Drug Interactions between clonidine and Maalox Advanced Maximum Strength Chewable
This report displays the potential drug interactions for the following 2 drugs:
- clonidine
- Maalox Advanced Maximum Strength Chewable (calcium carbonate/simethicone)
Interactions between your drugs
No interactions were found between clonidine and Maalox Advanced Maximum Strength Chewable. However, this does not necessarily mean no interactions exist. Always consult your healthcare provider.
clonidine
A total of 375 drugs are known to interact with clonidine.
- Clonidine is in the drug class antiadrenergic agents, centrally acting.
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Clonidine is used to treat the following conditions:
- ADHD
- Alcohol Withdrawal (off-label)
- Anxiety (off-label)
- Atrial Fibrillation (off-label)
- Benzodiazepine Withdrawal (off-label)
- Bipolar Disorder (off-label)
- High Blood Pressure
- Hyperhidrosis (off-label)
- Hypertensive Emergency (off-label)
- Insomnia, Stimulant-Associated (off-label)
- Migraine Prevention (off-label)
- Opiate Withdrawal (off-label)
- Pain
- Perimenopausal Symptoms (off-label)
- Pheochromocytoma Diagnosis (off-label)
- Postanesthetic Shivering (off-label)
- Postherpetic Neuralgia (off-label)
- Postural Orthostatic Tachycardia Syndrome (off-label)
- Restless Legs Syndrome (off-label)
- Smoking Cessation (off-label)
- Tardive Dyskinesia (off-label)
- Tourette's Syndrome (off-label)
- Ulcerative Colitis (off-label)
Maalox Advanced Maximum Strength Chewable
A total of 223 drugs are known to interact with Maalox Advanced Maximum Strength Chewable.
- Maalox advanced maximum strength chewable is in the drug class antacids.
- Maalox advanced maximum strength chewable is used to treat GERD.
Drug and food interactions
calcium carbonate food
Applies to: Maalox Advanced Maximum Strength Chewable (calcium carbonate / simethicone)
ADJUST DOSING INTERVAL: Administration with food may increase the absorption of calcium. However, foods high in oxalic acid (spinach or rhubarb), or phytic acid (bran and whole grains) may decrease calcium absorption.
MANAGEMENT: Calcium may be administered with food to increase absorption. Consider withholding calcium administration for at least 2 hours before or after consuming foods high in oxalic acid or phytic acid.
References (6)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- Canadian Pharmacists Association (2006) e-CPS. http://www.pharmacists.ca/function/Subscriptions/ecps.cfm?link=eCPS_quikLink
- Cerner Multum, Inc. "Australian Product Information."
- Agencia Española de Medicamentos y Productos Sanitarios Healthcare (2008) Centro de información online de medicamentos de la AEMPS - CIMA. https://cima.aemps.es/cima/publico/home.html
- Mangels AR (2014) "Bone nutrients for vegetarians." Am J Clin Nutr, 100, epub
- Davies NT (1979) "Anti-nutrient factors affecting mineral utilization." Proc Nutr Soc, 38, p. 121-8
cloNIDine food
Applies to: 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. Patients should also avoid driving or operating hazardous machinery until they know how the medications affect them.
References (10)
- Sternbach H (1991) "Fluoxetine-associated potentiation of calcium-channel blockers." J Clin Psychopharmacol, 11, p. 390-1
- Shook TL, Kirshenbaum JM, Hundley RF, Shorey JM, Lamas GA (1984) "Ethanol intoxication complicating intravenous nitroglycerin therapy." Ann Intern Med, 101, p. 498-9
- Feder R (1991) "Bradycardia and syncope induced by fluoxetine." J Clin Psychiatry, 52, p. 139
- Ellison JM, Milofsky JE, Ely E (1990) "Fluoxetine-induced bradycardia and syncope in two patients." J Clin Psychiatry, 51, p. 385-6
- Rodriguez de la Torre B, Dreher J, Malevany I, et al. (2001) "Serum levels and cardiovascular effects of tricyclic antidepressants and selective serotonin reuptake inhibitors in depressed patients." Ther Drug Monit, 23, p. 435-40
- Cerner Multum, Inc. "Australian Product Information."
- Pacher P, Kecskemeti V (2004) "Cardiovascular side effects of new antidepressants and antipsychotics: new drugs, old concerns?" Curr Pharm Des, 10, p. 2463-75
- Andrews C, Pinner G (1998) "Postural hypotension induced by paroxetine." BMJ, 316, p. 595
- (2023) "Product Information. Buprenorphine (buprenorphine)." G.L. Pharma UK Ltd
- (2023) "Product Information. Temgesic (buprenorphine)." Reckitt Benckiser Pty Ltd
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.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
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. | |
No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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