Naltrexone Hydrochloride 8mg + Bupropion Hydrochloride 90mg ER Tablets

Naltrexone Hydrochloride 8mg + Bupropion Hydrochloride 90mg ER Tablets are used with a reduced-calorie diet and increased physical activity for chronic weight management in eligible adults with obesity, or overweight adults with a weight-related condition.
Swallow extended-release tablets whole; do not cut, crush or chew them. The regimen is increased gradually to improve tolerability. Avoid high-fat meals because they increase drug exposure and seizure risk. Do not take another bupropion product or an opioid alongside this combination.
Bupropion and naltrexone act on hypothalamic appetite regulation and reward pathways involved in eating behavior and cravings.
Possible effects include nausea, constipation, headache, vomiting, dizziness, dry mouth, insomnia, anxiety, and raised blood pressure. Serious concerns include seizures, suicidal thoughts, severe hypertension, allergic reaction, angle-closure glaucoma, liver injury, and opioid withdrawal or overdose risk.
Do not use during pregnancy, with uncontrolled hypertension, seizure disorders, anorexia or bulimia, chronic opioid use, acute opioid withdrawal, another bupropion product, or an MAO inhibitor within the previous 14 days. Abrupt withdrawal from alcohol, benzodiazepines, barbiturates or antiepileptic medicines increases seizure risk. Tell your doctor about bipolar disorder, suicidal thoughts, glaucoma, kidney or liver disease, and diabetes medicines. Monitor blood pressure, pulse and mood.
May support clinically meaningful weight loss in selected patients by reducing appetite and reward-driven eating when lifestyle therapy continues.
Naltrexone 8mg + Bupropion HCL 90mg ER is used for chronic weight management in selected adults along with diet and physical activity.
Gradual titration helps reduce nausea and improves tolerability while reaching the target regimen.
It must not be used with a seizure disorder, anorexia or bulimia, uncontrolled hypertension, chronic opioid treatment or acute opioid withdrawal. Concurrent bupropion, recent MAO-inhibitor treatment and abrupt withdrawal of certain sedatives or alcohol are also contraindications.
Bupropion-containing medicines can affect mood and suicidal thoughts, especially after starting or dose changes.
No routine opioid use should be combined because naltrexone blocks opioids and can trigger withdrawal or complicate pain treatment.
Response is assessed after 12 weeks at the maintenance dose. Treatment is stopped if at least 5% of starting body weight has not been lost, because continued use is unlikely to give meaningful sustained benefit. This is 12 maintenance weeks, not 12 weeks including initial titration.
Extended release: gradual medicine release over time. BMI: body mass index, a measure relating weight to height. Maintenance dose: the ongoing dose after initial increases. Opioid blockade: prevention of opioid effects through receptor blocking. Seizure threshold: the level of stimulation at which a seizure can occur.; AR: Naltrexone 8mg + Bupropion HCL 90mg ER أقراص; FR: Naltrexone 8mg + Bupropion HCL 90mg ER comprimé; PT: Naltrexone 8mg + Bupropion HCL 90mg ER comprimido; ES: Naltrexone 8mg + Bupropion HCL 90mg ER tableta; RU: Naltrexone 8mg + Bupropion HCL 90mg ER таблетки; ID: Naltrexone 8mg + Bupropion HCL 90mg ER tablet; VI: Naltrexone 8mg + Bupropion HCL 90mg ER viên nén; MS: Naltrexone 8mg + Bupropion HCL 90mg ER tablet; TL: Naltrexone 8mg + Bupropion HCL 90mg ER tableta; ZH-SG: Naltrexone 8mg + Bupropion HCL 90mg ER 片剂
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Naltrexone Hydrochloride 8mg + Bupropion Hydrochloride 90mg ER Tablets