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Lccc drugs to know

common drugs

drug nameside effectsclassificationuses/drug actionspecial concernsoutcomesPeaks/half life/duration
MORPHINE constipation, seizures, cardiac arrest, shock, respiratory distress opiod analgesic treat pain by binding with opiate receptors in CNS, altering perception of and emotional esponse to pain keep opioid antagonist and resuscitation equipment ready, check respiratory rate & depth Q 30-60min for first 24 hours. decrease pain
TYLENOL few when taken in usual therapeutic doses non-narcotic analgesic control of pain due to headache, earache, dysmenorrhea, arthralgia, myalgia, musculoskeletal pain, arthritis, immunizations, teething, tonsillectomy, reduce fever in bacterial or viral infections Route: oral decrease pain & fever Peak plasma levels 30-120 min/ half life 45 min-3 hr.
ASA (aspirin) heartburn, dyspepsia, anorexia, nausea, occult blood loss, epigastic discomfort, GI bleeding Nonsteroidal, anti-inflammatory drug, analgesic, antipyretic pain, gout, arthritis, osteoarthritis, SLE, acute rheumatic fever, Route: caplets, gum, tablets, suppositori don't use in children and teenagers with flu or chickenpox may result in the development of Reye's syndrome. moniter kids and elderly closely. may have drug/herb interaction. may potentiate antidiabetic drugs. relief of pain/discomfort, improved joint mobility/function, decreased fever and vascular mortality, decreased inflammation, proplylaxis of MI/TIA half life asprin 15-20 min: salicylic acid, 2-20 hr depends on dose
DARVOCET dizziness, sedation, respiratory depression, nausea, vomiting non-narcotic analgesic mild to moderate pain (may be used if fever is present) Route: Tablets Use during pregnancy only if benefits outweigh risks. anticipate reduced dose in the elderly and in those with renal and hepatic dysfunction. control of pain'discomfort (blank)
DURAGESIC PATCH (fENTANYL) seizures, arrythmias, respiratroy problems, apnea narcotic analgesic continuous delivery of fentanyl up to 72 hrs. Used for severe chronic pain that cannot be managed with less powerfull drugs. Route: transdermal (film); moniter circulatory, respiratory, bladder and bowel function carefully. desired pain control it may take 24 hr for affect. provide short-acting analgesic until analgesic efficacy is reached with transdermal system.
HEPARIN hemmorhage, overly prolonged clotting time, thrombocytopnia, chills, fever, urticaria, headache, N&V anticoagulant Pulmonary/peripheral arterial embolism, proplylaxis and treatment of venous thrombosis, atrial fibrillation with embolization, prevent DVT an PE in pregnant clients Routes: IV & Deep Sub Q; Lab Tests: CBC, PT, PTT, renal and LFTs, INR; use with caution in mestruation and pregnant women PTT: 2-2.5 times the control/normal, prevention of trombus formation, clot prophylaxis/treatment, indewelling catheter patency Onset: IV immediately, Deep Sub Q 20-60 min. Peak plasma levels after Sub Q 2-4 hr. half life 30-180 min in healthy person. half time increases with dose, sever renal disease and cirrhosis
COUMADIN (Warfarin) Hemorrhage may occur from tissue or organ, headache, paralysis, pain in the joints, abdomen, or chest, difficulty in breathing or swallowing, SOB,re-orange urine anticoagulant Prophylaxis and treatment of veous thrombosis and its extension. Prophylaxis and treatment of atrial fibrillation with embolization. Prophylaxis and treatment of pulmonary embolism Routes: oral, IV; LAB Test PT and INR, Has many drug interactions regularly inspect patient for bleeding bums, bruises on body, petechiae, nosebleeds, tarry stools, hematuria and hematemesis, PT within desired rant (1.5-2 times control), INR within desired range (2.0-3.0 with standard therapy; 2.5-4.0 with high-dose therapy, decreased risk of thromboembolism with prosthetic heart valves, resolution/prophylaxis of DVT usually takes 36-48 hr for drug to reach steady state, peak activity 1.5-3 days, duration 2-5 days, half life 1-2.5 days
NEURONTIN usually well tollerated, dizziness, drowsiness, and peripheral edema, fatigue, weight gain, tremor, dental abnormalities anticonvulsant treatment of seizures, epilepsy, used to relieve pain, especially neuropathic pain Route: oral some drug interaction control of seizure activity, chronic pain control half life 5-7 hr.
LASIX fluid and electrolyte depletion leading to dehydration, hypovolemia, thromboembolism, hypokalemia and hypochloremia may cause metabolic alkalosis. nausea, oral and gastric irritation, vomiting, anorexia, diarrhea, or constipation, cramps diuretic, loop edema associated with CHF, nephrotic syndrome, hepatic cirrhosis, and ascites. IV for acute pulmonary edema, PO to treat hypertension in conjunction with spironolactone, triamterene, and other diuretics. Route: oral, IV, IM enhanced diuresis, resolution of pulmonary edema, decreased dependent edema, decreased serum calcium levels onset PO, IM 30-60 min; IV 5 min. Peak:PO, IM 1-2 hr; IV: 20-60 min, half life about 2 hr after PO use. Duration : PO, IM 6-8 hr; IV: 2 hr
GUAIFENESIN (ROBITUSSIN) N&V, GI upset, dizziness, headache, rash, urticaria Expectorant Dry, nonproductive cough due to colds and minor upper respiratory tract infections when there is mucus in the respiratory tract, to loosen phlegm and thin bronchial secretions Route: oral, liquid, syrup, tablets control of coughing episodes, mobilization of mucus half life 1 hr.
DILANTIN (PHENYTOIN) drowsiness, ataxia, dysarthria, confusion, insomnia, nervousness, irritability, depression, tremor, numbness, headache, psychoses, nystagmus anticonvulsant/ as an antiarrhythmic it increases the electrical stimulation threshold of the heart muscle. chronic epilepsy,Phenytoin acts to damp the unwanted, runaway brain activity seen in seizure by reducing electrical conductance among brain cells. Route: oral, IV, IM LAB TEST: monitor drug levels in the blood ECG, CBC, liver, and renal function studies. (may lower, serum Mg, folate, calcium and Vitamin D, watch for gingival hyperplasia control of seizures, termination of ventricular arrhythmias, stable cardiac rhythm, therapeutic drug levels (5-20 mcg/mL) Peak serum levels: 4-8 hr. IM, 24 hrs, half life 8-60 hr (average 20-30 hr), steady state 7-10 days after initiation
PREDNISONE may cause moderate fluid retention. pseudotumor cerebri, seizures, heart failure, thromboembolism, arrythmias, pancreatitis, acute adrenal insufficiency Glucocorticoid effective as an immuno suppresant, Autoimmune diseases, inflammatory diseases (such as sever asthma, sever poison ivy, and Crohn’s disease) Various kidney diseases including nephritic syndrome, and to 3 to 5 times as potent as cortisone or hydrocortisone Route: oral dose is individualized, LAB TEST monitor CBC, ESR, electrolytes, blood sugar, weights and mental staus. relief of allergic, immune, and inflammatory manifestations, control of pain (blank)
ALBUTEROL (Salbutamol) Dronchospasms, tremor, dizziness, headache, tachycardia, diarrhea, drymouth appetite loss or stimulation, epigastric pain, excitement, nervousness, tension, vertigo, drowsiness, fatigue, lightheadedness Sympathomimetic (bronchodilator) in conditions such as asthma and COPD.relaxes bronchial, uterine and vascular smooth muscle by stimulating beta2 receptors Route: oral, inhalation Document PFTs, CXR and lung sounds, monitor pulmonary status VS, peak flow or ABGs improved breathing patterns/airway exchange Onset PO 15-30 min, inhalation, within 5 min, Peak effect PO 2-3 hr; inhalation 60-90 min after 2 inhalations, Duration PO 4-8 hr (upto 12 for extended-release. inhalation 3-6 hr.
Created by: slofin
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