
to the major tranquilizers used to treat
psychosis.
 Changes in appearance and behaviour that
affect relationships and work performance.
Warning signs in teenagers include abrupt
changes in mood or sudden deterioration of
school performance.
Drug Effectiveness
 Refers to the ability of a drug to produce a
beneficial effect. A distinction is made between
'method' effectiveness which describes the
effect achievable if the drug was taken as
prescribed and 'use' effectiveness which is the
effect obtained under typical use
circumstances when adherence is not 100%.
 Drugs can have more than one effect
 The effectiveness of a drug is considered
relative to its safety
Drug Literature
 It is a document provided along with
a prescription medication to provide additional
information about a drug.
 It follows a standard format for every
medication and include the same types of
information.
Drug Literature Format
 Clinical pharmacology - tells how the medicine
works in the body, how it is absorbed and
eliminated, and what its effects are likely to be
at various concentrations.
 Indications and usage - uses (indications) for
which the drug has been FDA-approved (e.g.
migraines, seizures, high blood pressure).
 Contraindications - lists situations in which the
medication should not be used.
 Warnings - covers possible serious side
effects that may occur.
 Precautions - explains how to use the
medication safely including physical
impairments and drug interactions.
 Adverse reactions - lists all side effects
observed in all studies of the drug (as opposed
to just the dangerous side effects which are
separately listed in "Warnings" section)
 Drug abuse and Dependence - provides
information regarding whether prolonged use
of the medication can cause physical
dependence
 Overdosage - gives the results of
an overdose and provides recommended
action in such cases
 Dosage and Administration - gives
recommended dosage(s); may list more than
one for different conditions or different patients
(e.g., lower dosages for children)
 How supplied - explains in detail the physical
characteristics of the medication including
color, shape, markings, etc., and storage
information
Site of Action
 l. Enzyme Inhibition:
 Drugs act within the cell by modifying normal
biochemical reactions. Enzyme inhibition may
be reversible or non reversible; competitive or
non-competitive. Antimetabolites may be used
which mimic natural metabolites. Gene
functions may be suppressed.
 2. Drug-Receptor Interaction:
 Drugs act on the cell membrane by physical and/or
chemical interactions. This is usually through specific
drug receptor sites known to be located on the
membrane. A receptor is the specific chemical
constituents of the cell with which a drug interacts to
produce its pharmacological effects. Some receptor
sites have been identified with specific parts of proteins
and nucleic acids. In most cases, the chemical nature
of the receptor site remains obscure.
 3. Non-specific Interactions:
 Drugs act exclusively by physical means
outside of cells. These sites include external
surfaces of skin and gastrointestinal tract.
Drugs also act outside of cell membranes by
chemical interactions. Neutralization of
stomach acid by antacids is a good example.
Drug Interaction with Receptor Site
 A neurotransmitter has a specific shape to fit
into a receptor site and cause a
pharmacological response such as a nerve
impulse being sent. The neurotransmitter is
similar to a substrate in an enzyme interaction.
 After attachment to a receptor site, a drug may
either initiate a response or prevent a response
from occurring. A drug must be a close "mimic"
of the neurotransmitter.
 An agonist is a drug which produces a
stimulation type response. The agonist is a
very close mimic and "fits" with the receptor
site and is thus able to initiate a response.
 An antagonist drug interacts with the receptor
site and blocks or depresses the normal
response for that receptor because it only
partially fits the receptor site and can not
produce an effect. However, it does block the
site preventing any other agonist or the normal
neurotransmitter from interacting with the
receptor site.
Alcohol-Placebo Effect
 A simulated or otherwise medically ineffectual
treatment for a disease or other medical
condition intended to deceive the recipient.
Sometimes patients given a placebo treatment
will have a perceived or actual improvement in
a medical condition, a phenomenon commonly
called the placebo effect.
Effects of Repeated Administration
 Repeated administration of a drug can alter its
subsequent effectiveness:
 Tolerance: Repeated drug administration
results in diminished drug effect (or requires
increased dosage to maintain constant effect)
 Tolerance can reflect decreased drug-receptor
binding or reduced postsynaptic action of the
drug
 Sensitization: Repeated drug administration
results in heightened drug effectiveness
 Withdrawal effects: Abnormal physical or
psychological features that follow the
abrupt discontinuation of a drug that has the
capability of producing physical dependence.
Pharmacokinetics
 is the study of drug absorption, distribution
within body, and drug elimination
 Absorption depends on the route of administration
 Drug distribution depends on how soluble the drug
molecule is in fat (to pass through membranes) and on
the extent to which the drug binds to blood proteins
(albumin)
 Drug elimination is accomplished by excretion into
urine and/or by inactivation by enzymes in the liver
Routes of Drug Administration
 Intravenous (IV): into a vein (rapid absorption).
A method of introducing a drug into the body
with a hollow needle and a syringe which is
pierced through the skin into the body
 Intraperitoneal (IP): into the gut (used in lab
animals). is the injection of a substance into
the peritoneum (body cavity).
 Intramuscular (IM): into a muscle.
The injection of a substance directly into
a muscle.
 Oral Administration: orally as liquids, capsules,
tablets, or chewable tablets. Oral route is the
most convenient and usually the safest and
least expensive, it is the one most often used.
 Sublingual Administration: The dosage form is
placed under the tongue.
 Intrarectal Administration: Uses the rectum as
a route of administration for medication and
other fluids, which are absorbed by the
rectum's blood vessels.
 Inhalation Administration: via nose. Smoking or
inhalation of a substance is likely the most
rapid way to deliver drugs to the brain, as the
substance travels directly to the brain without
being diluted in the systemic circulation.
 Topical Administration: is the application of a
drug directly to the surface of the skin.
 Includes administration of drugs to any mucous
membrane
 eye – vagina
 nose – urethra
 ears – colon
 lungs
 Intracerebral Administration: (into the
cerebrum) direct injection into the brain. Used
in experimental research of chemicals and as a
treatment for malignancies of the brain. The
intracerebral route can also interrupt the blood
brain barrier from holding up against
subsequent routes.[15]
 Intracerebroventricular (into the cerebral
ventricles) administration into the ventricular
system of the brain. One use is as a last line of
opioid treatment for terminal cancer patients
with intractable cancer pain.
PSYCHOPHARMACOLOGY: THE STUDY OF DRUG-INDUCED CHANGES

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PSYCHOPHARMACOLOGY: THE STUDY OF DRUG-INDUCED CHANGES

  • 2. Psychopharmacology  (from Greek, psȳkhē, "breath, life, soul"; pharmakon, "drug"; and, -logia “study”)  Psychopharmacology is the study of drug- induced changes in mood, thinking, and behavior.  These drugs may originate from natural sources such as plants and animals, or from artificial sources such as chemical syntheses in the laboratory.
  • 3. Early Psychopharmacology  Hunter-gatherer or surviving tribal cultures used drugs depends on what the particular ecosystem a given tribe lives in can support, and are typically found growing wild.  These societies generally attach spiritual significance to such drug use, and often incorporate it into their religious practices.
  • 4.  With the dawn of the Neolithic and the proliferation of agriculture, new drugs came into use as a natural by-product of farming. Among them were opium, cannabis, and alcohol derived from the fermentation of cereals and fruits.
  • 5. Drugs  Drug is “a chemical substance used in the treatment, cure, prevention, or diagnosis of disease or used to otherwise enhance physical or mental well-being”.  Pharmaceutical Drugs  Recreational Drugs
  • 6. Over-the-Counter Drug  Medicines sold directly to a consumer without a prescription from a healthcare professional, as compared to prescription drugs, which may be sold only to consumers possessing a valid prescription.  OTC drugs are selected by a regulatory agency to ensure that they are ingredients that are safe and effective when used without a physician's care.
  • 7. Drugs and its effects  Depressants (Downers) - Chemicals that slow down the central nervous system and suppress brain activity causing relief from anxiety.  CANNABIS- make users feel relaxed and heighten their sensory awareness. Thus, users may experience a more vivid sense of sight, smell, taste and hearing.
  • 8.  HALLUCINOGENS- drugs that alter users' state of consciousness and produce different kinds of hallucinations. Leads to strong changes in thought, mood and senses in addition to feelings of empathy and sociability.
  • 9.  Stimulants (Upper) - act on the central nervous system and are associated with feelings of extreme well-being, increased mental and motor activity.  Cocaine can make users feel exhilarated and euphoric. Furthermore, users often experience a temporary increase in alertness and energy levels, and a postponement of hunger and fatigue.
  • 10.  ECSTASY- can heighten users' empathy levels and induce a feeling of closeness to people around them. It is often used at "rave parties" to increase participants' sociability and energy levels.
  • 11.  Opiates & Opioids- Drugs provide pain relief, euphoria, sedation and in increasing doses induce coma.  HEROIN-Can make users feel an initial surge of euphoria, along with a feeling of warmth and relaxation. Users also often become detached from emotional or physical distress, pain or anxiety.
  • 12.  METHAMPHETAMINE- stimulates a feeling of physical and mental well being, as well as a surge of euphoria and exhilaration. Users experience a temporary rise in energy, often perceived to improve their performance at manual or intellectual tasks. Users also feel postponement of hunger and fatigue.
  • 13.  Methadone- is a synthetic opioid that is used medically as a painkiller and as a substitute for addiction to narcotics such as heroin.  drowsiness, weakness, nausea, insomnia, itching, lack of appetite, mood swings, skin rashes, difficulty urinating, insomnia, headaches. When taken in larger doses it can cause slow breathing, irregular heartbeat and death.
  • 14.  Antipsychotics- class of psychiatric medication primarily used to manage psychosis (including delusions, hallucinations, or disordered thought), in particular in schizophrenia and bipolar disorder.  Include nausea, emesis, anorexia , anxiety, agitation, restlessness, and insomnia.
  • 15.  Barbiturates- sedatives prescribed to patients with sleep disorders and other mental illnesses to calm them down and put them to sleep.  Constant falling, bruised legs, excessive nervousness, shaking, sensitivity to noise, restlessness, sweating, hallucinations and insomnia.
  • 16.  Benzodiazepine- type of medication known as tranquilizers or minor tranquilizers, as opposed to the major tranquilizers used to treat psychosis.  Changes in appearance and behaviour that affect relationships and work performance. Warning signs in teenagers include abrupt changes in mood or sudden deterioration of school performance.
  • 17. Drug Effectiveness  Refers to the ability of a drug to produce a beneficial effect. A distinction is made between 'method' effectiveness which describes the effect achievable if the drug was taken as prescribed and 'use' effectiveness which is the effect obtained under typical use circumstances when adherence is not 100%.  Drugs can have more than one effect  The effectiveness of a drug is considered relative to its safety
  • 18. Drug Literature  It is a document provided along with a prescription medication to provide additional information about a drug.  It follows a standard format for every medication and include the same types of information.
  • 19. Drug Literature Format  Clinical pharmacology - tells how the medicine works in the body, how it is absorbed and eliminated, and what its effects are likely to be at various concentrations.  Indications and usage - uses (indications) for which the drug has been FDA-approved (e.g. migraines, seizures, high blood pressure).
  • 20.  Contraindications - lists situations in which the medication should not be used.  Warnings - covers possible serious side effects that may occur.  Precautions - explains how to use the medication safely including physical impairments and drug interactions.
  • 21.  Adverse reactions - lists all side effects observed in all studies of the drug (as opposed to just the dangerous side effects which are separately listed in "Warnings" section)  Drug abuse and Dependence - provides information regarding whether prolonged use of the medication can cause physical dependence
  • 22.  Overdosage - gives the results of an overdose and provides recommended action in such cases  Dosage and Administration - gives recommended dosage(s); may list more than one for different conditions or different patients (e.g., lower dosages for children)
  • 23.  How supplied - explains in detail the physical characteristics of the medication including color, shape, markings, etc., and storage information
  • 24. Site of Action  l. Enzyme Inhibition:  Drugs act within the cell by modifying normal biochemical reactions. Enzyme inhibition may be reversible or non reversible; competitive or non-competitive. Antimetabolites may be used which mimic natural metabolites. Gene functions may be suppressed.
  • 25.  2. Drug-Receptor Interaction:  Drugs act on the cell membrane by physical and/or chemical interactions. This is usually through specific drug receptor sites known to be located on the membrane. A receptor is the specific chemical constituents of the cell with which a drug interacts to produce its pharmacological effects. Some receptor sites have been identified with specific parts of proteins and nucleic acids. In most cases, the chemical nature of the receptor site remains obscure.
  • 26.  3. Non-specific Interactions:  Drugs act exclusively by physical means outside of cells. These sites include external surfaces of skin and gastrointestinal tract. Drugs also act outside of cell membranes by chemical interactions. Neutralization of stomach acid by antacids is a good example.
  • 27. Drug Interaction with Receptor Site  A neurotransmitter has a specific shape to fit into a receptor site and cause a pharmacological response such as a nerve impulse being sent. The neurotransmitter is similar to a substrate in an enzyme interaction.  After attachment to a receptor site, a drug may either initiate a response or prevent a response from occurring. A drug must be a close "mimic" of the neurotransmitter.
  • 28.  An agonist is a drug which produces a stimulation type response. The agonist is a very close mimic and "fits" with the receptor site and is thus able to initiate a response.
  • 29.  An antagonist drug interacts with the receptor site and blocks or depresses the normal response for that receptor because it only partially fits the receptor site and can not produce an effect. However, it does block the site preventing any other agonist or the normal neurotransmitter from interacting with the receptor site.
  • 30. Alcohol-Placebo Effect  A simulated or otherwise medically ineffectual treatment for a disease or other medical condition intended to deceive the recipient. Sometimes patients given a placebo treatment will have a perceived or actual improvement in a medical condition, a phenomenon commonly called the placebo effect.
  • 31. Effects of Repeated Administration  Repeated administration of a drug can alter its subsequent effectiveness:  Tolerance: Repeated drug administration results in diminished drug effect (or requires increased dosage to maintain constant effect)  Tolerance can reflect decreased drug-receptor binding or reduced postsynaptic action of the drug
  • 32.  Sensitization: Repeated drug administration results in heightened drug effectiveness  Withdrawal effects: Abnormal physical or psychological features that follow the abrupt discontinuation of a drug that has the capability of producing physical dependence.
  • 33. Pharmacokinetics  is the study of drug absorption, distribution within body, and drug elimination  Absorption depends on the route of administration  Drug distribution depends on how soluble the drug molecule is in fat (to pass through membranes) and on the extent to which the drug binds to blood proteins (albumin)  Drug elimination is accomplished by excretion into urine and/or by inactivation by enzymes in the liver
  • 34. Routes of Drug Administration  Intravenous (IV): into a vein (rapid absorption). A method of introducing a drug into the body with a hollow needle and a syringe which is pierced through the skin into the body  Intraperitoneal (IP): into the gut (used in lab animals). is the injection of a substance into the peritoneum (body cavity).
  • 35.  Intramuscular (IM): into a muscle. The injection of a substance directly into a muscle.  Oral Administration: orally as liquids, capsules, tablets, or chewable tablets. Oral route is the most convenient and usually the safest and least expensive, it is the one most often used.
  • 36.  Sublingual Administration: The dosage form is placed under the tongue.  Intrarectal Administration: Uses the rectum as a route of administration for medication and other fluids, which are absorbed by the rectum's blood vessels.
  • 37.  Inhalation Administration: via nose. Smoking or inhalation of a substance is likely the most rapid way to deliver drugs to the brain, as the substance travels directly to the brain without being diluted in the systemic circulation.
  • 38.  Topical Administration: is the application of a drug directly to the surface of the skin.  Includes administration of drugs to any mucous membrane  eye – vagina  nose – urethra  ears – colon  lungs
  • 39.  Intracerebral Administration: (into the cerebrum) direct injection into the brain. Used in experimental research of chemicals and as a treatment for malignancies of the brain. The intracerebral route can also interrupt the blood brain barrier from holding up against subsequent routes.[15]
  • 40.  Intracerebroventricular (into the cerebral ventricles) administration into the ventricular system of the brain. One use is as a last line of opioid treatment for terminal cancer patients with intractable cancer pain.

Hinweis der Redaktion

  1. These drugs interact with particular target sites or receptors found in the nervous system to induce widespread changes in physiological or psychological functions. The specific interaction between drugs and their target sites or receptors is referred to as drug action. The widespread changes in physiological or psychological function is referred to as drug effect. In psychopharmacology, researchers are interested in a wide range of drug classes such as antidepressants and stimulants. Drugs are researched for their pharmaceutical properties, physical side effects, and psychological side effects.
  2. Such drugs include various psychedelic mushrooms containing psilocybin, muscimol, and muscarine (to name a few), and cacti containing mescaline and other chemicals, along with myriad other psychoactive-chemical-containing plants
  3. Opium (poppy tears, lachryma papaveris) is the dried latex obtained from the opium poppy (Papaver somniferum).[3][4] Opium latex contains approximately 12% of the analgesic alkaloid morphine, which is processed chemically to produce heroin and other synthetic opioids for medicinal use and for the illegal drug trade. relaxation, pain relief, reduced anxiety and impaired alertness and coordination. 
  4. A pharmaceutical drug (medicine or medication and officially medicinal product) is a drug used in health care. Such drugs aid thediagnosis, cure, treatment, or prevention of disease. Recreational drug use is the use of a drug (legal, controlled, or illegal) with the primary intention to alter the state of consciousness(through disruption of the CNS) in order to recreate positive emotions and feelings.  Alcohol, tobacco, cannabis, cocaine, caffeine, mushrooms, lsd Lysergic acid diethylamide, mdma methylenedioxy-methamphetamine ecstasy, meth
  5. Increased appetite and pulse rate, intellectual and physical abilities are impaired, sensory perceptions and slow and confused thinking, may cause anxiety, panic and even psychotic episodes. Cannabis euphoria and anxiety.[1][2] Concerns have been raised about the potential for long-term cannabis consumption to increase risk for schizophrenia, depersonalization disorder, bipolar disorders, and major depression,
  6. Short-term, LSD produces delusions and distorted perceptions. The user´s sense of depth and time changes and colours, sound and touch seem more intense. Some LSD users experience severe, terrifying thoughts and feelings such as fear of losing control, fear of insanity and death, and despair. The physical effects are small compared to the psychological and emotional effects. They include dilated pupils, increased heart rate and blood pressure, loss of appetite, sleeplessness, dry mouth and tremors.
  7. make the body ignore distress signals such as dehydration, dizziness and exhaustion, and it can also interfere with the body's ability to regulate temperature. Furthermore, ecstasy can severely damage internal organs such as the liver and the kidneys, and sometimes lead to convulsions and heart failure. Large doses of ecstasy also cause restlessness, anxiety and severe visual and auditory hallucinations. Longer-term ecstasy use can damage certain brain regions, resulting in serious depression and memory loss.
  8. Short-term effects include constricted pupils, nausea, vomiting, drowsiness, inability to concentrate and apathy. Furthermore, heroin is very addictive, and development of tolerance and physical and psychological dependence occurs rapidly. Long-term heroin use has a variety of severe health effects. Among other things, it can cause severe weight loss and malnutrition that can lead to damaged veins and liver disease. It can also lead to menstrual irregularity, sedation and chronic apathy. Abruptly quitting heroin use leads to moderate/severe withdrawal symptoms such as cramps, diarrhea, tremors, panic, running nose, chills and sweats.
  9. Short-term, users can lose their appetite and start breathing faster. Their heart rate and blood pressure may increase and the body temperature may go up and cause sweating. With large doses, users may feel restless and irritable and they may experience panic attacks. Excessive doses of methamphetamine can lead to convulsions, seizures and death from respiratory failure, stroke or heart failure. Long-term methamphetamine use can lead to malnutrition, weight loss and the development of psychological dependence. Once chronic users stop taking methamphetamine, a long period of sleep, and then depression, usually follows.
  10. High doses of barbiturates depress both nerve and muscle activity and inhibit oxygen consumption in the tissues. In low doses barbiturates act as a sedative, in other words they have a tranquilizing effect. Increased doses have a hypnotic or sleep-inducing effect and still larger doses have an anticonvulsant and anesthetic effect. Short term effects of barbiturates include: slurred speech, shallow breathing, sluggishness, fatigue, disorientation, lack of coordination, dilated pupils, impaired judgment, irritability, mild euphoria, lack of inhibition and drowsiness. Long-term effects of barbiturates include: chronic tiredness, lack of coordination, vision problems, dizziness, slowed reflexes, sexual dysfunction and breathing disorders.
  11. Familiar names of these drugs include diazepam (Valium), lorazepam (Ativan),clonazepam (Klonopin), and alprazolam (Xanax). Benzodiazepines slow down the workings of the central nervous system. In addition to their effects of lowering anxiety levels, they're also used as sedatives and as anticonvulsant medications. They have muscle relaxant properties as well. They are used medically to reduce anxiety, to help people sleep and to relax the body. They should only be prescribed for short periods of time as there is a risk of addiction. Long-term use of benzodiazepines increases the risk of dementia. Benzodiazepines cause brain damage and also put one at risk for certain types of cancer. Premature death is also a possibility from taking benzodiazepines. Benzodiazepine addiction is more likely to occur in individuals with certain anxiety disorders, sleep disorders, and mood disorders. Oftentimes, individuals diagnosed with anxiety disorders or sleep disorders will find the effects of benzodiazepines helpful, and will pursue higher and higher doses in order to increase or simply maintain the effects. This tends to lead to a physical dependence, and individuals may continue seeking high doses to ward off withdrawal symptoms. 
  12. adhering; especially : the act of doing what is required by a rule, belief, etc. A major part of the drug development process is to weed out those compounds whose side effects overwhelm their therapeutic effects. This gets to the fundamental issue of efficacy vs effectiveness. A drug's efficacy is a measure of the ability of the drug to treat whatever condition it is indicated for. It is not a statement about the drug's tolerability or ease of use. Effectiveness is a measure of how well the drug works and encompasses all 3 of these issues. A drug may have very good efficacy but is so unpleasant to take that its actual utility is extremely limited. This would be determined in clinical trials, and the development of such a compound would cease. For those drugs that do make it to market, there usually is a qualitative difference between side effects and therapeutic effects. The side effects of most compounds, psychiatric or otherwise, are transient. A drug company is much more likely to market a compound if whatever side effects it has go away in a few weeks. All of us who prescribe medications spend a great deal of our time with our patients reassuring them that the difficulties they may be having with their medication are temporary. Drugs vary in effectiveness Different sites of action Different affinities for receptors
  13. Clinical pharmacology - May also contain results of various clinical trials (studies) and/or explanations of the medication's effect on various populations (e.g. children, women, etc.). Indications and usage - Physicians legally can and often do prescribe medicines for purposes not listed in this section (so-called "off-label uses").
  14. Contraindications - for example in patients with other medical conditions such as kidney problems or allergies Warnings - covers possible serious side effects that may occur Precautions - for example "Do not drink alcohol while taking this medication" or "Do not take this medication if you are currently taking MAOI inhibitors"
  15. Adverse reactions - lists all side effects observed in all studies of the drug (as opposed to just the dangerous side effects which are separately listed in "Warnings" section) Drug abuse and dependence - provides information regarding whether prolonged use of the medication can cause physical dependence (only included if applicable)
  16. Overdosage - gives the results of an overdose and provides recommended action in such cases Dosage and administration - gives recommended dosage(s); may list more than one for different conditions or different patients (e.g., lower dosages for children)
  17. How supplied - explains in detail the physical characteristics of the medication including color, shape, markings, etc., and storage information (e.g., "Do not store above 95°")
  18. A biochemical reaction is the transformation of one molecule to a different molecule inside a cell. Biochemical reactions are mediated by enzymes, which are biological catalysts that can alter the rate and specificity of chemical reactions inside cells. Enzymes /ˈɛnzaɪmz/ are molecules that accelerate, or catalyze, chemical reactions. In these reactions, the molecules at the beginning of the process are called substrates and the enzyme converts these into different molecules, called products. Almost all metabolic processesin the cell need enzymes in order to occur at rates fast enough to sustain life.  An antimetabolite is a chemical that inhibits the use of a metabolite, which is another chemical that is part of normalmetabolism.[ Metabolites are the intermediates and products of metabolism. The term metabolite is usually restricted to small molecules. Metabolites have various functions, including fuel, structure, signaling, stimulatory and inhibitory effects on enzymes, catalytic activity of their own (usually as a cofactor to an enzyme), defense, and interactions with other organisms (e.g. pigments, odorants, and pheromones). 
  19. Experimental evidence indicates that drugs interact with receptor sites localized in macromolecules which have protein-like properties and specific three dimensional shapes. A minimum three point attachment of a drug to a receptor site is required. In most cases a rather specific chemical structure is required for the receptor site and a complementary drug structure. Slight changes in the molecular structure of the drug may drastically change specificity.
  20. Antacids are agents that neutralize the gastric acid and raise the gastric pH, so are used to treat dyspepsia and are used as symptomatic relief of peptic ulcer. Antacids in common use salts of magnesium, aluminium and calcium.
  21. Agonist drugs mimic the effects of neurotransmitters naturally found in the human brain. There are two main categories of agonist drugs: direct-binding agonists and indirect-acting agonists.
  22. In contrast to agonist drugs which bind to the neurotransmitters in the brain, antagonist drugs do the opposite: they block the brain’s neurotransmitters Inverse agonist- an inverse agonist is an agent that binds to the same receptor as an agonist but induces a pharmacological response opposite to that agonist. Partial agonist- partial agonists are drugs that bind to and activate a given receptor, but have only partial efficacy at the receptor relative to a full agonist.
  23. Tolerance is a person's diminished response to a drug, which occurs when the drug is used repeatedly and the body adapts to the continued presence of the drug. Resistance refers to the ability of microorganisms or cancer cells to withstand the effects of a drug usually effective against them.
  24. Drug sensitization occurs in drug addiction, and is defined as an increased effect of drug following repeated doses (the opposite of drug tolerance). Such sensitization involves changes in brain mesolimbic dopamine transmission, as well as a molecule inside mesolimbic neurons called delta FosB. An associative process may contribute to addiction, for environmental stimuli associated with drug taking may increase craving. This process may increase the risk for relapse in addicts attempting to quit. withdrawal symptoms include sweating, goosebumps, vomiting, anxiety, insomnia, and muscle pain.
  25. The albumins (formed from Latin: albumen[3] "(egg) white; dried egg white") are a family of globular proteins, the most common of which are serum albumins. The albumin family consists of all proteins that are water-soluble, are moderately soluble in concentrated salt solutions, and experience heat denaturation. Albumins are commonly found in blood plasma, and are unique from other blood proteins in that they are not glycosylated.
  26. intravenous -- Drug injection is a method of introducing a drug into the body with a hollow needle and a syringe which is pierced through the skin into the body (usually intravenous, but also intramuscular or subcutaneous)  This act is often colloquially referred to as "slamming", "shooting [up]", "banging", "pinning", or "jacking-up", often depending on the specific drug subculture in which the term is used (i.e. heroin, cocaine, methamphetamine). IP injection is more often applied to animals than to humans. In general, it is preferred when large amounts of blood replacement fluids are needed, or when low blood pressure or other problems prevent the use of a suitable blood vessel for intravenous injection.
  27. Sublingual (abbreviated SL), from the Latin for "under the tongue", refers to the pharmacological route of administration by which drugs diffuse into the blood through tissuesunder the tongue. Many drugs are designed for sublingual administration, including cardiovascular drugs, steroids, barbiturates, enzymes and, increasingly, vitamins andminerals.