Drug REWIEW

acetaminophen (Tylenol paracetamol APAP
Click the card to flip 👆
1 / 20
Terms in this set (20)
Inhibits the synthesis of prostaglandins, In CNS only, inhibits COX (enzyme that forms prostaglandins in hypothalamic heat regulation center -> decreased pain & fever
- does not have antiinflamtory
- overdose can harm liver max dose 4000 mg/day don't use with chronic alcocholicks
- Safe in pregnancy cat B
- can cause hypokalemia and Hypoglycemia
Image: acetaminophen (Tylenol paracetamol APAP
Adrenergic -Beta2 Agonist (symphatetic nervosystem)
- inhaled : Used as a quick-relief agent for acute bronchospasm and for prevention of exercise-induced bronchospasm. Can be PO
RISK :
headache
tachycardia hypertension
Hypokalemia
CNS Stimulation
DD interaction
- beta blockers will block effect
- TCA MAOi Oxytocin - increase hypertension
amoxicillin + clavulanate acid= Augmentin PNC - brakes down bacteria clavulanate - prevents bacteria to destroy amoxicillin RISK: - anaphylaxis - SJSampicillin/sulbactamsimilar to Augmentinamphotericin B FungizoneBinds to fungal cell membrane, allowing leakage of cellular contents RISK -hemmerage renal failure liver failure PancutopiniaASPIRINProduce analgesia and reduce inflammation and fever by inhibiting the production of prostaglandin. Analgesic anti-inflammatory - don't use in children to treat fever - Rey syndrome - give immediately to hurt attack victims 19:51atenolol (Tenormin)Antihypertensive Beta Blocker Cardioselectiv B1 (smiler effect in lungs) chronotrope (slow the hurt rate ) - can couse BRoNCHOSPASMatorvastatin LipitorInhibition of HMG CoA reductase: Lovastatin simvastatin, pravastatin , atorvastatin , fluvastatin , pitavastatin and rosuvastatin are analogs of HMG, the precursor of cholesterol. Because of their strong affinity for the enzyme, all compete effectively to inhibit HMG CoA reductase, the rate-limiting step in cholesterol synthesis. By inhibiting de novo cholesterol synthesis, they deplete the intracellular supply of cholesterol. - Drug interactions: The HMG CoA reductase inhibitors may also increase warfarinatropine- Cardiovascular: Atropine produces divergent effects on the cardiovascular system, depending on the dose - At low doses, the predominant effect is a decreased cardiac rate (bradycardia). - With higher doses of atropine, the M2 receptors on the sinoatrial node are blocked, and the cardiac rate increases modestly. at least 1 mg of atropine, -Eye: Atropine blocks all cholinergic activity on the eye, resulting in persistent mydriasis - Secretions: Atropine blocks the salivary glands, producing a drying effect on the oral mucous membranes (xerostomia - Gastrointestinal (GI): Atropine can be used as an antispasmodic to reduce activity of the GI tract- to reduce daierhia . Although gastric motility is reduced, hydrochloric acid production is not significantly affected -Urinary system: Atropine-like drugs are also used to reduce hypermotility states of the urinary bladder. It is still occasionally used in enuresis (involuntary voiding of urine) among -antidote for cholinergic agonists: Atropine is used for the treatment of overdoses of cholinesterase inhibitor insecticides and some types of mushroom poisoningazithromycinantibiotic - community required pneumonia clamydiaTypical therapeutic applications of macrolides.Benztropine (COGENTIN)...