"The U.S. Food and Drug Administration today approved Orbactiv (oritavancin), a new antibacterial drug to treat adults with skin infections.
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Eurax Side Effects Center
Medical Editor: John P. Cunha, DO, FACOEP
Eurax (crotamiton) topical is a scabicide used to treat scabies and to reduce itching associated with certain conditions. Eurax is available in generic form. Serious side effects of Eurax are not likely to occur. Common side effects of Eurax include itching, burning, or stinging upon application, or worsening skin irritation (such as itching, redness).
To treat scabies, thoroughly massage into the skin of the whole body from the chin down, paying attention to all folds and creases. Apply a second dose 24 hours later. Clothing and bed linen should be changed the next morning. A cleansing bath should be taken 48 hours after the last application. To treat pruritus (itch), apply as recommended by your doctor. Do not apply other topical preparations to the affected area during treatment with Eurax topical. Other drugs may also interact with Eurax topical. Tell your doctor all medications you use. During pregnancy, Eurax should be used only when prescribed. It is unknown if this drug passes into breast milk. Consult your doctor before breast-feeding.
Our Eurax (crotamiton) 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.
Eurax in Detail - Patient Information: Side Effects
Serious side effects are not likely to occur. Stop using crotamiton topical and seek emergency medical attention if you experience an allergic reaction (shortness of breath; closing of your throat; swelling of your lips, face, or tongue; or hives).
Mild itching, burning, or stinging may occur upon application.
Notify your doctor if your condition worsens or if unusual itching, redness, swelling, burning, or a rash occurs.
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.
Read the entire detailed patient monograph for Eurax (Crotamiton Cream, Lotion)
What is Patient Information Overview?
A concise overview of the drug for the patient or caregiver from First DataBank.
Eurax 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.
A very serious allergic reaction to this drug is rare. However, seek immediate medical attention 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 Eurax (Crotamiton Cream, Lotion)
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
Eurax FDA Prescribing Information: Side Effects
Additional Eurax Information
Eurax - User Reviews
Eurax 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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