Sulbutiamine

Each coated tablet also contains the following excipients: Maize starch, starch, anhydrous glucose, lactose monohydrate, magnesium stearate, talc, sodium hydrogen carbonate, carmellose sodium, white beeswax, titanium dioxide (E171), ethylcellulose, sunset yellow FCF (E110) aluminium lake, glycerol mono-oleate, polysorbate 80, povidone, saccharose, anhydrous colloidal silica (Aerosil 130).

Symptomatic treatment of all forms of functional asthenia, eg: Physical and intellectual overwork; memory disorders, difficulty in concentration; fatigue not overcome by rest; decreased intellectual efficiency and lucidity especially in the elderly.

FOR ADULT USE ONLY

2 to 3 tablets daily.

Duration of Treatment: Limited to 4 weeks.

Administration: Tablets should be swallowed whole with a large glass of water, dividing the doses between the morning and midday meals.

Previous history of allergy to Sulbutiamine or to any of the ingredients of Sulbutiamine.

Due to the presence of lactose, Sulbutiamine should not be used in the case of galactosemia, malabsorption syndrome of glucose and galactose, or a deficiency in lactase (rare metabolic diseases).

No drug interactions have been reported. Sulbutiamine can be combined with other drugs.

See also:
What are the possible side effects of Sulbutiamine?

Like any active substance, Sulbutiamine may induce unpleasant effects of varying severity in some individuals: Possibility of skin allergy, digestive disorders, agitation, headaches, tremor and malaise.

Due to the presence of sunset yellow FCF, there is risk of allergic reactions.

Inform the physician if any undesirable and unpleasant effects not mentioned previously are experienced.