Library

Баклофен

Baclofen is a depressant and muscle relaxant of the butyric acid class that acts as a GABA-B receptor agonist. Originally synthesized in 1962 to treat epilepsy, it proved ineffective for that purpose but was later approved in 1977 for managing muscle spasticity. Chemically related to phenibut, pregabalin, and gabapentin, it produces sedation, anxiety suppression, and moderate euphoria. It has also been researched as a potential treatment for alcohol dependence.

Баклофен molecular structure
Баклофен molecular structure diagram from the DrugsPRO substance library.

Also known as: Liofen, Ozobax, Kemstro, Lioresal, Gablofen

Classification

  • Chemical: Gabapentinoid
  • Chemical: Medicine
  • Psychoactive: Depressant
  • Tag: Anxiolytic
  • Tag: Butyric acid
  • Tag: GABA analogue
  • Tag: GABAergic
  • Tag: Habit-Forming
  • Tag: Muscle Relaxant
  • Tag: Pharmaceutical
  • Tag: Sedative

Effects

  • Respiratory Depression
  • Sedation
  • Muscle Relaxation
  • Physical Fatigue
  • Nausea
  • Headache
  • Anxiety Suppression
  • Euphoria
  • Memory Suppression
  • Focus Suppression
  • Motor Control Loss
  • Dizziness
  • Dulled Perception
  • Disinhibition
  • Increased Libido
  • Spatial Disorientation
  • Dehydration
  • Open Eye Visuals

Routes of Administration

Oral

Dosage

  • Heavy: 75-125 mg
  • Light: 5 – 20 mg
  • Common: 20 – 50 mg
  • Strong: 50 – 75 mg
  • Threshold: 5 mg

Duration

  • Onset: 0.25-1.25 h
  • Comeup: 1-1.5 h
  • Peak: 1-2 h
  • Offset: 1.5-2.5 h
  • After Effects: 6-12 h

Harm Reduction

Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.

Sources

Substance data is aggregated from the following public harm-reduction and reference sources.

Links

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Baclofen - DrugsPRO ръководство за вещества

Baclofen: Baclofen is a depressant and muscle relaxant of the butyric acid class that acts as a GABA-B receptor agonist. Originally synthesized in 1962 to treat epilepsy, it proved ineffective for that purpose but was later approved in 1977 for managing muscle spasticity. Chemically related to pheni

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