Cefuroxime Sodium for Injection (Dalixin)
Function and Efficacy
1 Levobunolol is a non-selective β-adrenal receptor blocker that blocks both β1 and β2 receptors. Levobunolol's receptor blocking effect is 60 times stronger than its dextrorotatory isomer, but its direct myocardial depressant effect is the same, so the levorotatory isomer - levobunolol is used. Levobunolol has no obvious local anesthetic effect and intrinsic sympathomimetic effect. 2 This product has an intraocular hypotensive effect on patients with high and normal intraocular pressure. The intraocular hypotensive effect is the same as timolol, and the maximum intraocular hypotensive amplitude is 7mmHg. 3 The drug effect of this product can be detected within one hour after taking a drop, and the effect reaches a peak in 2 to 6 hours. The drug effect can be maintained for 24 hours after a single dose. The long duration of pharmacological action is the biggest advantage of this product. Its mechanism is that the plasma half-life of the main drug levobutafil olol is longer, which is 6 hours, while its main metabolite dihydrobutafil olol has the same intraocular hypotensive effect as the main drug, and the half-life is longer, up to 7 hours. 4 The intraocular pressure-lowering mechanism of this product is mainly to reduce the production of aqueous humor. This product has no effect on the outflow of aqueous humor through the uveal sclera, the ease of aqueous humor outflow and the episcleral venous pressure.
Ingredients
The main ingredient of this product is: Levobunolol hydrochloride. Its chemical name is: Racemic-5-[3-tert-butylamino-2-hydroxypropoxy]3,4-dihydro-1-(2H)naphthone. Molecular formula: C17H25NO3HCl Molecular weight: 327.85
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| Levobunolol hydrochlorideIngredients |
A non-selective β-adrenergic receptor blocker, it blocks both β1 and β2 receptors, has no obvious local anesthetic effect and intrinsic sympathomimetic effect; it has an intraocular pressure-lowering effect on patients with both high and normal intraocular pressure, with a maximum intraocular pressure-lowering amplitude of 7 mmHg; the drug effect can be detected within one hour of instillation, reaches a peak in 2 to 6 hours, and can last for 24 hours after a single dose; the intraocular pressure-lowering mechanism is mainly to reduce the production of aqueous humor More |
27912-14-7 | 6 |
Appearance
This product is a colorless clear solution.
Indication
It has a good effect of reducing intraocular pressure in primary open-angle glaucoma. For some secondary glaucoma, ocular hypertension, closed-angle glaucoma that is not completely controlled after surgery, and other glaucoma that is ineffective with other drugs and surgery, the addition of this product to the eye drops can further enhance the effect of reducing intraocular pressure.
Usage and Dosage
Eye drops, 1 drop at a time, 1-2 times a day. Drop into the conjunctival sac, and press the inner corner of the lacrimal sac with your fingers for 3-5 minutes after dropping.
Adverse Reactions
One-third of patients experienced temporary eye burning and stinging. 5% of patients developed conjunctivitis. Some patients experienced a slow heart rate and a drop in blood pressure. 1Other rare adverse eye reactions include: changes in heart rhythm, dyspnea, iridocyclitis, headache, dizziness, transient ataxia, drowsiness, itching and urticaria. 2The following very rare adverse reactions may also occur with this product: (1) Systemic symptoms: weakness, chest pain. (2) Cardiovascular system: bradycardia, arrhythmia, hypotension, syncope, heart block, cerebrovascular accident, cerebral ischemia, heart failure, angina pectoris, palpitations, cardiac arrest. (3) Digestive system: nausea, diarrhea. (4) Nervous system: depression, mental confusion, aggravated symptoms of myasthenia gravis, paresthesia. (5) Skin: allergic reactions, including local
Precautions
1. Patients with bronchial asthma or a history of bronchial asthma, severe chronic obstructive pulmonary disease. 2. Sinus bradycardia, Ⅱ or Ⅲ degree atrioventricular block, obvious heart failure, cardiogenic shock. 3. Patients who are allergic to this product.
Drug Interactions
1. When used in combination with adrenaline, it can cause pupil dilation. 2. Patients who are taking catecholamine-depleting drugs (such as reserpine) should be closely observed when using this product, because it can cause hypotension and significant bradycardia, the latter of which can cause dizziness, syncope or orthostatic hypotension. 3. It is not recommended to use two local beta-receptor blockers at the same time. 4. This product should be used with caution in combination with calcium channel antagonists, because it can cause atrioventricular conduction block, left ventricular failure and hypotension. For patients with impaired cardiac function, the two drugs should be avoided in combination. 5. This product can further prolong atrioventricular conduction time when used in combination with digitalis and calcium channel antagonists. 6. Phenothiazines can increase the antihypertensive effect of beta-receptor blockers because they can inhibit each other's metabolic pathways.
Storage
Keep away from light and store in a sealed container.
Packaging Specification
0.75g (calculated based on C16H16N408 tablets)
Manufacturer
Sinopharm ZHIJUN(Shenzhen)PHARMACEUTICAL Co., Ltd.
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Founded in:
1985-12-11 -
Address:
No. 16, Lanqing 1st Road, Guanlan High-tech Park, Longhua New District, Shenzhen -
Tax NO.:
91440300192190290M -
Registered Funds:
200 million yuan -
Website:
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Email: