Specifications 3 ml, 5 ml per bottle, 10 ml.
Formulated liniment
Ingredients: menthol, camphor, methyl salicylate, eucalyptus oil, borneol and lavender oil.
Matters needing attention
1. This product is for external use.
2. If there is obvious burning or itching, local redness, etc. In the coated area, stop using the medicine, clean it and consult a doctor if necessary.
3. Pregnant women should use it with caution.
4. It is forbidden for those who are allergic to this product, and should be used with caution for those who are allergic.
5. It is forbidden to use this product when its characteristics change.
6. Children must use it under the supervision of adults.
7. Please keep this product out of the reach of children.
8. If you are using other drugs, please consult a doctor or pharmacist before using this product.
dosage
External use, applied to the affected area; Take orally, 3 ~ 5 drops at a time, and reduce the amount for children.
Character; Role; letter
This product is colorless or yellowish transparent liquid; It has a strong special fragrance.
taboo
Don't use it on broken skin. Product name Baoji oil
Specifications 20ml per bottle
Formulated liniment
Comprise peppermint oil, camphor, menthol, fennel oil, eucalyptus oil, cinnamon oil, borneol and methyl salicylate; The auxiliary material is liquid paraffin.
Matters needing attention
1. This product is for external use.
2. If there is obvious burning or itching, local redness, etc. In the coated area, stop using the medicine, clean it and consult a doctor if necessary.
3. It is forbidden for those who are allergic to this product, and should be used with caution for those who are allergic.
4. Pregnant women should use it with caution.
5. It is forbidden for those who are allergic to this product, and should be used with caution for those who are allergic.
6. It is forbidden to use this product when its characteristics change.
7. Children must use it under the supervision of adults.
8. Please keep this product out of the reach of children.
9. If you are using other drugs, please consult a doctor or pharmacist before using this product.
Character; Role; letter
The scent of mint and camphor.
taboo
Don't use it on broken skin. Product Name Buflomedil Hydrochloride Capsules
English name buflomedily hydrochlorides
Specification 0. 15g
Dose capsule
Matters needing attention
1. contraindications (1) are allergic to this drug. (2) Angina pectoris or acute myocardial infarction. (3) Paroxysmal tachycardia. (4) Patients with hyperthyroidism. (5) Postpartum hemorrhage, severe arterial hemorrhage, cerebral hemorrhage, recent massive blood loss or other bleeding tendency.
2. Use with caution in patients with liver and renal insufficiency (1). (2) Patients taking antihypertensive drugs. (3) Patients with hypotension [systolic blood pressure lower than 12kPa(90mmHg)].
3. The influence of drugs on children. Children should not use this medicine.
4. The effect of drugs on the elderly elderly patients should use this drug with caution, because their liver metabolism slows down and their excretion through urine and feces also slows down.
5. Effects of drugs on pregnancy Pregnant women (especially in early pregnancy) should use this drug with caution.
6. Effects of drugs on breastfeeding. Breast-feeding women should use this medicine with caution.
counteraction
1. Cardiovascular system can cause hypotension with dizziness, palpitation, atrial fibrillation and hypertension.
2. The central nervous system may have short-term mild headache, dizziness and syncope, dizziness, lethargy and insomnia, and convulsions may occur at extremely high doses.
3. Gastrointestinal tract may have mild and temporary gastrointestinal dysfunction, including aversion to food, nausea, vomiting, diarrhea and stomach discomfort (such as burning sensation and stomachache).
4. Slight and transient itching and erythema, as well as burning sensation of limbs can appear on the skin, and there are few reports of psoriasis. There may be fever and swelling at the injection site.
5. Allergic reactions include rubella, itching and hypotension. Body temperature may also rise.
6. Other rare reports about serum creatinine increase, urine volume increase, menstrual flow change and nosebleeds.
Management description
1. Combined with antihypertensive drugs, heart rate and blood pressure should be closely monitored.
This medicine can cause dizziness or drowsiness, so you should avoid driving or operating the machine during taking the medicine.
3. Excessive use can lead to severe hypotension, tachycardia, emotional excitement, vomiting, convulsions, convulsions, etc. And should be treated in time, and diazepam drugs can be used for antagonistic treatment.
dosage
adult
Conventional dose
take orally
1. Tablets, capsules and oral liquid: 450-600mg per day, taken 2-3 times.
2. Sustained release tablets: 600mg once,/kloc-0 once a day.
Intravenous drip 1 time, 100-200mg once a day. Dilute with 250-500ml of 5% glucose injection or physiological saline, and then slowly drip intravenously. When using this medicine powder for injection, it should be completely dissolved with 2ml sterile water for injection, and then used according to the above method.
Dose of renal insufficiency
Patients with renal insufficiency should adjust the dose appropriately.
Partial dose of liver dysfunction
Patients with hepatic insufficiency should adjust the dose appropriately.
[Refer to foreign usage and dosage]
adult
Conventional dose
take orally
1. Dementia: It is recommended to take 450-600mg every day, 2-3 times with meals. 600mg controlled release tablets should be taken at breakfast.
2. When microalbuminuria is caused by diabetic retinopathy and diabetic nephropathy: 300mg once, twice a day.
3. Peripheral vascular diseases (used to control the symptoms of intermittent claudication and Raynaud's disease): 150mg once, four times a day. Or 300mg once, twice a day.
intramuscular injection
1. Cerebrovascular diseases: 50mg once, three times a day. The drug should not be used for more than 14 days, and the maximum dose is 100mg once.
2. Peripheral vascular diseases: a maximum dose 100mg.
Intravenous administration of dementia: the recommended dose is 100-200mg a day, which is used twice. Intravenous injection or infusion should be carried out slowly within 5- 10 minutes. After 2-4 weeks of intravenous administration, oral treatment can be changed.
Dose of renal insufficiency
Patients with renal insufficiency (creatinine clearance greater than or equal to 10ml/min) may not need to adjust the dose. At present, it is necessary to further study and evaluate the pharmacokinetic changes of patients with creatinine clearance below 10ml/min.
Partial dose of liver dysfunction
After a single intravenous injection of 100mg, the pharmacokinetic parameters of patients with chronic liver disease did not change significantly. However, when the coagulation factor II index is about 50%, accompanied by low albumin and low coagulation factor V, the clearance half-life of patients with chronic liver disease can be extended to 7.2 hours, so it is suggested to reduce the oral dose by 50%.
Dose during dialysis
There is no need to adjust the dose.
Preparation and specifications
Buflomedil tablets (1) 150mg. (2)300 mg.
Buflomedil hydrochloride tablets 150mg.
Storage method: sealed and stored in a dry place.
Buflomedil hydrochloride capsules 150mg.
Storage method: sealed storage.
Buflomedil sustained-release tablets 600mg.
Buflomedil hydrochloride sustained-release tablets 600mg.
Storage method: Keep away from light and keep it sealed.
Buflomedil hydrochloride oral solution 10ml: 150mg.
Storage method: sealed storage.
Buflomedil injection 5ml:50mg.
Buflomedil hydrochloride injection 5ml:50mg.
Storage: Keep away from light and shade.
Buflomedil hydrochloride and sodium chloride injection (Buflomedil hydrochloride 0. 1g, sodium chloride 2.25g).
Storage method: sealed and stored in a cool and dry place.
Buflomedil hydrochloride for injection 50 mg.
Storage method: sealed storage.
taboo
(1) is allergic to this drug. (2) Angina pectoris or acute myocardial infarction. (3) Paroxysmal tachycardia. (4) Patients with hyperthyroidism. (5) Postpartum hemorrhage, severe arterial hemorrhage, cerebral hemorrhage, recent massive blood loss or other bleeding tendency. Product name berberine trimethoprim capsules
Berberine trimethoprim hydrochloride capsules
Specification berberine hydrochloride 0. 1 g trimethoprim 50mg.
Dose capsule
Ingredients This product is a compound preparation, which consists of berberine hydrochloride 0.2g and trimethoprim 0.1g..
Matters needing attention
Not suitable for pregnant women, lactating women and newborns.
counteraction
Occasionally, nausea, vomiting and rash disappeared after stopping taking the medicine.
dosage
Oral. 1 capsule once, 3 times a day; Still follow the doctor's advice.
Preparation and specifications
Specification: each capsule contains berberine hydrochloride 0.2g and trimethoprim 0.1g.
Storage and shading, sealed preservation.
Packaging aluminum foil board, 9 pieces/box.
The validity period is tentatively set at 2 years.
taboo
Severe liver and kidney diseases and blood system diseases (such as leukopenia, thrombocytopenia, purpura, etc.). ) is forbidden.