Milgamma compositum Tablets n / o, # 30
Category
Neurological disorders
Scope of the drug
Neurology, psychiatry
Release form
Tablet
Manufacturer country
Germany
Package quantity, pcs
thirty
Round, biconvex, white film-coated tablets.
Name ENG
MILGAMMA COMPOSITUM
Clinical and pharmacological group
B complex vitamins
ATX code
Combination of vitamin B1 with vitamins B6 and / or B12
Dosage
100mg + 100mg
Structure
1 coated tablet contains:
active substances: benfotiamine 100 mg,
pyridoxine hydrochloride 100 mg.
Excipients:
composition of the coated tablet core: microcrystalline cellulose - 222.0 mg, povidone (K value = 30) - 8.0 mg, high-chain partial glycerides - 5.0 mg, colloidal silicon dioxide - 7.0 mg, croscarmellose sodium - 3.0 mg, talc - 5.0 mg
shell composition:
shellac 37% on a dry matter basis - 3.0 mg, sucrose - 92.399 mg, calcium carbonate - 91.675 mg, talc - 55.130 mg, acacia gum - 14.144 mg, corn starch - 10.230 mg, titanium dioxide (E 171) - 14.362 mg, colloidal silicon dioxide - 6.138 mg, povidone (K value = 30) - 7.865 mg, macrogol-6000 - 2.023 mg, glycerol 85% in terms of dry matter - 2.865 mg, polysorbate-80 - 0.169 mg, mountain wax glycol - 0.120 mg
Indications
Neurological diseases with confirmed deficiency of vitamins B1 and B6.
Contraindications
Hypersensitivity to thiamine, benfotiamine, pyridoxine or other components of the drug.
The period of pregnancy and breastfeeding.
(See section Use during pregnancy and breastfeeding").
Childhood due to lack of data.
Each tablet contains 92.4 mg sucrose.
Therefore, the drug should not be used by persons with congenital fructose intolerance, glucose-galactose malabsorption syndrome or glucose-isomaltase deficiency.
If you have any of the listed diseases, be sure to consult your doctor before taking this medicine.
Application during pregnancy and during breastfeeding:
use of the drug is contraindicated during pregnancy and breastfeeding.
(See section "Contraindications").
INN / Active ingredient
Benfotiamine, Pyridoxine
Storage conditions and periods
At a temperature not higher than 25 degrees.
Expiration date: 5 years
Specifications
Category
Neurological disorders
Scope of the drug
Neurology, psychiatry
Release form
Tablet
Manufacturer country
Germany
Package quantity, pcs
thirty
Scope of application
Neurology
Way of introduction
Through the mouth
Vacation conditions
Without recipe
Brand name
ToExternalID_146958738
The amount of the dosage form in the primary package
15 pcs.
Primary packaging type
Blister
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
B vitamins
Dosage form
Film-coated tablets
Packaging
Box
Dosage (volume) of the substance in the preparation
1 tablet: benfotiamine 100 mg, pyridoxine 100 mg
The target audience
Adult
Expiration date in days
1825
Package weight, g
thirty
Mode of application
:
Inside.
The tablet should be taken with plenty of liquid.
Unless otherwise prescribed by the attending physician, an adult patient should take 1 tablet per day.
In acute cases, after consulting a doctor, the dose may be increased to 1 tablet 3 times a day.
After 4 weeks of treatment, the doctor must decide whether to continue taking the drug in an increased dose and consider reducing the increased dose of vitamins B6 and B1 to 1 tablet per day.
If possible, the dose should be reduced to 1 tablet per day in order to reduce the risk of neuropathy associated with the use of vitamin B6.
Anatomical and therapeutic characteristics
:
A11DB Vitamin B1 in combination with vitamin B6 and / or vitamin B12
"