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63 Cards in this Set
- Front
- Back
Codeine
Metabolised by? |
CYP2D6
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Codeine/morphine
agonist or antagonist at what receptor? |
agnoist at mu receptor
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Codeine/morphine
Adverse effects? |
nausea and vomit
dyspepsia drowsiness dizziness heaache drymouth constricted pupil urinary retentioin constipation |
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Codeine/morphine
Antidote? |
Naloxone
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Naloxone
Agonist or antagonist at which receptor? |
antagonist at mu receptor
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Promethazine
What is it? |
sedating anti-histamine
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Promethazine
ago or antago? At What receptor? |
antagonist at H1 and muscarinic receptors
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Promethazine
actions? |
antihistamine
decrease mucus secretion |
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Promethazine
adverse reactions? |
oral health issues (reduced salivary flow)
Avoid alcohol since it is sedating drug |
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Pseudoephedrine
actions? receptor? adverse effects? |
Relief of nasal congestion associated with acute and chronic rhinitis. It is sympathomimetic and acts (agonist) at the alpha adrenergic receptors (α1 and α2). It relieves nasal congestion by causing the nasal blood vessels to constrict. It can also dry salivary flow. Main adverse effect is increase in BP.
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Chlorpheniramine
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sedating anti-histamine. Antagonist at H1 receptor. ADR: drowsiness.
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Pilocarpine
include ADR |
primarily used to treat glaucoma but also is diluted and used to stimulate salivary flow. It is an agonist at the muscarinic receptor. Not to be used on asthmatics (since it causes bronchial constriction), and cardiac conditions (reduces HR)
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Paracetamol
what detoxifies paracetamol if overdosed? how to treat overdose? |
analgesic. Works by inhibition of central prostaglandin synthesis. Works on CNS. Overdose can cause liver damage. Chronic liver disease pts at high risk. Prolonged fasting or malnutrition depletes glutathione stores. Glutathione is used to detoxify the toxic metabolite of overdosed paracetamol. If it is depleted liver damage occurs. Acetyl cysteine or charcoal are antidotes for paracetamol overdose
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Ibuprofen
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An NSAID analgesic. Non-selective. Inhibits synthesis of prostaglandins by inhibiting cyclo-oxygenase (COX). ADR include nausea, dyspepsia, GI ulceration or bleeding, raised liver enzymes, diarrhoea, headache, dizziness, salt and fluid retention, hypertension. Ibuprofen can reduce the antiplatelet activity of low-dose aspirin and potentially reduce or negate its cardioprotective effect.
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Naproxen
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Nonselective NSAID
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Aspirin
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Aspirin has analgesic, antipyretic, anti-inflammatory and antiplatelet actions. It is a nonselective NSAID, preventing synthesis of prostaglandins by noncompetitively inhibiting both forms of cyclo-oxygenase (COX1 and 2).
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Diclofecnac
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Nonselective NSAID. (found in Voltaren)
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Precautions from NSAIDs:
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Allergic reactions to NSAIDs, including aspirin—contraindicated, see also Practice points.
Asthma —NSAIDs may increase risk of bronchospasm. Coagulation disorders—nonselective NSAIDs increase risk of bleeding (antiplatelet effect); selective NSAIDs (COX-2 inhibitors) and possibly diclofenac increase risk of thrombosis. Cardio- or cerebrovascular NSAIDs increase risk of cardiovascular events Heart failure and hypertension may worsen due to sodium and fluid retention from NSAID-induced reduction in glomerular filtration rate and renal blood flow. Gastrointestinal Contraindicated in active peptic ulcer disease or GI bleeding. Renal Pre-existing renal impairment increases the risk of NSAID-induced impairment; nonselective NSAIDs increase risk of bleeding. Hepatic Use with caution in severe impairment; nonselective NSAIDs increase risk of bleeding; selective NSAIDs (COX-2 inhibitors) are not recommended. Excessive bleeding with warfarin |
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Choline salicylate
include ADR |
: Found in Bonjella, the teething gel. Non-acetyl salicylate medicament that has anti-inflammatory properties but less analgesic and antiplatelet actions than aspirin. Not to be used for children under 16 since it has same effect as aspirin which is contraindicated for children. Risk of Reye’s syndrome (causes serious liver and brain damage). Alternatives include chewing on cold towel, carrot, ice, teething ring or give paracetamol/ibuprofen
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Clove oil/Eugenol
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Main constituent is eugenol which inhibits prostaglandin synthesis via COX1,2 and depresses the sensory receptros involved in pain perception. Adverse reactions include: allergic rashes, burning, loss of sensation, local tissue damage, dental pulp damage, lip sores, increased risk of cavities.
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Salbutamol
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B2 agonist (but can also act as B1 agonist). Used in MDI to relieve acute asthma attack. Can also cause tremor and palpitations because it acts on B2 receptors in skeletal muscles. When it acts on B1 it can cause increase HR.
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Fluticasone
what does it do? mechanism of action? ADR? |
A corticosteroid which reduces airway inflammation and bronchial hyper-reactivity. This is to treat asthma. It doesn’t work straight away since it works by protein synthesis. Adverse reactions include dysphonia, oropharyngeal candidiasis, and bruising. Always use spacer with MDI and rinse out mouth with water after using it. Adrenal suppression can occur with high doses so only used for short courses (10 days or less). Long term use can cause adrenal insufficiency and Cushing’s syndrome.
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Prednisolone
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A corticosteroid which suppresses inflammation and immune response. Hence it is used for treating asthma. Long term use can cause adrenal insufficiency and Cushing’s syndrome.
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Fexofenadine
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Non sedating antihistamine (Selectively antagonise the action of histamine at H1 receptors).
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Terbutaline
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B2 agonist. Used for acute asthma. Tremor and palpitations.
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Salmeterol
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B2 agonist. For maintenance of asthma and not for acute asthma relief (slow onset) Symptom controller
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Ipratropium
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muscarinic antagonist. Prevent secretion of mucus. ADR: dry mouth, throat irritations
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Tiotropium
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muscarinic antagonist. Prevent secretion of mucus. ADR: dry mouth, throat irritations.
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Theophylline
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Acts on two sites. 1 inhibits PDE from metabolising cAMP into AMP leading to accumulation of cAMP which increases bronchodilation. 2 decreases bronchoconstriction. Hence very effective for acute asthma treatment or airway obstruction.
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Metaprolol
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Selective B1 blocker (antagonist). Used for treating hypertension, angina, MI, tachyarrythmia. This is safe for asthmatics since it B1 is only found in the heart.
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Propanolol
Cautions? |
non selective Beta blocker (blocks B1 and B2 receptors). Don’t give it to asthmatic since blocking B2 will prevent bronchodilation
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Budesonide
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Inhaled corticosteroid drug. Reduces airway inflammation and bronchial hyper-reactivity. ADR: adverse effects from corticosteroids
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Nystatin
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Antifungal for treating oral candidiasis.
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Miconazole
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An azole antifungal which works by inhibiting ergosterol synthesis. Azole antifungals may reduce warfarin metabolism hence increase risk of bleeding.
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Amphotericin
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Antifungal works by binding irreversibly to ergosterol in fungal cell membranes causing cell death by altering their permeability and allowing leakage of intracellular material.
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Aciclovir
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Antiviral for treating cold cores
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Terbinafine
Include drug interactions |
Inhibits ergosterol synthesis. Does not inhibit CYP450 unlike other azoles. It is both fungicidal (for fungal infections) and fungistatic (for yeast infections). Symptoms relieved very quickly (2 to 3 days).
It inhibits CYP206 codeine enzyme which breakes down morphine. So don’t give with codeine. |
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Imidazole
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Group of antifungal drugs (includes metronidazole). All fungistatic and inhibits CYP450. Overdose can cause drug poisoning. Symptoms relieved within 7 days.
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Amoxicillin
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is a beta-lactam penicillin antibiotic. It contains beta-lactam ring. It is bactericidal and inhibits bacterial wall synthesis. But it can be deactivated by beta-lactamase enzyme which some bacteria resistant to amoxicillin have. Its adverse reactions include gastrointestinal symptoms such as nausea, vomiting, diarrhoea.
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Clavulanic acid
Include ADR |
Inhibits beta-lactamase in beta-lactam resistant bacteria. Often given along with amoxycillin for such bacterial infection. It can cause hepatotoxicity.
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Cephalexin
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It is a cephalosporin antibiotic. Beta lactam. Can cause diarrhoea.
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Clindamycin
all about it including ADR |
: Lincosamide antibiotic. Bacteriostatic; inhibit protein synthesis by binding to the 50S ribosomal subunit. Alternative in patients with severe allergy to penicillins and cephalosporins. A serious adverse effect of it is pseudomembranous colitis which is characterised by explosive diarrhoea.
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Glycopeptides
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Include teicoplanin and vancomycin. These are not broad spectrum which are active only against gram +ve organisms. Adverse reactions include, nausea, vomiting, diarrhoea, chills and fever. All administered via IV. Poor renal function pts in risk of ototoxicity, nephrotoxicity
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Red man syndrome
when does it occur? what are the symptoms? |
Occurs when vancomycin is infused too quickly. Pt turns red showing fever, chill, erythema, uppor torso rash
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Macrolides
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Group of antibiotics. Has similar spectrum of antibiotic activity as penicillin. Includes, azithromycin, clarithromycin, erythromycin, roxithromycin
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Clarithromycin
type? durg interactions? |
: a macrolide antibiotic. Inhibits CYP 450 3A4 which breaks down midazolam. Don’t prescribe with midazolam
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Midazolam
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sedative. Clarithromycin prevents midazolam metabolim.
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Metronidazole
include drug interactions |
Antibiotic. Fast absorbing. Can be given rectally or intravenously. ADR: nausea, diarrhea, and/or metallic taste in the mouth. Avoid alcohol due to disulfram-like reaction. Metronidazole inhibits warfarin metabolism, increasing its concentration and risk of bleeding.
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Doxycycline
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: A tetracycline. Bacteriostatic; inhibit bacterial protein synthesis by reversibly binding to 30S subunit of the ribosome. Avoid antacids since it can chelate with Fe3+. Must be taken with water – if sticks to throat, it may cause a hole in the throat. Becomes photosensitive and easily sunburnt. Avoid sun. Avoid in growing children. Causes tooth discolouration and bone defect.
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Oxymetazoline
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: Agonist at α1 and α2 receptor. Produce vasoconstriction in nasal mucosa; decrease nasal blood flow and congestion. Used in nasal sprays. ADR: increase in BP but small since it is in topical form. Avoid using it long term (restrict to 5 days) since it develops rebound congestion (desensitisation).
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Pholcodine
include ADR |
Opioid derivative. Agonist at mu receptor. Used in cough syrups for dry irritating cough.
ADR: constipation, sedation. Increase effects of alcohol. |
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Guaifenesin
include ADR |
Expectorant (loosens and expels mucus). Cough symptom relief. ADR: laxative effect, diarrhoea. Take with water and don’t use if hypersensitive
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Pethidine
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Opioid analgesics. It has active metabolite – norpethidine. The effect of the drug is prolonged.
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Diazepam
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A benzodiazepam psychotic drug. Benzodiazepines potentiate the inhibitory effects of GABA throughout the CNS, resulting in anxiolytic, sedative, hypnotic, muscle relaxant and antiepileptic effects
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Example of selective NSAID?
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Celecoxib
Rofecoxib |
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ADR of Celecoxib?
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Increased risk of CVS
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ADR of Sedating Antihistamines?
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Dry mouth
Dry eyes Blurred vision Hot Flushed |
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What drugs have the following ADRs?
Dry mouth Dry eyes Blurred vision Hot Flushed |
sedating antihistamine
Tricyclic Antidepressants Anticholinergics (atropine) Benzodiazepines (diazepam) |
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Relationship between OC and grapefruit?
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grapefruit will inhibit enzyme that metabolises OC. OC levels will be high.
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Relationship between OC and rifampicin?
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rifampicin will induce enzymes that metabolises OC. OC levels will be low.
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Relationship between OC and St Johns Worts?
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St John's Worts will induce enzymes that metabolises OC. OC levels will be low.
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Serotonin Syndrome?
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– Nausea, vomiting, diarrhoea
– Tachycardia – Agitation, anxiety, headache – Tremor – Sweating |
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What are Phase I and Phase II reactions?
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Phase I reactions:
Transform the drug to a more hydrophilic (more polar) metabolite by adding -OH -NH2 -SH Phase II reactions: Metabolites are made more hydrophilic (more polar) to enable them to be excreted by the kidneys by adding liver conjugates e.g. acetyl, glycine, methyl, glutathione. Thus it makes the molecule a lot heavier, more polar and less activity(toxicity). |