“Compound
The active ingredients of the drug are: magnesium citrate (Magnesii citras) and vitamin B6, i.e. pyridoxine hydrochloride (Pyridoxini hydrochloride).
1 film-coated tablet contains 60 mg of magnesium ions in the form of magnesium citrate and 6.06 mg of vitamin B6.
Excipients: tablet core: microcrystalline cellulose, crospovidone (type A), croscarmellose sodium, colloidal anhydrous silicon dioxide, magnesium stearate; tablet shell: polyvinyl alcohol, talc, titanium dioxide (E 171), glycerol monocaprylocaproate (type 1), sodium lauryl sulfate.
Dosage
Magnefar B6 Bio is used orally with meals.
If, despite using the drug for a month to compensate for magnesium deficiency, the symptoms do not subside, the use of the drug should be discontinued.
Age Body weight Dose of medication
from 6 to 14 years from 21 to 30 kg 3-4 tablets per day in several divided doses with meals
from 31 to 39 kg 4-5 tablets per day in several doses with meals
from 14 to 18 years 40 kg or more 5-6 tablets per day in several doses with meals
Adults 40 kg and more 5-6 tablets per day in several doses with meals
Action
Magnefar B6 Bio replenishes magnesium deficiency in the body. The preparation contains magnesium ions, which are necessary for many biochemical processes – magnesium cations are necessary for the activation of a number of enzymes. Magnesium also affects, among other things, heart muscle contractions and neuromuscular excitability.
The second active ingredient of Magnefar B6 Bio, that is, vitamin B6, is responsible for the absorption of magnesium citrate.
Indications
Magnefar B6 Bio is used in the treatment and prevention of magnesium deficiency, which can manifest itself in:
nervousness, irritability, mood swings, anxiety, temporary fatigue, lethargy, minor sleep disturbances,
fear,
muscle spasms, tingling, eyelid twitching.
Contraindications
When you should not use Magnefar B6 Bio:
if you are allergic to the active substances or any of the ingredients of the drug,
in people with hypermagnesemia (high levels of magnesium in the blood),
in patients with significant arterial hypotension, atrioventricular block, voluntary myasthenia.”
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