Примери за използване на Fampridine на Английски и техните преводи на Български
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The active substance is fampridine.
Fampridine has a narrow therapeutic index.
Prescription drugs listed.Substance:"Fampridine".
Fampridine is not a substrate for P-glycoprotein.
Fampyra 10 mg prolonged-release tablets fampridine.
Fampridine has a volume of distribution of approximately 2.6 l/kg.
If you are taking any other medicine containing fampridine.
Fampyra(fampridine)- Summary of product characteristics- N07XX07.
OCT2 is the transporter responsible for the active secretion of fampridine.
Treatment with fampridine increases seizure risk(see section 4.8).
Do not take Fampyra if you are taking any other medicine containing fampridine.
It is unknown whether fampridine is excreted in human or animal milk.
Concurrent treatment with other medicinal products containing fampridine(4-aminopyridine).
Fampyra(fampridine)- Conditions or restrictions regarding supply and use- N07XX07.
The active substance in Fampyra, fampridine, is a potassium channel blocker.
Fampridine is a lipid-soluble medicinal product which readily crosses the blood-brain barrier.
Assessment of symptomatic treatment with Fampridine in multiple sclerosis patients.
These clinical signs were not unexpected andrepresent exaggerated pharmacology of fampridine.
Fampridine is largely unbound to plasma proteins(bound fraction varied between 3-7% in human plasma).
Your doctor will consider the benefit of you being treated with fampridine against the risk to your baby.
Fampridine is eliminated mainly via the kidneys with active renal secretion accounting for about 60%(see section 5.2).
No pharmacological activity was found for the fampridine metabolites against selected potassium channels in vitro.
Fampridine is eliminated mainly via the kidneys with active renal secretion accounting for about 60%(see section 5.2).
Fampyra contains the active substance fampridine which belongs to a group of medicines called potassium channel blockers.
The clinical relevance of these findingsremains to be elucidated, but a causal relationship with fampridine treatment cannot be excluded.
In a battery of in vitro andin vivo studies fampridine did not show any potential to be mutagenic, clastogenic or carcinogenic.
Fampridine is metabolised in humans by oxidation to 3-hydroxy-4-aminopyridine and further conjugated to the 3-hydroxy-4-aminopyridine sulfate.
Concurrent treatment with other medicinal products containing fampridine(4-aminopyridine) is contraindicated(see section 4.3).
Baclofen: fampridine has been administered concomitantly with baclofen and no pharmacokinetic medicinal product interactions were observed.
There is no evidence of clinically relevant accumulation of fampridine taken at the recommended dose in patients with full renal function.