drug study for itp

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  • 8/9/2019 Drug Study for ITP

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    DRUG

    STUDY

    Petal Rose T. Madiam

    Group 9E

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    (ROCEPHIN)

    y anti infective

    :y Meningitis and bone/joint infection. Septicemia, Otitis

    Media, Peri operative Prophylaxis, Lyme dse.

    y Bind to the bacterial cell wall membrane causing celldeath.Therapeutic effect: bactericidal action against

    susceptible bacteria.

    :y Hypersensitivity to cephalosporin

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    pain, tenderness, hardness, or warmth in the place whereceftriaxone was injected

    headache

    dizziness

    sweating

    flushing

    diarrhea

    y Usual Adult Dose for Intra abdominal Infection:

    2 g IV 24 hours for 7 to 14 days, depending on the nature andseverity of the infection

    y Intermittent Infusion: reconstitute

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    (COZAAR)

    y anti hypertensives

    y Alone or with other agents in the management ofhypertension .Prevention of stroke in patients with

    hypertension.

    :y Lowering of blood pressure. decreased risk of stroke in

    patients with hypertension

    y Hypersensitivity; OB: can cause injury or death of fetus.

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    Dizziness,

    anxiety,

    depression,

    fatigue,

    headache,

    insomnia,

    weakness,

    hypotension,

    chest pain edema,

    tachycardia,

    diarrhea, nausea,

    and vomiting

    y Adults: PO hypertension-50 mg once daily initial

    y Correct volume depletion, if possible, prior to initiation of therapy

    y PO: May be administered without regard to meals

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    (LOPRESOR)

    y Anti Hypertensive

    y Hypertension. Angina Pectoris. Prevention of MI anddecreased mortality in patients with recent MI.

    y Decreased blood pressure and heart rate. Decreasedfrequency of attacks of angina pectoris. Decreasedrate of cardiovascular mortality and hospitalization in

    patient with heart failure.

    y Uncompensated CHF; Pulmonary edema:Cardiogenic shock; Bradycardia

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    Fatigue,

    weakness,

    anxiety,

    depression, dizziness,

    drowsiness,

    insomnia,

    memory loss,

    blurred vision,

    hypotension,

    diarrhea,

    dry mouth,

    flatulence,

    heart burn,

    urinary frequency.

    y Adults: PO; Anti Hypertensive / Anti anginal -25-100mg/day as a single

    dose initially or two divided doses.

    :

    y PO: Take apical pulse before administering, If

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    (LASIX)

    y Diuretics

    y Treatment of edema ,associated w/ CHF renal & hepaticdisorders. Management of oliguria due to renal failure &insufficiency. Mild to moderate HTN. Severe hypercalcemia.

    Adjunct to other antihypertensive agents.

    y Rapid-acting potent sulfonamide loop diuretic andantihypertensive with pharmacologic effects and usesalmost identical to those of ethacrynic acid. Exact mode ofaction not clearly defined; decreases renal vascular

    resistance and may increase renal blood flow.

    y Severe renal or hepatic dysfunction. Addison's disease.Electrolyte imbalance.

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    Fluid & electrolyte imbalance including :

    hyponatremia,

    hypokalemia

    hypochloremic alkalosis;

    hyperuricemia

    y Treatment of HTN AdultUsually, 40-80 mg daily either alone or in

    conjunction w/ anti hypertensives. Amp Adult20-40 mg IV/IM once

    daily to bid, may be increase at 2-hrly interval by 20 mg.

    :y Do not administer discolored solution or tablets.

    y PO: May be taken with food or milk to minimize gastric irritation.

    Tablets may be crushed if the patients has difficulty swallowing.

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    (ALDACTONE)

    y Diuretics

    y Counteract potassium loss caused by other diuretics .

    Used with other agents to treat edema or hypertension.

    y Inhibition of sodium re-absorption in the kidney whilesaving potassium and hydrogen ions

    y Hypersensitivity; Hyperkalemia; anuria, acute renalinsufficiency.

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    y Dizziness,

    y clumsiness,

    y headache,y constipation,

    y nausea,

    y vomiting,

    y breast tenderness,

    y irregular menses,

    y voice deepening.

    y Adults: PO: Edema-25-200mg/day in 1-2 divided doses.

    y Diuretic Induced hypokalemia-25-100mg/day in 1-2divided doses

    y PO: Administer in A.M. to avoid interrupting sleep pattern.

    y Administer with food or milk to minimize gastric irritation andto increase bioavailability.

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    (CITROCARBONATE)

    y anti ulcer agents

    y PO,IV: Management of metabolic Acidosis; Used toalkanalize urine and promote excretion of certain

    drugs in over dosage situations; Antacids

    y Acts as an alkalinizing agent by releasingbicarbonate ions. Following oral administration,releases bicarbonate, which is capable of

    neutralizing gastric acid.

    y Metabolic or respiratory alkalosis; Hypocalcemia;Excessive chloride loss; Patients on sodium restricteddiets; renal failure

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    y Edema

    y

    Flatulencey Gastric distention

    y ALKALINIZATION OF URINE: 48 meq(4g) initially. Then12-24 meq (1-2g) q 4hr.

    y ANTACID: tab/powder-325mg-2g,1-4 times daily or tsp. of powder q 4 hr as needed

    y This medication may cause premature dissolution ofenteric coated tablets in the stomach.

    y When used in treatment of peptic ulcers, may beadministered 1&3 hr after meals and at bedtime

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    (CIPRO)

    y anti-infectives

    y Infections of the resp. tract, middle ear, sinuses, eyes,kidneys &/or UTI, genital organs (including gonorrhea),

    abdominal cavity (eg bacterial infections of the GIT,biliary tract, peritonitis), skin & soft tissues, bones &joints; septicemia, infections in patients w/reduced hostdefenses, selective gut decontamination.

    y

    Death of susceptible bacteria.

    y Hypersensitivity. Cross sensitivity among agents withinclass may occur.

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    Nausea,

    diarrhea,

    vomiting,

    abdominal pain,

    flatulence

    anorexia.

    Dizziness,

    headache,

    tiredness,

    agitation

    trembling.

    Skin rashes,

    drug fever.

    Joint pains.

    y Tab Uncomplicated upper & lower UTI 100-125 mg bid.

    y Complicated urinary & resp tract infections (eg bronchitis) 250-500 mg bid.

    :y If gastric irritation occurs, ciprofloxacin may be administered with meals

    y Do confuse norfloxacin with norflex

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    (CATAPRES)

    y anti hypertensives

    y PO,Transdermal: Management of mild to

    moderate hypertension.

    y Decreased Blood Pressure, Decreased pain

    y

    Hypersensitivity; Epidural- injection, anti coagulanttherapy

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    Dizziness,

    headache,

    sedation,

    depression,

    hallucination,

    decreased libido,

    nightmare,

    sleep disorder,

    nasal dryness,

    rash,

    fatigue,

    constipation,

    nausea, ,

    vomiting.

    y Adult; PO: HPN -100 mcg bid, increase by 100-200mcg/day in 2-4days; Usualmaintenance dose is 200-600 mcg/day in 2-3 divided doses.

    y PO: Administer last dose of the day at the bedtimey Transdermal: Transdermal system should be applied once every 7 days. May

    be applied to any hairless site; avoid cuts or calluses

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    (MAALOX)

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    tingling

    arrhythmias

    bradycardia

    constipation

    nausea

    vomiting

    y Adults: PO; Prevention of hypocalcemia, treatment ofdepletion -1-2g/day

    y PO: Administer calcium carbonate or phosphate 1-1.5hr. after meals and at bed time.

    y Follow oral doses with a full glass of water, Administer onan empty stomach to optimize effectiveness.

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    (ZOCOR)

    y Lipid lowering agents

    y Secondary prevention of cardiovascular

    events(decreased risk of MI, stroke, and cardio vascularmortality) in patients with clinically evident CHD or thoseat high risk for CHD.

    y Lowers total and LDL cholesterol. Slightly increase HDL..

    Slows the progression of coronary atherosclerosis withresultant decrease in CHD.

    y Hypersensitivity; Active liver dse, OB/LACTATION:pregnancy or lactation

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    Dizziness

    Headache

    Insomnia

    Weakness

    Chest pain

    Abdominal cramps

    Constipation

    Diarrhea

    Flatus

    Heartburn

    Nausea

    y Adults PO: 5-80 mg once daily in the evening

    y Avoid Large amounts of grape fruit juice during therapy; mayincrease risk of toxicity

    y Administer extended release tablets at bed time. Extended releasetablets should be swallowed whole.

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    (ERYTHROPOIETIN)

    y anti anemics

    y Anemia associated with chronic renal failure.

    Reduction of need for transfusions after surgery.

    y Maintains and may elevate RBCs, decreasing theneed for transfusions.

    y Hypersensitivity to albumin or mammalian cell-

    derived products. Uncontrolled HPN.

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    y Headache

    y Hypertensions

    y Transient rashes

    y ANEMIA OF CHRONIC RENAL FAILURE-subcut, IV -50-100 units/kg 3times weekly initially, then adjust dose based on hematocrit.

    y Do not shake the vial; inactivation of medication may occur.discard vial immediately after drawing dose from single use.

    y Transfusions are still required for severe symptomatic anemia.

    Supplemental iron should be initiated and continue throughouttherapy

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    (ANTARA)

    y Lipid lowering Agents

    y With dietary therapy to decrease LDL cholesterol, total

    cholesterol, and triglycerides.

    y Lowering of cholesterol and triglycerides withsubsequent decreased risk of pancreatitis

    y Hypersensitivity; severe hepatic and renal impairment.Unexplained persistent liver function abnormality andprimary biliary cirrhosis; preexisting gall bladder disease.Pregnancy, lactation

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    Headache, dizziness

    fatigue, arrhythmia,

    dizziness, vaginitis,,

    rhinitis,

    cough,

    sinusitis,, polyuria,

    y Antara-43mg/day; Lofibra -67 mg/day, Tricor-48mg/day

    y Patients should be placed on a triglyceride lowering dietbefore therapy and remain on this diet throughouttherapy.

    y Brands are not interchangeable