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Liver function monitoring

On rare occasions, pemoline can cause a chemical hepatitis (liver dysfunction). For this reason, patients with known liver disease should not be prescribed pemoline. A baseline laboratory assessment of liver enzymes before starting therapy with pemoline is advised, and liver function monitoring must be repeated periodically. If liver abnormalities are detected, then pemoline must be discontinued. The recognition of this side effect resulting from therapy with pemoline has markedly restricted its use. [Pg.279]

Esophagitis 200 mg bid hepatotoxiq long-term use requires liver function monitoring poorabsorptbn in low gastric acid states use with astemizole cisapride may cause QT prolongation. [Pg.91]

Geriatric Considerations - Summary Tolcapone inhibits peripheral COMT and increases levodopa s effects. Its primary role is as adjunct therapy to prolong the beneficial effects of levodopa and to decrease end-of-dose fluctuations in response to treatment. Due to the potential to cause serious hepatotoxicity, tolcapone requires frequent liver function monitoring and because of this risk,is rarely used. [Pg.1239]

Landau J, Martin A. Is liver function monitoring warranted during risperidone treatment J Am Acad Child Adolesc Psychiatry 1998 37(10) 1007-8. [Pg.359]

Thus, liver function monitoring is a necessary component of pemoline therapy... [Pg.360]

Information is limited. However, it would seem prudent to avoid the use of androgens or anabolic steroids in patients taking ciclosporin wherever possible. If no alternative is available it may be prudent to increase the frequency of liver function monitoring. [Pg.1014]

The authors highlighted the need for liver function monitoring in the first few weeks of buprenorphine treatment in susceptible patients, such as those with hepatitis, alcohol abuse, or concomitant use of drugs that cause mitochondrial toxicity. [Pg.225]

PYRAZINAMIDE Patients should have baseline liver functions tests to use as a comparison when monitoring liver function during pyrazinamide therapy. The nurse should monitor the patient closely for symptoms of a decline in hepatic functioning (ie, yellowing of the skin, malaise, liver tenderness, anorexia, or nausea). The primary health care provider may order periodic liver function tests. Hepatotoxicity appears to be dose related and may appear at any time during therapy. [Pg.114]

ITRACONAZOLE Although rare, die patient may develop hepatitis during itraconazole administration. The nurse closely monitors die patient for signs of hepatitis, including anorexia, abdominal pain, unusual tiredness, jaundice, and dark urine. The primary healtii care provider may order periodic liver function tests. [Pg.136]

MTX is potentially toxic. Therefore, the nurse observes closely for development of adverse reactions, such as thrombocytopenia (see Nursing Alert in Gold Compounds section) and leukopenia (see discussion of adverse reactions associated with hydroxychloroquine). Hematology, liver, and renal function studies are monitored every 1 to 3 months with MTX therapy. The primary care provider is notified of abnormal hematology, liver function, or kidney function finding. The nurse immediately brings all adverse reactions or suspected adverse reactions to the attention of the primary health care provider. [Pg.196]

A serious and potentially fatal adverse reaction to tolcapone ishepatic injury. Regular blood testing to monitor liver function is usually prescribed. The phys dan may order testing of serum transaminase levels at frequent intervals(eg, every 2 weeks for the first year and every 8 weeks thereafter). Treatment is discontinued if the ALT (SOFT) exceeds the upper normal limit or sgns or symptoms of liver failure develop. [Pg.271]

FAT EMULSIONS. When a fat emulsion is administered, the nurse must monitor the patient s ability to eliminate the infused fat from the circulation. The lipidemia must clear between daily infusions. The nurse monitors for lipidemia through assessing the result of the following laboratory exams hemogram, blood coagulation, liver function tests, plasma lipid profile, and platelet count. The nurse reports an increase in any of these laboratory examinations as abnormal. [Pg.637]

Monitor for adequate perfusion of vital organs through assessment of mental status, creatinine clearance, liver function tests, and a stable HR between 50 and 100 beats per minute. Additionally, adequate skin and muscle blood perfusion and normal pH is desirable. [Pg.59]

Prior to initiating methotrexate therapy, obtain complete blood count, serum creatinine, liver function tests, chest x-ray, and pregnancy test (if female). Monitor blood counts weekly for 1 month, then monthly thereafter. [Pg.293]

Carbamazepine Manufacturer recommends CBC and platelets (and possibly reticulocyte counts and serum iron) at baseline, and that subsequent monitoring be individualized by the clinician (e.g., CBC, platelet counts, and liver function tests every 2 weeks during the first 2 months of treatment, then every 3 months if normal). Monitor more closely if patient exhibits hematologic or hepatic abnormalities or if the patient is receiving a myelotoxic drug discontinue if platelets are less than 100,000/mm3, if white blood cell (WBC) count is less than 3,000/mm3 or if there is evidence of bone marrow suppression or liver dysfunction. Serum electrolyte levels should be monitored in the elderly or those at risk for hyponatremia. Carbamazepine interferes with some pregnancy tests. [Pg.598]

It is important to carefully document core ADHD symptoms at baseline to provide a reference point from which to evaluate effectiveness of treatment. Improvement in individualized patient outcomes are desired, such as (1) family and social relationships, (2) disruptive behavior, (3) completing required tasks, (4) self-motivation, (5) appearance, and (6) self-esteem. It is very important to elicit evaluations of the patient s behavior from family, school, and social environments in order to assess the preceding. Using standardized rating scales (e.g., Conners Rating Scales-Revised, Brown Attention-Deficit Disorder Scale, and IOWA Conners Scale) in both children and adults with ADHD helps to minimize variability in evaluation.29 After initiation of therapy, evaluations should be done every 2 to 4 weeks to determine efficacy of treatment, height, weight, pulse, and blood pressure. Physical examination or liver function tests may be used to monitor for adverse effects. [Pg.641]

Major adverse events Edema, weight gain disconti nue use if alanine aminotranferase (ALT) greater than 3 times normal monitor liver function tests at baseline and periodically thereafter ... [Pg.655]

Methotrexate Monitor complete blood cell count and liver function tests at baseline and regularly, and consider liver biopsy prior to treatment and at a cumulative dose of 1.5 g. If available, monitor PIIINP at least three times yearly. [Pg.957]

Acitretin Monitor serum lipids and liver function tests. [Pg.957]

All azole antifungals carry the potential for rash, photosensitivity, and hepatotoxicity. In general, hepatotoxicity is mild and reversible, presenting as asymptomatic increases in liver transaminases. However, fulminant hepatic failure has been reported with itraconazole. Therefore, serial monitoring of liver function... [Pg.1216]

Laboratory monitoring is performed before initiating therapy and before each cycle of chemotherapy. A complete blood count should be obtained prior to each course of chemotherapy to ensure that hematologic values are adequate. In particular, white blood cell counts and absolute neutrophil counts can be decreased in patients receiving chemotherapy such as irinote-can and 5-FU and increase the risk of infection. Baseline liver function tests and an assessment of renal function should be done prior to and periodically during therapy. Other selected laboratory tests include checking for the presence of protein in the urine in patients receiving oxaliplatin and bevacizumab. [Pg.1353]


See other pages where Liver function monitoring is mentioned: [Pg.114]    [Pg.170]    [Pg.410]    [Pg.481]    [Pg.407]    [Pg.412]    [Pg.422]    [Pg.114]    [Pg.170]    [Pg.410]    [Pg.481]    [Pg.407]    [Pg.412]    [Pg.422]    [Pg.340]    [Pg.595]    [Pg.135]    [Pg.128]    [Pg.186]    [Pg.544]    [Pg.544]    [Pg.598]    [Pg.603]    [Pg.710]    [Pg.874]    [Pg.884]    [Pg.955]    [Pg.964]    [Pg.1017]    [Pg.1206]    [Pg.1209]    [Pg.1439]    [Pg.1464]    [Pg.1507]    [Pg.128]   
See also in sourсe #XX -- [ Pg.202 ]




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