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INJ. CRYCEF-S 1.5

INJ. CRYCEF-S 1.5
INJ. CRYCEF-S 1.5

INJ. CRYCEF-S 1.5 Specification

  • Salt Composition
  • Ceftriaxone 1000 mg + Sulbactam 500 mg
  • Dosage Form
  • Injection
  • Origin of Medicine
  • India
  • Indication
  • Treatment of various infections like respiratory tract infections, urinary tract infections, skin and soft tissue infections, etc.
  • Brand Name
  • CRYCEF-S
  • Packaging Type
  • Vial with sterile water for injection
  • Pacakaging (Quantity Per Box)
  • 1 vial per box
  • Life Span
  • 24 months from manufacturing date
  • Drug Type
  • Allopathic
  • Ingredients
  • FLUCONAZOLE 150 MG
  • Physical Form
  • Tablets
  • Function
  • Antibiotic
  • Recommended For
  • Bacterial Infections
  • Dosage
  • As directed by the physician
  • Dosage Guidelines
  • Intravenous or Intramuscular use only
  • Suitable For
  • Adults and Children
  • Quantity
  • 1.5 g/vial
  • Storage Instructions
  • Store below 25C, protected from light and moisture
 
 

About INJ. CRYCEF-S 1.5

INJ. CRYCEF-S 1.5

Product Details

Form

Liquid

Storage

Store in cool & dry place at room temperature

Dosage Form

As Per Doctor Prescription

Type of Medicine

Allopathic

Pack Contain

1.5gm

Best Before

2 Years from manufacturing

Usage

Clinical, Hospital

Side Effects

Nill

Dosage

As prescribed by doctor

Care Instruction

Keep out of reach of children.

Function

Health-care



 



How to Use CRYCEF-S 1.5 Injection

CRYCEF-S 1.5 is intended for intravenous (IV) or intramuscular (IM) injection only. The powder must be reconstituted with the sterile water provided in the packaging by a qualified healthcare professional. The dosage and administration schedule will be determined by your physician, according to the type and severity of the infection.


Benefits of Third Generation Cephalosporin with Beta-lactamase Inhibitor

CRYCEF-S 1.5 combines Ceftriaxone and Sulbactam, offering broad-spectrum action against resistant bacterial strains. This combination extends protection against beta-lactamase-producing organisms, increasing its effectiveness in treating serious bacterial infections in adults and children.


Storage and Handling Guidelines

CRYCEF-S 1.5 should be stored below 25C and protected from direct light and moisture to maintain its efficacy. Always keep the vial in its original packaging and ensure it is out of reach of children. Discard any unused solution as instructed by medical professionals.

FAQ's of INJ. CRYCEF-S 1.5:


Q: How is CRYCEF-S 1.5 administered?

A: CRYCEF-S 1.5 is given by intravenous (IV) or intramuscular (IM) injection. The dry powder is first reconstituted using the sterile water provided and then administered by a trained healthcare professional.

Q: What conditions does CRYCEF-S 1.5 treat?

A: This medication is recommended for the treatment of various bacterial infections, including those affecting the respiratory tract, urinary tract, skin, and soft tissues.

Q: Who should not receive CRYCEF-S 1.5?

A: CRYCEF-S 1.5 is contraindicated in individuals with known hypersensitivity to cephalosporins, penicillins, or sulbactam. Always inform your physician of any allergies before starting treatment.

Q: When should CRYCEF-S 1.5 be used?

A: Use CRYCEF-S 1.5 only when prescribed by your doctor for a confirmed or suspected bacterial infection susceptible to this antibiotic formulation. Do not use for self-medication or without medical supervision.

Q: What are the possible side effects of CRYCEF-S 1.5?

A: Reported side effects may include rash, diarrhea, nausea, and pain at the injection site. If you experience any severe or persistent symptoms, contact your healthcare provider promptly.

Q: Where should CRYCEF-S 1.5 be stored?

A: Store the vial below 25C, away from direct sunlight and heat sources. Keep it in a cool, dry place, protected from moisture, and out of reach of children.

Q: What is the process for preparing CRYCEF-S 1.5 for injection?

A: A healthcare professional should reconstitute the off-white to pale yellow powder in the vial with the sterile water supplied, following aseptic techniques to ensure safety and effectiveness before administering it by the prescribed route.

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