High-Quality Cefazolin sodium for injection Suppliers, Service

[Drug name]
General name: Cefazolin sodium for injection
Trade name: Cefazolin sodium for injection
English name: Cefazolin Sodium for Injection

[Composition and traits]
Main ingredients: The main ingredient of this product is cefazolin sodium.
Character: This product is white or like white powder or crystalline powder, odorless.

[indication]
For the treatment of bronchitis, respiratory tract infections, urinary tract infections, skin and soft tissue infection caused by sensitive bacteria; it is also used as preventive medication before surgical operation. This product is not suitable for central nervous system infection; For chronic urinary tract infections, especially for patients with urinary tract anatomical abnormalities; not for gonorrhea and syphilis.

[Specifications and Packaging]
Single-dose specification: 500MG
Packaging specification: 1 + 1 piece

[usage and dosage]
1. It can be slowly injected intravenously, intravenously or intramuscular.
(1) Intravenous injection: slow intravenous injection in 3-5 minutes.
(2) Intravenous infusion: dissolve with appropriate injection water, and then dilute with 100ml of sodium chloride or glucose injection.
(3) intramuscular injection: before use, add water for injection or sodium chloride injection before use. It can also be dissolved in 2-3ml of 5% lidocaine hydrochloride injection.
2. Dosage
(1) Adult dose: 0.5-1g once, 2-4 times a day, severe infection can be increased to 6g a day, and given 2-4 times IV.
(2) Dose for children: 50-100mg / kg per day, 2-3 times of slow intravenous infusion, intravenous infusion or intramuscular injection.

[untoward effect]
1. Skin and subcutaneous tissues: rash, pruritus, hyperhidrosis, flushing, angioedema, allergic purpura, urticaria, erythema multiforme, exfoliative dermatitis, Stevenson-Johnson-Johnson (Stevens-Johnson) syndrome, toxic epidermal necrolysis, acute generalized pustular skin disease.
2. Digestive system: oral candidiasis, dry mouth, bitter mouth, oral ulcer, nausea, vomiting, stomach cramps, abdominal pain, abdominal distension, diarrhea, constipation, hepatitis, jaundice, anorexia, and pseudomembranous colitis.
3. Systemic and administration site reactions: drug fever, chest discomfort, fatigue, rare thrombophlebitis arising from intravenous injection, rash, itching and swelling at the injection site.
4. Immune system: hypersensitivity reaction, anaphylactic shock.

[taboo]
1. Cefazolin allergy is prohibited.
2. People who are allergic to other cephalosporin drugs are prohibited.
3. Patients with a history of severe allergy to penicillin or other β -lactams are not allowed.

[matters need attention]
1. Cross allergic reaction: Patients allergic to one cephalosporin or penicillin (cephamycin) may also be allergic to other cephalosporins or penicillin; patients allergic to penicillin, penicillin derivatives or penicillamine may also be allergic to cephalosporin or penicillin.
2. Patients must be asked about their prior allergy to cefazolin, other cephalosporins, penicillin, or other drugs.
3. Interference with diagnosis: 1% of patients with cefazolin may have positive direct or indirect antiglobulin Coombs test and false positive urine sugar (copper sulfate method).
4. Patients with low urine volume caused by impaired renal function or renal insufficiency should use this product with caution, and the amount must be reduced when applied.
5. Patients with liver impairment, renal impairment or malnutrition, patients with a longer course of treatment and patients with previous stable anticoagulant therapy may be at risk of cefazolin-related prothrombin activity.
6. Like all cephalosporins, this product should be used with caution in patients with gastrointestinal diseases, especially those with a history of colitis.

[condition of storage]
Keep sealed below 25℃.

[term of validity]
24 Months

Product Description

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Frequently Asked Questions
What does GMP/BP/USP stand for in your products?
GMP stands for Good Manufacturing Practice, while BP and USP refer to British Pharmacopoeia and United States Pharmacopeia standards respectively. These certifications ensure that our pharmaceutical products like Doxycycline and Vitamin B12 meet international quality, safety, and purity requirements.
How should these injections and capsules be stored?
Generally, pharmaceutical products should be stored in a cool, dry place away from direct sunlight. Injections like Vitamin B12 or Enoxaparin Sodium may have specific temperature requirements. Always refer to the specific storage instructions provided on the packaging.
What are the main applications of Enoxaparin Sodium Injection?
Enoxaparin Sodium is an anticoagulant used to prevent and treat deep vein thrombosis (DVT) and pulmonary embolism. Our injection is manufactured under strict GMP standards to ensure maximum efficacy.
Are the Doxycycline Capsules available in different dosages?
Our Doxycycline Capsules are produced following BP/USP specifications. For specific dosage availability and technical details, please review the product specifications as outlined in our catalog.
How is the quality of the Amoxicillin Capsules ensured?
Quality is ensured through a stable manufacturing process and rigorous testing of raw materials. Each batch of Amoxicillin Capsules undergoes quality control checks to meet stable quality parameters and international pharmaceutical standards.
What makes your Vitamin B12 injections reliable?
Our Vitamin B12 injections are produced in GMP-certified facilities. The use of high-grade raw materials and adherence to BP/USP pharmacopoeia standards ensures a high level of purity and patient safety.

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