Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)

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  • Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)
  • Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)
  • Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)
  • Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)
  • Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)
  • Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)
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Basic Info.

Model NO.
Powder Injection
Specification
1.2g
Trademark
Sinolead
Origin
China

Product Description

 

Basic Info.

Model NO.
Powder Injection

Product Description

Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)
 
Generic Name Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g
Strength 1.2g
Packing 10 vials/box
Origin China

Component:
This product is a compound preparation, its group is divided into: amoxicillin sodium and clavulanate potassium. Each 1.2g This product contains 1.0g amoxicillin and 0.2g clavulanic acid.

Character:
This product is white or white powder.

Indications:

1. Upper respiratory tract infection: sinusitis, tonsillitis, pharyngitis.

2. Lower respiratory tract infections: acute bronchitis, acute episodes of chronic bronchitis, pneumonia, lung abscess, and bronchiectasis.

3. Urinary system infection: cystitis, urethritis, pyelonephritis, prostatitis, pelvic inflammation, Neisseria gonorrhoea urinary tract infection.

4. Skin and soft tissue infections: furuncle, abscess, cellulitis, wound infection, intra-abdominal sepsis, etc.

5. Other infections: otitis media, osteomyelitis, septicemia, peritonitis and post-operative infections.


 

Matters needing attention:

A severe and occasionally fatal allergic reaction (anaphylactic shock) has been reported in patients treated with penicillin, only in those allergic to penicillin (see Contraindications).

There are some patients taking this product have liver function changes. Because the clinical significance of this change has not been determined, it must be used with caution in patients with hepatic insufficiency. Severe and reversible obstructive jaundice has rarely been reported, and symptoms and symptoms may also appear up to six weeks after discontinuing the drug.

For patients with moderate or severe renal insufficiency, the dosage of this product should be adjusted according to the [usage and dosage] of patients with renal insufficiency.

Patients with infectious mononucleosis who use amoxicillin are prone to erythema rash. Patients suspected of infectious mononucleosis should avoid use of this product.

Long-term use of this product may cause the growth of resistant bacteria.

If a patient needs to receive a large dose of this product by injection, the amount of sodium contained in this product should be included in the total sodium intake for patients on a sodium-restricted diet.

Crystalluria is rare in patients with reduced urine output, especially when treated with parenteral administration. When taking high doses of amoxicillin, it is recommended that patients take adequate fluid intake and ensure sufficient urine output to reduce the likelihood of amoxicillin crystalluria.

[Impact on drivers and mechanics]

No adverse effects have been found.
6 Use with caution if you are allergic to penicillin or allergic to it. 2 About 1% of patients on the drug may have direct and indirect Coombs test positive and urine sugar false positive reaction (copper sulfate method).
Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)

Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)

Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)Amoxicillin Soudium and Clavulanate Potassium for Injection 1.2g (10vials/box)

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