Lincomycin Hydrochloride Injection
Function and Efficacy
This product has high antibacterial activity against common aerobic Gram-positive bacteria, such as Staphylococcus aureus (including those resistant to penicillin G), Staphylococcus epidermidis, beta-hemolytic Streptococcus, viridans Streptococcus and Streptococcus pneumoniae. It has good antibacterial effect on anaerobic bacteria, including Clostridium tetani, Corynebacterium diphtheriae and Clostridium perfringens. It has no activity against Gram-negative bacteria such as Enterococcus, meningococci, Neisseria gonorrhoeae and Haemophilus influenzae, as well as fungi. There is no cross-resistance between this product and penicillin, chloramphenicol, cephalosporins and tetracyclines, and there is partial cross-resistance with macrolides. This product acts on the 50S subunit of the ribosome of sensitive bacteria, preventing the extension of the peptide chain, thereby inhibiting the protein synthesis of bacterial cells. It is generally an antibacterial agent, but at high concentrations, it also has a bactericidal effect on certain bacteria.
Ingredients
The main ingredient is lincomycin hydrochloride, and its chemical name is 6-(1-methyl-trans-4-propyl-L-2-pyrrolidinecarboxamido)-1-thio-6,8-dideoxy-D-erythro-alpha;-D-galacto-octinopyranoside hydrochloride hydrate. Its structural formula is: Molecular formula: C18H34N2O6SHClH2O Molecular weight: 461.02
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| Lincomycin hydrochlorideIngredients |
It has high antibacterial activity against common aerobic Gram-positive bacteria, such as Staphylococcus aureus (including those resistant to penicillin G), Staphylococcus epidermidis, beta-hemolytic Streptococcus, viridans Streptococcus and Streptococcus pneumoniae. It has good antibacterial effect on anaerobic bacteria, including Clostridium diphtheriae, and Clostridium perfringens. It has no activity against Gram-negative bacteria such as Enterococcus, meningococci, Neisseria gonorrhoeae, and Haemophilus influenzae, as well as fungi. There is no cross-resistance with penicillin, chloramphenicol, cephalosporins and tetracyclines, and there is partial cross-resistance with macrolides. It acts on the 50S subunit of the ribosome of sensitive bacteria, preventing the extension of the peptide chain, thereby inhibiting the protein synthesis of bacterial cells. It is generally an antibacterial agent, but at high concentrations, it also has a bactericidal effect on certain bacteria. More |
859-18-7 | 30 |
Indication
This product is suitable for respiratory tract infections, skin and soft tissue infections, female reproductive tract infections, pelvic infections and abdominal infections caused by sensitive Staphylococcus, Streptococcus, Streptococcus pneumoniae and anaerobic bacteria. The latter two diseases can be used alone or in combination with other antibacterial drugs according to the situation. In addition, for patients with indications for the use of penicillin, such as patients who are allergic to penicillin or are not suitable for penicillin, this product can be used as an alternative drug.
Usage and Dosage
Intramuscular injection: 0.6-1.2g per day for adults, 10-20mg/kg per day for children, divided into several injections. Intravenous drip: Generally, 0.6g per time for adults, once every 8 hours or 12 hours, each 0.6g is dissolved in 100-200ml of infusion solution, and dripped for 1-2 hours. For children, 10-20mg/kg per day is based on body weight. It should be noted that each 0.6g is dissolved in no less than 100ml of solution during intravenous drip, and the drip time is no less than 1 hour. It is not used for infants less than 4 weeks old.
Adverse Reactions
1. Gastrointestinal reactions: symptoms such as nausea, vomiting, abdominal pain, diarrhea, etc.; severe cases may include abdominal cramps, abdominal tenderness, severe diarrhea (watery or purulent), accompanied by fever, abnormal thirst and fatigue (pseudomembranous enteritis); diarrhea, enteritis and pseudomembranous enteritis may occur in the early stage of medication or several weeks after discontinuation of medication. 2. Blood system: leukopenia, neutropenia, neutropenia and thrombocytopenia may occur occasionally, and aplastic anemia is rare. 3. Allergic reactions: rash, itching, etc. may be seen, urticaria, angioedema and serum sickness reactions may be seen occasionally, and epidermal excoriation, bullous dermatitis, erythema multiforme and S-J syndrome may be reported rarely. 4. Occasionally, there are reports of jaundice caused by the use of this product. 5. Hypotension, electrocardiogram changes and even cardiac and respiratory arrest may occur when this product is rapidly infused. 6. Intravenous administration may cause thrombophlebitis.
Precautions
It is contraindicated in patients with a history of hypersensitivity to lincomycin and clindamycin.
Drug Interactions
1. It can enhance the neuromuscular blockade of inhaled anesthetics, leading to skeletal muscle weakness and respiratory depression or paralysis (apnea). Caution should be taken when used in combination during or after surgery. Treatment with anticholinesterase drugs or calcium salts is expected to be effective. 2. When used in combination with antiperistaltic antidiarrheal drugs and antidiarrheal drugs containing white clay, this product may cause pseudomembranous colitis with severe watery diarrhea during the course of treatment or even a few weeks after the course of treatment. Because it can delay the excretion of colonic endotoxins, thereby causing prolonged and aggravated diarrhea, antiperistaltic antidiarrheal drugs should not be used in combination. When this product is used in combination with antidiarrheal drugs containing white clay, the absorption of the former will be significantly reduced, so the two should not be taken at the same time, and a certain interval (at least 2 hours) is required. 3. This product has a neuromuscular blocking effect. When used in combination with anti-myasthenic drugs, the latter will weaken the effect on skeletal muscles. In order to control the symptoms of myasthenia gravis, the dose of anti-myasthenic drugs should be adjusted when used in combination. 4. Chloramphenicol or erythromycin can replace this product at the target site, or inhibit the latter from binding to the bacterial ribosome 50S subunit. In vitro tests show that lincomycin and erythromycin have antagonistic effects, so lincomycin should not be used in combination with chloramphenicol or erythromycin. 5. When used in combination with opioid analgesics, the respiratory depressant effect of this product and the central respiratory depressant effect of opioids may lead to prolonged respiratory depression or respiratory paralysis (apnea) due to cumulative phenomena, so patients must be closely observed or monitored. 6. This product can enhance the effect of neuromuscular blocking drugs, and the two should be avoided in combination. 7. It is incompatible with neomycin and kanamycin when intravenously dripped in the same bottle.
Storage
Keep tightly closed.
Packaging Specification
2ml:0.6g (calculated as C18H34N2O6S)
Manufacturer
Wuhan Aimin Pharmaceutical Co., Ltd.
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Founded in:
1990-03-17 -
Address:
No. 10, Chuangye Avenue, Gedian Economic Development Zone, Ezhou City, Hubei Province -
Tax NO.:
91420700177707714R -
Registered Funds:
100.52 million yuan -
Website:
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Email: