Baclofen
Appearance
Baclofen
Lioresal (oral, intrathecal pump), Ozobax / Fleqsuvy (oral suspension), Gablofen (intrathecal), Lyvispah (oral granules)
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Summary
Common uses
Spasticity in multiple sclerosis (FDA, oral and intrathecal)0, Spasticity in spinal cord injury (FDA, oral and intrathecal)0, Cerebral palsy spasticity (FDA intrathecal; off-label oral)0, Alcohol use disorder (off-label, evidence-supported, generally third-line)0, Persistent hiccups (off-label)0, GERD with esophageal motility dysfunction (off-label)0, Trigeminal neuralgia adjunct (off-label)0
Pharmacy
Starting dose
Oral: 5 mg PO TID, titrate by 5 mg per dose every 3 days. Intrathecal: bolus test dose, then continuous infusion via implanted pump
Preparations
Tablets 5, 10, 20 mg; oral suspension 5 mg/5 mL (Ozobax, Fleqsuvy); intrathecal injection 50, 500, 1000, 2000 mcg/mL (Lioresal Intrathecal, Gablofen); oral granules (Lyvispah)
US FDA Max
80 mg/day oral (higher off-label)
Pharmacology
Routes
Oral, intrathecal (via implanted infusion pump)
Onset
1-2 hours (oral)
Duration
4-6 hours (oral, TID-QID dosing)
Half-life
3-4 hours[1]
Bioavailability
~70-85% (oral)[1]
Pregnancy
Limited human data.[citation needed]
Purported mechanism
Selective agonist at the GABA-B receptor (the only metabotropic GABA receptor; distinct from the ionotropic GABA-A targeted by benzodiazepines and Z-class hypnotics). Reduces excitatory neurotransmitter release presynaptically and hyperpolarizes postsynaptic membranes, producing antispastic effect particularly at spinal cord interneurons.0 Severe withdrawal syndrome is the marquee adverse-event concern, especially with abrupt cessation of intrathecal administration: hyperthermia, altered mental status, hyperreflexia, rhabdomyolysis, and multiorgan failure can develop within 24-72 hours and progress to death. Gradual taper is essential after extended use; intrathecal pump failures are a recognized emergency[1].
References
- ↑ 1.0 1.1 1.2 1.3 FDA Prescribing Information, Lioresal (baclofen), Saol Therapeutics/Novartis, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/017851s019lbl.pdf