Actimmune

Side Effects
Interactions

SIDE EFFECTS

The following data on adverse reactions are based on the subcutaneous administration of ACTIMMUNE (interferon gamma 1 b) at a dose of 50 mcg/m2, three times weekly, in patients with Chronic Granulomatous Disease (CGD) during an investigational trial in the United States and . Europe.

The most common adverse events observed in patients with CGD are shown in the following table:

  Percent of Patients
Clinical Toxicity ACTIMMUNE (interferon gamma 1 b)
CGD
(n=63)
Placebo
CGD (n=65)
Fever 52 28
Headache 33 9
Rash 17 6
Chills 14 0
Injection site erythema
or tenderness
14 2
Fatigue 14 11
Diarrhea 14 12
Vomiting 13 5
Nausea 10 2
Myalgia 6 0
Arthralgia 2 0
Injection site pain 0 2

Miscellaneous adverse events which occurred infrequently in patients with CGD and may have been related to underlying disease included back pain (2 percent versus 0 percent), abdominal pain (8 percent versus 3 percent) and depression (3 percent versus 0 percent) for ACTIMMUNE (interferon gamma 1 b) and placebo treated patients, respectively.

Similar safety data were observed in 34 patients with severe malignant osteopetrosis.

ACTIMMUNE (interferon gamma 1 b) has also been evaluated in additional disease states in studies in which patients have generally received higher doses ( > 100 mcg/m2/three times weekly) administered by intramuscular or subcutaneous injection, or intravenous infusion. All of the previously described adverse reactions which occurred in patients with Chronic Granulomatous Disease have also been observed in patients receiving higher doses. Adverse reactions not observed in patients with Chronic Granulomatous Disease but reported in patients receiving ACTIMMUNE (interferon gamma 1 b) (Interferon gamma-1b) in other studies include:

Cardiovascular- hypotension, syncope, tachyarrhythmia, heart block, heart failure, and myocardial infarction. Central Nervous System-confusion, disorientation, gait disturbance, Parkinsonian symptoms, seizure, hallucinations, and transient ischemic attacks.Gastrointestinal-hepatic insufficiency, gastrointestinal bleeding, and pancreatitis, including pancreatitis with fatal outcome. Hematologic-deep venous thrombosis and pulmonary embolism. Immunological- increased autoantibodies, lupus-like syndrome. Metabolic- hyponatremia, hyperglycemia and hypertriglyceridemia. Pulmonary-tachypnea, bronchospasm, and interstitial pneumonitis. Renal-reversible renal insufficiency. Other- chest discomfort, exacerbation of dermatomyositis.

Abnormal Laboratory Test Values: Elevations of ALT and AST, neutropenia, thrombocytopenia, and proteinuria have been observed (see WARNINGS and PRECAUTIONS: Laboratory Tests).

No neutralizing antibodies to ACTIMMUNE (interferon gamma 1 b) have been detected in any Chronic Granulomatous Disease patients receiving ACTIMMUNE (interferon gamma 1 b) .

Post-Marketing Experience

Children with CGD less than 3 years of age

Data on the safety and activity of ACTIMMUNE (interferon gamma 1 b) in 37 patients under the age of 3 years was pooled from four uncontrolled post-marketing studies. The rate of serious infections per patient-year in this uncontrolled group was similar to the rate observed in the ACTIMMUNE (interferon gamma 1 b) treatment groups in controlled trials. Developmental parameters (height, weight and endocrine maturation) for this uncontrolled group conformed to national normative scales before and during ACTIMMUNE (interferon gamma 1 b) therapy.

In 6 of the 10 patients receiving ACTIMMUNE (interferon gamma 1 b) therapy before age one year 2-fold to 25- fold elevations from baseline of AST and/or ALT were observed. These elevations occurred as early as 7 days after starting treatment. Treatment with ACTIMMUNE (interferon gamma 1 b) was interrupted in all 6 of these patients and was restarted at a reduced dosage in 4. Liver transaminase values returned to baseline in all patients and transaminase elevation recurred in one patient upon ACTIMMUNE (interferon gamma 1 b) rechallenge. An 11-fold alkaline phosphatase elevation and hypokalemia in one patient and neutropenia (ANC= 525 cells/mm3) in another patient resolved with interruption of ACTIMMUNE (interferon gamma 1 b) treatment and did not recur with rechallenge.

In the post-marketing safety database clinically significant adverse events observed during ACTIMMUNE (interferon gamma 1 b) therapy in children under the age of three years (n=14) included: two cases of hepatomegaly, and one case each of Stevens-Johnson syndrome, granulomatous colitis, urticaria, and atopic dermatitis.

Read the Actimmune (interferon gamma 1 b) Side Effects Center for a complete guide to possible side effects

DRUG INTERACTIONS

interactions between ACTIMMUNE (interferon gamma 1 b) and other drugs have not been fully evaluated. Caution should be exercised when administering ACTIMMUNE (interferon gamma 1 b) in combination with other potentially myelosuppressive agents (see WARNINGS).

Preclinical studies in rodents using species-specific interferon-gamma have demonstrated a decrease in hepatic microsomal cytochrome P-450 concentrations. This could potentially lead to a depression of the hepatic metabolism of certain drugs that utilize this degradative pathway.

Read the Actimmune Drug Interactions Center for a complete guide to possible interactions

Last reviewed on RxList: 2/19/2008
This monograph has been modified to include the generic and brand name in many instances.

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