Peginterferon Beta-1a Side Effects
Medically reviewed by Drugs.com. Last updated on Dec 28, 2023.
Applies to peginterferon beta-1a: solution.
Serious side effects
Along with its needed effects, peginterferon beta-1a may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following side effects occur while taking peginterferon beta-1a:
More common
- blue-green to black skin discoloration
- chills
- cough
- diarrhea
- dizziness
- extremely high fever or body temperature
- fast, shallow breathing
- fast, weak heartbeat
- fever
- general feeling of discomfort or illness
- joint pain
- muscle aches, cramps, and pains
- pale, clammy skin
- runny nose
- seizures
- shivering
- sore throat
- sweating
- thirst
- trouble sleeping
- unusual tiredness or weakness
- vomiting
Less common
- dark urine
- decreased appetite
- itching skin
- light-colored stools
- stomach pain
- yellow eyes or skin
Rare
- chest tightness
- difficulty with swallowing
- hives or welts, skin rash
- large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or genitals
- puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue
- redness of the skin
Other side effects
Some side effects of peginterferon beta-1a may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
More common
- difficulty with moving
- itching, rash, redness, soreness, swelling, or warmth at the injection site
- lack or loss of strength
- muscle aches, cramps, pains, or stiffness
- pain, redness, or sloughing of the skin at the injection site
For healthcare professionals
Applies to peginterferon beta-1a: intramuscular solution, subcutaneous kit, subcutaneous solution.
General
The most common side effects were injection site erythema, influenza-like illness, pyrexia, headache, myalgia, chills, injection site pain, asthenia, injection site pruritus, and arthralgia.[Ref]
Dermatologic
Gastrointestinal
Cardiovascular
- Frequency not reported: Congestive heart failure[Ref]
Hematologic
- Frequency not reported: Decreased peripheral blood counts[Ref]
Hepatic
- Common (1% to 10%): Alanine aminotransferase increased, aspartate aminotransferase increased, gamma-glutamyl-transferase increased
- Frequency not reported: hepatic injury[Ref]
Hypersensitivity
- Uncommon (0.1% to 1%): Anaphylaxis, angioedema, urticaria[Ref]
Immunologic
- Very common (10% or more): Influenza like illness (47%)
- Frequency not reported: Autoimmune disorders[Ref]
Local
- Very common (10% or more): Injection site erythema (62%), injection site pain (15%), injection site pruritus (13%)
- Common (1% to 10%): Injection site edema, injection site warmth, injection site hematoma, injection site rash[Ref]
Musculoskeletal
- Very common (10% or more): Myalgia (19%), arthralgia (11%)[Ref]
Nervous system
- Very common (10% or more): Headache (44%)
- Uncommon (0.1% to 1%): Seizures[Ref]
Other
- Very common (10% or more): Pyrexia (45%), chills (17%), asthenia (13%)
- Common (1% to 10%): Hyperthermia, pain[Ref]
Psychiatric
- Common (1% to 10%): Depression, suicide[Ref]
References
1. (2014) "Product Information. Plegridy (peginterferon beta-1a)." Biogen Idec Inc
Frequently asked questions
- What are the new drugs used for multiple sclerosis (MS)?
- What is Plegridy used for and is it an immunosuppressant?
- How do you use the Plegridy pen and where do you inject?
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Further information
Peginterferon beta-1a side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.