Roferon-A: Side Effects, Overdose and Pregnancy Information

Main ingredient in Roferon-A injection are interferon alfa-2a and interferon beta-1a. Interferons are small protein molecules that are produced by body in response to viral and other infections. Three major classes of interferons are alfa, beta and gamma. They are believed to enhance the immune system, causing it to attack infected or abnormal cells. Roferon-A is used to treat multiple sclerosis (MS). Roferon-A helps to reduce the frequency and severity of the relapses. Roferon-A is given by injection into a muscle once a week. Roferon-A is not effective in all people with MS and since it can have major side effects, it is recommended that all patients are evaluated by a neurologist before starting treatment.

ROFERON-A SIDE EFFECTS

Side effects of Roferon-A may include flu-like symptoms such as aches and pains, fever, chills, sweating, headache, fatigue and nausea. They tend to be worse at the start of treatment and improve with continued treatment, dry mouth and dry eyes. Rare side effects of Roferon-A include injection site reactions such as pain, redness or bruising, weakness, rigidity of muscles right after the injection, rash, pain in the muscles, joints, back or neck, muscle cramps or stiffness, heavy or irregular menstrual bleeding, dizziness, flushing, runny nose, appetite loss, diarrhea, insomnia, depression, under or overactive thyroid, confusion, seizures, and hair loss.

Roferon-A Warning and Caution

Treatment with Roferon-A should only be started by a physician specializing in MS.

Different injection site should be used each week.

Roferon-A can cause flu-like symptoms such as aches and pains, fever, chills, sweating, headache, fatigue and nausea. These tend to be worse at the start of treatment and improve with continued treatment.

Roferon-A has been associated with depression that can occur at any time during treatment.

Roferon-A has rarely been associated with liver problems and may decrease the number of blood cells in your blood.

Roferon-A should be used in with caution in seizure disorders, history of depression, heart disease, arrhythmias, decreased blood cell production by the bone marrow, causing lower than normal levels of blood cells in the blood, decreased kidney/liver function/disease, history of alcohol abuse, and overactive or underactive thyroid gland.

Roferon-A should not to be given to children under 12.

Roferon-A and Pregnancy

Roferon-A should not be used during pregnancy because it may be harmful to the fetus and may increase the risk of miscarriage.

Roferon-A passes into breast milk. Nursing mothers should switch to bottle-feed while taking Roferon-A.

Roferon-A Interaction

There may be an increased risk of side effects on the liver or blood cells if other drugs that can affect the liver or blood cells are used in combination with Roferon-A.

Roferon-A may increase the blood level of the following drugs:

Antiepileptic drugs

Certain antidepressants

Zidovudine

Roferon-A Overdose

In case of Roferon-A overdose, seek medical attention right away.