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Intron
A and Roferon A
What Is Interferon Alfa?
Which Patients with Hepatitis
B Should Use Interferon?
What Are the Doses
Used?
What Are the Side Effects
of Treatment?
Intron
A Prescribing Information 
| WARNING
- Alpha interferons, including INTRON® A, cause
or aggravate fatal or life-threatening neuropsychiatric,
autoimmune, ischemic, and infectious disorders. Patients
should be monitored closely with periodic clinical and
laboratory evaluations. Patients with persistently severe
or worsening signs or symptoms of these conditions should
be withdrawn from therapy. In many but not all cases these
disorders resolve after stopping INTRON A therapy. |

What
Is Interferon Alfa?

Natural
interferon is a protein produced by the body's cells in response
to viral infections. There are three types: alfa, beta and
gamma. Commercially-produced (genetically-engineered) interferon
alfa mimics the activity of naturally-occuring interferon
alfa produced by the body, although the mechanism of action
of the drug is not well understood.
Intron A (interferon alfa-2b) is one commercial form of interferon
approved by the US Food and Drug Administration for the treatment
of Hepatitis B and C.
Roferon A (interferon alfa-2a), and Infergen ("consensus"
interferon) are also FDA-approved for treatment of chronic
hepatitis C, but not for chronic hepatitis B.
Which Patients with Hepatitis B Should Use Interferon?

Less
than 50% of patients with chronic hepatitis B infection are
eligible for interferon therapy. Patients should have infection
documented for at least six months, elevated liver enzymes
(AST or SGOT, and ALT or SGPT tests) and an actively replicating
virus in their blood (hepatitis "e" antigen [HBeAg]
and/or hepatitis B virus DNA [HBV DNA] positive tests).
Patients with normal liver enzymes are less likely to respond
to therapy. Patients with low hepatitis B virus DNA levels
and elevated liver enzymes are more likely to benefit than
those with high HBV DNA levels.
A biopsywhere a needle is inserted into the liver to
obtain a small sample of tissueis helpful to determine
liver damage prior to treatment. Patients with acute infection,
cirrhosis or other
major medical problems should not be treated.
What
Are the Doses Used?

The FDA-approved dose of standard interferon alfa for treatment
of hepatitis. FDA-approved treatment for hepatitis B is five
million units daily for 16 weeks. The dose may be modified
for significant side effects.
However, lower doses may result in lower rates of response.
Higher doses, more frequent doses, longer therapy, and combination
therapies are being tested.
What
Are the Side Effects of Treatment?

The most common serious side effect is depression,
particularly in patients with a prior history. Most patients
will have muscle aches, fatigue and low grade fevers. These
can be minimized by taking low doses of acetaminophen (e.g.
Tylenol) at night. Nausea and diarrhea are common as is irritation
of the skin at the injection site.
Patients may experience significant weight loss, and if this
occurs the dose should be adjusted. Patients often complain
of irritability and headaches. A small number of patients
may develop thyroid disease.
Normal thyroid function should be documented prior to treatment.
Hair loss is not uncommon, but usually reversible. Few side
effects are severe or persist after treatment.
When
Is Treatment Not Indicated?

Patients with chronic hepatitis B or C, with fluid
in the abdomen (ascites), bleeding from dilated veins in the
esophagus (variceal bleeding), or mental confusion (encephalopathy)
should be treated only in a clinical trial.
Others not suitable for treatment are those with symptomatic
heart, lung or kidney disease, with human immunodeficiency
virus (HIV) infection or organ transplant recipients on prednisone,
cyclosporine and FK-506 and patients on antidepressants or
with a history of suicide attempts.
Interferon should not be given to women considering pregnancy,
nor to the intended father. Patients with active substance
abuse (alcohol or illegal drugs) should not be offered this
therapy.
What
Can Be Expected from Treatment?

Approximately
40%-50% of patients with chronic hepatitis C receiving full
dose therapy will have a normalization of their liver enzymes,
usually by the third month. With normal liver tests, the virus
may become undetectable in blood. If no response is seen by
three months, most researchers advocate stopping therapy.
A few patients who respond to therapy may see their liver
enzymes rise towards the end of treatment. The reason for
this is unknown. When interferon is stopped after six months,
more than half of the patients with hepatitis C who have responded
will experience a rise in their liver tests. Patients will
usually respond again if given further therapy. Therefore,
10%-15% will have a long lasting positive response. Longer
treatments will likely result in longer positive responses.
However, there is no evidence that this affects the relapse
rate when treatment is stopped. Few patients will eradicate
the virus using this therapy alone.
What
Happens if Interferon Is Not Given?

The
long term prognosis of hepatitis C is poorly understood. However,
hepatitis C is generally a slowly progressive disease, with
evolution over years if not decades. There is no proof that
six months of treatment with interferon alters this.
The changes vary from mild chronic hepatitis (least amount
of liver damage) to moderate or severely active chronic hepatitis,
with or without fibrosis or cirrhosis (most amount of liver
scar damage). It is not known who will develop complications
including chronic liver disease, liver failure and liver cancer.
What New Drugs Are Available?

Much
is unknown about treatment with interferon. Therefore, when
possible, patients should consider participating in clinical
trials.
Different kinds of interferons and other new drugs, by themselves
or in combination with other drugs, are being evaluated for
both hepatitis B and C.
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