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Albenza Side Effects Center
Medical Editor: John P. Cunha, DO, FACOEP
Albenza (albendazole) is used to treat certain infections caused by worms such as pork tapeworm and dog tapeworm. Albenza is a broad spectrum anthelmintic, or anti-worm medication. Common side effects include nausea, vomiting, abdominal pain, headache, or temporary hair loss.
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 breast-feeding.
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.
What is Patient Information in Detail?
Easy-to-read and understand detailed drug information and pill images for the patient or caregiver from Cerner Multum.
Albenza in Detail - Patient Information: Side Effects
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)
What is Patient Information Overview?
A concise overview of the drug for the patient or caregiver from First DataBank.
Albenza Overview - Patient Information: Side Effects
Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.
Tell your doctor right away if you have any serious side effects, including: vision changes, yellowing eyes/skin, severe stomach/abdominal pain, dark urine, unusual tiredness, easy bruising/bleeding, signs of infection (e.g., fever, persistent sore throat), change in the amount of urine, severe/persistent headache, seizures, confusion, very stiff neck.
A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.
This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.
In the US -
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.
Read the entire patient information overview for Albenza (Albendazole)
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
Albenza FDA Prescribing Information: Side Effects
The adverse event profile of albendazole differs between hydatid disease and neurocysticercosis. Adverse events occurring with a frequency of ≥ 1% in either disease are described in the table 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 events that were reported by investigators to be at least possibly or probably related to albendazole.
Adverse Event Incidence ≥ 1% in Hydatid Disease and Neurocysticercosis
|Adverse Event||Hydatid Disease||Neurocysticercosis|
|Abnormal Liver Function Tests||15.6||< 1.0|
|Raised Intracranial Pressure||0||1.5|
|Reversible Alopecia||1.6||< 1.0|
The following adverse events were observed at an incidence of < 1%:
Blood and Lymphatic System Disorders: Leukopenia. There have been rare reports of granulocytopenia, pancytopenia, agranulocytosis, or thrombocytopenia (see WARNINGS). Patients with liver disease, including hepatic echinococcosis, appear to be more at risk of bone marrow suppression (see WARNINGS and PRECAUTIONS).
Postmarketing Adverse Reactions: In addition to adverse events reported from clinical trials, the following events have been identified during world-wide post-approval use of ALBENZA (albendazole) . Because they are reported voluntarily from a population of unknown size, estimates of frequency cannot be made. These events have been chosen for inclusion due to a combination of their seriousness, frequency of reporting, or potential causal connection to ALBENZA (albendazole) .
Blood and Lymphatic System Disorders: Aplastic anemia, bone marrow suppression, neutropenia.
Renal and Urinary Disorders: Acute renal failure.
Read the entire FDA prescribing information for Albenza (Albendazole)
Additional Albenza Information
Albenza - User Reviews
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Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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