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diltiazem, enalapril, phenytoin, fluconazole, haloperidol, itraconazole, macrolides, nifedipine, quinidine, rapamycin, simvastatin, theophylline, and verapamil. Haloperidol adalah obat yang dikategorikan ke dalam agen antipsikotik, antidiskinetik, Efek samping haloperidol berbeda pada berbagai tingkatan usia . efek. Pada pasien skizofrenia penurunan konsentrasi haloperidol 70 % sehingga efek antipsikosis menurun. Litium dapat meningkatkan efek samping peningkatan.

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These patients should be closely monitored and should undergo clinical examination and laboratory tests more frequently than is necessary for patients haloperidil liver disease. Clinically significant interactions with drugs used in the treatment of tuberculosis. Hypotension and circulatory collapse may be counteracted by using IV fluids, plasma, or concentrated albumin, and vasopressor agents such as metaraminol, phenylephrine and norepinephrine.

However, due to the important role that rifampin plays in tuberculosis treatment regimens, the drug is generally included, with the proviso that the patients be closely monitored szmping frequent clinical evaluations and laboratory tests see also Drug-induced hepatitis.

The treatment must be discontinued, and, in patients using multiple-drug regimens, the causative drug must be identified see also Hepatotoxicity. In non-gouty patients haloperudol pyrazinamide, hyperuricemia commonly leads to arthralgia. Data was taken retrospectively from medical record. Severe systemic lupus erythematosus induced by isoniazid [Article in French].

Isoniazid drug and food interactions. For emergency control of severely disturbed patients: Oral Short-term adjunct in severe anxiety or behavioral disturbances Adult: Prospective randomized control trial of isoniazid chemoprophylaxis during renal replacement therapy. That meaned patient who used haloperidol could 5 more time got extrapiramidal side effects than haloperidol unused and patient who used chlorpromazine could 3 more time got hypotension orthostatic side effects than chlorpromazine unused.


The Treatment of Tuberculosis Guidelines. INH induced status epilepticus: Programa Nacional de Controle da Tuberculose. In these cases, serology for viral hepatitis should be ordered. In vitro resistance to ethambutol develops slowly and is probably due to mutations in the embB gene. Incidence, clinical and epidemiological risk factors, and outcome of drug-induced hepatitis due to antituberculous agents in new tuberculosis cases.

Isoniazid is a prodrug and must be activated by the M. Tajender V, Saluja J. However, these reactions are severe and call for a change in the therapeutic regimen.

Haloperidol: Indication, Dosage, Side Effect, Precaution | Indonesia

Risperidone vs haloperidol in schizophrenia Documents. Patients should be alerted to the possibility that rifampin administration can cause discoloration of body fluids. Isoniazid administration can also worsen preexisting lupus.

The mechanism of action of pyrazinamide has yet to be fully understood. The administration of isoniazid in isolation, at doses adjusted to the weight of the patient, rarely produces drug-induced hepatitis, which is practically nonexistent in children but is more common in alcoholic and elderly individuals. The drug has been used since and the MIC of rifampin for M. If exanthema occurs, treatment should be discontinued, and the drugs should be subsequently reintroduced, one by one, in order to identify the causative drug.

Adverse reactions to firstline antituberculosis drugs. Crosses the blood-brain barrier; enters breast milk. Antacids containing aluminum hydroxide or ranitidine should be administered 1 h after the administration of isoniazid. The WHO considers it safe to use pyrazi amide during pregnancy.


Treatment of tuberculosis in presence of hepatic and renal impairment. Risks of antibacterial agents in pregnancy [Article in Italian]. The half-life of pyrazinamide is h but can be as long as 26 h in patients with kidney failure if the doses are not adjusted. Restlessness and confusion mg 8 hrly. In addition, rifampin induces uridine diphosphate-glucuronosyltransferase, an enzyme that has also been implicated in the metabolism of various drugs, the plasma levels of which can be reduced when such drugs are administered in combination with rifampin.

However, there is a risk of developing hepatitis in the postpartum period.

Perbandingan Risperidone Dengan Haloperidol

Vieira DE, Gomes M. Halo;eridol rifampin is compatible with breastfeeding, the infant should be monitored for jaundice. Discontinue upon signs of neurological toxicity in patients taking haloperidol and lithium.

Drug-induced hepatitis due to interactions among antituberculosis drugs. View original from publikasiilmiah. The absorption of rifampin competes with the absorption and conjugation of bilirubin for the inhibition of glucuronosyltransferase.

Drugs that increase the gastric pH delay the absorption of isoniazid. Antacids containing aluminum hydroxide delay the absorption of rifampin. The mechanism is related to pyrazinoic acid, the principal metabolite of pyrazinamide, which inhibits the renal tubular secretion of uric acid.

Pyrazinamide is bactericidal and has a potent sterilizing effect, principally in the acid medium within macrophages and at sites of acute inflammation.

The reaction is dosedependent.