Xinjiang Biochemical Pharmaceutical Co., Ltd.

It can inhibit the body's prostaglandin synthase, reduce the synthesis of prostaglandins and produce a good antipyretic and analgesic effect. It can treat cold symptoms such as headache, fever, limb pain, muscle pain, and general discomfort.

It can specifically inhibit influenza A virus and interfere with RNA virus penetration into host cells. It can also inhibit virus uncoating and nucleic acid release, and can be used for the prevention and treatment of influenza A.

It has the effects of clearing the heart and detoxifying, relieving fever and anti-inflammatory, and is used to treat cold symptoms such as headache, fever, sore throat, etc.

It has an excitatory effect on the cerebral cortex and is mainly used to counteract the central nervous system inhibition state. Oral administration can relieve drowsiness. In addition, since caffeine can constrict cerebral blood vessels and reduce the amplitude of cerebral blood vessel pulsation, it can enhance the analgesic effect when combined with the above-mentioned antipyretic analgesics to treat general headaches.

1. Gankang is an antipyretic, analgesic and antiviral cold medicine. 2. The amantadine in this prescription can specifically inhibit influenza A virus and interfere with RNA virus penetration into host cells. It can also inhibit viral uncoating and nucleic acid release, and can be used for the prevention and treatment of influenza A. Acetaminophen can inhibit the body's prostaglandin synthase, reduce prostaglandin synthesis and produce good antipyretic and analgesic effects. It can treat cold symptoms such as headache, fever, limb pain, muscle pain, and general discomfort. 3. Artificial bezoar has the effects of clearing the heart and detoxifying, antipyretic and anti-inflammatory, and is used to treat cold symptoms such as headache, fever, sore throat, etc. 4. Caffeine has an excitatory effect on the cerebral cortex, mainly used to counteract the central inhibition state, and can relieve drowsiness after oral administration; in addition, because caffeine has the effect of constricting cerebral blood vessels and reducing the amplitude of cerebral blood vessel pulsation, it can be used in combination with the above-mentioned antipyretic and analgesic drugs to treat general headaches, which can enhance the analgesic effect.

This product is a new type of non-narcotic analgesic, with mild antipyretic and muscle relaxant effects. It is effective for moderate and severe pain. An intramuscular injection of 20 mg of this product is equivalent to the effect of 12 mg of morphine. It has a mild respiratory depressant effect. It has no depressant effect on the circulatory system. There is no tolerance and dependence.

This product is an analogue of diphenhydramine, which mainly suppresses cough center and relieves cough. It also has a weak antihistamine effect and has no dependence or tolerance. It takes effect 20-30 minutes after taking it and the effect lasts for 3-4 hours.

The structure is similar to that of papaverine. Single or continuous administration can increase blood flow to the brain, heart, kidneys and limbs. It can directly relax vascular smooth muscle to dilate blood vessels, and has a selective and sustained dilation effect on the brain, kidneys, blood vessels and coronary arteries, thereby increasing blood flow. The effect is weaker and more lasting than that of papaverine. This product can also promote collateral circulation. It has almost no effect on respiration, heart rate, cardiac output, myocardial oxygen consumption, blood pressure, etc.

This product is a blood lipid regulating drug of clofibric acid derivatives. It reduces blood low-density lipoprotein, cholesterol and triglycerides by inhibiting the production of very low-density lipoprotein and triglycerides and increasing their catabolism at the same time; it also increases the production of apolipoprotein A1 and A11, thereby increasing high-density lipoprotein. This product also has the effect of reducing blood uric acid in normal people and patients with hyperuricemia. Animal experiments have shown that fenofibrate is teratogenic and carcinogenic.