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Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
By mouth
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only)
Pharmacokinetic data
Bioavailability100% (oral)
Elimination half-life10 hours
CAS Number
PubChem CID
ECHA InfoCard100.012.357 Edit this at Wikidata
Chemical and physical data
Molar mass602.63 g·mol−1
3D model (JSmol)
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Lymecycline is a tetracycline broad-spectrum antibiotic marketed by the pharmaceutical company Galderma. It is approximately 5,000 times more soluble than tetracycline base and is unique amongst tetracyclines in that it is absorbed by an active transport process across the intestinal wall, making use of the same fast and efficient mechanism by which carbohydrates are absorbed.[1]

The greater absorption of lymecycline allows for lower dosages to be used; the standard dose of 408 mg is equivalent to 300 mg tetracycline base and, in its action, to 500 mg tetracycline hydrochloride. Lymecycline, unlike tetracycline hydrochloride, is soluble at all physiological pH values.


Lymecycline was released into the pharmaceutical market in 1963.


Lymecycline, like other tetracyclines, is used to treat a range of infections. Its better absorption profile makes it preferable to tetracycline for moderately severe acne and typically prescribed for 8 weeks at a time, but alternatives should be sought if no improvement occurs by 3 months.[2]

Lymecycline capsules

Side effects[edit]

Lymecycline's side effects can include rash, headache, diarrhoea, nausea, vomiting, dermatitis, dysphasia, inflammation of the liver, hypersensitive reactions, and visual disturbances. When taken for a long period of time, it can cause reflux oesophagitis.[3]


  1. ^ New Zealand Datasheet Archived 2006-03-03 at the Wayback Machine August 2003
  2. ^ British National Formulary 45 March 2003
  3. ^ Dr Wang, Peter. "Side effects of Tetralysal". Retrieved 23 March 2011.

See also[edit]