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Drug Interactions between Enduron and iodamide

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Moderate

methyclothiazide iodamide

Applies to: Enduron (methyclothiazide) and iodamide

MONITOR: Forced diuresis during administration of radiocontrast agents may increase the risk of renal impairment in patients who are at high risk for contrast-induced nephropathy. Patients considered at high risk include those with diabetes (especially diabetic nephropathy), preexisting renal insufficiency (serum creatinine >1.5 mg/dL or GFR <60 mL/min/1.73 m2), volume depletion, advanced age (>70 years), congestive heart failure, and/or concurrent use of nephrotoxic drugs (e.g., NSAIDs). Diuretics have been studied for use in the prevention of contrast-induced nephropathy because investigators theorized that they may reduce medullary ischemia by decreasing oxygen demands. In published studies, however, maintenance intravenous fluids plus forced diuresis with furosemide, mannitol, or a combination of both given at the time of radiocontrast exposure generally produced similar or even higher rates of nephropathy compared with intravenous fluids alone. Meta-analyses of published data suggest that furosemide-based interventions significantly increase the risk of contrast-induced nephropathy compared with hydration alone, and one study found that hospitalization for all patients who developed contrast-induced nephropathy was increased by 4 days in those who received concomitant diuretic therapy. Contrast-induced nephropathy is most commonly defined as an increase in serum creatinine >=0.5 mg/dL or 25% from baseline within 48 to 72 hours of intravascular contrast administration in the absence of alternative etiologies, although nephropathy may occur up to a week after contrast exposure. While the condition is usually transient and asymptomatic, it can be associated with increased risk of renal failure, dialysis, prolonged hospitalization, significant long-term morbidity, and mortality.

MANAGEMENT: Whenever possible, alternative imaging techniques should be considered in patients who are at high risk for contrast-induced nephropathy. Otherwise, some experts recommend discontinuing diuretics 1 to 2 days before administration of contrast media, depending on the clinical feasibility of doing so. The smallest effective dose of a nonionic, hypo- or iso-osmolar contrast medium (e.g., iohexol, iodixanol, iopamidol) should be used, since the risk of nephropathy is increased with increasing contrast dose and/or osmolarity. Repeat procedures with contrast media, if necessary, should not occur until at least 72 hours after the previous contrast exposure and renal function has fully recovered. Although it is not necessary to measure the serum creatinine levels of every patient before contrast administration, measurements should generally be made in patients receiving contrast agent by intraarterial administration (which is associated with increased risk of nephropathy relative to intravenous administration) and patients with a history of kidney disease, proteinuria, kidney surgery, diabetes, hypertension, gout, or other risk factors for nephropathy. Creatinine measurements should be continued for 24 to 48 hours after administration of contrast medium. It is important that patients be adequately hydrated with either saline or sodium bicarbonate.

References

  1. "Product Information. Lasix (furosemide)." sanofi-aventis PROD (2007):
  2. Weinstein J-M, Heyman S, Brezis M "Potential deleterious effect of furosemide in radiocontrast nephropathy." Nephron 62 (1992): 413-5
  3. Solomon R, Werner C, Mann D, D'Elia J, Silva P "Effects of saline, mannitol, and furosemide on acute decreases in renal function induced by radiocontrast agents." N Engl J Med 331 (1994): 1416-20
  4. Costa N "Understanding contrast media." J Infus Nurs 27 (2004): 302-12
  5. Stevens MA, McCullough PA, Tobin KJ, et al. "A prospective randomized trial of prevention measures in patients at high risk for contrast nephropathy: results of the P.R.I.N.C.E. Study. Prevention of Radiocontrast Induced Nephropathy Clinical Evaluation." J Am Coll Cardiol 33 (1999): 403-11
  6. Barrett BJ, Parfrey PS "Clinical practice. Preventing nephropathy induced by contrast medium." N Engl J Med 354 (2006): 379-86
  7. Briguori C, Marenzi G "Contrast-induced nephropathy: Pharmacological prophylaxis." Kidney Int 69(S100) (2006): S30-S38
  8. Tepel M, Aspelin P, Lameire N "Contrast-induced nephropathy: a clinical and evidence-based approach." Circulation 113 (2006): 1799-806
  9. Meschi M, Detrenis S, Musini S, Strada E, Savazzi G "Facts and fallacies concerning the prevention of contrast medium-induced nephropathy." Crit Care Med 34 (2006): 2060-80
  10. Stacul F, Adam A, Becker CR, et al. "Strategies to reduce the risk of contrast-induced nephropathy." Am J Cardiol 98(6S1) (2006): 59-77
  11. Ho KM, Sheridan DJ "Meta-analysis of frusemide to prevent or treat acute renal failure." BMJ 333 (2006): 420
  12. Kelly AM, Dwamena B, Cronin P, Bernstein SJ, Carlos RC "Meta-analysis: effectiveness of drugs for preventing contrast-induced nephropathy." Ann Intern Med 148 (2008): 284-94
  13. Venkataraman R "Can we prevent acute kidney injury?" Crit Care Med 36(4 Suppl) (2008): S166-71
  14. Fishman EK, Reddan D "What are radiologists doing to prevent contrast-induced nephropathy (CIN) compared with measures supported by current evidence? A survey of European radiologists on CIN associated with computed tomography." Acta Radiol 49 (2008): 310-20
  15. Massicotte A "Contrast medium-induced nephropathy: strategies for prevention." Pharmacotherapy 28 (2008): 1140-50
View all 15 references

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Drug and food interactions

Moderate

methyclothiazide food

Applies to: Enduron (methyclothiazide)

MONITOR: Many psychotherapeutic and CNS-active agents (e.g., anxiolytics, sedatives, hypnotics, antidepressants, antipsychotics, opioids, alcohol, muscle relaxants) exhibit hypotensive effects, especially during initiation of therapy and dose escalation. Coadministration with antihypertensives and other hypotensive agents, in particular vasodilators and alpha-blockers, may result in additive effects on blood pressure and orthostasis.

MANAGEMENT: Caution and close monitoring for development of hypotension is advised during coadministration of these agents. Some authorities recommend avoiding alcohol in patients receiving vasodilating antihypertensive drugs. Patients should be advised to avoid rising abruptly from a sitting or recumbent position and to notify their physician if they experience dizziness, lightheadedness, syncope, orthostasis, or tachycardia.

References

  1. Sternbach H "Fluoxetine-associated potentiation of calcium-channel blockers." J Clin Psychopharmacol 11 (1991): 390-1
  2. Shook TL, Kirshenbaum JM, Hundley RF, Shorey JM, Lamas GA "Ethanol intoxication complicating intravenous nitroglycerin therapy." Ann Intern Med 101 (1984): 498-9
  3. Feder R "Bradycardia and syncope induced by fluoxetine." J Clin Psychiatry 52 (1991): 139
  4. Ellison JM, Milofsky JE, Ely E "Fluoxetine-induced bradycardia and syncope in two patients." J Clin Psychiatry 51 (1990): 385-6
  5. Rodriguez de la Torre B, Dreher J, Malevany I, et al. "Serum levels and cardiovascular effects of tricyclic antidepressants and selective serotonin reuptake inhibitors in depressed patients." Ther Drug Monit 23 (2001): 435-40
  6. Cerner Multum, Inc. "Australian Product Information." O 0
  7. Pacher P, Kecskemeti V "Cardiovascular side effects of new antidepressants and antipsychotics: new drugs, old concerns?" Curr Pharm Des 10 (2004): 2463-75
  8. Andrews C, Pinner G "Postural hypotension induced by paroxetine." BMJ 316 (1998): 595
View all 8 references

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Therapeutic duplication warnings

No warnings were found for your selected drugs.

Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.