C C C Vertigo,: Electrolyte and Water Balance Agent
C C C Vertigo,: Electrolyte and Water Balance Agent
C C C Vertigo,: Electrolyte and Water Balance Agent
Action Inhibits reabsorption of sodium and chloride from the proximal and distal tubular and ascending limb of the loop of Henle, leading to a sodiumrich diuresis.
Adverse Effect CNS: vertigo, paresthesia, weakness, headache, drowsiness, fatigue, blurred vision EENT: Blurred vision; hearing impairment; tinnitus; xanthopsia (yellow vision). CV: orthostatic hypotension, cardiac arrhythmias, thromboplhebitis DERMA: photosensitivity, rash, pruritus, urticaria, purpura, dermatitis. GI: nausea, anorexia, vomiting, oral and gastric irritation, constipation, diarrhea GU: polyuria, glycosuria, nocturia, urinary bladder
Indication Management of edema associated with congestive heart failure and hepatic or renal disease; used alone or in combination with antihypertensives in treatment of hypertension
Contraindication Allergy with furosemide, sulfonamides; allergy to tartazine( in oral solution); anuria, severe renal failure; hepatic coma; pregnancy; lactation. Use cautiously with SLE, gout, DM
Nursing Consideration Determine allergy to furosemides, tatrtazine; electrolyte depletion anuria, severe renal failure, hepatic coma; gout;SLE; DM; lactation; pregnancy Assess for skin color, lesions, edema,orientation , reflexes, hearing, pulses Administer with food or milk to prevent GI upset Decrease dosage if given with other antihypertensive; readjust dosage gradually as blood pressure responds Measure and record weight to monitor fluid changes Advise patient to
spasm HEMA: leukopenia, anemia, thrombocytopenia, fluid and electrolyte imbalance, hyperglycemia OTHER: muscle cramps, muscle spasm
get up slowly when rising from a seated or lying position to minimize dizziness.
Action prevents a decrease in intracellular adenosine triphosphate levels, thereby ensuring the proper functioning of ionic pumps and transmembranous sodium-potassium flow whilst maintaining cellular homeostasis
Adverse Effect GI: nausea, vomiting and other gastrointestinal disorders RESPI: respiratory illness HEMA:anemia
Contraindication Do not take Vastarel MR if you are allergic to any of the constituents. This drug is generally not recommended during breast feeding
Nursing Consideration use cautiously in patients with heart failure or hypertension and in elderly patients
Name of Drug
Action
Adverse Effect
Indication
Contraindication
Nursing Consideration Monitor apical pulse for 1 minute before administering; hold dose if pulse lower than 60bpm in adult and lower than 90bpm in infant Monitor I&O ratio during digitalization, particularly in patients with impaired renal function. Also monitor for edema daily and auscultate chest for rales. Avoid giving with meals; this may delay absorption Monitor for S/S of drug toxicity: In children, cardiac arrhythmias are usually reliable
prevents a decrease in intracellular adenosine triphosphate levels, thereby ensuring the proper functioning of ionic pumps and transmembranous sodium-potassium flow whilst maintaining cellular homeostasis
CNS: headache, dizziness, weakness, drowsiness, mental status change GI:nausea, vomiting, abdominal pain, anorexia CV: heart block, rapid heartbeat, and slow heart rate DERMA: EENT: visual disturbance (blurred or yellow vision, light flashes, halos around bright objects) HEMA:high calcium and low magnesium blood levels OTHERS:Personality
Preventive treatment for episodes of angina pectoris (Chronic stable angina). prophylactic management and treatment of CHF, control of ventricular rate in patients with atrial fibrillation. treatment and prevention of recurrent paroxysmal atrial tachycardia
contraindicated with allergy to digitalis preparations, ventricular tachycardia, ventricular fibrillation, heart block, sick sinus syndrome, acute MI This drug is generally not recommended during breast feeding
signs of early toxicity. Early indicators in adults (anorexia, nausea, vomiting, diarrhea, visual disturbances) are rarely initial signs in children. Weigh each day under standard conditions. Assess for GI disturbances, neurologic abnormalities (signs of toxicity) every 2-4 hours during digitalization (daily during maintenance).
Action normalizes the metabolism of lipids and proteins, improves the detoxification function of the liver, restores the cellular structure of the liver and retards the producing of conjunctive tissue
Adverse Effect CNS: nausea GU:abdominal pain, diarrhea and DERMA: skin rash
Indication
Contraindication
Hepatic protectors
Hepatitis(acute hypersensitivity and chronic), toxic or allergy to any hepatitis, ingredients of the medicinal and preparation alcoholic hepatitis, children, pregnat poisonings woman Diseases of the cardiovascular system: coronary heart disease, stable stenocardia, post-infarction condition, disturbance of the cerebral and peripheral circulation, Hypertension, thrombembolia prophylaxis, atherosclerosis, diabetic angiopathy, thrombembolia prophylaxis and fat embolism(solution for injection)
Nursing Consideration Do not use Essentialein hypersensitivity or allergy to any ingredientsof the preparation. Theapplication of Essentialein newborn children isnot safe. Duringpregnancy women arerecommended to consulttheir health careprovider prior to takingEssentiale.
Action Inhibits prostaglandin synthesis, acts on the hypothalamus heat-regulating center to reduce fever, blocks prostaglandin synthetase action which prevents formation of the platelet-aggregating substance thromboxane A2
Adverse Effect CNS: fatigue GI: gastrointestinal ulceration, nausea, dyspepsia, anorexia RESPI: dyspnea DERMA: rash, urticaria NEURO&MUSCU: weakness HEMA:hemolytic anemia, occult blood loss OTHERS: anaphylactic shock High dosages: gastroinestinal bleeding or gastric mucosal lesions Low grade toxicity : ringing in the ears, generalized pruritus, headache, dizziness, flushing, tachycardia, hyperventilation, sweating, and thirst. Febrile dehydrated children can reach
Indication treatment of mild to moderate pain, inflammation, and fever may be used as prophylaxis for myocardial infarction and transient ischemic episodes management for rheumatoid arthritis, rheumatic fever, osteoarthritis, and gout (high dose)
Nursing Consideration hypersensitivity to monitor for signs salisylates or other or symptoms of NSAIDs; bleeding adverse effects with special disorders; allergy attention to 8th to tartazine dye; cranial nerve asthma diagnosis function use cautiously with Assess type, impaired renal function; location, duration chickenpox, of pain, and influenza inflammation. Inspect appearance of affected joints for immobility, deformities, and skin condition. Monitor urinary pH (pH from 6.5 to 5.5), may result in toxicity. Assess skin for evidence of bruising. When given as an antipyretic, assess body temperature before and 1 hour after giving
Contraindication
medication. Evaluate for therapeutic response: relief of pain, stiffness, swelling; increase in joint mobility, reduced joint tenderness, and improved grip strength.
Action Inhibits prostaglandin synthesis in the CNS and blocks the pain impulse through a peripheral action. It acts on the hypothalamic heatregulating center, producing peripheral vasodilation. It results in antipyresis and produces analgesic effect.
Adverse Effect Hematologic: hemolytic anemia, neutropenia, leucopenia, pancytopenia. Hepatic: Jaundice Metabolic: Hypoglycemia Skin: rash, urticaria Early signs of toxicity: Anorexia, nausea, diaphoresis (excessive sweating), generalized weakness within the first 12-24 hours. Late signs of toxicity: Vomiting, right upper quadrant tenderness, elevated liver function tests within 48-72 hours
Contraindication Contraindicated in patients hypersensitive to drug. Use cautiously in patients with long term alcohol use because therapeutic doses cause hepatotoxicity in these patient
Nursing Consideration Assess temperature directly before and 1 hour after giving medication. Use liquid form for children and patients who have difficulty swallowing. In children, don t exceed five doses in 24 hours. Advise patient that drug is only for short term use and to consult the physician if giving to children for longer than 5 days or adults for longer than 10 days. Advise patient or caregiver that many over the counter products contain acetaminophen;
be aware of this when calculating total daily dose. Warn patient that high doses or unsupervised long term use can cause liver damage Give drug with food if GI upset occurs Evaluate for therapeutic response: relief of pain, stiffness, swelling; increasing in joint mobility; reduced joint tenderness; improve grip strength.
Action
Adverse Effect
Indication malnutrition, protein and vitamin deficiencies, anemia, convalescence, restoration and maintenance of body resistance, pregnancy and lactation, adjuvant in the therapy of peptic ulcer and TB
Stimulates hypervitaminosis normalerythropoiesi (large doses) s andStimulates normalerythropoiesi s andneucloproteinsy nthesis. NutritionalSuppleme nt
Nursing Consideration Assess patient for signs of vitamin deficiency before and periodically throughout therapy. Assess nutritional status through 24 h diet recall. Determine frequency of consumption of vit rich food Assess patient sfolic aciddeficiency beforestarting therapystarting therapy Evaluate CBC and assess patient s physical statusthroughout therapy.
Action Adrenergic bronchodilators and phosphodiesterase inhibitors both work by increasing intracellular level of cyclic-3 ,5 adenosine monophosphate (cAMP)
Adverse Effect Nausea, vomiting, epigastric pain, cephalalgia, irritability, insomnia, tachycardia, extrasystole, tachypnea, hyperglycemia, albuminuria
Nursing Consideration Assess lung sounds, pulse and blood pressure before administration and during peak of medication. Not amount, color, and character of sputum produced. Monitor pulmonary function tests before initiating therapy and periodically during therapy to determine effectiveness of medication. Observe for paradoxical bronchospasm (wheezing). If conditions occur, withhold medication and