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Product details

Product Listing: Mero-SB 1.5 g Injection

Brand Name: Mero-SB™ 1.5 g
Manufacturer: Aristo Pharmaceuticals Private Limited
Formulation Type: Sterile Dry Powder for Intravenous (I.V.) Injection / Infusion.

Product Overview

Mero-SB 1.5 g Injection is a premium, dual-component broad-spectrum antibiotic engineered to combat severe and multi-drug resistant (MDR) bacterial infections. By combining a high-potency carbapenem antibiotic with a powerful beta-lactamase inhibitor, this clinical-grade formulation overcomes bacterial defensive enzymes to ensure maximal therapeutic efficacy in acute care settings.

Ingredient & Salt Composition

Each single-use vial delivers a high-precision therapeutic load:

Meropenem IP (Equivalent to Anhydrous Meropenem 1000 mg): A powerful, ultra-broad-spectrum carbapenem antibiotic that works by disrupting and breaking down the bacterial protective cell wall, leading to rapid bacterial elimination. [1, 2]
Sulbactam Sodium IP (Equivalent to Sulbactam 500 mg): A dedicated beta-lactamase enzyme inhibitor. While it carries no standalone antibiotic properties, it permanently blocks the protective enzymes produced by resistant bacteria, safeguarding Meropenem from degradation and dramatically expanding its antibacterial spectrum.
Sodium Carbonate IP (90.2 mg): Included within the dry mix formulation as a critical pH buffering agent to optimize structural stability.
Companion Solvent Pack: Each commercial carton includes one 20 ml ampoule of Sterile Water for Injection IP for immediate clinical reconstitution.

Key Therapeutic Indications

This advanced dual-salt combination is typically utilized within hospital environments to treat critical bacterial pathologies:

Respiratory Tract Infections: Severe or hospital-acquired pneumonia.
Abdominal Infections: Complicated intra-abdominal infections and peritonitis.
Central Nervous System Infections: Acute bacterial meningitis.
Complicated URO-Genital Pathologies: Advanced or resistant urinary tract infections (UTIs).
Systemic Crises: Severe bloodstream infections, septicemia, and soft-tissue conditions.

Reconstitution & Administration Instructions

Preparation: Refer exclusively to the enclosed pack insert for specialized handling and reconstitution ratios.
Immediate Action Mandate: The reconstituted solution must be administered immediately after preparation. Any unused portion of the dissolved fluid must be discarded.
Critical Visual Inspection Safety Warning: Users and healthcare providers must inspect the solution thoroughly. If any particulate matter, crystallization, or discoloration remains visible in the vial after dissolving the dry powder, do not use the solution.

Storage Parameters

Store the un-reconstituted dry pack in a dry, cool space at a temperature not exceeding 25°C.
Keep the vial tightly packed inside its external carton to shield the powder from direct light exposure and humidity.
Keep securely stored completely out of reach of children.

Documented Potential Side Effects

While clinically vital, patients undergoing IV treatment should be monitored for general side effects: []

Localized injection site pain, swelling, inflammation, or redness.
Mild to moderate gastrointestinal distress (including nausea, vomiting, or diarrhea).
Headaches, skin rashes, or localized itching.

Safety Disclaimers

⚠️ Schedule H1 Prescription Drug Warning: This product is classified under Schedule H1. It is dangerous to take this preparation except under strict professional medical supervision. This product is strictly not to be sold via retail channels without a valid, authentic prescription from a Registered Medical Practitioner.

⚠️ Clinical Administration Notice: This medication is a dry powder for intravenous infusion and must never be used for self-administration at home. It must be prepared and infused exclusively by a trained nurse or medical practitioner in a verified clinical or hospital ecosystem.

Medical Disclaimer: The product details provided above are gathered exclusively from public medical literature for general informational and online index cataloging purposes only. It does not constitute direct medical advice or formal diagnostic instruction. Web store users must explicitly double-check their physical label text, batch variations, and expiry dates before any clinical deployment.

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