It inhibits the synthesis and release of prostaglandins in the hypothalamus, restores the normal responsiveness of the sensory neurons in the temperature regulation center, and has an antipyretic effect; it has an analgesic effect by inhibiting the synthesis of prostaglandins, etc.; it inhibits the synthesis and release of prostaglandins in the local tissue of inflammation, stabilizes lysosomal enzymes, and affects the phagocytic function of phagocytes, thus playing an anti-inflammatory role

It inhibits the synthesis and release of prostaglandins in the hypothalamus, restores the normal responsiveness of the receptor neurons in the temperature regulation center, and has an antipyretic effect; it has an analgesic effect by inhibiting the synthesis of prostaglandins, etc.

It excites the cerebral cortex, increases sensitivity to the outside world, constricts cerebral blood vessels, and enhances the effect of aminopyrine and phenacetin in relieving headaches

It has sedative, hypnotic and anticonvulsant effects, can enhance the analgesic effect of aminopyrine and phenacetin, and prevent convulsions caused by fever

Vitamin B1 is an important component of coenzymes required for sugar metabolism

Vitamin B2 is an important coenzyme component required for tissue respiration

Vitamin B6 is a cofactor for many enzymes and is involved in the metabolism of amino acids and fats.

Nicotinamide is a component of coenzymes I and II, essential for lipid metabolism and oxidation of tissue respiration

Calcium pantothenate is a component of coenzyme A and is involved in the metabolism of sugar, fat, and protein.

This product has the function of regulating autonomic nervous system dysfunction and endocrine balance disorders.

After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration (Cmax) is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration (Cmax) is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

This product cannot be taken at the same time as enteric-coated tablets. If used at the same time with other drugs, drug interactions may occur. Please consult your doctor or pharmacist for details.

This product cannot be taken at the same time as enteric-coated tablets. If used at the same time with other drugs, drug interactions may occur. Please consult your doctor or pharmacist for details.