GNH USA

Europe — EMA

Kemicetine

GNH USA supplies Kemicetine (Chloramphenicol Sodium Succinate), an antibiotic for meningitis, typhoid fever and rickettsial disease. Request a quote today.

Chloramphenicol Sodium Succinate

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What is Chloramphenicol Sodium Succinate?

Chloramphenicol sodium succinate, the active ingredient in Kemicetine, is an amphenicol antibiotic presented as an injection for intramuscular and intravenous use. It treats severe bacterial infections such as meningitis, typhoid fever and rickettsial diseases in hospitalized patients.

GNH USA supplies Kemicetine as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides reliable cold‑chain logistics for injectable medicines. Clients benefit from consistent batch release, regulatory documentation, and on‑time delivery across multiple continents.

What is Chloramphenicol Sodium Succinate used for?

Chloramphenicol sodium succinate is used to treat serious bacterial infections by targeting susceptible organisms within the amphenicol class. - Severe bacterial infections: Provides systemic antibacterial activity for life‑threatening infections. - Meningitis: Achieves rapid bacterial clearance in cerebrospinal fluid to reduce morbidity. - Typhoid fever: Eradicates Salmonella Typhi organisms, aiding recovery in acute systemic illness. - Rickettsial infections: Controls intracellular rickettsiae, improving clinical outcomes in spotted fever and related diseases.

What are the side effects of Chloramphenicol Sodium Succinate?

Adverse reactions to chloramphenicol sodium succinate vary in frequency and severity. Common Side Effects: - Nausea: mild gastrointestinal upset. - Rash: skin erythema or itching. - Bone marrow suppression (dose‑related): mild reduction in blood cell counts. Serious or Rare Side Effects: - Aplastic anemia: irreversible bone marrow failure. - Gray syndrome: fatal metabolic acidosis in neonates. - Hepatic toxicity: elevated liver enzymes or jaundice.

What precautions apply to Chloramphenicol Sodium Succinate?

Key safety considerations for chloramphenicol sodium succinate include patient monitoring and handling precautions. - Renal impairment: monitor kidney function and adjust therapy as needed. - Hepatic dysfunction: assess liver enzymes before and during treatment. - Neonates and infants: avoid use due to risk of Gray syndrome. - Pregnancy: prescribe only when benefit outweighs potential risk. - Blood monitoring: perform regular complete blood counts to detect marrow suppression. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Chloramphenicol Sodium Succinate interact with?

Chloramphenicol sodium succinate can interact with other medicines, affecting efficacy or safety. Major Interactions (Avoid): - Concurrent bone marrow suppressants: increased risk of severe aplastic anemia. - Alcohol: may exacerbate hepatic toxicity. Moderate Interactions (Monitor Closely): - NSAIDs: potential additive renal toxicity. - Loop diuretics: may alter renal clearance of chloramphenicol. - Anticoagulants: possible enhancement of bleeding tendency.

Frequently asked questions

What is Kemicetine used for?+
Kemicetine contains chloramphenicol sodium succinate and is indicated for the treatment of severe bacterial infections such as meningitis, typhoid fever and rickettsial diseases. It is administered in hospital settings where rapid, systemic antibacterial activity is required.
How does chloramphenicol sodium succinate work?+
The drug penetrates bacterial cells and binds to the 50S ribosomal subunit, blocking the peptidyl transferase activity essential for protein synthesis. This inhibition stops bacterial growth, providing a bacteriostatic effect that can become bactericidal at higher concentrations.
What is the usual dose of Kemicetine?+
The dosage of Kemicetine is determined by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and route of administration. No fixed regimen is provided here; the prescriber sets the appropriate dose.
Is Kemicetine safe in pregnancy or breastfeeding?+
Safety data for chloramphenicol sodium succinate in pregnancy and lactation are limited. It is classified as pregnancy category unknown, and use is generally reserved for situations where the potential benefit justifies any potential risk to the fetus or infant.
How do I order Kemicetine from GNH USA?+
To order Kemicetine, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.
How does Kemicetine compare with the main alternative drug or class?+
Kemicetine (chloramphenicol) differs from many beta‑lactam antibiotics such as ceftriaxone by inhibiting protein synthesis rather than cell‑wall synthesis. It offers broad‑spectrum coverage, including some resistant organisms, but carries a higher risk of bone‑marrow suppression, requiring careful monitoring compared with alternatives.
How should Kemicetine be stored and handled?+
Kemicetine should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. The product should remain in its original packaging until use to maintain sterility and potency.
How is Kemicetine administered?+
Kemicetine is supplied as a sterile injection for intramuscular or intravenous administration. The preparation is reconstituted according to the label instructions and delivered by a qualified healthcare professional using aseptic technique.
What are the most serious risks associated with Kemicetine?+
The most serious risks include aplastic anemia, Gray syndrome in neonates, and severe hepatic toxicity. These adverse events are rare but can be life‑threatening, necessitating immediate discontinuation of therapy and appropriate medical intervention.
Who should not use Kemicetine?+
Kemicetine is contraindicated in neonates and infants due to the risk of Gray syndrome, in patients with known hypersensitivity to chloramphenicol, and in individuals with pre‑existing severe bone‑marrow suppression. Caution is also advised for pregnant or lactating women and those with significant liver or kidney disease.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Chloramphenicol Sodium Succinate
Route
Intramuscular Use , Intravenous Use
Manufacturer
Essential Pharma
Origin
EU

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