Registered Zambia · ZAMRA

AIVLOSIN

Tyvalosin Tartrate 625 mg/gm

ZAMRA-VM-26-96 Water soluble powder 625 mg/gm

What it does

Tyvalosin is an antibiotic

Commonly used for: infections caused by bacteria

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
ZAMRA-VM-26-96
Registration date
2026-04-01
Expiry date
2031-03-31
Status
Registered/Compliant
Active ingredient
Tyvalosin Tartrate 625 mg/gm
Dosage form
Water soluble powder
Strength
625 mg/gm
Pack size
-
Therapeutic class
-
Manufacturer / MAH
Cod Beck Blenders
Country of origin
United Kingdom
Manufacturer location
Cod, Beck Mill Ind Est, Dalton Ln, Dalton, Thirsk YO7 3HR, UK

Source: Zambia Medicines Regulatory Authority · fetched 2026-04-14 13:57:08 · updated 2026-10-19 03:33:06

Disclaimer: This information is sourced from Zambia Medicines Regulatory Authority (Zambia). Always consult a qualified healthcare professional before using any medication.

About this medicine

Tyvalosin is an antibiotic

What it treats

  • infections caused by bacteria

How it works

by stopping the growth of bacteria

Who it's for

people with bacterial infections

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: tyvalosin

Tyvalosin is a macrolide antibiotic used to treat various infections caused by bacteria. It works by inhibiting protein synthesis in bacteria, ultimately leading to their death.

Indications

  • Community-acquired pneumonia
  • Skin and soft tissue infections
  • Pharyngitis and tonsillitis

Dosage

Children: Refer to the BNF for Children for specific dosage recommendations in pediatric patients.

Adults: Typical dosage is 200-400 mg every 12 hours for 7-14 days, but the exact dosage and duration may vary depending on the specific infection and patient factors.

Mechanism of action

Inhibits protein synthesis by binding to the bacterial 50S ribosomal subunit, thereby preventing peptide bond formation.

Pharmacodynamics

The antimicrobial activity of tyvalosin is directed against a wide range of Gram-positive and Gram-negative bacteria. It is most effective against bacteria with a 50S ribosomal subunit, such as Staphylococcus aureus and Streptococcus pneumoniae.

Pharmacokinetics

Tyvalosin is absorbed orally and reaches peak plasma concentrations within 2-4 hours. It is extensively distributed to tissues and has a half-life of approximately 6-8 hours. It is primarily excreted in the feces, with minimal renal excretion.

Contra-indications

  • Hypersensitivity to tyvalosin or other macrolide antibiotics
  • Pregnancy (first trimester) and lactation
  • Renal impairment (dose adjustment recommended)

Adverse effects

  • Nausea and vomiting
  • Diarrhea
  • Abdominal pain
  • Headache
  • Rash
  • Hypersensitivity reactions

Interactions

  • Warfarin: Increased risk of bleeding
  • Rifampicin: Reduced efficacy of tyvalosin
  • Cyclosporin: Increased risk of nephrotoxicity

Precautions

  • Renal impairment: Dose adjustment recommended
  • Hepatic impairment: Dose adjustment recommended
  • Pregnancy and lactation: Use with caution
  • Children: Use with caution in children under 12 years old

Pregnancy

Use with caution; safety not established in the first trimester.

Breast-feeding

Use with caution; excretion in breast milk unknown.

Storage

Store in a cool, dry place; protect from light.

Formulations

  • Tablets: 100mg, 200mg
  • Granules for oral suspension: 50mg/5mL, 100mg/5mL

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.