Contract Manufactured Cefixime Dispersible Tablets 100mg

Product Details
Customization: Available
Application: Internal Medicine
Usage Mode: For oral administration
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  • Contract Manufactured Cefixime Dispersible Tablets 100mg
  • Contract Manufactured Cefixime Dispersible Tablets 100mg
  • Contract Manufactured Cefixime Dispersible Tablets 100mg
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Basic Info.

Suitable for
Elderly, Children, Adult
State
Solid
Shape
Tablet
Type
Organic Chemicals
Pharmaceutical Technology
Chemical Synthesis
Drug Reg./Approval No.
Available
Drug Ad Approval No.
Available
Quality Standard
Bp, USP, Cp
Shelf Time
36month
MOQ
10000 Boxes
Sample
Available
Storage
Sealed, Stored in a Cool Place
Transport Package
Box/Carton
Specification
100mg, 200mg, 400mg
Trademark
Private logo service
Origin
China
Production Capacity
100000000000PCS/Month

Product Description

                                                                                    Cefixime Dispersible Tablets
Ingredients
The main ingredient of this product is cefixime
Molecular formula: C16H15N5O7S2· 3H2O
Molecular weight: 507.50

character
This product is film coated tablets, white or yellowish after removing coating.

indication
It is effective for the following infections caused by cefixime sensitive bacteria in Streptococcus (except Enterococcus), pneumococcus, Neisseria gonorrhoeae, hantavirus catarrhalis, Escherichia coli, Klebsiella, Serratia, Proteus and influenza.
Acute attack of chronic bronchitis, acute bronchitis with bacterial infection, bronchiectasis with infection, pneumonia;
Pyelonephritis, cystitis and gonococcal urethritis;
Acute bacterial infection of biliary system (cholecystitis, cholangitis);
Scarlet fever;
Otitis media, sinusitis.

Usage and dosage
Oral administration.
Dosage for adults and children weighing more than 30 kg:
Oral, 0.1g (1 tablet), twice a day; adult severe infection, can be increased to 0.2g (2 tablets), twice a day.
Children:
The dosage was 1.5-3.0 mg / kg, twice a day. Or follow the doctor's advice.

Adverse reactions
In the total 12879 cases, 249 cases (2.58%) of adverse reactions were found, including abnormal clinical examination values. These adverse reactions included diarrhea and other gastrointestinal symptoms in 112 cases (0.87%), skin rash and other skin symptoms in 29 cases (0.23%). In addition, abnormal clinical examination values included elevated GPT in 78 cases (0.61%), elevated got in 58 cases (0.45%), and eosinophilia in 26 cases (0.20%).
(1) Serious adverse reactions were observed
1.Shock: due to the possibility of causing shock (< 0.1%), close observation should be carried out. In case of discomfort, abnormal feeling in mouth, asthma, dizziness, defecation, tinnitus, sweating, etc., the administration should be stopped and appropriate measures should be taken;
2.Anaphylactic symptoms: the possibility of anaphylactic symptoms (including dyspnea, systemic flushing, vascular edema, urticaria, etc.) (< 0.1%) should be closely observed. If there is any abnormality, stop the administration and take appropriate measures;
3. Skin lesions: the possibility of skin and mucous membrane eye syndrome (Stevens Johnson syndrome, < 0.1%) and toxic epidermal necrosis (Lyell syndrome, < 0.1%) should be closely observed. If there are symptoms such as fever, headache, joint pain, skin or mucous erythema, blisters, skin tension, burning sensation and pain, the administration should be stopped and appropriate treatment should be taken;
4.Blood disorders: the possibility of agranulocytosis (< 0.1%, early symptoms: fever, sore throat, headache, burnout, etc.), hemolytic anemia (< 0.1%, early symptoms: fever, hemoglobinuria, anemia, etc.), thrombocytopenia (< 0.1%, early symptoms: punctate hemorrhage, purpura, etc.) and other cephalosporins causing pancytopenia Therefore, close observation should be carried out, such as regular inspection, etc. in case of any abnormality, the administration should be stopped and appropriate measures should be taken;
5.Renal dysfunction: due to the possibility of causing severe renal dysfunction (< 0.1%) such as acute renal insufficiency, close observation should be carried out, such as regular examination, etc. in case of abnormality, drug administration should be stopped and appropriate treatment should be taken;
6.Colitis: may cause severe colitis with bloody stool, such as pseudomembranous colitis (< 0.1%). In case of abdominal pain and recurrent diarrhea, the administration should be stopped immediately and appropriate measures should be taken;
7. Interstitial pneumonia, PTE syndrome: interstitial pneumonia with fever, cough, dyspnea, chest X-ray abnormalities, eosinophilia and other symptoms, and the possibility of PTE syndrome (0.1% respectively). If the above symptoms occur, the administration should be stopped, and appropriate treatment such as glucocorticoid should be taken;
(2) Other adverse reactions: the incidence of adverse reactions in 0.1-5% is common, and less than 0.1% is rare.
Allergy: common rash, urticaria, erythema, rare pruritus, fever, edema;
Blood: eosinophilia was common (0.1% - 5%), neutropenia was rare;
Liver: the levels of alanine aminotransferase (ALP / GPT) and alanine aminotransferase (AST / got) were increased, and jaundice was rare;
Kidney: rare increase of urea nitrogen (BUN);
Digestive system: common diarrhea, stomach discomfort, rare nausea, vomiting, abdominal pain, chest burning, loss of appetite, abdominal fullness, constipation;
Dysbacteriosis: stomatitis and oral candidiasis are rare;
Vitamin deficiency: rare vitamin K deficiency (hypothrombin, bleeding tendency, etc.), vitamin B deficiency (glossitis, stomatitis, loss of appetite, neuritis, etc.);
Others: headache, dizziness.
taboo
Allergic to this or other cephalosporins.
matters needing attention
1) In order to prevent the emergence of drug-resistant strains, the sensitivity should be confirmed in principle before using this product, and the dose should be controlled at the minimum dose required for disease control.
(2) For patients with severe renal dysfunction, because the drug concentration can be maintained in the blood, it should be reduced according to the renal function, and the interval of administration should be increased.
(3) The following patients were treated with caution:
1. Patients with a history of allergy to penicillins.
2. I or parents, brothers, with easy to cause bronchial asthma, rash, urticaria and other allergic symptoms of patients with physical constitution.
3. Patients with severe renal dysfunction.
4. Patients with oral administration difficulties or non oral nutrition, and patients with systemic cachexia. The symptoms of vitamin K deficiency should be observed.
(4) Due to the possibility of shock, the medical history should be fully inquired before administration.
(5) Do not mix milk, juice, etc. with medicine and place them.
(6) Influence on clinical test results:
1. In addition to the test paper reaction, we should pay attention to the possibility of false positive in urine sugar test of Benedict reagent, Fehling reagent and clinitest.
2. We should pay attention to the possibility of direct Coombs test positive.
 
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Contract Manufactured Cefixime Dispersible Tablets 100mg
Contract Manufactured Cefixime Dispersible Tablets 100mg
Contract Manufactured Cefixime Dispersible Tablets 100mg
 
Contract Manufactured Cefixime Dispersible Tablets 100mg
Contract Manufactured Cefixime Dispersible Tablets 100mg
Contract Manufactured Cefixime Dispersible Tablets 100mg

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