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Drug Interactions between Clorpres and Ritalin LA

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

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Interactions between your drugs

Moderate

cloNIDine methylphenidate

Applies to: Clorpres (chlorthalidone / clonidine) and Ritalin LA (methylphenidate)

MONITOR: Serious adverse events may occur during concomitant use of methylphenidate or dexmethylphenidate with centrally-acting alpha-2 agonists. The mechanism of interaction, if any, is unknown, and a causal relationship has not been established. The use of clonidine, with or without methylphenidate, has been associated with rare cases of sudden death and cardiotoxicity including sinus bradycardia and heart block. Electrocardiographic (ECG) abnormalities have also been demonstrated in patients treated with clonidine, even at low dosages. However, some investigators suggest these findings may reflect the pharmacologic effects of the drug and not necessarily cardiotoxic effects. Although the existence of a methylphenidate-clonidine interaction is questionable, it is possible that the combination may be more dangerous than either drug alone with respect to drug discontinuation. Specifically, methylphenidate may exacerbate the rebound hypertension and hyperadrenergic state associated with abrupt withdrawal of clonidine, and methylphenidate withdrawal may aggravate the bradycardia and hypotension associated with clonidine use.

MANAGEMENT: The safety of using methylphenidate (racemic) or dexmethylphenidate (the more pharmacologically active d-enantiomer) in combination with clonidine or other centrally-acting alpha-2 agonists has not been established. Patients being considered for alpha-2 agonist therapy, alone or with methylphenidate or dexmethylphenidate, should have cardiovascular status and history evaluated. Vital signs, including pulse and blood pressure, should be monitored prior to and during therapy. The routine use of ECGs in patients being treated for behavioral disorders is controversial, since it is uncertain what findings may indicate actual risk for sudden death. However, ECG monitoring may be appropriate in cases of preexisting cardiac disease or abnormal finding on physical examination. Finally, patients should be advised not to abruptly discontinue the alpha-2 agonist, methylphenidate, or dexmethylphenidate following chronic use unless otherwise directed by their physician.

References

  1. Roden DM, Nadeau JH, Primm RK "Electrophysiologic and hemodynamic effects of chronic oral therapy with the alpha 2-agonists clonidine and tiamenidine in hypertensive volunteers." Clin Pharmacol Ther 43 (1988): 648-54
  2. Brest AN "Hemodynamic and cardiac effects of clonidine." J Cardiovasc Pharmacol 2 (1980): s39-46
  3. Maloney MJ, Schwam SJ "Clonidine and sudden death." Pediatrics 96 (1995): 1176-7
  4. "Product Information. Ritalin (methylphenidate)." Novartis Pharmaceuticals PROD (2001):
  5. "Product Information. Focalin (dexmethylphenidate)." Mikart Inc (2001):
  6. Blackman JA, Samson-Fang L, Gutgesell H "Clonidine and electrocardiograms." Pediatrics 98((6 Pt 1)) (1996): 1223-4
  7. Wilens TE, Spencer TJ, Swanson JM, Connor DF, Cantwell D "Combining methylphenidate and clonidine: a clinically sound medication." J Am Acad Child Adolesc Psychiatry 38 (1999): 614-9; discussion 619-22
  8. Popper CW "Combining methylphenidate and clonidine: pharmacologic questions and news reports about sudden death." J Child Adolesc Psychopharmacol 5 (1995): 157-66
  9. Swanson JM, Flockhart D, Udrea D, Cantwell D, Connor D, Williams L "Clonidine in the treatment of ADHD: questions about safety and efficacy." J Child Adolesc Psychopharmacol 5 (1995): 301-4
View all 9 references

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Moderate

chlorthalidone methylphenidate

Applies to: Clorpres (chlorthalidone / clonidine) and Ritalin LA (methylphenidate)

MONITOR: Methylphenidate and other derivative amphetamines may decrease the therapeutic effects of antihypertensive drugs. According to serdexmethylphenidate label information, CNS stimulants cause a mean increase in blood pressure of approximately 2 to 4 mmHg and a mean increase in heart rate of approximately 3 to 6 beats per minute. With some individuals having larger increases.

MANAGEMENT: Caution and monitoring of blood pressure is recommended if methylphenidate, dexmethylphenidate or serdexmethylphenidate are administered with antihypertensives agents such as: potassium-sparing and thiazide diuretics, calcium channel blockers, angiotensin-converting-enzyme (ACE) inhibitors, angiotensin II receptor blockers (ARBs), beta blockers or centrally acting alpha-2 receptor agonists. The dosage of the antihypertensive drug should be adjusted as needed.

References

  1. "Product Information. Ritalin (methylphenidate)." Novartis Pharmaceuticals PROD (2001):
  2. "Product Information. Metadate CD (methylphenidate)." Celltech Pharmaceuticals Inc (2022):
  3. "Product Information. Focalin (dexmethylphenidate)." Mikart Inc (2001):
  4. "Product Information. Metadate ER (methylphenidate)." Celltech Pharmaceuticals Inc (2002):
  5. Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
  6. Cerner Multum, Inc. "Australian Product Information." O 0
  7. "Product Information. Ritalin LA (methylphenidate)." Quality Care Products/Lake Erie Medical (2013):
  8. "Product Information. Azstarys (dexmethylphenidate-serdexmethylphenidate)." Corium, Inc. (2021):
View all 8 references

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Drug and food interactions

Moderate

methylphenidate food

Applies to: Ritalin LA (methylphenidate)

GENERALLY AVOID: Alcohol may exacerbate the adverse central nervous system effects of psychoactive drugs, including methylphenidate.

GENERALLY AVOID: Consumption of alcohol while taking certain sustained-release formulations of methylphenidate may cause rapid release of the drug, resulting in increased systemic levels of methylphenidate. In vitro studies have been conducted using Metadate CD 60 mg and Ritalin LA 40 mg capsules, as well as Concerta 18 mg tablet. At an alcohol concentration of 40%, an increase in the release rate of methylphenidate was observed in the first hour for Metadate CD and Ritalin LA, resulting in 84% and 98% of the methylphenidate being released, respectively. In contrast, there was no increased release of methylphenidate in the first hour for Concerta. These results are considered to be representative of the other available strengths of the corresponding product.

MANAGEMENT: Patients treated with methylphenidate should be advised to avoid alcohol or medications that contain alcohol.

References

  1. "Product Information. Metadate CD (methylphenidate)." Celltech Pharmaceuticals Inc (2022):
  2. "Product Information. Concerta (methylphenidate)." Alza (2002):
  3. "Product Information. Ritalin LA (methylphenidate)." Quality Care Products/Lake Erie Medical (2013):

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Moderate

cloNIDine food

Applies to: Clorpres (chlorthalidone / clonidine)

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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Moderate

chlorthalidone food

Applies to: Clorpres (chlorthalidone / clonidine)

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.