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Bioclavid (Augmentin)

Bioclavid is a prescription antibiotic medication. It's used to treat infections caused by bacteria. Bioclavid belongs to the penicillin class of antibiotics. Bioclavid contains two drugs: amoxicillin and clavulanic acid. Bioclavid is used in adults and children to treat the following infections: middle ear and sinus infections; respiratory tract infections; urinary tract infections; skin and soft tissue infections including dental infections; bone and joint infections.

Other names for this medication:
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Take Bioclavid exactly according to your doctor’s instructions. You might start to feel better before you finish your entire treatment. But even if you do feel better, don’t stop taking Bioclavid. In many cases, it’s important to finish the entire treatment to ensure that the infection does not come back.

If you’re feeling better and want to stop Bioclavid early, be sure to ask your doctor if it’s safe to do so.


Bioclavid is taken two or three times daily. If you take it twice daily, spread out the doses so that they’re roughly 12 hours apart. If you take it three times daily, spread out the doses so that they’re roughly eight hours apart.

Bioclavid XR is taken twice daily. Spread out the doses so that they’re about 12 hours apart.

Taking Bioclavid with food

You can take Bioclavid on an empty stomach or with a meal. Taking it with a meal may reduce stomach upset and help your body absorb the drug better.

You should take Bioclavid XR at the start of a meal. This increases the amount of medication your body absorbs and helps reduce stomach upset.

Can Bioclavid be crushed?

Bioclavid can be crushed. However, Bioclavid XR should not be crushed. If either type of tablet is scored (has an indented line across it), it can be split in half.

If you have trouble swallowing pills, ask your doctor or pharmacist about taking Bioclavid liquid suspension instead.

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Using an indirect estimation technique based on observed lung cancer mortality from 1931 to 2012, we estimated lifetime smoking prevalence and smoking-attributable mortality. These findings suggest previously unobserved roles for bile acids as physiologically relevant molecules targeting hypoxic tumour progression. Results of extensive evaluation of the proposed approach on three different retinal image datasets are reported, and used to highlight the promise in the presented strategy.

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