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    Autonomous University of Tlaxcala School of

    Integrative activity.

    Pharmacokinetics and Pharmacodynamics o

    Michelle Alison Ochoa

    Jessica Fernanda Lp

    Jorge Daniel Campos

    Leobardo Flores Cuah

    Jess Antonio Snche

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    Dialogue------------------ Leobardo y A

    Alison: Hi good morning Leobardo: Hello

    Alison: Sorry that medication can recommend me is that myhurts and I'm swollen.

    Leobardo: I recommend an NSAID

    Alison: A NSAIDs, What is an NSAID?

    Leobardo: Do not look worry you'll explain ...

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    Fernanda:

    Introduccin. Los antiinflamatorios no esteroideos comparten

    actividades teraputicas y efectos colaterales, su mecanismo

    est mediado por la inhibicin de la Ciclooxigenasa (COX 1 y 2

    encargada de la biosntesis de prostaglandinas. Casi tantiinflamatorios no esteroideos utilizados en la actualidad, in

    actividades de la ciclooxigenasa 1 constitutiva y la ciclooxig

    inducida en el sitio de la inflamacin. Mtodo. Para lo

    investigacin se busc informacin principalmente en journa

    complementndose con la de libros, artculos y pginas web. Co

    Los AINEs se presentan como un grupo farmacolgico su

    heterogneo en lo que a estructuras qumicas se refiere. Sin emba

    ellos comparten un principio de accin fundamental, el bloqu

    sntesis de prostaglandinas a travs de la inhibicin de la

    ciclooxigenasa.

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    Fernanda:

    Pharmacokinetics

    Pharmacokinetics is the branch of pharmacology that studies the

    processes to which a drug is submitted by its passage through the

    body. Try to explain what happens to a drug from the time it is used

    until complete elimination from the body.

    The detailed stepwise traversing the drug in the body, the study are

    grouped LADME acronym:

    Release of the active ingredient.

    Absorption of it.

    Distribution by the body.

    Metabolism.

    Excretion of the drug or the waste that remains the same.

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    Ferananda:

    NSAIDs

    Nonsteroidal antiinflammatory

    drugs (NSAIDs) are a diverse

    group of mainly anti-inflammatory

    drugs, analgesics and antipyreticsgroup, thereby reducing the

    symptoms of inflammation, pain

    and fever.

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    Jesus:

    Mechanism of Action

    Activation of phospholipase A2 in response to various stimuli, hydroly

    membrane phospholipids releasing arachidonic acid in cytoplasm. Thserves as a substrate for two enzmicas pathways: cyclooxygenase a

    lipoxygenase. By way of COX prostaglandin (PG) H2, which stimulat

    formation of various prostanoids generated, including various prosta

    thromboxane A2.

    Of particular importance in anti-inflammatory therapy was the identifidifferent forms of the cyclooxygenase enzyme: cyclooxygenase-1 (C

    cyclooxygenase-2 (COX-2). COX-1 is an enzyme involved in the ove

    homeostasis and is present in most tissues and organs. COX-2 is no

    tissues, appears only in the presence of certain stimuli. By way of lipo

    leukotrienes, lipoxins and other products are formed.

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    Mechanism of Action

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    Jesus:

    Inflammation

    The inflammatory process involves a series ofevents that can be triggered by various stimuli

    (infectious agents, ischemia, antigen-antibody

    interactions).

    Which will be five signs of inflammation:

    Blush: Redness mainly due to the phenomena

    of increased pressure by vasodilation.

    Tumor: Increased interstitial fluid and edema

    formation.

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    Heat: Temperature increase

    Pain: Symptom subjective in nature while the rest a

    an objective nature

    Loss of function: Changes caliber vascular flow and

    in vascular permeability.

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    Leobardo

    Pain:Almost always inflammatory drugs

    are classified as mild analgesics.

    Pain that accompanies inflammation

    and tissue injury results from perhaps

    local stimulation of pain fibers and

    increased sensitivity to it.

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    Leobardo

    Fever:

    The fever may result from

    infection or tissue injury

    sequel, inflammation, graft

    rejection, cancer or other

    pathogens pictures.

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    Pharmacodynamics

    The main action of all NSAIDs is inhibition of

    cyclooxygenase. Inhibiting the synthesis of

    prostaglandins and thromboxanes NSAID

    would be responsible for their therapeutic

    activity and various toxic effects of this class

    of drugs.

    The fundamental action of NSAIDs areessentially threefold: - Relieve pain for their

    analgesic actions Reduce inflammation for

    their anti-inflammatory actions Reduce fever

    antipyretic actions.

    Leobardo

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    Alison

    Analgesic Action

    And a peripheral effect is related to the

    inhibition of prostaglandin synthesis in the

    place where it is perceived. All NSAIDs

    inhibit the cyclooxygenase activity. They

    prevent sensitization of nociceptors. As will

    be useful in pain with acute or chronic

    inflammatory component, such as renal

    colic pain or bilar.

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    Alison

    Anti-Inflammatory Action

    NSAIDs also act directly or indirectly modifyingother inflammatory mediators. This ability of

    NSAIDs peripherally to block or inhibit any or all

    mediators of inflammation factors. The reducing

    inflammation with NSAIDs often brings clinical

    improvement for important periods of time. In

    dentistry, NSAIDs frequently indicated for relief

    of mild to moderate pain of dental origin and

    subsequent dental procedures

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    Daniel

    Ibuprofen

    First member of the family of propionic acid

    NSAIDs, their pharmacokinetics in plasma

    proteins absorbed reached 90% plasma at

    30 minutes dental indications concentrations

    processes, presentations are 200,400,600

    and 800 mg and 200 mg suspensions their

    dosage one capsule every 6 to 8 hour dose6-11 months is 10 ml of 12 to 23 months and

    12.5 ml of 2-5 years is 15 ml trade names

    are tabalon, actron, motrin, advil not for

    hypertensive patients

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    Ketorolac

    Ketorolac is to treat short-term pain (posttraumatic,

    postoperative) pharmacokinetics bound to plasma

    protein 99% is metabolized in the liver via renal

    excretion is 92% and the rest by feces indicated for

    dental processes (not as antipyretic) presentations

    tablet 10 mg, 1 ml ampoules their dosage 10 mg

    tablet every 4 to 6 hours not to exceed 20 mg

    ampule every 4-6 hours. dolac Supradol tradenames, mavidol.

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    Hypersensitivity

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    Pregnancy and lactation

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    coagulation defects

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    Renal impairment

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    Cardiac disorders

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    Gastric Pathology

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    Conclusion

    NSAIDs are a group of commonly used in clinical practi

    variety of indications drugs. In general, NSAIDs should

    short cycles and lowest doses possible, always within r

    effectiveness, and monitoring specifically digestive,

    cardiovascular, renal, hepatic and hematologic complicEach patient may respond to a specific NSAIDs, while a

    require a different product, however the best benefit r

    ibuprofen.

    Fernanda