Drug Interactions between naloxegol and naloxone
This report displays the potential drug interactions for the following 2 drugs:
- naloxegol
- naloxone
Interactions between your drugs
naloxone naloxegol
Applies to: naloxone and naloxegol
GENERALLY AVOID: Concomitant use of peripherally-acting mu-opioid receptor antagonists, such as methylnaltrexone, naldemedine and naloxegol, with other opioid antagonists may result in additive pharmacologic effects and increased risk of opioid withdrawal. Symptoms consistent with opioid withdrawal including hyperhidrosis, chills, diarrhea, abdominal pain, nausea, vomiting, anxiety, irritability, increased lacrimation, rhinorrhea, and yawning have occurred in patients treated with peripherally-acting mu-opioid receptor antagonists. Patients with disruptions to the blood-brain barrier may be at increased risk.
MANAGEMENT: Concomitant use of peripherally-acting mu-opioid receptor antagonists with other opioid antagonists should generally be avoided.
References (3)
- (2008) "Product Information. Relistor (methylnaltrexone)." Wyeth Laboratories
- (2014) "Product Information. Movantik (naloxegol)." Astra-Zeneca Pharmaceuticals
- (2017) "Product Information. Symproic (naldemedine)." Shionogi USA Inc
Drug and food interactions
naloxegol food
Applies to: naloxegol
GENERALLY AVOID: Grapefruit juice may significantly increase the plasma concentrations of naloxegol. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. In pharmacokinetic studies, naloxegol systemic exposure (AUC) was increased approximately 3.5-fold by the moderate CYP450 3A4 inhibitor diltiazem and nearly 13-fold by the potent inhibitor ketoconazole. The interaction has not been studied with grapefruit juice. In general, the effect of grapefruit juice is concentration-, dose- and preparation-dependent, and can vary widely among brands. Certain preparations of grapefruit juice (e.g., high dose, double strength) have sometimes demonstrated potent inhibition of CYP450 3A4, while other preparations (e.g., low dose, single strength) have typically demonstrated moderate inhibition. Increased exposure to naloxegol may precipitate opioid withdrawal symptoms such as hyperhidrosis, lacrimation, rhinorrhea, chills, diarrhea, abdominal pain, anxiety, insomnia, irritability, restlessness, and yawning.
ADJUST DOSING INTERVAL: Food may increase the rate and extent of naloxegol absorption. When administered with a high-fat meal, naloxegol peak plasma concentration (Cmax) and systemic exposure (AUC) increased by approximately 30% and 45%, respectively. In clinical trials, naloxegol was given on an empty stomach approximately 1 hour prior to the first meal in the morning.
MANAGEMENT: Patients treated with naloxegol should avoid consumption of grapefruit and grapefruit juice. Naloxegol should be taken on an empty stomach at least 1 hour prior to the first meal of the day or 2 hours after the meal.
References (1)
- (2014) "Product Information. Movantik (naloxegol)." Astra-Zeneca Pharmaceuticals
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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