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Albenza

Last reviewed on RxList: 4/3/2017
Albenza Side Effects Center

Last reviewed on RxList 9/28/2016

Albenza (albendazole) is a broad spectrum anthelmintic, or anti-worm medication used to treat certain infections caused by worms such as pork tapeworm and dog tapeworm. Common side effects of Albenza include:

  • nausea,
  • vomiting,
  • stomach and abdominal pain,
  • headache,
  • dizziness, or
  • temporary hair loss.

Tell your doctor if you have serious side effects of Albenza including:

  • vision changes,
  • yellowing eyes or skin,
  • severe stomach or abdominal pain,
  • dark urine,
  • unusual tiredness,
  • easy bruising or bleeding,
  • signs of infection (e.g., fever, persistent sore throat),
  • changes in the amount of urine,
  • severe or persistent headache,
  • seizures,
  • confusion, or
  • very stiff neck.

Dosing of Albenza varies, depending upon which parasitic infection is being treated. Albenza may interact with other medications including antibiotics, cimetidine, dexamethasone, praziquantel, or theophylline. Tell your doctor all medications you are taking. During pregnancy, Albenza should be used only when prescribed. It may harm a fetus. Women of child-bearing age should have a negative pregnancy test before starting this medication. If you become pregnant, tell your doctor immediately. It is recommended that men and women use 2 effective forms of birth control (e.g., condoms and birth control pills) while taking Albenza and for 1 month after stopping the medication. It is not known if Albenza passes into breast milk. Consult your doctor before breastfeeding.

Our Albenza (albendazole) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Albenza Consumer Information

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have any of these serious side effects:

  • easy bruising or bleeding, unusual weakness;
  • fever, sore throat, and headache with a severe blistering, peeling, and red skin rash; or
  • fever with chills, body aches, or flu-like symptoms.

Less serious side effects may include:

  • stomach pain;
  • nausea, vomiting;
  • headache, dizziness; or
  • temporary hair loss.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may report side effects to FDA at 1-800-FDA-1088.

Read the entire detailed patient monograph for Albenza (Albendazole)

Albenza Professional Information

SIDE EFFECTS

Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

The adverse reaction profile of ALBENZA differs between hydatid disease and neurocysticercosis. Adverse reactions occurring with a frequency of 1% or greater in either disease are described in Table 2 below.

These symptoms were usually mild and resolved without treatment. Treatment discontinuations were predominantly due to leukopenia (0.7%) or hepatic abnormalities (3.8% in hydatid disease). The following incidence reflects adverse reactions that were reported to be at least possibly or probably related to ALBENZA.

Table 2: Adverse Reaction Incidence 1% or Greater in Hydatid Disease and Neurocysticercosis

Adverse Reaction Hydatid Disease Neurocysticercosis
Gastrointestinal
Abdominal Pain 6 0
Nausea 4 6
Vomiting 4 6
General disorders and administration site conditions
Fever 1 0
Investigations
Elevated Hepatic Enzymes 16 less than 1
Nervous system disorders
Dizziness 1 less than 1
Headache 1 11
Meningeal Signs 0 1
Raised Intracranial Pressure 0 2
Vertigo 1 less than 1
Skin and subcutaneous tissue disorders
Reversible Alopecia 2 less than 1

The following adverse events were observed at an incidence of less than 1%:

Blood and Lymphatic System Disorders: There have been reports of leukopenia, granulocytopenia, pancytopenia, agranulocytosis, or thrombocytopenia [see WARNINGS AND PRECAUTIONS].

Immune System Disorders: Hypersensitivity reactions, including rash and urticaria.

Postmarketing Experience

The following adverse reactions have been identified during post-approval use of ALBENZA. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Blood and Lymphatic System Disorders: Aplastic anemia, bone marrow suppression, neutropenia.

Eye Disorders: Vision blurred.

Gastrointestinal Disorders: Diarrhea.

General System Disorders: Asthenia.

Hepatobiliary Disorders: Elevations of hepatic enzymes, hepatitis, acute liver failure.

Musculoskeletal and Connective Tissue Disorders: Rhabdomyolysis.

Nervous System Disorders: Somnolence, convulsion.

Renal and Urinary Disorders: Acute renal failure.

Skin and Subcutaneous Tissue Disorders: Erythema multiforme, Stevens-Johnson syndrome.

Read the entire FDA prescribing information for Albenza (Albendazole)

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© Albenza Patient Information is supplied by Cerner Multum, Inc. and Albenza Consumer information is supplied by First Databank, Inc., used under license and subject to their respective copyrights.

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