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Budeprion XL and Rebif Rebidose

Determining the interaction of Budeprion XL and Rebif Rebidose and the possibility of their joint administration.

Check result:
Budeprion XL <> Rebif Rebidose
Relevance: 25.11.2022 Reviewer: Shkutko P.M., M.D., in

In the database of official manuals used in the service creation an interaction registered by statistical results of studies was found, which can either lead to negative consequences for the patient health or strengthen a mutual positive effect. A doctor should be consulted to address the issue of joint drug administration.

Consumer:

Using buPROPion together with interferon beta-1a can increase the risk of seizures and liver injury. This may be more likely to occur in older adults or those with a history of seizures or liver problems. Risk factor for seizures are: head trauma, excessive use of alcohol or sedatives, addiction to opiates, cocaine, or stimulants, severe liver cirrhosis, and diabetes. Call your doctor if you have symptoms of seizures, muscle stiffness, hallucinations, fainting, fast or uneven heartbeat, shallow breathing, or heart failure. If your doctor prescribes these medications together, you may need a dose adjustment or special tests to safely take both medications. You should be advised to notify your doctor if you experience signs and symptoms of liver problems such as fever, rash, loss of appetite, nausea, vomiting, fatigue, right upper back pain, dark urine, and jaundice (yellow skin). If liver injury is suspected, interferon beta-1a therapy should be stopped. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.

Professional:

MONITOR CLOSELY: The use of bupropion is associated with a dose-related risk of seizures. The estimated incidence of seizures is approximately 0.1% at dosages up to 300 mg/day and 0.4% at dosages between 300 to 450 mg/day, but increases almost tenfold between 450 mg and 600 mg/day. The risk may also be increased during coadministration of bupropion with other potentially epileptogenic agents such as interferons.

MONITOR CLOSELY: Coadministration of beta interferons with other agents known to induce hepatotoxicity may potentiate the risk of liver injury. Use of beta interferons has been associated with rare cases of liver injury, including autoimmune hepatitis and severe liver damage leading to hepatic failure, some of which required transplantation. In some cases, these events have occurred in the presence of other drugs that have been associated with hepatic injury. Symptoms of liver dysfunction typically began from 1 to 6 months following the initiation of therapy. Asymptomatic elevation of hepatic transaminases (particularly SGPT) have also been reported but is common with interferon therapy.

MANAGEMENT: Caution is advised if bupropion is administered with beta interferons, particularly in the elderly and in patients with a history of seizures or other risk factors for seizures (e.g., head trauma; brain tumor; severe hepatic cirrhosis; metabolic disorders; CNS infections; excessive use of alcohol or sedatives; addiction to opiates, cocaine, or stimulants; diabetes treated with oral hypoglycemic agents or insulin). The manufacturer recommends a lower initial dosage of bupropion and gradual dosage increments in patients receiving concurrent treatment with other potentially epileptogenic drugs. The total dose of bupropion should generally not exceed 450 mg/day (or 150 mg every other day in patients with severe hepatic cirrhosis). Bupropion should be discontinued and not restarted in patients who experience a seizure during treatment.

The risk of hepatic injury should also be considered with this combination. Liver function tests should be monitored at regular intervals and the interferon dosage reduced if SGPT rises above 5 times the upper limit of normal. The dosage may be gradually re-escalated when enzyme levels return to normal. Patients should be advised to notify their physician if they experience signs and symptoms of hepatotoxicity such as fever, rash, anorexia, nausea, vomiting, fatigue, right upper quadrant pain, dark urine, and jaundice. If liver injury is suspected, interferon therapy should be promptly discontinued due to the potential for rapid progression to liver failure.

References
  • "Product Information. Wellbutrin (bupropion)." Glaxo Wellcome, Research Triangle Park, NC.
  • "Product Information. Betaseron (interferon beta-1b)." Berlex, Richmond, CA.
  • "Product Information. Avonex (interferon beta-1a)." Biogen, Cambridge, MA.
  • "Product Information. Rebif (interferon beta-1a)." Serono Laboratories Inc, Norwell, MA.
Budeprion XL

Generic Name: bupropion

Brand name: Aplenzin, Budeprion XL, Forfivo XL, Wellbutrin XL, Buproban, Wellbutrin SR, Zyban, Zyban Advantage Pack

Synonyms: n.a.

Rebif Rebidose

Generic Name: interferon beta-1a

Brand name: Rebif, Rebif Rebidose, Rebif Rebidose Titration Pack, Rebif Titration Pack, Avonex, Avonex Prefilled Syringe, Avonex Pen

Synonyms: n.a.

In the course of checking the drug compatibility and interactions, data from the following reference sources was used: Drugs.com, Rxlist.com, Webmd.com, Medscape.com.

Interaction with food and lifestyle
Disease interaction