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53 Cards in this Set

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Diphenhydramine ( Benadryl, others)

First generation h1- receptors antagonist whose primary use is to treat minor symptoms of allergy and the common cold such as sneezing , runny nose , and tearing of the eyes . Administered topically to treat rashes, IM and IV forms are available for severe allergic reactions. Other uses are for Parkinson's disease, motion sickness , and insomnia.

Dyphenhydramine (Benadryl) administration alerts

Increased risk of anaphylactic shock when administered parentally


Administering IV, inject at a rate 25 mg/min to reduce risk of shock


Administering IM, inject deep into large muscle to minimize tissue irritation.

Dyphenhydramine (Benadryl) pharmacokinetics

PO: 15-30 min


Peak: 1-4 h


Duration: 4-7 h

Dyphenhydramine (Benadryl) adverse effects

First generation H1- antagonist cause significant drowsiness, occasionally paradoxical CANS stimulation and excitability will be observed rather than drowsiness. Excitation is more frequent in children. Anticholinergic effects such as dry mouth. Tachycardia and mild hypotension. May cause hyperthyroidism.

Dyphenhydramine ( Benadryl) contraindications

Hypersensitivity to the drug , benign prostatic hypertrophy (BPH) , narrow -angle glaucoma , and GI obstruction. Used cautiously in patients with asthma or hyperthyroidism.

Diphenhydramine ( Benadryl) interactions

Drug - drug - use with CNS depressants like alcohol or opiods can increase sedation. OTC cold preparations may increase anticholinergic side effects. Monoamine oxidase inhibitors may cause hypertensive crisis.



Labs - drug discontinued at least four days before allergy testing , otherwise false negative may results



Herbal/food- henbane may increase anticholinergic effects .



Treatment of overdose - over may cause CNS depression or excitation. No specific treatment for overdose.

Diphenhydramine (Benadryl) route and dose

PO: 20-59 mg tid to qid ( max : 300 mg / day ).

Dyphenhydramine( Benadryl) therapeutic class and pharmacologic class

Therapeutic class- drug to treat allergies


Pharmacologic class- H1 receptor antagonist; antihistamine.

Fluticasone (Flonase, veramyst, others) therapeutic class and pharmacologic class

Therapeutic class - drug for allergic rhinitis


Pharmacologic class - intranasal corticosteroids.

Fluticasone (veramyst, flonase,) actions and uses

Intranasal corticosteroids to treat allergic rhinitis. Two sprays in each nostril, twice daily , decreases to one dose per day. Acts to decrease local inflammation in nasal passages reducing nasal stuffiness.


Approved for both seasonal and perennial allergic rhinitis.


2012 dymista was approved which combines fluticasone with azelastine, H2-receptor antagonist .


Fluticasone is available in oral inhalation to reduce bronchial inflammation for copd and asthma.


2014 second oral formulation of fluticasone (arnuity ellipta) for maintenance of asthma.


Topical fluticasone treat various inflammation condition including atopic dermatitis, eczema, psoriasis, and contact dermatitis.

Fluticasone (veramyst flonase) administration alerts

Instruct pt to carefully follow the directions for use provided by manufacturer.


Pregnancy category C

Fluticasone ( veramyst flonase) adverse effects

Swallowing large amounts increase potential for systemic corticosteroids adverse effects. Nasal irritation and epistaxis occur in small number of patients.


Administered intranasally , adverse effects of fluticasone are rare.


When inhaled to treat COPD , most frequent side effects are headache and nasopharyngitis.

Fluticasone (veramyst flonase) contraindications

Prior hypersensitivity to drug


Can mask signs of infection


Pts with known MO infections, especially in respiratory tract, should not receive corticosteroids.

Fluticasone (veramyst flonase) interactions

Drug -drug concomitant use of intranasal decongestant increase the risk of nasal irritation or bleeding.


Use with ritonavir should be avoided because drug increases plasma fluticasone levels.


Lab test-unknown


Herbal/food- caution with licorice which my potentiate the effects of corticosteroids


Treatment of overdose- no specific treatment

Leukotriene modifiers

Montelukast singular


Therapeutic-anti inflammatory drug for asthma, prophylaxis

Leukotriene modifiers contraindications

Hypersensitivity


Rare cases hepatic failure

Leukotriene modifiers adverse effects

Headache


Nausea diarrhea


Rare cases - suicidal ideation, hallucinations, aggressiveness, depression

Leukotriene modifiers administration

Don't use to terminate acute asthma attacks


Take drug two hours before exercising to prevent exercise-induced bronchospasms.


Pregnancy B

Leukotriene modifiers action

Given PO and acts rapidly. Only agent in it's class approved for pediatrics. Available in chewable tablets and granules.


Prevents airway edema and inflammation by blocking leukotriene receptors in the airway.

Leukotriene modifiers


Pharmacokinetics

Rapid 3-4 hours and duration is unknown.

Allergic rhinitis of hay fever

Inflammation of the nasal mucosa die to exposure to allergens.


Symptoms - tearing eyes, sneezing, nasal congestion, postnasal drip, itching of the throat.


Potential complications_-Loss of taste , smell, sinusitis, chronic cough, hoarseness, middle ear infections in children.

Asthma

Chronic pulmonary disease with inflammatory and bronchospasms components.


Characteristics-acute bronchospasms, intense breathlessness , coughing , and gasping for air.


Acute inflammatory response stimulates secretion of histamine and other inflammatory mediators , increasing mucus and edema in airways.

Beta2-adrenergic agonist actions

Albuterol-saba, relieve bronchospasms of asthma. Rapid onset and excellent for termination of acute bronchospasms.


Facilitates mucus drainage and can inhibit the release of inflammatory chemicals from mast cells.


Inhaled 15-30 min before physical acitivty can prevent excercise induced bronchospasms. Not recommended for asthma prophylaxis.

Beta2-adrenergic agonist administration

Albuterol- use only the actuator that comes with the canister. Observe and instruct patient in proper use.


Pregnancy C


Beta2-adrenergic agonist adverse effects

Uncommon serious effects


Some experience palpations, headaches, restlessness, and tachycardia


Less common - insomnia and dry mouth.

Beta2-adrenergic agonist contraindications

Albuterol- contraindicated in patients with hypersensitivity to the drug. Caution required when administering to patient with history of cardiac disease or hypertension.

Beta2-adrenergic agonists pharmacokinetics

5-15 min inhalation , 0.5-2 h for peak and lasts 2-6 h


30 min PO , peak is the same as inhalation, and lasts 8-12 h PO, sustained release.

Methylxanthines

Theophylline and aminophylline


Bronchodilators chemically related to caffeine.


Used as long-term management of persistent asthma that is unresponsive to beta2-adrenergic agonist or inhaled corticosteroids.


Have narrow safety margin


Adverse effects are nausea, vomiting, CANS stimulation, dysrhythmias, can cause nervousness and insomnia.


Administered IV or PO.

Inhaled corticosteroids action and therapeutic class

Beclomethasone qvar-anti-inflammatory drug for asthma and allergic rhinitis.


Available as inhalation for asthma (qvar) or nasal spray(beconase AQ, Qnasl) for allergic rhinitis. Preferred long time management of asthma in children and adults


3-4 weeks of therapy before peak is obtained


Acts by reducing inflammation, decreasing frequency of asthma attacks. Not a bronchodilators and should not be used to terminate asthma attacks in progress.

Inhaled corticosteroids administration

Do not use if patient is experiencing acute asthma attacks


Oral inhalation products and nasal spray products are not to be used interchangeably


Pregnancy C

Inhaled corticosteroids pharmacokinetics

1-4 wk onset, 30-70 min peak, and unknown duration.

Inhaled corticosteroids adverse effects

Few systemic adverse effects


Patient should be observed for sign of corticosteroid toxicity.


Local effects may include hoarseness, dry mouth , changes in taste.


Cataract in adults


Long term basis patients may develop oralpharyngeal candidiasis, a fungal infection in the throat.

Inhaled corticosteroids contraindications

Can mask signs of infection if an active infection is present.


In those with hypersensitivity to the drug


May reduce growth velocity in some children.

Sympathetic nervous system and the respiratory system ?

Constricts arterioles in the nose , reducing thickness of mucosal layer= wider airway and allow more air to enter.

Parasympathetic nervous system and the respiratory system ?

Arterioles dilate and more mucus is produced

Administration of sympathomimetic ?

Will shrink nasal mucosa, relieving nasal stuffiness associated with the common cold.

Most common agents for allergic rhinitis ?

Pollen from weeds, grasses, trees ,molds spores, dust mites , certain foods, and animal dander.

Diphenhydramine Benadryl contraindications

Hypersensitivity to the drug , benign prostatic hypertrophy BPH, narrow-angle glaucoma and GI obstruction. Used cautiously in patients with asthma or hyperthyroidism.

Intranasal corticosteroids are also known as what and applied where ?

Glucocorticoids and applied directly to the nasal mucosa to prevent symptoms of allergic rhinitis.

Intranasal corticosteroids produce virtually no and are often the first line drugs in treatment of allergic rhinitis

Serious adverse effects

When sprayed into the nasal mucosa , corticosteroids decrease?

Inflammation mediators, reduce tissue edema, and cause mild vasoconstriction.

Fluticasone veramyst flonase route and dose

1 spray in each nostril once (veramyst) twice (Flonase)

Intranasal sympathomimetic can cause ?

Rebound congestion.

Expectorant route and dose

Guaifenesin(Mucinex)


PO:200-400 mg q4h(max 2.4 g/day)-drowsiness, headache, GI upset


Extended release PO 600-1200 mg q12h(max 2400 mg/day)- no serious adverse effects

Mucolytic route and dose

Acetylcysteine ( mucomyst )


Inhalation : 1-10 ml of 20 %- unpleasant odor, nausea


Solution q4-6h or 2-20 ml of 10%


Solution q4-6h - severe nausea and vomiting, bronchospasms

Antitussives

Medications that control cough

Codeine and hydrocodone are ?

The most effective opioid antitussives - act by raising the cough threshold in the CNS.

Dextromethorphan Deslym Robitussin DM route and dose

PO 10-20 mg q4h or 30 mg 6-8h(max:120 mg /day)

Dextromethorphan has the potential abuse in which age group ?

Teens

Define expectorant

Drugs that reduce the thickness or viscosity of bronchial secretions , thus increasing mucus flow that can be more easily removed by coughing.

Mucolytics define

Break down the chemical structure of mucus molecules. Not OTC and delivered inhalation route. Has an offensive odor resembling rotten eggs.


Administered IV for pts who overdosed on acetaminophen

Sympathetic branch on the lower respiratory

Activated beta2-adrenergic receptors , cause bronchiolar smooth muscle to relax, airway diameter increase, bronchodilation occurs.

Parasympathetic nervous system on lower respiratory

Causes bronchiolar smooth muscle to contact, airway diameter to narrow, bronchoconstriction occurs.